Fact-checked by Grok 2 weeks ago

Neuron

A neuron, also known as a nerve cell, is the fundamental structural and functional unit of the nervous system, responsible for receiving, processing, and transmitting information through electrical and chemical signals to enable sensory perception, motor control, and cognitive functions throughout the body.^[1]^[2]^[3] Neurons are electrically excitable cells that maintain a resting membrane potential of approximately -70 mV due to ion gradients, primarily involving sodium (Na⁺), potassium (K⁺), and chloride (Cl⁻) ions, and generate action potentials to propagate signals along their length.^[3] The typical neuron consists of three main components: the soma (cell body), which houses the nucleus and organelles for protein synthesis and metabolic activities; dendrites, branched extensions that receive incoming signals from other neurons or sensory receptors; and the axon, a long, slender projection that conducts outgoing electrical impulses away from the soma toward target cells.^[2]^[1]^[3] Axons are often insulated by a myelin sheath formed by glial cells, which accelerates signal transmission via saltatory conduction, and terminate in synaptic terminals that release neurotransmitters to communicate across synapses.^[3] Structurally, neurons are classified into several types based on the number and arrangement of processes extending from the soma: multipolar neurons, which have one axon and multiple dendrites and are the most common type in the central nervous system; bipolar neurons, featuring one axon and one dendrite, typically found in sensory pathways like the retina and olfactory epithelium; pseudounipolar (or unipolar) neurons, with a single process that bifurcates into axon-like and dendrite-like branches, common in sensory ganglia; and anaxonic neurons, lacking a distinct axon, such as those in the retina or cerebellum.^[3] Functionally, neurons are categorized into three primary groups: sensory (afferent) neurons, which convey information from peripheral sensory organs to the central nervous system; motor (efferent) neurons, which transmit commands from the central nervous system to muscles or glands for action; and interneurons, which integrate signals within the central nervous system to facilitate processing and coordination between sensory and motor pathways.^[2]^[3] In the human brain and spinal cord, there are approximately 86 to 100 billion neurons, forming vast networks that underpin complex behaviors and cognition, with most generated during prenatal development though limited neurogenesis persists in regions like the hippocampus into adulthood.^[1]^[2] Once mature, neurons generally do not divide but can undergo plasticity, strengthening or weakening connections through synaptic remodeling in response to experience or injury.^[3]

Role in the Nervous System

Definition and Basic Functions

A neuron is an electrically excitable cell specialized for communication through the transmission of electrochemical signals across the nervous system.^[3] These cells form the fundamental building blocks of the nervous system, enabling rapid information processing and coordination of bodily functions.^[4] The primary functions of neurons involve receiving inputs from other cells via synapses, integrating these signals through summation of excitatory and inhibitory influences, and generating outputs in the form of action potentials that propagate along the axon to influence target cells such as muscles or other neurons.^[3] This process allows neurons to act as decision-making units, firing only when integrated inputs reach a threshold, thereby ensuring efficient signal relay without constant activity.^[5] Through interconnected networks, neurons collectively facilitate essential processes including sensory perception by converting environmental stimuli into neural signals, motor control by directing muscle contractions and glandular secretions, and higher cognitive functions such as learning and memory formation.^[6] Neurons are among the longest-lived cells in the human body, with many post-mitotic neurons persisting for the entire lifespan, often exceeding a century in long-lived individuals.^[7]^[8]

Distribution Across Nervous System Components

Neurons are distributed throughout the central nervous system (CNS), which comprises the brain and spinal cord, and the peripheral nervous system (PNS), which includes cranial and spinal nerves as well as ganglia.^[9] The vast majority of neurons reside in the CNS, where they form complex networks for processing and integration, while PNS neurons primarily serve as conduits for sensory input and motor output between the CNS and the body's periphery.^[10] In humans, the brain alone houses approximately 86 billion neurons, underscoring the CNS's role as the primary site of neural computation.^[11] Neuron density varies significantly across CNS regions to support specialized functions; for instance, the cerebellum contains about 80% of the brain's total neurons despite comprising only 10% of its mass, due to the high packing of small granule cells.^[12] In the spinal cord, motor neurons are concentrated in the ventral horn, where their cell bodies give rise to axons that innervate skeletal muscles via the ventral roots.^[13] Interneurons, which facilitate local circuit integration, are abundant in the cerebral cortex, comprising 20-30% of its neuronal population and providing essential inhibitory and excitatory connections.^[14] Within the PNS, sensory neurons are clustered in dorsal root ganglia adjacent to the spinal cord, with their cell bodies pseudounipolar and axons bifurcating to convey peripheral stimuli to the CNS.^[15] Adaptations in myelination reflect functional demands: many PNS axons, particularly large-diameter motor and proprioceptive sensory fibers, are myelinated by Schwann cells to enable saltatory conduction and rapid signal transmission over long distances.^[16] In contrast, unmyelinated fibers predominate in the autonomic nervous system, such as postganglionic sympathetic and parasympathetic axons, allowing slower, modulatory influences on visceral organs like heart rate and glandular secretion.^[17]

Anatomy

Somatic Structure

The soma, or cell body, of a neuron is a compact, spherical or polygonal structure that serves as the central hub of the cell, housing the nucleus and various organelles essential for cellular maintenance and function. It typically constitutes about one-tenth of the neuron's total volume and contains the nucleus, which encloses the genetic material (DNA) required for cellular operations, along with organelles such as the endoplasmic reticulum (both smooth and rough), Golgi apparatus, mitochondria, microtubules, and lysosomes.^[18] A prominent feature within the soma are the Nissl bodies, specialized clusters of rough endoplasmic reticulum (rER) studded with ribosomes, which are rich in RNA and responsible for synthesizing proteins critical to neuronal structure and activity, including secretory, membrane, and cytoskeletal proteins.^[19] These Nissl bodies, named after Franz Nissl, appear as dense granules or blocks in the cytoplasm—larger in motor neurons and more dust-like in sensory cells—and are absent from the axon, facilitating the neuron's high metabolic demands for protein production.^[19] Extending from the soma are dendrites, which form a highly branched, tree-like network of short, tapering processes that increase the neuron's surface area for receiving inputs. These structures, often numbering several from each neuron, consist of dendritic shafts covered in numerous small protrusions called dendritic spines, which provide sites for synaptic contacts and compartmentalize signaling.^[18] Dendrites contain organelles similar to those in the soma, including Nissl bodies in their proximal regions, supporting local protein synthesis and structural integrity.^[19] The integration of inputs occurs primarily at the soma, where signals from dendrites converge to influence the neuron's overall activity.^[18] The axon emerges as a single, elongated fiber from the soma, specialized for transmitting signals over distances, and originates at the axon hillock—a cone-shaped junction devoid of large organelles like Nissl bodies or the Golgi apparatus.^[20] Adjacent to the hillock is the initial segment, a short region (approximately 30-40 micrometers long) that extends from the soma and contains dense concentrations of neurofilaments, microtubules, mitochondria, and possibly residual Nissl substance, marking it as a key structural zone for signal initiation.^[20] Axons vary widely in length, from millimeters in interneurons to up to 1 meter in projection neurons such as those in the human sciatic nerve, which spans from the spinal cord to the foot.^[20] Their diameters, ranging from 1 to 25 micrometers, also differ significantly, with larger diameters generally permitting faster signal conduction along the axon.^[20]

Membrane Properties and Ion Channels

The plasma membrane of a neuron consists of a fluid phospholipid bilayer, formed by two layers of amphipathic lipid molecules with hydrophilic heads facing the aqueous environments inside and outside the cell, and hydrophobic tails forming the inner core. This structure creates a semipermeable barrier that restricts passive ion diffusion, while embedded proteins, including transporters and channels, facilitate selective ion movement essential for electrical signaling.^[21]^[22] The resting membrane potential of neurons is typically around -70 mV, with the cell interior negative relative to the exterior, primarily due to higher permeability to K⁺ ions and the active maintenance of ion gradients by the Na⁺/K⁺-ATPase pump. This electrogenic pump hydrolyzes ATP to export three Na⁺ ions and import two K⁺ ions per cycle, counteracting passive leaks and sustaining the unequal ion distributions (high intracellular K⁺ ~140 mM and low Na⁺ ~10 mM; high extracellular Na⁺ ~145 mM and low K⁺ ~4 mM).^[23] Neuronal excitability arises from specialized ion channels that regulate membrane permeability to ions like Na⁺, K⁺, and Ca²⁺. Voltage-gated ion channels open or close in response to changes in membrane potential, enabling rapid depolarization (via Na⁺ influx through voltage-gated Na⁺ channels) and repolarization (via K⁺ efflux through voltage-gated K⁺ channels), while voltage-gated Ca²⁺ channels support processes like synaptic transmission by allowing Ca²⁺ entry. Ligand-gated channels, activated by neurotransmitter binding, mediate synaptic integration by permitting ion fluxes that either depolarize (e.g., Na⁺ or Ca²⁺ permeable) or hyperpolarize (e.g., Cl⁻ or K⁺ permeable) the membrane. Leak channels, which are constitutively open, provide background permeability—predominantly to K⁺—that stabilizes the resting potential and sets the baseline for excitability.^[24]^[25] The Goldman-Hodgkin-Katz (GHK) equation provides a quantitative model for the membrane potential under steady-state conditions, incorporating relative permeabilities (P) and concentrations of multiple permeant ions, unlike the Nernst equation which applies to single ions. Derived from the constant-field theory, it assumes a uniform electric field across the membrane and derives ion fluxes as functions of concentration gradients and voltage, setting net current to zero at equilibrium. The unidirectional flux of an ion species (e.g., cation X) through the membrane is given by the Goldman flux equation: J_X = -P_X \frac{z_X F V_m}{RT (1 - e^{z_X F V_m / RT})} \left( [X]_i - [X]_o e^{z_X F V_m / RT} \right) where P_X is permeability, z_X is valence, F is Faraday's constant, R is the gas constant, T is temperature, V_m is membrane potential, and subscripts i/o denote intra/extracellular concentrations. The net flux is J_X^{net} = J_X^i - J_X^o, but at steady state with no net current, the sum of fluxes for all ions (considering opposite signs for anions) equals zero. For monovalent cations (Na⁺, K⁺) and anions (Cl⁻), this simplifies to the GHK voltage equation: V_m = \frac{RT}{F} \ln \left( \frac{P_K [K^+]_o + P_{Na} [Na^+]_o + P_{Cl} [Cl^-]_i}{P_K [K^+]_i + P_{Na} [Na^+]_i + P_{Cl} [Cl^-]_o} \right) Here, parameters reflect typical neuronal values: P_K : P_{Na} : P_{Cl} \approx 1 : 0.04 : 0.45, yielding V_m \approx -70 mV when combined with measured concentrations. This equation highlights how permeability ratios, rather than concentrations alone, determine the potential.^[26]^[27] Mutations in genes encoding neuronal ion channels, termed channelopathies, alter channel function and thereby disrupt membrane excitability; for instance, such genetic defects have been linked to epilepsy through impaired voltage-gated Na⁺ or K⁺ channel activity.^[28]

Internal Histology

The internal histology of neurons reveals a highly organized cytoplasm rich in specialized structures that support cellular architecture, energy production, and intracellular trafficking. The neuronal cytoskeleton forms the foundational scaffold, comprising microtubules, neurofilaments, and actin filaments that provide mechanical support, maintain axonal and dendritic integrity, and facilitate the transport of organelles and molecules along the neuron's extensive processes. Microtubules, composed of tubulin dimers, are polar structures essential for intracellular transport and neuronal polarity, extending throughout the soma, dendrites, and axons. Neurofilaments, as type IV intermediate filaments primarily consisting of three subunits (NF-L, NF-M, NF-H), are abundant in axons and contribute to structural stability and caliber maintenance, particularly in long-projection neurons like motor neurons. Actin filaments, or microfilaments, form dynamic networks concentrated in the dendritic spines and growth cones, enabling motility, synaptic plasticity, and local cytoskeletal remodeling. Key organelles within the neuronal cytoplasm include mitochondria, the Golgi apparatus, and the endoplasmic reticulum, each adapted to meet the high metabolic demands of neurons. Mitochondria, distributed along axons and dendrites, generate ATP through oxidative phosphorylation to power energy-intensive processes such as ion pumping and synaptic transmission. The Golgi apparatus, often appearing as stacked cisternae in the soma, modifies and packages proteins and lipids received from the endoplasmic reticulum into vesicles for axonal transport and synaptic delivery. The rough endoplasmic reticulum, studded with ribosomes and visible as Nissl bodies, synthesizes proteins, while the smooth endoplasmic reticulum serves as a major intracellular store for calcium ions, regulating signaling and buffering during neuronal activity. Histological techniques have been instrumental in visualizing these internal components. Nissl staining, using basic dyes like cresyl violet, selectively highlights the rough endoplasmic reticulum in the neuronal soma and dendrites, allowing differentiation of neuronal populations based on their metabolic activity. Silver impregnation methods, such as Bielschowsky's technique, impregnate neurofibrils and axons to reveal their fine branching and connectivity in tissue sections. Electron microscopy provides ultrastructural detail, resolving individual microtubules (approximately 25 nm in diameter), mitochondrial cristae, and Golgi stacks, which are critical for understanding organelle distribution in three dimensions. Axoplasmic transport, powered by motor proteins kinesin and dynein along the microtubule tracks of the cytoskeleton, moves organelles, proteins, and other cargoes bidirectionally at rates ranging from 1 to 400 mm/day, ensuring the maintenance of distant axonal terminals. Kinesin drives anterograde transport toward the axon tip, while dynein mediates retrograde movement back to the soma.

Classification

Structural Types

Neurons are classified into structural types primarily based on their polarity, which refers to the number and arrangement of processes—dendrites and axons—extending from the cell body (soma). This morphological classification reflects adaptations for receiving and transmitting signals within neural circuits.^[29]^[30] Unipolar neurons feature a single process emerging from the soma, which typically branches into both dendritic and axonal components; they are common in invertebrate sensory systems but rare in vertebrates.^[29] Bipolar neurons possess two distinct processes: one dendrite and one axon, extending from opposite poles of the soma, facilitating direct sensory transduction; representative examples include retinal bipolar cells and olfactory receptor neurons.^[30]^[31] Multipolar neurons, characterized by one axon and multiple dendrites radiating from the soma, dominate vertebrate nervous systems and enable complex integration of inputs; they include pyramidal cells in the cerebral cortex and Purkinje cells in the cerebellum.^[29]^[30] Pseudounipolar neurons, a variant found in vertebrate peripheral nervous systems, have a single process that bifurcates shortly after leaving the soma into a peripheral branch (functioning as a dendrite) and a central branch (as an axon); these are typical of sensory neurons in dorsal root ganglia.^[29]^[30] In addition to these polar types, anaxonic neurons lack a clearly identifiable axon, with multiple short processes that may serve both input and output functions; prominent examples are amacrine cells in the retina, which form local connections within the inner plexiform layer.^[32] Axons in many neuron types, particularly multipolar and pseudounipolar, often give rise to collaterals—side branches that extend from the main axon to form additional synaptic connections, enhancing signal distribution to multiple targets.^[33] These collaterals typically terminate in arborizations, intricate bush-like networks that increase the axon's reach and connectivity within specific brain regions, such as the axonal arborizations of lateral geniculate neurons in the visual cortex. Dendritic branching patterns vary across structural types to optimize input reception: bipolar neurons show simple, elongated dendrites for localized sensory capture, while multipolar neurons display highly branched, tree-like dendrites—often with basal tufts and a prominent apical dendrite in pyramidal cells—to integrate diverse synaptic inputs over larger areas.^[34]^[35] Multipolar neurons predominate in mammalian brains, comprising over 99% of central nervous system neurons and underscoring their role in the majority of signal relay processes.^[31]

Functional Types

Neurons are functionally classified based on the direction of signal transmission relative to the central nervous system (CNS). Afferent neurons, also termed sensory neurons, convey sensory information from peripheral receptors toward the CNS, enabling the detection of environmental stimuli. Efferent neurons transmit commands from the CNS to peripheral effectors, such as skeletal muscles or glands, to elicit motor responses or secretory actions. Interneurons, comprising the majority of neurons in the CNS, integrate signals between afferent and efferent neurons, supporting complex information processing and reflex modulation within neural circuits. Another key functional classification distinguishes neurons by their postsynaptic effects and the neurotransmitters they employ. Excitatory neurons depolarize target cells to increase the likelihood of action potential generation, with glutamatergic neurons—predominantly using glutamate as their transmitter—serving as the primary mediators of excitation in the mammalian brain. Inhibitory neurons hyperpolarize postsynaptic membranes to suppress firing, chiefly through GABAergic neurons that release gamma-aminobutyric acid (GABA) or glycinergic neurons using glycine, thereby maintaining neural balance and preventing hyperexcitability. Neuromodulatory neurons exert prolonged, modulatory influences on circuit dynamics rather than direct excitation or inhibition, as seen in dopaminergic neurons that release dopamine to regulate reward processing, motivation, and plasticity in regions like the basal ganglia. Neurotransmitters further delineate functional neuron types into categories based on chemical structure. Small-molecule neurotransmitters include amino acids such as glutamate and GABA, which enable rapid synaptic transmission; monoamines like dopamine, serotonin, and norepinephrine, which often mediate slower modulatory effects; and acetylcholine, involved in both excitatory and modulatory roles at neuromuscular junctions and autonomic synapses. Neuropeptides, consisting of short amino acid chains (e.g., substance P or neuropeptide Y), typically co-released with small molecules, provide additional layers of signaling for pain modulation or stress responses. Many neurons exhibit multimodal functionality by co-releasing multiple transmitters from distinct vesicular pools, such as ventral tegmental area neurons that simultaneously release glutamate and GABA to fine-tune reinforcement learning. A specialized functional class, mirror neurons, exemplifies integrated sensory-motor processing unique to primates. Located in the ventral premotor cortex, these neurons discharge both during the execution of goal-directed actions, like grasping, and during the observation of similar actions performed by others, facilitating action understanding and social cognition. This dual activation underscores their role in bridging perception and intention, with evidence primarily from macaque monkeys and homologous systems in humans.

Electrophysiology

Action Potential Generation

Action potentials in neurons are brief, stereotyped electrical events lasting approximately 1-2 ms, first quantitatively modeled in 1952 using squid giant axons. These events are initiated at the axon hillock, the junction between the neuronal soma and axon, where excitatory and inhibitory synaptic inputs are spatially and temporally integrated as graded postsynaptic potentials.^[36] If the net depolarization reaches the threshold potential of about -55 mV, voltage-gated sodium channels open rapidly, triggering the action potential.^[37] This threshold serves as a critical detection mechanism, where the density and properties of voltage-gated ion channels, particularly sodium channels like Nav1.6 clustered at the axon hillock, determine the sensitivity to depolarizing inputs.^[36] The action potential unfolds in distinct phases driven by the sequential activation of voltage-gated ion channels. The rising phase begins with the influx of Na⁺ ions through opening sodium channels, rapidly depolarizing the membrane from threshold to a peak of around +40 mV. This is followed by the falling phase, where sodium channels inactivate and voltage-gated potassium channels open, allowing K⁺ efflux that repolarizes the membrane toward the potassium equilibrium potential. The process concludes with an afterhyperpolarization, a brief period of hyperpolarization below the resting potential due to lingering potassium conductance, which helps reset the membrane.^[37] The biophysical basis of these phases is captured by the Hodgkin-Huxley model, which mathematically describes the membrane currents underlying action potential generation. The model treats the neuronal membrane as a capacitor with parallel ionic conductances, governed by the equation:

C_m \frac{dV}{dt} = - \bar{g}_\mathrm{Na} m^3 h (V - E_\mathrm{Na}) - \bar{g}_\mathrm{K} n^4 (V - E_\mathrm{K}) - g_\mathrm{L} (V - E_\mathrm{L}) + I

where V is the membrane potential, C_m is the membrane capacitance (1 μF/cm²), I is the applied current, and the ionic currents depend on voltage-sensitive gating variables m, h, and n for activation and inactivation of sodium and potassium channels. The sodium conductance is given by g_\mathrm{Na} = \bar{g}_\mathrm{Na} m^3 h, with maximum conductance \bar{g}_\mathrm{Na} = 120 mS/cm², reversal potential E_\mathrm{Na} = 50 mV (adjusted from intracellular recordings); potassium by g_\mathrm{K} = \bar{g}_\mathrm{K} n^4, \bar{g}_\mathrm{K} = 36 mS/cm², E_\mathrm{K} = -77 mV; and leak g_\mathrm{L} = 0.3 mS/cm², E_\mathrm{L} = -54.4 mV. The gating variables follow first-order kinetics:

\frac{dm}{dt} = \alpha_m (1 - m) - \beta_m m, \quad \frac{dh}{dt} = \alpha_h (1 - h) - \beta_h h, \quad \frac{dn}{dt} = \alpha_n (1 - n) - \beta_n n

with voltage-dependent rate constants \alpha and \beta defined as:

\alpha_m = \frac{0.1 (V + 40)}{1 - \exp(-(V + 40)/10)}, \quad \beta_m = 4 \exp(-(V + 65)/18)

\alpha_h = 0.07 \exp(-(V + 65)/20), \quad \beta_h = \frac{1}{1 + \exp(-(V + 35)/10)}

\alpha_n = \frac{0.01 (V + 55)}{1 - \exp(-(V + 55)/10)}, \quad \beta_n = 0.125 \exp(-(V + 65)/80)

(Here, V is in mV, shifted from the original squid axon values for standardization.) These equations, solved numerically, simulate the rapid Na⁺ activation (m rises quickly near threshold) and delayed K⁺ activation (n slower), reproducing the observed phases and enabling predictions of excitability under varying conditions. The model highlights how threshold detection emerges from the nonlinear voltage dependence of channel gating, ensuring regenerative depolarization once initiated.^[38]

Propagation Mechanisms

In unmyelinated axons, action potentials propagate via continuous conduction, where local circuit currents depolarize adjacent membrane segments sequentially along the entire axon length, resulting in conduction velocities of 0.5 to 10 m/s.^[39] This mechanism relies on the passive spread of voltage changes through the axoplasm, limited by the axon's membrane capacitance and resistance.^[39] Myelinated axons employ saltatory conduction, in which the action potential regenerates only at the nodes of Ranvier—short, periodic gaps (typically 1-2 μm long) in the myelin sheath that concentrate voltage-gated sodium channels—allowing the impulse to "jump" between nodes at speeds up to 150 m/s.^[39]^[40] This leaping process minimizes the energy and time required for ion channel activation across the insulated internodal segments, which can span 0.2 to 2 mm depending on axon diameter.^[40] The myelin sheath enabling saltatory conduction is a multilayered lipid-rich membrane, comprising 70-85% lipids such as cholesterol (about 40%), phospholipids (40%), and glycolipids (20%), with 15-30% proteins including myelin basic protein (MBP), which stabilizes the compact spiral wrapping by interacting with lipid bilayers.^[41] In the peripheral nervous system (PNS), Schwann cells form myelin by extending and spiraling their plasma membrane around a single axonal segment, producing one internode per cell.^[42] In the central nervous system (CNS), oligodendrocytes similarly wrap axons but extend processes to myelinate multiple internodes across different axons, up to 50 or more.^[42] Demyelination disrupts this insulation, forcing continuous conduction and slowing velocities by 50-100 fold, as the loss of myelin exposes the axon to excessive current leakage and requires reactivation along the full length, a hallmark of disorders like multiple sclerosis.^[39]^[43] Cable theory models the passive electrotonic spread of signals in axons as a leaky cable, where the length constant λ quantifies the distance over which a steady voltage decays to 1/e (about 37%) of its initial value.^[44] The length constant is derived from the core conductor model and given by

\lambda = \sqrt{\frac{r_m}{r_i}},

where r_m is the membrane resistance per unit length (Ω·cm) and r_i is the intracellular (axial) resistance per unit length (Ω/cm).^[44]^[45] To derive this, consider the steady-state case along an infinite uniform cable. The axial current at position x is I_i(x) = -\frac{1}{r_i} \frac{dV}{dx}, where V(x) is the transmembrane voltage. The divergence of axial current equals the outward membrane current per unit length, i_m = \frac{V}{r_m}, so \frac{dI_i}{dx} = -i_m = -\frac{V}{r_m}. Differentiating the expression for I_i gives \frac{d^2 I_i}{dx^2} = -\frac{1}{r_i} \frac{d^2 V}{dx^2}. Substituting \frac{dI_i}{dx} = -\frac{V}{r_m} yields \frac{d^2 V}{dx^2} = \frac{r_i}{r_m} V = \frac{V}{\lambda^2}, confirming the exponential decay solution V(x) = V_0 e^{-x/\lambda} with \lambda = \sqrt{r_m / r_i}.^[44]^[45] In myelinated axons, high r_m due to insulation increases λ, facilitating faster saltatory jumps by reducing signal attenuation between nodes.^[44]

All-or-None Principle

The all-or-none principle describes the binary nature of action potentials in neurons, where the response is either a full-amplitude spike or no spike at all, provided the stimulus depolarizes the membrane to threshold. Once threshold is reached—typically around -55 mV—the action potential propagates with invariant amplitude (approximately 100 mV peak-to-peak) and duration (about 1-2 ms), regardless of further increases in stimulus intensity. This principle was established for single nerve fibers by Edgar Adrian in his 1914 experiments on frog sciatic nerves, building on Keith Lucas's earlier demonstrations in skeletal muscle fibers. The fixed characteristics ensure that the signal remains consistent over long distances, preventing degradation that would occur with analog-like variations. In contrast to the all-or-none output of action potentials, synaptic inputs to neurons generate graded potentials, such as excitatory postsynaptic potentials (EPSPs), which are analog signals varying proportionally in amplitude with the stimulus strength. These graded potentials decrement with distance and can summate spatially and temporally at the axon hillock to reach threshold, thereby triggering the digital, all-or-none action potential that serves as the neuron's output. This hybrid system—analog integration followed by digital transmission—allows neurons to process nuanced inputs while reliably conveying information along axons without loss of fidelity. Action potentials are further constrained by refractory periods that enforce discrete timing and prevent signal overlap. The absolute refractory period, lasting about 1 ms, occurs during depolarization and early repolarization when voltage-gated sodium channels are inactivated, rendering the neuron incapable of firing another action potential irrespective of stimulus strength. This is followed by the relative refractory period, approximately 2-4 ms, during which the membrane is hyperpolarized due to lingering potassium efflux, requiring a suprathreshold stimulus to initiate a new action potential. These periods, first characterized in detail through intracellular recordings in the mid-20th century, limit maximum firing rates to around 500 Hz and ensure unidirectional, non-overlapping propagation for accurate neural signaling.

Synaptic Connectivity

Synapse Structure and Formation

Synapses are specialized junctions that facilitate communication between neurons, primarily classified into two main types based on their mechanism of signal transmission: chemical and electrical. Chemical synapses, the most prevalent type in the vertebrate nervous system, operate through the release of neurotransmitters from synaptic vesicles in the presynaptic terminal into a narrow synaptic cleft, allowing for unidirectional signaling modulated by specific receptors on the postsynaptic side. In contrast, electrical synapses enable direct bidirectional flow of ions and small molecules through gap junctions formed by connexin proteins, which create low-resistance channels between adjacent neuronal membranes. These gap junctions typically consist of paired hemichannels, each composed of six connexin subunits, permitting rapid synchronization of electrical activity across coupled cells. Morphologically, chemical synapses exhibit distinct ultrastructural features that correlate with their functional roles. Asymmetric synapses, often associated with excitatory transmission, feature a prominent postsynaptic density (PSD) and spherical synaptic vesicles clustered near the presynaptic membrane, as first described in electron microscopy studies. Symmetric synapses, typically linked to inhibitory signaling, display more evenly thickened pre- and postsynaptic membranes with flatter vesicles and less pronounced PSDs. The presynaptic terminal, an expansion of the axon, contains these vesicles and active zones for release machinery, while the synaptic cleft spans approximately 20-40 nm, filled with extracellular matrix proteins that regulate diffusion and adhesion. The PSD, a protein-dense specialization on the postsynaptic side (often 30-50 nm thick), anchors ionotropic receptors such as AMPA and NMDA types for glutamate, along with scaffold proteins like PSD-95 that organize signaling cascades. Synapse formation, or synaptogenesis, begins during neural development through coordinated processes involving axonal guidance and target recognition. Axonal growth cones are directed by extracellular cues, including netrins that promote attraction and semaphorins that mediate repulsion, enabling precise navigation to postsynaptic partners such as dendrites or somata. Initial contacts form transient adhesions via cell adhesion molecules like neurexins and neuroligins, which trigger assembly of presynaptic and postsynaptic components. Activity-dependent mechanisms then stabilize these nascent synapses; correlated presynaptic and postsynaptic firing strengthens connections, following the Hebbian principle that "cells that fire together wire together," as proposed in foundational work on synaptic modification. A typical mature neuron in the cerebral cortex forms between 10,000 and 100,000 such synapses, enabling extensive network integration.

Neurotransmitter Release and Action

Upon arrival of an action potential at the presynaptic terminal, depolarization opens voltage-gated calcium channels, allowing Ca²⁺ influx into the axon terminal.^[46] This Ca²⁺ binds to synaptotagmin-1, the primary Ca²⁺ sensor, which interacts with the SNARE complex to trigger rapid fusion of synaptic vesicles with the presynaptic membrane.^[47] The SNARE proteins—syntaxin-1 and SNAP-25 on the plasma membrane, and synaptobrevin (VAMP2) on the vesicle—form a four-helix bundle that zippers the membranes together, driving exocytosis and releasing neurotransmitter into the synaptic cleft in discrete packets known as quanta.^[48] The quantal nature of release was established by the quantal hypothesis, which posits that neurotransmitters are packaged and released in fixed units corresponding to vesicle contents, as evidenced by fluctuations in end-plate potentials at the neuromuscular junction.^[49] Each synaptic vesicle typically contains approximately 5,000 molecules of neurotransmitter, such as glutamate or acetylcholine, leading to miniature postsynaptic potentials (minis) upon spontaneous release of single quanta even in the absence of stimulation.^[50] These minis represent the unitary response to one vesicle's contents and sum to produce larger evoked potentials during synaptic transmission.^[49] In the synaptic cleft, approximately 20-50 nm wide, the released neurotransmitter diffuses rapidly to bind postsynaptic receptors.^[46] Ionotropic receptors, which are ligand-gated ion channels, mediate fast synaptic transmission by directly opening upon binding, allowing ion flux that generates excitatory postsynaptic potentials (EPSPs) via Na⁺/K⁺ influx or inhibitory postsynaptic potentials (IPSPs) via Cl⁻ influx, typically within milliseconds.^[46] Metabotropic receptors, coupled to G-proteins, produce slower effects (hundreds of milliseconds to seconds) by activating intracellular signaling cascades that modulate ion channels or second messengers, often leading to prolonged EPSPs or IPSPs.^[46] Spatial and temporal summation of multiple EPSPs and IPSPs at the postsynaptic neuron determines whether the membrane potential reaches threshold for action potential initiation.^[46] To terminate signaling and recycle neurotransmitters, mechanisms include reuptake via plasma membrane transporters and enzymatic degradation.^[51] For monoamines like serotonin, the serotonin transporter (SERT) facilitates reuptake into the presynaptic terminal or glia, where the neurotransmitter is repackaged or degraded.^[52] Acetylcholine, for example, is rapidly hydrolyzed in the cleft by acetylcholinesterase into inactive choline and acetate, preventing prolonged activation.^[51] These clearance processes ensure precise control of synaptic strength and prevent spillover to adjacent synapses.^[51]

Nonelectrochemical Communication

Nonelectrochemical communication in neurons encompasses non-synaptic mechanisms that enable signaling through diffusion of messengers or direct intercellular channels, contrasting with targeted synaptic transmission. Volume transmission represents a key mode, where neuromodulators diffuse extracellularly to act on multiple distant targets, facilitating broader integration of neural activity. This process involves the release of diffusible substances such as nitric oxide (NO) and cytokines, which operate extrasynaptically to modulate neuronal excitability and plasticity over extended ranges.^[53]^[54] Nitric oxide exemplifies volume transmission as a gasotransmitter synthesized on demand by neuronal nitric oxide synthase (nNOS) enzymes within the neuronal cytoplasm, without requiring vesicular packaging or synaptic specializations. Once produced, NO diffuses freely through cell membranes, reaching effective distances of 100-300 μm, thereby influencing surrounding neurons and glia in a non-point-to-point manner. This diffusion modulates synaptic plasticity, such as long-term potentiation, by activating pathways like NO-soluble guanylyl cyclase-cyclic GMP, which fine-tunes network dynamics across volumes containing multiple synapses.^[55]^[56] Neurotransmitter spillover provides an additional nonelectrochemical pathway, where synaptically released molecules like glutamate escape the cleft and activate extrasynaptic receptors on nearby or distant sites. This phenomenon occurs due to incomplete clearance by transporters such as excitatory amino acid transporters (EAATs), allowing glutamate to bind high-affinity extrasynaptic NMDA receptors and alter circuit-wide excitability. Such spillover can induce heterosynaptic effects, including enhanced long-term potentiation at adjacent synapses, and is implicated in broader neural integration beyond discrete synaptic contacts.^[57]

Neural Information Processing

Neural Coding Mechanisms

Neural coding refers to the strategies by which neurons represent and transmit information about sensory stimuli, motor commands, or internal states through patterns of action potentials, the basic unit of neural signaling. These discrete electrical events, typically lasting 1-2 milliseconds, allow neurons to encode information in a reliable yet efficient manner across diverse brain regions. Key mechanisms include rate coding, where the frequency of spikes conveys stimulus intensity; temporal coding, which relies on the precise timing of spikes; population coding, involving coordinated activity across groups of neurons; and sparse coding, which uses minimal neural activation for high-fidelity representation. Rate coding is one of the earliest identified mechanisms, in which the firing rate of a neuron—measured in spikes per second—varies proportionally with the strength or intensity of the input stimulus. For instance, in sensory neurons innervating muscle spindles, the frequency of action potentials increases linearly with applied stretch force, ranging typically from 0 to 100 Hz, allowing graded encoding of mechanical stimuli. This approach is prevalent in somatosensory and motor systems, where sustained firing rates correlate with ongoing stimulus features, though it may lose temporal precision for rapidly changing inputs. Temporal coding complements rate coding by exploiting the exact timing or intervals between spikes to convey information, such as the phase of oscillatory inputs or rapid stimulus onsets. In systems like the auditory pathway, neurons use spike bursts or precise latencies relative to stimulus cycles to encode timing differences with resolutions down to milliseconds, enabling discrimination of frequencies or motion directions.00709-X) This mechanism is particularly effective in rhythmic environments, where spike timing relative to network oscillations carries additional information beyond average rates. Population coding involves the collective activity of many neurons to represent multidimensional features, such as stimulus orientation in the visual cortex, where the vector sum of individual neuron tuning preferences forms a population vector that accurately predicts perceived direction.^[58] In primary visual cortex, ensembles of orientation-selective neurons encode angles through their relative firing rates, providing robustness against noise in single-cell responses. This distributed strategy enhances coding capacity and precision, as information emerges from correlations across the group rather than isolated neurons.^[59] Sparse coding achieves efficiency in neural representation by activating only a small fraction of neurons for any given stimulus, minimizing metabolic costs while maximizing discriminability. In the olfactory bulb, mitral and tufted cells exhibit highly selective responses, with fewer than 10% typically active for monomolecular odorants, promoting combinatorial patterns that distinguish thousands of scents using a limited repertoire of cells.^[60] This sparsity is quantified using information theory, where mutual information—measuring shared bits between stimuli and spike patterns—reaches up to several bits per spike in optimized sensory systems, underscoring the informational efficiency of such codes.

Discharge Patterns and Firing Modes

Neurons exhibit a variety of intrinsic discharge patterns that determine how they encode and transmit information, ranging from regular spiking to complex bursting behaviors. Tonic firing, characterized by sustained, regular action potentials at a relatively constant rate in response to depolarizing inputs, is common in many cortical and subcortical neurons and supports the representation of steady-state signals. In contrast, phasic firing involves brief bursts of spikes at the onset of stimulation, followed by silence or reduced activity, enabling neurons to detect and respond to transient changes in input. These patterns arise from the interplay of voltage-gated ion channels and can be modulated by synaptic inputs, contributing to diverse computational roles within neural circuits.^[61] Bursting and pacemaker activities represent more specialized firing modes, where groups of spikes occur in rapid succession, often separated by quiescent periods. In thalamic relay neurons, for instance, cells can switch between tonic firing during alert states and burst mode during sleep or sensory gating, with bursts generated by low-threshold calcium currents that promote rebound excitation after hyperpolarization.^[62] Pacemaker activity, seen in these neurons and others like those in central pattern generators, maintains rhythmic firing independently of synaptic drive, facilitating oscillatory behaviors such as sleep spindles.^[63] Spike frequency adaptation and fatigue further shape these patterns, where prolonged depolarization leads to a progressive decrease in firing rate due to calcium-dependent potassium currents, preventing overstimulation and allowing recovery. Ionic conductances play a key role in influencing discharge patterns and enabling resonance properties. The hyperpolarization-activated cation current (Ih), mediated by HCN channels, promotes membrane resonance at theta frequencies (4-8 Hz), enhancing the neuron's responsiveness to rhythmic inputs and facilitating transitions between firing modes.^[64] Neuromodulators, such as norepinephrine and acetylcholine, can dynamically alter these modes by modulating ion channel expression or kinetics; for example, they increase excitability to favor bursting over tonic firing in locus coeruleus neurons.^[61] In the visual cortex, chattering cells—superficial pyramidal neurons—exhibit intrinsic repetitive bursts at 20-60 Hz, which are thought to contribute to synchronous oscillations that aid in feature binding during visual processing.^[65] These single-neuron patterns complement rate-based coding strategies by providing temporal structure to neural signals.

Development and Plasticity

Embryonic Development

Neurogenesis in the embryonic brain begins with the proliferation of neural progenitors within the neural tube, which forms early in gestation from the neural plate. These progenitors, initially neuroepithelial cells, undergo asymmetric cell divisions to produce one progenitor cell that retains stem-like properties and one daughter cell that differentiates toward a neuronal fate. This process ensures a balance between progenitor maintenance and neuronal production, with divisions oriented along the apical-basal axis of the neural tube.^[66]^[67] Radial glial cells emerge as key precursors during this phase, serving as neural stem cells that line the ventricular surface and generate the majority of neurons through self-renewing asymmetric divisions. These cells extend processes from the ventricular zone to the pial surface, providing a scaffold for subsequent neuronal migration while contributing directly to the neuronal pool via intermediate progenitors. In humans, neurogenesis peaks during the second trimester, when the fetal brain produces approximately 250,000 neurons per minute to establish the foundational neuronal population. However, this overproduction is followed by a critical period of programmed cell death, where apoptosis prunes about 50% of the excess neurons to refine neural circuits and match target availability.^[68]^[69]^[70]^[71] Newly generated neurons then migrate from the proliferative zones to their final positions, employing both radial and tangential paths. Radial migration follows the radial glial scaffold, allowing neurons to ascend toward the cortical surface, while tangential migration occurs parallel to the ventricular surface and is crucial for populating specific layers or interneurons. This migration is guided by extracellular cues such as reelin, a glycoprotein secreted by Cajal-Retzius cells in the marginal zone, which regulates the radial translocation and layering of neurons by modulating integrin-mediated adhesion and cytoskeletal dynamics. In the developing cerebral cortex, these processes contribute to the inside-out formation of layers, where earlier-born neurons occupy deeper layers and later-born ones settle superficially.^[72]^[73]^[74]^[75] Following migration, neuronal differentiation establishes cellular identity and polarity, driven by transcription factors that specify neurotransmitter phenotypes and structural features. For instance, NeuroD1 promotes the glutamatergic fate in cortical and hippocampal neurons by activating genes for excitatory neurotransmission and dendrite morphogenesis. Concurrently, axon guidance ensures proper connectivity, with the Slit/Robo signaling pathway providing repulsive cues to direct axonal outgrowth away from midline barriers and toward target regions during embryonic pathfinding. These mechanisms collectively shape the nascent neural architecture, setting the stage for synaptic integration.^[76]^[77]^[78]^[79]

Neural Plasticity

Neural plasticity refers to the ability of neurons to modify their structure and function in response to experience, learning, or injury. A key mechanism is synaptic plasticity, which involves changes in the strength of synaptic connections. Long-term potentiation (LTP) strengthens synapses through repeated stimulation, primarily via N-methyl-D-aspartate (NMDA) receptor activation and calcium influx, leading to insertion of AMPA receptors and enhanced signal transmission. Conversely, long-term depression (LTD) weakens synapses, contributing to circuit refinement. These Hebbian processes underpin learning and memory formation. Structural plasticity includes dendritic spine remodeling and axonal arborization, driven by activity-dependent cytoskeletal changes and neurotrophins like BDNF. In adulthood, plasticity enables adaptive responses, such as recovery after stroke through cortical remapping.^[80]^[81] Adult neurogenesis, the generation of new neurons postnatally, occurs primarily in the subgranular zone of the hippocampus and the subventricular zone of the lateral ventricles. In humans, it persists at low levels into adulthood, producing thousands of new neurons daily in the hippocampus, which integrate into existing circuits to support functions like spatial memory and mood regulation. This process is regulated by factors such as exercise, environmental enrichment, and BDNF, and declines with age.^[82]^[83]

Regeneration and Repair Processes

In the peripheral nervous system (PNS), neuronal regeneration following injury involves a well-orchestrated sequence beginning with Wallerian degeneration, where the distal axon segment degenerates and is cleared by macrophages, creating a pathway for regrowth.^[84] This process facilitates axonal sprouting from the proximal stump, guided by motile growth cones that sense and respond to environmental cues to extend new axons toward their targets.^[85] The rate of this axonal regeneration typically ranges from 1 to 3 mm per day, influenced by factors such as injury type and neuronal subtype.^[86] In contrast, the central nervous system (CNS) exhibits limited regenerative capacity due to intrinsic neuronal constraints and an inhibitory extracellular environment. Reactive astrocytes form a glial scar at the injury site, secreting chondroitin sulfate proteoglycans (CSPGs) that bind to neuronal receptors, such as PTPσ, to inhibit axon extension and prevent regrowth.^[87] This scar, while stabilizing the lesion to limit secondary damage, creates a persistent barrier that, combined with the neurons' reduced intrinsic growth potential after maturity, severely hampers repair compared to the supportive milieu of the PNS.^[88] Therapeutic strategies aim to overcome these barriers by enhancing regenerative signals. Neurotrophins like nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) promote axonal sprouting and survival by activating Trk receptors, stimulating intracellular pathways such as PI3K/Akt to support growth cone advance and synapse formation in both PNS and CNS contexts.^[89] Similarly, BDNF has been shown to drive regenerative sprouting in serotonergic neurons post-injury, independent of direct survival effects.^[90] Stem cell transplants, including neural stem cells or mesenchymal stem cells, further aid repair by secreting trophic factors, modulating inflammation, and potentially differentiating into supportive glia, thereby fostering endogenous axonal regrowth and functional recovery after CNS trauma like stroke or spinal cord injury.^[91] As of 2025, emerging therapies include CRISPR/Cas9 gene editing to enhance intrinsic growth programs by targeting PTEN or KLF4, optogenetics for precise stimulation of regrowth, and neural stem cell-derived extracellular vesicles that deliver miRNAs to reduce inflammation and promote axon extension. These approaches show promise in preclinical models for improving CNS repair.^[92]^[93]^[94] A notable example of species-specific differences is optic nerve regeneration, which fails in mammals due to the inhibitory CNS environment but succeeds robustly in fish through macrophage-derived oncomodulin, a calcium-binding protein that activates RGC axons via cAMP pathways to enable long-distance regrowth. In mammals, where full regeneration is absent, neuronal plasticity compensates via collateral sprouting, where intact axons from nearby neurons extend branches to reinnervate denervated targets, partially restoring function through adaptive circuit reorganization.^[80]

History and Etymology

Key Historical Discoveries

The earliest microscopic observations of neural structures date to the late 17th century, when Dutch microscopist Antonie van Leeuwenhoek examined bovine optic nerves and described myelinated nerve fibers as tube-like structures filled with fluid, marking the first documented visualization of such elements using his handmade single-lens microscope.^[95] In the 19th century, Czech anatomist Jan Evangelista Purkinje advanced this work by identifying and describing ganglion cells—large neurons in the brain, spinal cord, and cerebellum—through improved light microscopy techniques during his 1837 presentation at the Congress of German Naturalists and Physicians in Prague.^[96] A pivotal advancement in visualizing neuron morphology occurred in 1873, when Italian histologist Camillo Golgi developed the "black reaction" silver chromate stain, which selectively impregnated entire neurons with silver nitrate, revealing their intricate dendritic and axonal structures in unprecedented detail and enabling the study of individual cell architectures in fixed tissue.^[97] Building on Golgi's method, Spanish neuroscientist Santiago Ramón y Cajal produced highly detailed drawings of individual neurons starting in 1888, including the first illustrations of Golgi-impregnated preparations from the cerebellar cortex and the discovery of dendritic spines, which depicted neurons as discrete, polarized cells with branching processes throughout the 1880s and 1890s.^[98] In electrophysiology, Italian physician Luigi Galvani's experiments in the 1780s culminated in his 1791 publication "De Viribus Electricitatis in Motu Musculari Commentarius," where he demonstrated that electrical stimulation of frog nerves and muscles produced contractions, establishing the concept of "animal electricity" as an intrinsic bioelectric force driving neural and muscular activity.^[99] This laid the groundwork for later intracellular studies, notably in the 1920s when British physiologist Edgar Adrian, collaborating with Detlev Bronk, pioneered single-unit recording techniques using vacuum tube amplifiers to isolate and measure action potentials from individual motor nerve fibers and sensory neurons, as detailed in their 1928–1929 papers in The Journal of Physiology, which quantified firing rates and linked them to sensory stimuli.^[100] The advent of electron microscopy in the mid-20th century provided ultrastructural insights into neural components; in 1953–1954, researchers Sanford Palay and George Palade, along with Eduardo De Robertis and J. David Robertson, independently published the first high-resolution images of synaptic terminals, revealing clusters of synaptic vesicles—small, membrane-bound organelles approximately 40–50 nm in diameter—as key features of chemical synapses in vertebrate nervous tissue.^[101] By 2025, advancements in genetic tools enabled precise in vivo manipulation of neuron genes; for instance, a CRISPR-based screening method using AAV-delivered libraries (CrAAVe-seq) profiled thousands of neuron-essential genes across mouse brain subpopulations, identifying circuit-specific vulnerabilities and demonstrating efficient editing in diverse neuronal types without off-target effects.^[102]

Neuron Doctrine

The neuron doctrine, a foundational principle in neuroscience, posits that the nervous system is composed of discrete, individual cells called neurons, rather than a continuous network of fused protoplasm. This theory was formulated in the late 19th century through the pioneering histological work of Santiago Ramón y Cajal, who, using the Golgi staining method, demonstrated in the 1890s that neural elements are anatomically independent units with distinct morphologies. Cajal's detailed drawings of neuronal structures in various species provided compelling visual evidence against the prevailing reticular theory, which viewed the nervous system as an interconnected syncytium. In 1891, German anatomist Heinrich Waldeyer-Hartz formalized the concept by coining the term "neuron" (from the Greek for "sinew") in a seminal paper summarizing these findings and advocating for the application of cell theory to the nervous system.^[103]^[104]^[105] Central to the doctrine are several key principles: neurons function as autonomous cells with inherent polarity, where dendrites receive signals and axons transmit them unidirectionally; intercellular communication occurs via specialized contact points rather than cytoplasmic fusion; and growth or regeneration proceeds from the cell body outward along processes. These ideas emerged prominently from the scientific debate between Cajal and Camillo Golgi, the latter's reticular theory—supported by his silver chromate staining technique—positing a fused network, which Cajal refuted through meticulous observations of neuronal boundaries and directed outgrowth. The doctrine's tenets were later empirically validated in the mid-20th century by electron microscopy, which revealed synaptic clefts as discrete junctions between neurons, confirming the absence of continuity.^[106]^[107]^[104] The neuron doctrine profoundly shaped modern neuroscience by establishing neurons as the basic functional units, enabling subsequent advances in understanding neural circuits, signaling, and plasticity. It directly refuted Golgi's reticular theory, shifting the paradigm from a holistic network view to one emphasizing cellular individuality and specificity in connections. This conceptual framework was recognized with the 1906 Nobel Prize in Physiology or Medicine, jointly awarded to Golgi and Cajal for their work on the nervous system's microstructure, despite their opposing views—highlighting the doctrine's contentious yet transformative role. Throughout the 20th century, the doctrine evolved to incorporate glial cells into broader neuron-glia networks, acknowledging their active participation in signaling and support, as evidenced by studies on astrocytic modulation of synapses.^[108]^[109]

Terminology Origins

The term "neuron" derives from the ancient Greek word νεῦρον (neûron), signifying "sinew" or "nerve," a usage traceable to early anatomists such as Herophilus (c. 330–260 BCE), who applied it to components of the nervous system.^[110] In 1891, German anatomist Heinrich Waldeyer-Hartz formally coined the modern scientific term "Neuron" (in German, das Neuron) to designate the nerve cell and its extensions as the basic structural and functional unit of the nervous system.^[110] This introduction built on earlier histological observations and marked a pivotal linguistic formalization within the emerging framework of cellular neuroscience.^[110] Spelling variations emerged shortly after, with "neurone" appearing in French literature by 1893 and gaining traction in British English, as seen in early 20th-century texts and persisting in some contexts like the Motor Neurone Disease Association.^[110] However, by the post-1900 period, international standardization favored "neuron," as advocated by figures like William Gowers in 1899, who noted its near-universal adoption and declared it the correct form.^[110] This unification eliminated confusion and aligned with the term's Greek roots, reflecting a broader trend toward precise, etymologically consistent nomenclature in biology. Key related terms further illustrate the evolution of neural terminology during this era. The word "dendrite," from the Greek déndron meaning "tree," was coined in 1889 by Wilhelm His to describe the branching receptive processes of nerve cells, emphasizing their arboreal morphology.^[97] Similarly, "axon," derived from the Greek axōn for "axis," was introduced in 1896 by Albert von Kölliker to denote the elongated, directive outgrowth of the neuron.^[111] Santiago Ramón y Cajal, through his detailed illustrations and studies, popularized these terms, integrating them into the descriptive language of neuronal anatomy.^[97] The term "synapse," originating from Greek roots syn- ("together") and haptō ("to clasp"), was introduced in 1897 by Charles Sherrington in the seventh edition of Michael Foster's Textbook of Physiology to characterize the junction between neurons.^[110] These terms collectively embody the late 19th-century paradigm shift from conceptualizing nerves as holistic, continuous fibers to distinct cellular units, a transformation encapsulated in the neuron doctrine.^[110] By 2025, no significant alterations to this foundational nomenclature have occurred, affirming its stability in contemporary neuroscience.^[110]

Pathological Aspects

Common Neurological Disorders

Neurological disorders encompass a range of conditions that impair neuronal function or lead to neuronal death, disrupting communication within the nervous system and resulting in diverse symptoms such as cognitive decline, motor impairments, and seizures.^[112] These disorders often involve progressive degeneration or abnormal activity in specific neuronal populations, with global impacts including an estimated 57 million people living with dementia in 2021, projected to rise to approximately 78 million by 2030 due to aging populations.^[113] Research into these conditions increasingly employs techniques like optogenetics to probe and modulate neural circuits at a cellular level, offering insights into potential therapeutic interventions.^[114] Alzheimer's disease, a leading neurodegenerative disorder, is characterized by the accumulation of amyloid-β plaques extracellularly and hyperphosphorylated tau protein forming neurofibrillary tangles intracellularly, both contributing to synaptic dysfunction and widespread neuronal loss, particularly in the hippocampus and cortex.^[115] This neuronal damage correlates with cognitive symptoms like memory loss and behavioral changes, as plaques and tangles directly disrupt neuronal integrity and lead to atrophy.^[116] Similarly, Parkinson's disease involves the selective death of dopaminergic neurons in the substantia nigra pars compacta, reducing dopamine levels in the basal ganglia and causing motor symptoms such as tremors, rigidity, and bradykinesia.^[117] This loss, which can exceed 50% of neurons before symptoms manifest, underscores the vulnerability of these high-energy-demand neurons to oxidative stress and protein aggregation.^[118] Epilepsy arises from hypersynchronous firing of neuronal networks in the cortex, leading to recurrent seizures through imbalanced excitation and inhibition.^[119] This abnormal synchronization can be triggered by factors like stroke-induced ischemia, which deprives neurons of oxygen and glucose, causing acute neuronal damage and potentially epileptogenic foci.^[120] Huntington's disease results from expanded CAG trinucleotide repeats in the huntingtin gene, leading to toxic polyglutamine aggregates that impair neuronal function and cause progressive degeneration in the striatum and cortex.^[121] Genetic ataxias, such as spinocerebellar ataxias (SCAs), also genetic, involve Purkinje cell loss in the cerebellum due to repeat expansions, manifesting as coordination deficits and ataxia.^[122] Acquired neuropathies, often from trauma, diabetes, or toxins, damage peripheral neurons through mechanisms like axonal degeneration, resulting in sensory loss, pain, or weakness without central involvement.^[112]

Cellular Mechanisms of Damage

Neurons are particularly vulnerable to cellular damage due to their high metabolic demands, extensive axonal projections, and reliance on precise ion homeostasis for signaling. Damage mechanisms often involve disruptions in calcium regulation, energy production, and protein homeostasis, leading to dysfunction or death. These processes can be triggered by insults such as ischemia, toxins, or genetic factors, culminating in pathways like apoptosis or necrosis.^[123] Excitotoxicity represents a primary mechanism where excessive extracellular glutamate overactivates ionotropic receptors, particularly NMDA receptors, resulting in massive calcium influx. This calcium overload disrupts mitochondrial function, activates proteases and lipases, and initiates apoptotic cascades through cytochrome c release and caspase activation. In acute settings like stroke, this leads to rapid neuronal swelling and death, while chronic exposure contributes to progressive degeneration.^[124]^[125] Oxidative stress arises from an imbalance in reactive oxygen species (ROS) production, predominantly from dysfunctional mitochondria, which damage lipids, proteins, and DNA in neurons. During aging, mitochondrial electron transport chain leaks generate excess ROS, impairing ATP synthesis and promoting protein misfolding, such as in prion diseases or amyloid-beta aggregates. This stress exacerbates neuronal vulnerability by inactivating antioxidant defenses like superoxide dismutase.^[126]^[127] Axonal degeneration often follows injury or pathology, manifesting as Wallerian degeneration where the distal axon segment undergoes programmed fragmentation due to loss of trophic support from the cell body. This involves activation of nicotinamide mononucleotide adenylyltransferase 2 (NMNAT2) degradation and SARM1 signaling, leading to NAD+ depletion and axonal die-back. Synaptic stripping, mediated by activated microglia, removes presynaptic terminals from injured motoneurons, potentially isolating them from inputs and accelerating dysfunction. In immune-mediated contexts like multiple sclerosis, demyelination occurs through autoreactive T cells and macrophages attacking myelin sheaths, forming plaques that expose axons to ionic imbalances and mechanical stress.^[128]^[129]^[130] Programmed cell death (PCD) is a regulated process essential for neuronal refinement, with approximately 50% of developing neurons eliminated via caspase-dependent apoptosis to match target innervation. Caspases, such as caspase-3 and -9, are activated in response to trophic factor withdrawal, cleaving structural proteins and DNA repair enzymes. In pathological tauopathies, recent models reveal hyperphosphorylated tau aggregates disrupting microtubules, triggering caspase activation and non-apoptotic PCD forms like parthanatos, contributing to neuronal loss in disorders like Alzheimer's disease.^[131]^[132]^[133]

References

[1]
What is a neuron? - Queensland Brain Institute
Neurons (also called neurones or nerve cells) are the fundamental units of the brain and nervous system, the cells responsible for receiving sensory input ...Missing: authoritative | Show results with:authoritative
[2]
Brain Basics: The Life and Death of a Neuron
Feb 25, 2025 · Neurons are nerve cells that send messages all over your body to allow you to do everything from breathing to talking, eating, walking, and thinking.Missing: authoritative | Show results with:authoritative
[3]
Neuroanatomy, Neurons - StatPearls - NCBI Bookshelf
Neurons are electrically excitable cells that transmit signals throughout the body. Neurons employ both electrical and chemical components in the transmission ...Missing: authoritative | Show results with:authoritative
[4]
Introduction to Neurons and Neuronal Networks | Section 1, Intro ...
This chapter will begin with a discussion of the neuron, the elementary node or element of the brain, and then move to a discussion of the ways in which ...
[5]
Cells of the Nervous System: The Neuron
The main function of neurons is to send electrical signals over short and long distances in the body, and they are electrically and chemically excitable.
[6]
Information about the Brain - NIH Curriculum Supplement Series
When responding to input that requires a very fast response, our nervous system allows sensory neurons to relay information through only one interneuron, or to ...
[7]
Learning the secrets of neural longevity could benefit the aging ...
Oct 3, 2024 · Neurons in the brain can live for more than 90 years, making them exceptional examples of longevity among cells, but scientists know little ...
[8]
Stanford Medicine study hints at ways to generate new neurons in ...
Oct 2, 2024 · Most neurons in the human brain last a lifetime, and for good reason. Intricate, long-term information is preserved in the complex structural ...
[9]
Anatomy, Central Nervous System - StatPearls - NCBI Bookshelf - NIH
Oct 10, 2022 · First-order neurons receive impulses from skin and proprioceptors and send them to the spinal cord. They then synapse with second-order neurons.Introduction · Structure and Function · Embryology · Surgical Considerations
[10]
Neural Systems - Neuroscience - NCBI Bookshelf - NIH
The central nervous system comprises the brain (cerebrum, cerebellum, and brainstem) and the spinal cord. The peripheral nervous system includes sensory neurons ...
[11]
The Human Brain in Numbers: A Linearly Scaled-up Primate Brain
These authors estimated the number of neurons in the human brain at about 85 billion: 12–15 billion in the telencephalon (Shariff, 1953), 70 billion in the ...
[12]
Development and Evolution of Cerebral and Cerebellar Cortex - PMC
The cerebellum contains ~80% of the brain's neurons, but constitutes only ~10% of brain mass because most of its neurons are tiny granule cells packed into a ...
[13]
Neuroanatomy, Motor Neuron - StatPearls - NCBI Bookshelf
Jul 24, 2023 · The upper motor neurons originate in the cerebral cortex and travel down to the brain stem or spinal cord, while the lower motor neurons begin ...
[14]
GENERATION OF DIVERSE CORTICAL INHIBITORY ...
Inhibitory interneurons in the cerebral cortex constitute ~20–30% of the neuronal population. The rich array of interneuron subtypes endows local circuits with ...
[15]
Human Dorsal Root Ganglia - PMC - PubMed Central - NIH
Jun 19, 2019 · Sensory neurons with cell bodies situated in dorsal root ganglia convey information from external or internal sites of the body such as actual or potential ...
[16]
Myelin: A Specialized Membrane for Cell Communication - Nature
Myelinated axons are ensheathed along their entire length. The axon caliber (diameter) in mammalian PNS ranges from 0.1 μm to 20 μm, with unmyelinated axons ...
[17]
Neuroanatomy, Unmyelinated Nerve Fibers - StatPearls - NCBI - NIH
C-type fibers are unmyelinated fibers that form 1 of these groups, and they are involved in the afferent transfer of temperature, burning pain, and itch.
[18]
Parts of a neuron: Structure and functions | Kenhub
Dec 21, 2023 · The basic functions of neurons can be summarized into four main tasks: receiving signals, integrating these signals/generating signals and transmitting the ...
[19]
Nissl Body - an overview | ScienceDirect Topics
Nissl bodies are defined as specialized structures within the cytoplasm of neurons, composed of condensed endoplasmic reticulum and fine granules, ...
[20]
Histology, Axon - StatPearls - NCBI Bookshelf - NIH
In structural terms, the axon hillock may contain fragments of Nissl substance. ... Further study of soma, dendrite, and axon excitation in single neurons.
[21]
The Lipid Bilayer - Molecular Biology of the Cell - NCBI Bookshelf
Biological membranes consist of a continuous double layer of lipid molecules in which membrane proteins are embedded. This lipid bilayer is fluid, with ...
[22]
Structure of the Plasma Membrane - The Cell - NCBI Bookshelf
Proteins embedded within the phospholipid bilayer carry out the specific functions of the plasma membrane, including selective transport of molecules and cell- ...
[23]
Physiology, Resting Potential - StatPearls - NCBI Bookshelf - NIH
Since the plasma membrane at rest has a much greater permeability for K+, the resting membrane potential (-70 to -80 mV) is much closer to the equilibrium ...
[24]
Ion Channels and the Electrical Properties of Membranes - NCBI - NIH
They are responsible for the electrical excitability of muscle cells, and they mediate most forms of electrical signaling in the nervous system. A single neuron ...
[25]
Voltage-gated sodium channels at 60: structure, function and ...
Voltage-gated sodium channels initiate action potentials in nerve, muscle and other excitable cells. The sodium current that initiates the nerve action ...
[26]
POTENTIAL, IMPEDANCE, AND RECTIFICATION IN MEMBRANES ...
Impedance and potential measurements have been made on a number of artificial membranes. Impedance changes were determined as functions of current and of the ...
[27]
The effect of sodium ions on the electrical activity of the giant axon of ...
The effect of sodium ions on the electrical activity of the giant axon of the squid. A. L. Hodgkin,. A. L. Hodgkin. Search for more papers by this author.
[28]
Ion channels in genetic and acquired forms of epilepsy - PMC - NIH
Genetic mutations causing dysfunction of both voltage- and ligand-gated ion channels make a major contribution to the cause of many different types of familial ...Ion Channels In Genetic And... · Ion Channel Defects Modelled... · Table 3Missing: sources | Show results with:sources
[29]
Organization of Cell Types (Section 1, Chapter 8) Neuroscience ...
This section reviews the cellular components of nervous tissue. Students should be able to describe neurons and glia, their morphological components.Missing: somatic | Show results with:somatic
[30]
Neuroscience Review – Introduction to Sensation and Perception
Neurons are broadly divided into four main types based on the number and placement of axons: (1) unipolar, (2) bipolar, (3) multipolar, and (4) pseudounipolar ( ...
[31]
Neuron Structure and Classification - EdTech Books - BYU-Idaho
Multipolar neurons are defined as having three or more processes that extend out from the cell body. They comprise more than 99% of the neurons in humans ...
[32]
The Nervous System and Nervous Tissue - OERTX
Multipolar neurons are all of the neurons that are not unipolar or bipolar. ... Some sources describe a fourth type of neuron, called an anaxonic neuron.
[33]
Three-dimensional organization of dendrites and local axon ...
The group of neurons (n = 19) in which the entire neuron could be visualized, including the cell body, dendritic arborizations and local axon collaterals, was ...
[34]
Morphology of Dendrites | SynapseWeb - University of Texas at Austin
A neuron typically has many dendrites and one axon. The dendrites branch and terminate in the vicinity of the cell body.
[35]
Dendrites Contain a Spacing Pattern - PMC - NIH
The distinctive branching patterns of dendritic arbors are essential for neuronal information processing. The final shape of an arbor is the result of intrinsic ...
[36]
A Threshold Equation for Action Potential Initiation - PubMed Central
Jul 8, 2010 · ... threshold is Nav1.6, which is expressed in the spike initiation zone in the axon hillock [53]–[55]. Sodium channel inactivation and other ...
[37]
Physiology, Action Potential - StatPearls - NCBI Bookshelf - NIH
An action potential is a rapid voltage change across a membrane, involving depolarization (sodium) and repolarization (potassium) in neurons.Missing: squid | Show results with:squid
[38]
Action Potential Initiation in the Hodgkin-Huxley Model - PMC
In 1952, Hodgkin and Huxley explained how action potentials are generated through the electrical excitability of neuronal membranes [1]. Action potentials arise ...
[39]
Increased Conduction Velocity as a Result of Myelination - NCBI - NIH
Unmyelinated axon conduction velocities range from about 0.5 to 10 m/s, myelinated axons can conduct at velocities up to 150 m/s.
[40]
Neuroanatomy, Nodes of Ranvier - StatPearls - NCBI Bookshelf
The purpose of the myelin sheath is to increase the speed of transmission by acting as an electrical insulator. In non-myelinated axons, the action potential ...Introduction · Structure and Function · Embryology · Surgical Considerations
[41]
Characteristic Composition of Myelin - Basic Neurochemistry - NCBI
Myelin basic protein content in the PNS varies from approximately 5 to 18% of total protein, in contrast to the CNS, where it is on the order of 30%. In ...Missing: unmyelinated | Show results with:unmyelinated
[42]
The Myelin Sheath - Basic Neurochemistry - NCBI Bookshelf
CNS myelin is a spiral structure similar to PNS myelin; it has an inner mesaxon and an outer mesaxon that ends in a loop, or tongue, of glial cytoplasm (Fig. 4- ...
[43]
Myelination - an overview | ScienceDirect Topics
years ago as a mechanism to increase conduction velocity 100-fold without requiring an expansion of axon diameter (Zalc, 2015). Indeed, without myelin it is ...
[44]
Neuronal cable theory - Scholarpedia
Mar 17, 2022 · Neuronal cable theory is a set of assumptions and results relating to the propagation and interaction of electrical signals in spatially extended nerve cells.Motivation · Neurites as core conductors · Compartmental Modeling · History
[45]
[PDF] 580.439 Course Notes: Cable Theory Reading
To derive a linear cable equation, it will be assumed that gm is a constant, linear resistance equal to the resting conductance of the membrane. This is an ...
[46]
Two Families of Postsynaptic Receptors - Neuroscience - NCBI - NIH
The receptors in one family—called ionotropic receptors—are linked directly to ion channels (the Greek tropos means to move in response to a stimulus). These ...
[47]
Mechanism of neurotransmitter release coming into focus - PMC
Synaptotagmin‐1 functions as the major Ca2+ sensor that triggers release by binding to membrane phospholipids and to the SNAREs, in a tight interplay with ...
[48]
Molecular Mechanisms Underlying Neurotransmitter Release - PMC
May 9, 2023 · In this model, the SNARE proteins syntaxin-1, SNAP-25 and synaptobrevin form tight complexes that bring the membranes together and are crucial for membrane ...
[49]
Quantal components of the end-plate potential - PMC - NIH
1954 Jun 28;124(3):560–573. ... Quantal components of the end-plate potential. J del Castillo. J del Castillo. Find articles by J del Castillo. , B Katz. B Katz.Missing: hypothesis original
[50]
Number of molecules of neurotransmitter in one synaptic vesicle
Number of molecules of neurotransmitter in one synaptic vesicle ; 5000 unitless · Unspecified · link · Kandel et al., 2000, p. 277 · Many useful facts related to ...Missing: average per
[51]
Neurotransmitter Release and Removal - Neuroscience - NCBI - NIH
The mechanisms by which neurotransmitters are removed vary but always involve diffusion in combination with reuptake into nerve terminals or surrounding glial ...
[52]
Neurotransmitter transporters and their impact on the development ...
Jan 9, 2006 · The transporters for noradrenaline and serotonin are key targets for antidepressant drugs. Both noradrenaline-selective and serotonin-selective ...
[53]
Mechanisms of neuromodulatory volume transmission - Nature
May 24, 2024 · Here, we review literature on mechanisms of volume transmission and raise scientific questions that should be addressed in the years ahead. We ...
[54]
Four-Dimensional Neuronal Signaling by Nitric Oxide
Keywords: nitric oxide, diffusion, nitric oxide synthase, computational modeling, volume signaling, guanylyl cyclase ... distance of 225 μm from the center of the ...
[55]
NO as a signalling molecule in the nervous system - PMC
The distance of this NO diffusion (40 – 300 μm in diameter) implies that ... signal for neuronal nitric oxide. Nat. Cell Biol. 2001;3:193–197. doi ...
[56]
The role of glutamate transporters in the pathophysiology of ... - Nature
Sep 21, 2017 · Glutamate spillover occurs when synaptically released glutamate diffuses from the synapse and activates extrasynaptic receptors or different ...
[57]
Gap Junctions in the Nervous System: Probing Functional ... - Frontiers
Gap junctions are channels that physically connect adjacent cells, mediating the rapid exchange of small molecules, and playing an essential role in a wide ...
[58]
Neuronal Population Coding of Movement Direction - Science
The direction of movement was found to be uniquely predicted by the action of a population of motor cortical neurons.
[59]
Optimal population coding by noisy spiking neurons - PNAS
Here we study optimal coding by networks of noisy neurons with an architecture experimentally observed in retina, cortical culture, and cortical slice—i.e., ...Missing: seminal | Show results with:seminal
[60]
Sparse and Selective Odor Coding by Mitral/Tufted Neurons in the ...
Feb 21, 2007 · We found that M/T activation by odorants was markedly selective, with neurons responding robustly, sensitively, and reliably to only a highly restricted subset ...Missing: percentage | Show results with:percentage
[61]
Neural Burst Firing and Its Roles in Mental and Neurological Disorders
In this review, we summarize recent findings on the mechanisms underlying burst firing in various brain areas, as well as the roles of burst firing in several ...
[62]
Higher-order thalamic relays burst more than first-order relays - PNAS
A key feature of the thalamus is the ability of its relay cells to fire in two distinct modes (called tonic and burst), and the firing mode is determined by the ...
[63]
Distinct burst properties contribute to the functional diversity of ...
Thalamic neurons fire spikes in two modes, burst and tonic. The function of burst firing is unclear, but the evidence suggests that bursts are more effective at ...
[64]
Hyperpolarization-Activated Currents and Subthreshold Resonance ...
Oct 27, 2016 · The hyperpolarization-activated current (Ih) plays an essential role in neuronal function and network oscillatory dynamics throughout the ...
[65]
Chattering Cells: Superficial Pyramidal Neurons Contributing to the ...
... Chattering Cells: Superficial Pyramidal Neurons Contributing to the Generation of Synchronous Oscillations in the Visual Cortex. Charles M. Gray and David A ...
[66]
The Symmetry of Neural Stem Cell and Progenitor Divisions in the ...
May 25, 2022 · Here, we review these examples of cellular neural stem and progenitor cell asymmetries and will discuss how they fit into our current understanding of neural ...
[67]
The Evolution of Early Neurogenesis - PMC - PubMed Central - NIH
Jun 5, 2018 · Neural progenitors may divide in a “stem cell-like”, asymmetric pattern, as shown for the “apical progenitors” of the vertebrate neural tube ( ...
[68]
Radial glia – from boring cables to stem cell stars | Development
Feb 1, 2013 · The discovery in the year 2000 that radial glial cells act as neural stem and progenitor cells in development has led to a change in the ...
[69]
Radial Glia Serve as Neuronal Progenitors in All Regions of the ...
Radial glial cells function during CNS development as neural progenitors, although their precise contribution to neurogenesis remains controversial.
[70]
The Development and Shaping of the Brain - NCBI - NIH
To arrive at the more than 100 billion neurons that are the normal complement of a newborn baby, the brain must grow at the rate of about 250,000 nerve cells ...
[71]
Axon pruning: an essential step underlying the developmental ...
It is well known that approximately 50% of the post-mitotic neurons during development do not survive till adulthood. Many of these neurons die by a natural ...
[72]
Guiding Neuronal Cell Migrations - PMC - PubMed Central - NIH
Neurons use tangential and radial migration to reach their final destination; both strategies are used by the same neurons at different stages of development ( ...
[73]
Reelin Functions, Mechanisms of Action and Signaling Pathways ...
Reelin exerts several important functions in the brain including the regulation of neuronal migration, dendritic growth and branching, dendritic spine ...
[74]
Neuronal Migration During Development of the Cerebellum - Frontiers
Cajal-Retzius cells play an important role during neuronal migration as they secrete Reelin to guide the radial migration of the projection neurons of the ...
[75]
Cerebral cortex development: an outside‐in perspective - FEBS Press
Nov 30, 2017 · Cortical layering arises during embryonic development in an inside-out manner as forebrain progenitors proliferate and generate distinct waves ...Regulation of the biology of... · Local cues influencing the... · Pathophysiological...
[76]
NeuroD1 reprograms chromatin and transcription factor landscapes ...
Oct 29, 2015 · NeuroD1 binding initiates events that confer transcriptional competence to neuronal fate genes including conversion of heterochromatin to ...
[77]
The Role of Neurod Genes in Brain Development, Function, and ...
They control and direct progenitor cell decisions as well as the cellular fate choices to undergo glial or neuronal differentiation. An interesting trait of ...<|separator|>
[78]
The Role of the Slit/Robo Signaling Pathway - PMC - PubMed Central
The Slit/Robo pathway, involving secreted Slit proteins and Robo receptors, regulates neuronal axon guidance, angiogenesis, and tumor cell migration.
[79]
Slit-Robo signaling | Development | The Company of Biologists
Sep 1, 2016 · Slits are secreted proteins that bind to Roundabout (Robo) receptors. Slit-Robo signaling is best known for mediating axon repulsion in the developing nervous ...
[80]
Wallerian degeneration: gaining perspective on inflammatory events ...
Nevertheless, peripheral nervous system (PNS) axon regrowth is hampered by nerve gaps created by injury. In addition, the growth-supportive milieu of PNS axons ...
[81]
Current Status of Therapeutic Approaches against Peripheral Nerve ...
The frequency of regeneration of axon is estimated by alterations within the soma, growth cone stability at the axonal sprout tip, and the hindrance of damaged ...
[82]
Nerve Injury, Axonal Degeneration and Neural Regeneration
Nerve regeneration occurs at a rate of 3–4 mm/day after crush and 2–3 mm/day after sectioning a nerve. Nerve regeneration can be fostered pharmacologically.
[83]
Scar-mediated inhibition and CSPG receptors in the CNS - PMC
Chondroitin sulfate proteoglycans (CSPGs), which are generated by reactive scar tissues, are particularly potent contributors to the growth-limiting environment ...
[84]
The roles of neuronal and glial precursors in overcoming chondroitin ...
The limited regenerative capacity of CNS neurons and the formation of an inhibitory environment at the injury site represent major challenges for regeneration ...
[85]
Peripheral nerve regeneration and neurotrophic factors - PMC
After axotomy and during peripheral nerve regeneration, the neurotrophins NGF, NT-3 and BDNF show a well defined and selective beneficial effect on the survival ...
[86]
BDNF Promotes the Regenerative Sprouting, But Not Survival, of ...
The neurotrophin brain-derived neurotrophic factor (BDNF) has trophic effects on serotonergic neurons and thus is hypothesized to have a role in the treatment ...
[87]
Stem Cell Transplantation Enhances Endogenous Brain Repair after ...
Thus, it has been postulated that transplanted stem cells aid recovery after stroke through secretion of factors that enhance brain repair and plasticity.
[88]
Neuroplasticity - StatPearls - NCBI Bookshelf - NIH
Neuroplasticity can be broken down into two major mechanisms: Neuronal regeneration/collateral sprouting: This includes concepts such as synaptic plasticity and ...Introduction · Issues of Concern · Clinical Significance
[89]
The history of myelin - PMC - PubMed Central
The first to describe myelinated fibers is arguably Antoni van Leeuwenhoek (1632–1723†), draper from the Netherlands Delft (Fig. 1). He was extremely gifted, ...
[90]
Jan Evangelista Purkynje (1787–1869) - PMC - NIH
In 1837, he published a paper about the ganglion cells in the brain, spinal cord, and cerebellum [5]. He was the first to notice the significance of the grey ...Missing: neurons | Show results with:neurons
[91]
The Original Histological Slides of Camillo Golgi and His ...
Feb 18, 2019 · The metallic impregnation invented by Camillo Golgi in 1873 has allowed the visualization of individual neurons in their entirety, leading to a ...
[92]
The Histological Slides and Drawings of Cajal - PMC
There are also some drawings showing details of the cell biology of neurons ... The discovery of dendritic spines by Cajal in 1888 and its relevance in the ...Missing: timeline | Show results with:timeline
[93]
Luigi Galvani - Magnet Academy - National MagLab
Based on such unusual observations Galvani concluded that there was a type of electrical fluid inherent in the body, which he dubbed animal electricity.
[94]
a century of in vivo motor unit recordings is the legacy of Adrian and ...
Dec 7, 2023 · In two papers dated 1928 to 1929 in The Journal of Physiology, Edgar Adrian and Detlev Bronk described recordings from motor nerve and muscle fibres.
[95]
The discovery of synaptic vesicles - PMC - NIH
Jan 3, 2005 · When the Journal of Cell Biology was born, in 1955, electron microscopy (EM) was a new but booming source of biological information.
[96]
CRISPR screening by AAV episome-sequencing (CrAAVe-seq)
Aug 22, 2025 · Using CrAAVe-seq, we profiled neuron-essential genes in the mouse brain across different neuronal subpopulations, using libraries containing ~ ...
[97]
Life and discoveries of Santiago Ramón y Cajal - NobelPrize.org
Apr 20, 1998 · ... Cajal and of the “neuron doctrine,” which would be officially enunciated by Wilhelm Waldeyer (1836-1921) in 1891. Cajal was fiercely opposed ...
[98]
The Neuron Doctrine (1860-1895) | Embryo Project Encyclopedia
Jun 15, 2017 · Ramón y Cajal suggested that neural bodies are not connected with a continuous network of axons and dendrites. Rather, neural bodies function ...
[99]
The Neuron Doctrine: Santiago Ramón y Cajal and Camillo Golgi
Feb 16, 2023 · ... Cajal's neuron doctrine, the term used by Wilhelm Waldeyer (1836–1921) in 1891, who also invented the name “neuron.” Golgi's “reticularist ...<|control11|><|separator|>
[100]
Neuron Doctrine - an overview | ScienceDirect Topics
Electron microscopy conclusively shows that nerve cells are separate, but the neuron doctrine needs careful revision. Indeed, this has gone forward. Four issues ...
[101]
Observations of synaptic structures: origins of the neuron doctrine ...
Electron microscopic studies confirm this. They show that at synapses such as those made by mossy fibres or on motor neurons, the light microscopically ...
[102]
Speed read: Exposing the forest - NobelPrize.org
Sep 16, 2009 · The 1906 Nobel Prize in Physiology or Medicine was awarded to Camillo Golgi and Santiago Ramón y Cajal for revealing the inner beauty of the nervous system.
[103]
Reflecting on the Nobel Prize Awarded to Golgi and Cajal in 1906
The first conclusion became known as the neuron doctrine and, unlike the reticular theory, allowed for control points between neurons in a circuit—the ...
[104]
Etymology and the neuron(e) - PMC - PubMed Central
Dec 17, 2019 · Waldeyer coined the term 'die Neuronen' (singular 'das Neuron'), as an alternative for 'Nerveneinheiten' or 'nerve units': Figure 2. Figure 2.
[105]
1896–1996: The Centennial of the Axon - ScienceDirect.com
The term “axon” was coined by Koelliker in 1896. To celebrate the occasion of this centennial, the contributions made in the 19th century by Remak and ...
[106]
Peripheral Neuropathy | National Institute of Neurological Disorders ...
Aug 7, 2024 · Acquired neuropathies can be symptomatic (the result of another disorder or condition) or idiopathic (meaning it has no known cause). Diabetes ...Charcot-Marie-Tooth Disease · Guillain-Barré Syndrome · Friedreich Ataxia
[107]
Dementia - World Health Organization (WHO)
Mar 31, 2025 · In 2021, 57 million people had dementia worldwide, over 60% of whom live in low-and middle-income countries. Every year, there are nearly 10 ...
[108]
Development of an optogenetic toolkit for neural circuit dissection in ...
Apr 30, 2018 · Optogenetic tools have opened a rich experimental landscape for understanding neural function and disease. Here, we present the first ...
[109]
What Happens to the Brain in Alzheimer's Disease?
Jan 19, 2024 · Neurofibrillary tangles are abnormal accumulations of a protein called tau that collect inside neurons. Healthy neurons are supported internally ...
[110]
Amyloid-β and tau: the trigger and bullet in Alzheimer disease ...
The behavioral symptoms of AD correlate with the accumulation of plaques and tangles, and they are a direct consequence of the damage and destruction of ...
[111]
Determinants of dopaminergic neuron loss in Parkinson's disease
The cardinal motor symptoms of Parkinson's disease (PD) are caused by the death of dopaminergic neurons in the substantia nigra pars compacta (SNc).
[112]
Parkinson's Disease, the Dopaminergic Neuron and ...
Jan 24, 2018 · The high energy demands of the substantia nigra pars compacta dopaminergic (DASNc) neurons render these neurons vulnerable to degeneration.
[113]
Basic Mechanisms Underlying Seizures and Epilepsy - NCBI
Despite major differences in etiology, the outcome of synchronous bursting of cortical neurons may superficially appear to have a similar phenotype. Seizure ...
[114]
Synchronization and desynchronization in epilepsy - NIH
Epilepsy has been historically seen as a functional brain disorder associated with excessive synchronization of large neuronal populations leading to a ...
[115]
Huntington Disease - StatPearls - NCBI Bookshelf - NIH
Apr 6, 2025 · Huntington disease is a hereditary neurodegenerative disorder, inherited in an autosomal dominant manner, caused by an expansion of CAG trinucleotide repeats ...
[116]
Spinocerebellar Ataxia - StatPearls - NCBI Bookshelf
Sep 15, 2023 · Spinocerebellar ataxia (SCA) is a progressive neurodegenerative inherited (autosomal dominant) heterogeneous disease that mainly affects the cerebellum.
[117]
Molecular mechanisms of excitotoxicity and their relevance to ...
This review discusses the current understanding of excitotoxic mechanisms and how they are involved in the pathogenesis of neurodegenerative diseases.
[118]
Molecular mechanisms of excitotoxicity and their relevance to the ...
May 19, 2025 · Excitotoxicity is a key neurodegenerative mechanism that disrupts neuronal function and survival in CNS disorders [139]. Over the past decade, ...
[119]
Molecular mechanisms of ischemia and glutamate excitotoxicity
Sep 1, 2023 · Excitotoxicity is characterized by the extracellular accumulation of high concentrations of glutamate or other excitatory amino acids, leading to excessive ...
[120]
Oxidative Stress, Mitochondrial Dysfunction, and Aging - PMC
Many studies have demonstrated that oxidative stress and mitochondrial dysfunction are two important factors contributing to the aging process.
[121]
Mitochondria in oxidative stress, inflammation and aging - Nature
Jun 11, 2025 · This review hypothesizes that mitochondria serve as central hubs regulating oxidative stress, inflammation, and aging, and their dysfunction contributes to ...
[122]
Wallerian degeneration: From mechanism to disease to imaging
Jan 15, 2025 · Wallerian degeneration (WD) was first discovered by Augustus Waller in 1850 in a transection of the glossopharyngeal and hypoglossal nerves in frogs.Missing: stripping | Show results with:stripping
[123]
The role of microglia in synaptic stripping and synaptic degeneration
We review here the evidence for the involvement of microglia in synaptic stripping and synapse degeneration and we conclude that this is a case of guilt by ...
[124]
Multiple sclerosis: molecular pathogenesis and therapeutic ... - Nature
Oct 2, 2025 · Proinflammatory cytokines and matrix metalloproteinases degrade the BBB, allowing autoreactive lymphocytes to attack myelin sheaths, leading to ...
[125]
Regulation of Programmed Cell Death - The Cell - NCBI Bookshelf
Neurons are produced in excess, and up to 50% of developing neurons are eliminated by programmed cell death. Those that survive are selected for having made ...
[126]
Programmed cell death during neuronal development - Nature
Apr 25, 2014 · Apoptosis occurs extensively during the normal development of the mammalian nervous system and has been observed in populations of developing ...
[127]
Tau in neurodegenerative diseases: molecular mechanisms ...
Aug 6, 2024 · In this review, we briefly introduce several tauopathies and discuss the mechanisms mediating tau aggregation and propagation. We also describe ...