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Trisynaptic circuit

The trisynaptic circuit is a canonical neural pathway in the mammalian hippocampus that relays sensory and cognitive information from the entorhinal cortex through three sequential synaptic relays, forming a core component of hippocampal processing.^[1] It consists of the perforant pathway, which originates in layer II of the entorhinal cortex and projects to the granule cells of the dentate gyrus; the mossy fiber pathway, connecting dentate gyrus granule cells to pyramidal neurons in the CA3 subfield; and the Schaffer collaterals, which link CA3 pyramidal neurons to those in the CA1 subfield.^[2] This circuit extends longitudinally along the septotemporal axis of the hippocampus, enabling coordinated excitation and inhibition across its subregions.^[3] The trisynaptic circuit is essential for memory functions, particularly the acquisition and recall of episodic and spatial memories, by integrating neocortical inputs and facilitating their consolidation into long-term storage through outputs from CA1 and the subiculum to the limbic system and neocortex.^[2] Disruptions in this pathway, such as those observed in Alzheimer's disease, impair memory formation due to its role in synaptic plasticity mechanisms like long-term potentiation (LTP).^[1] First described in detail through anatomical studies in the early 20th century, the circuit has been a focal point of neuroscience research, revealing its involvement in network dynamics like high-frequency oscillations and feedforward inhibition that refine information flow.^[3]

Overview

Definition and Pathway

The trisynaptic circuit is the primary excitatory neural pathway within the mammalian hippocampus, characterized by a sequential flow through three major synaptic relays: from layer II neurons of the entorhinal cortex (EC) to granule cells in the dentate gyrus (DG), then to pyramidal cells in cornu ammonis 3 (CA3), and finally to pyramidal cells in cornu ammonis 1 (CA1).^[2]^[4] This circuit serves as the canonical route for information processing in the hippocampal formation, integrating cortical inputs for downstream functions.^[5] The pathway begins with the perforant path, where axons from EC layer II neurons project to the outer molecular layer of the DG, forming excitatory synapses onto the dendrites of granule cells.^[1] These granule cells then extend mossy fiber axons that synapse onto the proximal dendrites of CA3 pyramidal cells in the stratum lucidum, providing a high-fidelity relay with large, multivesicular boutons.^[6] From CA3, the Schaffer collaterals—axonal branches of pyramidal cells—project to the apical dendrites of CA1 pyramidal cells in the stratum radiatum, completing the trisynaptic loop and enabling output to subcortical and cortical targets.^[7]^[5] Transmission across all three synapses is predominantly glutamatergic, utilizing ionotropic receptors such as AMPA and NMDA subtypes to mediate fast excitatory postsynaptic potentials and plasticity mechanisms like long-term potentiation.^[2]^[8] This neurochemical uniformity supports efficient signal propagation and synaptic modification.^[6] The trisynaptic circuit exhibits evolutionary conservation across mammalian species, forming a core architectural feature of the hippocampal formation that has been maintained through phylogenetic adaptations.^[9]^[10] Its standardized connectivity has positioned it as a foundational model for investigating neural circuit dynamics, synaptic integration, and computational principles in the hippocampus.^[11]^[12]

Anatomical Significance

The trisynaptic circuit is situated within the hippocampal formation, a key component of the medial temporal lobe, positioned medial to the inferior horn of the lateral ventricle in each cerebral hemisphere.^[13] This formation encompasses the dentate gyrus, the cornu ammonis regions (CA1–CA3), and the subicular complex, which includes the subiculum, presubiculum, parasubiculum, and entorhinal cortex, all embedded as an integrated unit within the broader limbic system of the medial temporal lobe.^[13] The circuit's anatomical placement underscores its role as a gateway for cortical inputs to the hippocampus, facilitating structured information processing through its core structures. In terms of scale, the trisynaptic circuit involves approximately 1–2 million principal neurons across its primary components in rodents, with the dentate gyrus containing the highest density of granule cells, estimated at up to 1.2 million per hippocampal formation.^[14] These numbers reflect the circuit's capacity for extensive parallel processing, where granule cells in the dentate gyrus outnumber upstream entorhinal inputs, enabling sparse and patterned representation of sensory information.^[15] The circuit exhibits a strictly unidirectional flow of information, progressing from the entorhinal cortex through the dentate gyrus to CA3 and then CA1, in contrast to alternative monosynaptic paths (such as direct layer III entorhinal projections to CA1) or disynaptic routes (like entorhinal inputs bypassing the dentate to reach CA3 directly).^[16] This trisynaptic specificity ensures sequential elaboration of signals, introducing temporal delays and integrative opportunities not present in shorter pathways.^[17] Understanding the trisynaptic circuit is prerequisite to appreciating the hippocampal formation's laminar organization, where projections from the entorhinal cortex—particularly from its layer II—terminate in a highly ordered, trilaminar fashion within the dentate gyrus's molecular layer, dividing it into outer, middle, and inner sublayers based on input sources.^[15] This layered architecture, with entorhinal afferents occupying the outer two-thirds, exemplifies the circuit's precision in synaptic targeting and supports the broader trilaminar cytoarchitecture of allocortical regions like the entorhinal cortex itself.^[15]

Historical Development

Discovery and Early Descriptions

Theodor Meynert discussed the hippocampal formation in his 1868 book on brain anatomy, providing early observations on its organization and connections to adjacent cortical regions.^[18] These 19th-century accounts built on prior macroscopic views of the hippocampal formation but introduced microscopic insights into its laminar architecture, emphasizing the transitional nature of entorhinal-hippocampal interfaces. Meynert's work highlighted the layered cellular arrangement in the hippocampus, which would later inform interpretations of information flow through the region.^[18] Advancing into the late 19th and early 20th centuries, Santiago Ramón y Cajal employed the Golgi staining technique between 1893 and 1909 to visualize key cellular elements of the circuit, notably the granule cells in the dentate gyrus and their unmyelinated axons forming mossy fibers that project to the CA3 region.^[19] In his comprehensive 1911 publication Histologie du système nerveux de l'homme et des vertébrés, Cajal illustrated these connections with unprecedented clarity, revealing the mossy fibers' characteristic varicosities and thorny excrescences that synapse onto CA3 pyramidal cells, thus delineating a critical segment of the pathway.^[20] This Golgi-based approach not only confirmed the discrete neuronal elements but also suggested a sequential relay mechanism within the hippocampus, influencing subsequent anatomical models.^[19] In the 1930s and 1940s, Rafael Lorente de Nó extended these observations through meticulous Golgi analyses, producing detailed mappings of hippocampal intrinsic circuits in his seminal 1934 paper "Studies on the Structure of the Cerebral Cortex."^[21] Lorente de Nó integrated Cajal's cellular details into a cohesive framework for hippocampal intrinsic circuits, describing the connections from mossy fibers to CA3 and Schaffer collaterals to CA1, while defining the cytoarchitectonic subdivisions of the cornu Ammonis fields.^[22] His descriptions proposed a sequential pathway as the primary route for cortical-hippocampal processing.^[21] Early characterizations sparked debates on the pathway's completeness, particularly concerning the precise termination of entorhinal perforant path fibers and potential direct projections bypassing the dentate gyrus. These uncertainties were largely resolved by mid-20th-century tract-tracing studies, including Trygve Blackstad's 1958 application of the Nauta silver impregnation method, which confirmed the perforant path's dual projections to the dentate gyrus and CA fields while validating the loop's integrity.^[23] Such techniques provided unequivocal evidence of the circuit's sequential connectivity, solidifying the trisynaptic model against alternative reticular interpretations.^[24]

Key Researchers and Milestones

In the 1950s, John D. Green and colleagues pioneered the use of evoked potential recordings to map the sequential activation of the trisynaptic circuit in the hippocampus, demonstrating the flow from entorhinal cortex to dentate gyrus, CA3, and CA1 in anesthetized cats and rabbits.^[25] These electrophysiological studies provided the first functional confirmation of the circuit's relay-like organization, establishing a foundational model for subsequent investigations. During the 1970s and 1980s, Per Andersen and his team advanced this understanding through intracellular recordings in hippocampal slices, revealing synaptic potentiation mechanisms along the pathway, including frequency-dependent enhancement at perforant path-dentate and Schaffer collateral-CA1 synapses. Their work highlighted the circuit's capacity for activity-dependent plasticity, using in vitro preparations to isolate and characterize excitatory transmission dynamics.^[26] In the 1990s, Tim Bliss and Terje Lømo extended their seminal LTP discoveries to specific synapses within the trisynaptic circuit, showing robust long-term potentiation at mossy fiber-CA3 and Schaffer collateral-CA1 connections in rat hippocampal slices, which underscored the pathway's role in enduring synaptic strengthening. These findings linked circuit-level plasticity to potential memory mechanisms, with mossy fiber LTP exhibiting presynaptic expression and Schaffer collateral LTP involving NMDA receptor activation.^[27] From the 2000s onward, technological advances like optogenetics and viral tracing refined circuit mapping, with Menno Witter and colleagues in the 2010s delineating entorhinal layer-specific projections using anterograde tracers in rodents, clarifying how layer II inputs drive the dentate gyrus leg and layer III inputs bypass it to reach CA1 directly. By the 2020s, connectomics efforts in mouse models, including electron microscopy reconstructions of hippocampal subregions, confirmed the precision of trisynaptic wiring, revealing synaptic densities and convergence patterns that align with classical descriptions while identifying subtle variations in connectivity fidelity.^[28] Post-2020 milestones include human in vivo imaging studies using high-resolution functional imaging to examine hippocampal activity during memory tasks, such as episodic encoding, where signals in the hippocampus correlated with successful recall in healthy adults.^[29] These non-invasive approaches have bridged rodent models to human cognition, demonstrating circuit engagement in relational memory formation.^[29]

Core Structures

Entorhinal Cortex

The entorhinal cortex serves as the primary origin of the trisynaptic circuit, relaying cortical inputs to the hippocampus through its superficial layers. Layer II of the entorhinal cortex contains the principal neurons responsible for initiating this pathway, consisting predominantly of stellate cells and pyramidal cells. Stellate cells, characterized by their multipolar morphology and reelin expression, are abundant in the medial entorhinal cortex, while pyramidal cells, often calbindin-positive, are found in both medial and lateral regions. These layer II neurons extend glutamatergic axons that form the perforant path, projecting directly to the outer molecular layer of the dentate gyrus.^[30] The projections from the entorhinal cortex exhibit a distinct topographical organization, with the lateral entorhinal cortex (LEC) and medial entorhinal cortex (MEC) contributing differentially to the circuit. The LEC, connected to object- and feature-based sensory areas such as the perirhinal cortex, conveys non-spatial "what" information via the lateral perforant path, targeting the outer third of the dentate gyrus molecular layer. In contrast, the MEC, linked to spatial processing regions like the presubiculum, transmits "where" or spatial cues through the medial perforant path, innervating the middle third of the same layer. This segregation allows the trisynaptic circuit to integrate object recognition and navigational information at its input stage.^[31]^[32] Synaptically, the perforant path axons from layer II neurons form en passant synapses onto the distal dendrites of dentate granule cells, utilizing glutamate as the primary neurotransmitter to drive excitatory transmission. These synapses are distributed along the axonal trajectory, enabling broad convergence onto multiple granule cells and facilitating pattern separation in the circuit. In humans, layer II of the entorhinal cortex contains approximately 650,000 neurons per hemisphere, underscoring its substantial contribution to hippocampal input.^[33]^[34] Notably, the MEC harbors grid cells, which fire in a hexagonal lattice pattern during spatial navigation and provide periodic spatial representations that influence the trisynaptic circuit's processing of environmental geometry. These cells, primarily located in superficial layers including layer II, encode self-motion and distance metrics, enhancing the circuit's role in path integration.^[35]

Dentate Gyrus

The dentate gyrus serves as the primary relay station in the trisynaptic circuit, receiving inputs from the entorhinal cortex via the perforant path and relaying processed signals to CA3 through its principal granule cells. These granule cells are small, spindle-shaped neurons densely packed in a V-shaped layer, with an estimated 10-15 million cells in the human hippocampus, far outnumbering pyramidal cells in other hippocampal subfields. Each granule cell features a compact soma and extensive apical dendrites that extend into the molecular layer to receive excitatory glutamatergic inputs primarily from the perforant path, enabling integration of spatial and contextual information.^[36]^[15] The output of granule cells occurs via mossy fibers, which are unmyelinated axons that project to the CA3 region, forming the second leg of the trisynaptic pathway. These fibers are characterized by large, thorn-like boutons that synapse onto the proximal dendrites of CA3 pyramidal cells, with each granule cell axon contacting up to 15-50 such targets, facilitating powerful but divergent excitation. Mossy fibers also release zinc ions upon activation, which can modulate synaptic transmission and contribute to network dynamics within the hilus.^[15]^[37]^[38] A key functional feature of the dentate gyrus is its implementation of sparse coding, where granule cells exhibit high activation thresholds, resulting in only a small fraction (typically 1-4%) firing in response to inputs, which helps orthogonalize similar patterns for enhanced discriminability. This sparse representation is thought to underlie pattern separation, a computational process that reduces overlap between similar sensory inputs, such as distinguishing contexts that differ subtly in space or time, thereby supporting distinct memory engrams. Hilar interneurons, including GABAergic basket cells that provide perisomatic inhibition and glutamatergic mossy cells that offer excitatory feedback, modulate granule cell activity to refine this sparsity and prevent overexcitation.^[39]^[40]^[41] Adult neurogenesis continuously replenishes the granule cell population in the subgranular zone of the dentate gyrus, with approximately 700 new neurons added daily in each human hippocampus, integrating into the existing circuit to potentially enhance plasticity and adaptability. These newborn granule cells initially exhibit heightened excitability before maturing to adopt the sparse firing properties of the resident population, contributing to the circuit's role in learning and memory formation.^[42]

Cornu Ammonis 3 (CA3)

The Cornu Ammonis 3 (CA3) region serves as a critical associative hub within the trisynaptic circuit of the hippocampus, characterized by its dense network of pyramidal neurons that integrate and process inputs from the dentate gyrus via mossy fibers. These pyramidal cells, numbering approximately 200,000 to 330,000 per hippocampus in rodents, feature large apical dendrites with specialized thorny excrescences that receive mossy fiber inputs on their proximal portions, facilitating strong excitatory drive.^[43]^[44] The basal dendrites of these neurons, in contrast, primarily accommodate recurrent collateral inputs from other CA3 cells, while the distal apical dendrites extend into the stratum lacunosum-moleculare to receive direct perforant path projections from the entorhinal cortex. This dendritic architecture enables CA3 pyramidal cells to perform complex computations, with their somata concentrated in the stratum pyramidale and axons forming extensive recurrent connections that span the region.^[44]^[45] A defining feature of CA3 is its recurrent collateral system, where axons of pyramidal cells form excitatory synapses onto the dendrites of neighboring pyramidal cells, creating an auto-associative network capable of pattern completion. This recurrent connectivity, with connection probabilities around 4-6% between pyramidal cells, allows partial or degraded input patterns to retrieve complete stored representations, a process essential for memory recall and associative learning. Theoretical and experimental models demonstrate that this network's high recurrent excitation supports the storage of thousands of memory patterns, with synaptic weights adjusted via Hebbian plasticity to enhance recall fidelity. The system's symmetry in bidirectional connectivity further enables efficient auto-association, distinguishing CA3 from upstream sparse-coding stages like the dentate gyrus.^[46]^[47]^[48] Synaptic dynamics at mossy fiber-CA3 synapses exhibit a high initial vesicle release probability (approximately 0.2-0.4), which facilitates rapid short-term facilitation and supports the quick induction of long-term potentiation (LTP) during high-frequency stimulation. This high release probability, coupled with multivesicular release from large boutons, ensures robust transmission of dentate gyrus signals into CA3, promoting associative integration while minimizing failure rates under physiological conditions. Such properties underlie CA3's role in rapid plasticity, where even brief bursts can trigger associative changes that propagate through the recurrent network.^[49]^[50]^[51] Place cells emerge prominently in CA3, where they encode spatial maps with greater overlap and complexity compared to the sparser representations in the dentate gyrus, allowing for the integration of contextual and episodic information. These cells fire in multiple, distinct place fields that can remap independently across environments, reflecting CA3's capacity for orthogonal storage of spatial memories through its recurrent dynamics. Inhibitory networks in CA3, dominated by parvalbumin-expressing basket interneurons, provide precise perisomatic control, targeting the soma and proximal dendrites of pyramidal cells to regulate firing rates and synchronize population activity during theta rhythms. These fast-spiking interneurons, comprising about 10-15% of local GABAergic cells, enforce sparse activity patterns and prevent runaway excitation in the recurrent network.^[52]^[53]^[54]^[55]

Cornu Ammonis 1 (CA1)

The Cornu Ammonis 1 (CA1) region serves as the primary output station of the trisynaptic circuit in the hippocampus, characterized by its distinct laminar architecture that enables segregated processing of convergent inputs. The stratum lacunosum-moleculare (SLM) occupies the outermost layer and receives direct excitatory inputs from layer III of the entorhinal cortex via the temporoammonic pathway, providing non-spatial contextual information. In contrast, the stratum radiatum, located below the pyramidal cell layer, is the primary site for Schaffer collateral inputs originating from CA3 pyramidal neurons, which convey processed spatial and associative data from upstream circuit stages. This layered organization allows CA1 to integrate disparate signals in a spatially organized manner, with dendritic compartments in each stratum tuned to specific afferent sources.^[56] CA1 is predominantly composed of pyramidal neurons, numbering approximately 5 million in the human hippocampus, which feature prominent apical dendrites extending upward through the stratum radiatum and branching tufts in the SLM to maximize input reception. These apical dendrites are smooth and lack the thorny excrescences characteristic of CA3 neurons, instead forming numerous spines that support glutamatergic synapses. Schaffer collateral synapses onto these dendrites in the stratum radiatum exhibit particularly high susceptibility to long-term potentiation (LTP), a form of Hebbian plasticity essential for strengthening connections following coincident activity, as demonstrated in foundational slice physiology studies. This LTP induction typically requires NMDA receptor activation and is a key mechanism for activity-dependent modifications in CA1 output.^[57] Through its integrative role, CA1 synthesizes temporal associations by combining sequential patterns from CA3 with contextual cues from the entorhinal cortex, supporting sequence learning in behavioral tasks such as trace conditioning. The axons of CA1 pyramidal neurons converge in the alveus, a superficial white matter bundle, before diverging to project heavily to the subiculum and layer V of the entorhinal cortex, thereby relaying processed hippocampal information back to neocortical circuits and facilitating memory consolidation. These projections form the gateway for hippocampal output to broader limbic and cortical networks.^[58]^[59] CA1 displays heightened vulnerability in neurodegenerative conditions, emerging as an early site of tau pathology in Alzheimer's disease, where hyperphosphorylated tau aggregates preferentially accumulate in pyramidal somata and proximal dendrites. This pathology disrupts synaptic function partly through alterations in NMDA receptor subtypes, notably GluN2B-containing receptors at Schaffer collateral synapses, leading to excitotoxicity and impaired LTP. Such selective degeneration in CA1 contributes to early episodic memory deficits observed in the disease.^[60]^[61]

Connections and Associated Areas

Afferent Inputs

The trisynaptic circuit receives a direct monosynaptic input from layer III of the entorhinal cortex to the CA1 region, bypassing the dentate gyrus and CA3, which provides an alternative pathway for cortical information to reach CA1 pyramidal cells and supports rapid temporal coding and spatial representation.^[62] This projection originates from glutamatergic neurons in both the lateral and medial entorhinal cortex, conveying non-spatial and spatial inputs, respectively, and is crucial for maintaining hippocampal output under conditions where the full trisynaptic loop may be less engaged.^[63] Lesions to this direct pathway impair spatial memory performance, highlighting its functional independence from the classical trisynaptic route.^[64] Cholinergic afferents to the trisynaptic circuit arise primarily from the medial septum and diagonal band of Broca, releasing acetylcholine that modulates synaptic plasticity and network dynamics across the entorhinal cortex, dentate gyrus, and CA regions.^[65] These inputs enhance attention-related gating by increasing the excitability of principal neurons and suppressing interneurons, thereby facilitating selective information processing during cognitive tasks.^[66] Septal cholinergic neurons exhibit target selectivity, with projections densely innervating the hippocampus to regulate theta oscillations, which are essential for coordinating circuit activity in response to behavioral demands.^[67] Dopaminergic modulation of the trisynaptic circuit stems from the ventral tegmental area, with projections targeting the dentate gyrus to influence granule cell activity and promote novelty detection.^[68] This input forms a functional loop with the hippocampus, where dopamine release signals environmental novelty, gating the entry of salient information into long-term memory storage.^[69] Activation of D1/D5 receptors in the dentate gyrus by these afferents strengthens synaptic plasticity for novel stimuli, enabling adaptive learning while weak or familiar inputs are filtered.^[70] Noradrenergic inputs from the locus coeruleus project densely to the hippocampus, particularly the dentate gyrus, where they enhance signal-to-noise ratios during stress by modulating neuronal excitability and synaptic transmission.^[71] Norepinephrine release under stress conditions activates β-adrenergic receptors, sharpening hippocampal responses to relevant stimuli and suppressing irrelevant noise, which supports adaptive behavioral adjustments.^[72] This modulation is phasic during acute stress, transiently boosting circuit gain to prioritize threat-related processing.^[73] Serotonergic projections from the raphe nuclei, including both dorsal and median raphe, innervate the trisynaptic circuit to regulate mood-related activity, with fibers targeting CA1 and other hippocampal subfields to influence emotional memory consolidation.^[74] These inputs fine-tune excitatory transmission and oscillatory patterns, promoting resilience to mood perturbations by modulating serotonin receptor-mediated inhibition in principal neurons.^[75] Dorsal raphe serotonin neurons projecting to CA1 are particularly involved in anxiety-like behaviors, where their activation suppresses excessive fear responses through circuit-wide dampening.^[76]

Efferent Outputs

The efferent outputs of the trisynaptic circuit primarily originate from the CA1 region and the entorhinal cortex, serving to relay processed information to downstream targets in subcortical and cortical structures. Pyramidal neurons in CA1 project their axons through the alveus, a layer of white matter on the ventricular surface, to the subiculum, which acts as a key gateway for further dissemination.^[24] From the subiculum, these projections continue via the postcommissural fornix, a major fiber bundle arching around the thalamus, to reach the mammillary bodies and anterior thalamic nuclei. Specifically, the medial mammillary nucleus receives light but direct input from ventral CA1 via this route, while projections to the paraventricular and interanteromedial nuclei of the anterior thalamus are similarly sparse but contribute to diencephalic relay.^[24] In primates, such as macaque monkeys, these subicular efferents to the medial mammillary nucleus are denser from caudal portions and travel exclusively through the fornix, with minimal direct contributions from CA1 itself. Layer V pyramidal cells in the entorhinal cortex provide additional efferent feedback, projecting to prefrontal and association cortices to facilitate reciprocal loops with neocortical areas. These projections target the prelimbic region of the medial prefrontal cortex, originating from distinct subregions of layers V and VI, and support the integration of hippocampal outputs with higher-order cognitive processing. In rodents, entorhinal layer V efferents to the medial prefrontal cortex exhibit topographic organization, with superficial neurons receiving stronger input from the medial entorhinal cortex to close memory-related circuits.^[77] A subset of CA1 pyramidal neurons, particularly in the ventral hippocampus, sends direct projections to the lateral septum, providing an additional outflow pathway for tagging information with emotional valence. These glutamatergic axons form unilateral connections, influencing septal GABAergic neurons and contributing to the modulation of social and anxiety-related behaviors.^[78]^[79] Topographically, approximately 80% of the total hippocampal output is channeled through the CA1-subiculum pathway, emphasizing its dominance in efferent signaling over direct CA1 projections to other sites. This route ensures efficient distribution to limbic and diencephalic targets, with dorsal CA1-subiculum fibers favoring anterior thalamic relays and ventral portions targeting mammillary regions.^[80] The axons in the fornix, including those from CA1-subiculum projections, are partially myelinated, enabling rapid conduction velocities essential for timely information relay across distant brain regions. Myelination in the fornix begins with large pyramidal cell axons from the hippocampus and subiculum, forming a compact white matter tract that supports the circuit's efficiency.^[13]^[81]

Integration with Limbic Structures

The trisynaptic circuit integrates with the basolateral amygdala (BLA) through reciprocal connections with the entorhinal cortex, enabling the incorporation of emotional information into hippocampal processing. The BLA sends direct projections to the medial entorhinal cortex, which serves as a gateway for amygdala influences on memory consolidation, particularly in contextual fear conditioning where BLA activity modulates the encoding of fear-associated spatial contexts.^[82] These projections facilitate the integration of aversive stimuli with hippocampal representations, as evidenced by optogenetic inhibition of BLA-entorhinal pathways impairing fear memory formation without affecting non-emotional spatial learning.^[83] Reciprocal inputs from the entorhinal cortex to the BLA further support bidirectional emotional modulation of trisynaptic activity, allowing fear signals to refine hippocampal output during threat detection.^[84] The anterior cingulate cortex (ACC) connects to the trisynaptic circuit indirectly via the medial septal pathway, contributing to conflict monitoring and motivational regulation of memory processing. ACC projections to the medial septum provide cholinergic modulation that influences hippocampal theta oscillations, enhancing attention to emotionally salient conflicts during decision-making tasks.^[85] This pathway allows the ACC to gate trisynaptic inputs for adaptive behavior, as disruptions in ACC-medial septum interactions impair error detection and conflict resolution linked to hippocampal-dependent learning.^[86] Outputs from the cingulate gyrus to entorhinal regions via diencephalic relays further integrate cognitive control over limbic-driven responses in the trisynaptic loop.^[87] The mammillary bodies form a critical diencephalic relay in the trisynaptic circuit through the mammillary-thalamus-fornix loop, supporting spatial memory consolidation. Hippocampal projections via the fornix terminate in the mammillary bodies, which in turn excite the anterior thalamic nuclei, relaying back to the cingulate and entorhinal cortices to reinforce episodic-spatial representations.^[88] Lesions in this loop disrupt consolidation of spatial memories, highlighting its role in stabilizing trisynaptic outputs for long-term storage without altering initial encoding.^[81] This circuit integrates limbic feedback to prioritize motivationally relevant spatial contexts, as seen in tasks requiring navigation under emotional duress.^[89] Hypothalamic links to the trisynaptic circuit occur primarily via the mammillary bodies, coupling hippocampal activity with autonomic responses for survival-oriented memory. The supramammillary nucleus, an extension of the hypothalamus, projects directly to the dentate gyrus and CA fields, modulating stress-induced plasticity in response to autonomic arousal.^[90] These connections enable hypothalamic regulation of hippocampal excitability during threat, linking emotional states to physiological adjustments like heart rate variability tied to memory retrieval.^[91] Functionally, these limbic integrations assign emotional valence to spatial and episodic memories processed by the trisynaptic circuit, enhancing adaptive encoding. Amygdala-entorhinal interactions imbue contextual memories with fear or reward salience, while mammillary-hypothalamic relays consolidate motivationally driven spatial maps.^[92] Cingulate modulation via septal pathways ensures conflict-sensitive prioritization, allowing the circuit to differentiate neutral from emotionally charged experiences for behavioral flexibility.^[93]

Physiological Functions

Role in Memory and Learning

The trisynaptic circuit in the hippocampus plays a pivotal role in memory formation and learning by enabling the orthogonalization, storage, and retrieval of episodic and spatial memories through specialized processing at each stage. In the dentate gyrus, pattern separation transforms similar input representations from the entorhinal cortex into distinct neural patterns, minimizing interference between overlapping experiences and facilitating the encoding of unique memory traces.^[94] This process is crucial for distinguishing subtle contextual differences, such as slight variations in spatial environments during navigation tasks. Subsequent transmission to CA3 supports pattern completion, where partial or degraded cues can reconstruct full memory representations via recurrent collaterals, allowing rapid recall of complete episodes from fragmentary reminders.^[95] Finally, CA1 integrates these signals for consolidation and output to cortical areas, refining memory traces for long-term storage and behavioral expression. A key mechanism underlying these functions is long-term potentiation (LTP), a form of synaptic plasticity that strengthens connections across the circuit. High-frequency stimulation of Schaffer collaterals (from CA3 to CA1) induces LTP, resulting in synaptic strengthening exceeding 200% of baseline efficacy, which persists for hours and models the cellular basis of memory engrams. This Hebbian learning principle—"cells that fire together wire together"—operates across the three synapses, promoting associative strengthening when correlated activity occurs, as seen in the co-activation of entorhinal inputs with dentate outputs or CA3 patterns with CA1 responses.^[96] Such plasticity ensures that repeated exposure to stimuli refines memory precision without overwriting prior traces. In spatial navigation, the circuit supports path integration through sequential activation of place and grid cells along the pathway. Entorhinal grid cells provide metric spatial scaling, which the dentate gyrus refines via sparse coding, enabling CA3 and CA1 place cells to form stable representations of locations and trajectories for efficient exploration. For episodic memory, the trisynaptic circuit serves as a primary engram storage site, where experience-specific neuronal ensembles form during encoding and replay during sleep to consolidate traces, bridging immediate learning with remote recall. This replay mechanism, supported by the core pathway's connectivity, reinforces memory stability without delving into oscillatory details.

Rhythm Generation and Synchronization

The trisynaptic circuit in the hippocampus generates distinct neural oscillations that coordinate activity across the entorhinal cortex, dentate gyrus, CA3, and CA1 regions. Theta rhythms, oscillating at 4-12 Hz, are primarily paced by rhythmic inputs from the medial septum, which synchronize hippocampal neurons through GABAergic and cholinergic projections.^[97] These inputs entrain pyramidal cells and interneurons, producing large-amplitude field potentials that facilitate temporal organization of neural firing. In the dentate gyrus and CA3, theta rhythms support phase precession, where place cells fire at progressively earlier phases of the theta cycle as an animal traverses its place field, enabling the encoding of spatial sequences.^[98] Dentate inputs are particularly crucial for this precession in CA3, sharpening spike timing and promoting sequential activation during navigation. Direct projections from entorhinal layer III to CA1 distal dendrites further modulate phase precession and theta sequences (6-10 Hz during active states), providing supervisory signals for learning and representational updates independent of the trisynaptic path.^[99]^[98] Gamma oscillations, ranging from 30-100 Hz, emerge intrinsically within the trisynaptic circuit through networks of fast-spiking GABAergic interneurons, such as parvalbumin-positive basket cells. These interneurons generate rhythmic inhibition via reciprocal synaptic connections, with slow decay kinetics of GABA_A receptors allowing population synchrony at gamma frequencies.^[100] This interneuron-driven rhythm imposes periodic inhibition on pyramidal cells across the dentate gyrus, CA3, and CA1, synchronizing their discharges and enhancing signal coherence along the circuit.^[100] Optimal synchronization occurs around 40 Hz, requiring modest network heterogeneity and sufficient synaptic contacts per interneuron.^[100] Sharp wave-ripples (SWRs), high-frequency oscillations at 150-250 Hz, arise from coordinated bursts in CA3 that propagate to CA1, forming transient population events lasting approximately 100-200 ms. These ripples, consisting of 3-9 fast waves per event, are generated by recurrent excitation in CA3 pyramidal networks interacting with perisomatic interneurons, producing synchronous discharges that replay spatial sequences.^[101] SWRs occur prominently during rest or slow-wave sleep, serving as a mechanism for memory consolidation by reactivating experience-related patterns in compressed time.^[101] Cross-frequency coupling within the trisynaptic circuit integrates theta and gamma rhythms, with theta phase modulating gamma amplitude to enable information multiplexing. This theta-gamma coupling peaks during active behaviors like locomotion, allowing nested gamma cycles to carry distinct computational signals within each theta phase, such as input-specific patterns in CA1.^[102] Theta harmonics up to 40 Hz further strengthen this coupling, coordinating activity across hippocampal subregions without strong reliance on gamma for inter-regional synchrony.^[102] Rhythm generation in the trisynaptic circuit is further supported by intrinsic cellular mechanisms, including gap junctions between interneuron dendrites that enhance gamma synchrony over distances up to 1 mm. These electrical synapses, with conductances of 0.5-1.5 nS, overcome conduction delays and heterogeneities, promoting coherent oscillations across distributed networks.^[103] In pyramidal cells, potassium-mediated M-currents (I_M) contribute to theta-frequency resonance at depolarized membrane potentials around -60 mV, amplifying subthreshold oscillations and facilitating entrainment to septal pacing.^[104] Together, these mechanisms ensure robust synchronization intrinsic to the circuit, with medial septal modulation providing extrinsic timing as detailed in afferent inputs.

Interactions with Other Systems

The trisynaptic circuit in the hippocampus interacts with non-limbic systems to integrate sensory, motor, and autonomic signals, enabling adaptive behaviors beyond core memory processing. Respiratory coupling represents a key modulatory influence, where hippocampal theta oscillations (typically 4-12 Hz) become entrained to breathing cycles through inputs from the olfactory bulb, facilitating the temporal alignment of olfactory stimuli with memory encoding. This entrainment supports odor-memory associations by synchronizing neural activity across olfactory and hippocampal networks during active sniffing, as observed in rodent models where respiration-driven rhythms in the hippocampus interact bidirectionally with olfactory bulb oscillations to enhance sensory processing for memory-guided navigation.^[105]^[106]^[107] Sensorimotor integration occurs via projections from the parietal association cortex to the entorhinal cortex, which updates visuo-spatial representations within the trisynaptic circuit to align with ongoing body movements and environmental changes. These inputs, primarily targeting the medial entorhinal cortex (MEC), incorporate multisensory spatial information from visual and somatosensory modalities, allowing the circuit to refine grid cell and place cell activity for precise navigation. In rodents, this pathway supports the transformation of allocentric spatial maps into egocentric coordinates, essential for sensorimotor coordination during exploration.^[108]^[109]^[110] Autonomic feedback from the vagus nerve modulates the excitability of the trisynaptic circuit, particularly during stress, through noradrenergic pathways originating from the locus coeruleus that project to hippocampal regions. Vagal stimulation enhances neurotransmitter release, including norepinephrine, which alters synaptic plasticity and circuit dynamics in CA1 and dentate gyrus, thereby influencing arousal states and adaptive responses to environmental stressors. This interaction helps regulate hippocampal activity under physiological stress, preventing maladaptive overexcitation while promoting resilience in sensory-motor tasks.^[111]^[112]^[113] Outputs from CA1 to the basal ganglia bridge spatial learning with habit formation, channeling hippocampal representations into striatal circuits for the consolidation of action sequences. These projections, primarily to the ventral striatum and nucleus accumbens, integrate declarative spatial knowledge with procedural motor learning, enabling the transition from goal-directed behaviors to efficient habits in complex environments. In learning paradigms, this hippocampal-striatal axis facilitates value-based decision-making by updating reward predictions with spatial context.^[114]^[115]^[116] Cross-system specificity is evident in the phase-locking of hippocampal theta (4-12 Hz) to sniffing-respiration cycles, particularly in rodents where respiration-entrained oscillations synchronize with olfactory bulb-driven rhythms during odor discrimination tasks. This coupling, observed during active exploration, ensures precise timing between respiratory phases and neural firing, optimizing sensory sampling and memory retrieval without relying on intrinsic hippocampal rhythms alone.^[117]^[118]^[119]

Clinical and Pathophysiological Relevance

Involvement in Epilepsy

The trisynaptic circuit in the hippocampus plays a central role in the pathophysiology of temporal lobe epilepsy (TLE), where disruptions lead to hyperexcitability and seizure propagation. In TLE, approximately 70% of cases involve hippocampal sclerosis, characterized by neuronal loss and gliosis that preferentially affect the trisynaptic pathway, including the dentate gyrus, CA3, and CA1 regions.^[120] This sclerosis disrupts the balance between excitation and inhibition, facilitating recurrent seizures originating in the temporal lobe.^[121] A key mechanism of hyperexcitability is mossy fiber sprouting, where granule cell axons in the dentate gyrus form aberrant excitatory synapses onto CA3 pyramidal cells and neighboring granule cells following injury or prolonged seizures. This sprouting creates recurrent excitatory loops within the trisynaptic circuit, acting as "spark plugs" that ignite synchronized neuronal firing and contribute to epileptogenesis.^[122] In post-injury states, such as after status epilepticus, these sprouted mossy fibers enhance synaptic efficacy in CA3, bypassing normal dentate gating and amplifying perforant path inputs.^[123] Seizure propagation in the trisynaptic circuit is exemplified by the entorhinal-dentate kindling model, where repeated stimulation of the entorhinal cortex progressively lowers the seizure threshold, leading to discharges that spread via the perforant path to the dentate gyrus and ignite hyperexcitable CA3 networks as a primary site of seizure initiation. In this model, CA3 back-projections reinforce entorhinal activity, sustaining limbic seizures characteristic of TLE.^[124] The kindling process mimics chronic epilepsy by inducing long-term plasticity changes that favor excitation over inhibition in the circuit.^[125] Animal models, such as pilocarpine-induced status epilepticus in rodents, replicate these disruptions by causing widespread neuronal hyperexcitability that imbalances the trisynaptic circuit, resulting in mossy fiber sprouting and reduced inhibitory control in the dentate gyrus. In pilocarpine-treated animals, the model induces chronic epilepsy with spontaneous seizures, highlighting how initial cholinergic overactivation leads to persistent alterations in CA3 synaptic transmission and circuit-wide synchronization.^[126] These changes underscore the circuit's vulnerability to acute insults that precipitate enduring epileptogenic states.^[127] Diagnostic markers of trisynaptic involvement in epilepsy include EEG patterns showing reduced dentate inhibition, manifested as diminished evoked potentials following perforant path stimulation, and enhanced excitability along the entorhinal-dentate pathway, often appearing as interictal spikes or rhythmic theta-like activity in TLE patients. High-frequency oscillations in EEG recordings from the hippocampus further indicate dentate hyperexcitability, correlating with seizure onset zones in the circuit.^[128] These electrophysiological signatures aid in identifying circuit dysfunction non-invasively.^[129]

Implications in Neurodegenerative Diseases

The trisynaptic circuit in the hippocampus exhibits particular vulnerability in Alzheimer's disease (AD), a primary neurodegenerative disorder characterized by progressive cognitive decline. Early pathological changes often begin in the entorhinal cortex, where layer II neurons are among the first to accumulate tau tangles, initiating degeneration of the perforant path that provides critical input to the dentate gyrus.^[130] This selective neuronal loss disrupts the circuit's foundational connectivity, contributing to the initial breakdown of memory processing pathways.^[131] In parallel, amyloid-beta accumulation in the synaptic cleft interferes with long-term potentiation (LTP) at Schaffer collateral synapses between CA3 and CA1 regions, thereby impairing synaptic strengthening essential for memory consolidation.^[132] Such disruptions manifest as early deficits in episodic memory, underscoring the circuit's role in AD pathogenesis. As AD advances, significant neuronal attrition occurs in the CA1 subfield, with studies reporting up to 46-50% reduction in pyramidal neuron numbers even in mild cognitive impairment stages preceding full dementia.^[133] This loss correlates with the Braak staging system, where tau pathology invades the trisynaptic circuit from stages I-II onward, starting in the entorhinal cortex and transentorhinal regions before spreading to hippocampal layers.^[134] These early-stage changes are tightly linked to emerging episodic memory impairments, as tau burden in entorhinal-hippocampal projections predicts declines in recall and recognition tasks.^[135] The progressive atrophy along the circuit's trisynaptic pathway thus serves as a neuropathological hallmark, distinguishing AD from normal aging.^[62] Structural imaging further highlights the circuit's degeneration, with magnetic resonance imaging (MRI) volumetry revealing 20-30% hippocampal shrinkage in early AD, attributable to atrophy in key trisynaptic components like the dentate gyrus and CA1.^[136] This volume loss reflects underlying synaptic and neuronal depletion within the circuit, providing a quantifiable biomarker for disease progression and cognitive correlates.^[137] Overall, these alterations emphasize the trisynaptic circuit's susceptibility to proteinopathies in AD, driving the selective impairment of memory functions central to daily cognition.^[130]

Therapeutic Targeting

Antiepileptic drugs such as carbamazepine modulate the trisynaptic circuit by targeting mossy fiber hyperexcitability through voltage-gated sodium channel blockade, thereby stabilizing neuronal firing in the dentate gyrus-CA3 pathway during epileptic activity.^[138] This mechanism reduces aberrant synchronization and seizure propagation in hippocampal networks, as demonstrated in ex vivo models of temporal lobe epilepsy where carbamazepine inhibits sharp wave-ripple complexes associated with mossy fiber reorganization.^[139] Clinical use of carbamazepine in patients with hippocampal epilepsy further supports its role in dampening trisynaptic hyperexcitability, though resistance can develop in chronic cases due to altered channel expression.^[140] In Alzheimer's disease therapies, anti-amyloid antibodies such as lecanemab (Leqembi) and donanemab (Kisunla) aim to preserve perforant path integrity within the trisynaptic circuit by promoting amyloid-beta plaque clearance in the entorhinal-hippocampal region.^[141]^[142] Lecanemab, approved by the FDA in 2023, and donanemab, approved in 2024, bind aggregated amyloid forms, facilitating microglial-mediated removal and reducing early synaptic disruption along the perforant path, which is vulnerable to amyloid accumulation.^[143]^[144] This preservation supports dentate granule cell function and downstream trisynaptic signaling, potentially slowing memory decline in mild cases.^[145] Deep brain stimulation via fornix electrodes enhances theta rhythms in the trisynaptic circuit to restore memory processes in mild cognitive impairment associated with Alzheimer's disease. Phase II trials have shown that chronic fornix stimulation increases theta-band power, correlating with improved verbal memory recall and hippocampal activation in patients.^[146] Theta-burst protocols specifically amplify entorhinal-hippocampal oscillations, promoting synaptic plasticity across the circuit without significant adverse effects.^[147] Optogenetic approaches in animal models target the trisynaptic circuit by silencing CA3 interneurons to prevent seizure propagation.^[148] Using archaerhodopsin for hyperpolarization, inhibition of CA3 interneuron activity disrupts recurrent excitation, attenuating kainic acid-induced seizures and reducing ictal discharge duration in hippocampal slices.^[149] This selective silencing restores balanced inhibition-excitation dynamics, offering a precise tool for circuit-specific seizure control in preclinical epilepsy research.^[150] Future prospects include gene editing technologies like CRISPR/Cas9 for Alzheimer's disease, which hold potential for addressing genetic factors contributing to neurodegeneration in the trisynaptic circuit.^[151]

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The supramammillary (SuM) nucleus of the hypothalamus is thought to serve as an 'interface' relaying inputs to hypothalamic and limbic structures involved in ...
[91]
The mammillary bodies and memory: more than a hippocampal relay
One suggestion is that the ventral tegmental nucleus of Gudden, via their connections with the mammillary bodies, may influence hippocampal function through ...
[92]
From Structure to Behavior in Basolateral Amygdala-Hippocampus ...
Oct 31, 2017 · The amygdala is specialized for input and processing of emotion, while the hippocampus is essential for declarative or episodic memory.
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Interactions between the Medial Prefrontal Cortex and Hippocampus
Apr 18, 2017 · This review will examine both spatial working memory and long-term memory interactions between the mPFC and HC, concentrating on whether these processes are ...
[94]
Pattern Separation in the Dentate Gyrus and CA3 of the Hippocampus
Feb 16, 2007 · The number of active cells was lower in the dentate gyrus than in CA3 (25), which confirmed previous indications of sparse firing in the granule ...
[95]
Direct Evidence for CA3 Pattern Completion and Dentate Gyrus ...
Jan 22, 2014 · Pattern completion refers to the ability of the network to retrieve stored output patterns when presented with partial or degraded input ...Results · Discussion · Experimental Procedures
[96]
A theory of hippocampal function: New developments - ScienceDirect
The theory is a quantitative model for hippocampal episodic memory storage and recall, using a CA3 attractor network, spatial view cells, and reward from the ...Missing: completeness | Show results with:completeness
[97]
The Theta Rhythm of the Hippocampus: From Neuronal and Circuit ...
Mar 4, 2021 · This review focuses on the neuronal and circuit mechanisms involved in the generation of the theta (θ) rhythm and of its participation in behavior.
[98]
Distinct roles of dentate gyrus and medial entorhinal cortex inputs for ...
Jan 2, 2025 · DG inputs are essential for preferential spiking of CA3 cells during late theta phases and for organizing the temporal order of neuronal firing, ...
[99]
Gamma Oscillation by Synaptic Inhibition in a Hippocampal ...
By contrast, the network synchronization was found to be high only within a frequency band coinciding with the gamma (20–80 Hz) range. We conclude that the GABA ...
[100]
Hippocampal sharp wave‐ripple: A cognitive biomarker for episodic ...
Sharp wave ripples (SPW‐Rs) represent the most synchronous population pattern in the mammalian brain. Their excitatory output affects a wide area of the cortex.
[101]
Theta dominates cross-frequency coupling in hippocampal-medial ...
Nov 18, 2022 · We found that theta is the dominant frequency of cross-frequency coupling between the MEC and hippocampus, with hippocampal gamma largely independent of ...
[102]
Gap Junctions between Interneuron Dendrites Can Enhance ... - PMC
Cortical and hippocampal interneuronal networks can, by virtue of mutual inhibitory chemical synaptic connections, generate gamma-frequency network oscillations ...
[103]
Two forms of electrical resonance at theta frequencies, generated by ...
The hippocampal pyramidal cells are equipped with two slow voltage-gated ionic currents that seem promising candidates for contributing to slow subthreshold ...
[104]
Hippocampal Respiration-Driven Rhythm Distinct from Theta ...
Jan 6, 2016 · We found mutual, state-dependent interactions between hippocampal and olfactory networks in both patterns: theta and respiration-coupled ...
[105]
https://www.jneurosci.org/content/36/1/162
[106]
Rhythmic coordination and ensemble dynamics in the hippocampal ...
Dec 8, 2022 · Our findings indicate that rhythmic coordination within the hippocampal-prefrontal-olfactory bulb network supports utilization of odor cues for memory-guided ...
[107]
A non-canonical visual cortical-entorhinal pathway contributes to ...
May 15, 2024 · The authors report a direct pathway from the secondary visual cortex to MEC layer 5a in mice and its involvement in memory-guided navigation.
[108]
The medial entorhinal cortex encodes multisensory spatial information
Oct 11, 2024 · The MEC enables accurate spatial encoding during multisensory navigation by computing spatial information in different sensory modalities and generating ...
[109]
Neurons and networks in the entorhinal cortex - Wiley Online Library
Aug 13, 2019 · In this review, we aim to reappraise the organization of intrinsic and extrinsic networks of the entorhinal cortex with a focus on the concept of parallel ...
[110]
Vagus nerve stimulation: mechanisms and factors involved in ...
Vagus nerve stimulation affects excitability in memory-associated pathways by altering brain neurotransmitters, such as γ-aminobutyric acid (GABA) and ...
[111]
Vagus Nerve as Modulator of the Brain–Gut Axis in Psychiatric and ...
Because the vagus nerve sends information to brain regions is important in the stress response (LC, orbitofrontal cortex, insula, hippocampus, and amygdala), ...
[112]
Enhancing Rehabilitative Therapies with Vagus Nerve Stimulation
Dec 15, 2015 · Serotonergic and noradrenergic pathways are required for the anxiolytic-like and antidepressant-like behavioral effects of repeated vagal ...<|separator|>
[113]
Integrating cortico-limbic-basal ganglia architectures for learning ...
Behaviour in spatial navigation is often organised into map-based (place-driven) versus map-free (cue-driven) strategies; behaviour in operant conditioning ...
[114]
The hippocampal–striatal axis in learning, prediction and goal ...
Strong evidence implicates the hippocampal–temporal lobe system in declarative memory and the striatum and connected basal ganglia structures in procedural ...
[115]
Dynamic reorganization of the cortico-basal ganglia-thalamo-cortical ...
Sep 20, 2022 · We reveal that functional networks encompassing basal ganglia, thalamus, neocortex, and hippocampus grow and stabilize upon learning, especially at stimulus ...
[116]
Whisking, Sniffing, and the Hippocampal θ-Rhythm: A Tale of Two ...
Feb 18, 2016 · The results from studies in rats and mice suggest that the most parsimonious hypothesis, at least for rodents, involves the rhythmic nature of ...
[117]
Delta-range coupling between prefrontal cortex and hippocampus ...
Apr 14, 2021 · ... Hz), overlapping in rodents with sniffing frequency. ... phase-lock to the olfactory bulb's respiratory rhythm in the freely behaving rat.
[118]
Multiple Modes of Phase Locking between Sniffing and Whisking ...
May 8, 2013 · Mean whisking as a function of sniffing phase was calculated by pooling all sessions for each rat and averaging whisking RMS over rats in 60 ...
[119]
Hippocampal sclerosis and temporal lobe epilepsy - Oxford Academic
Hippocampal sclerosis is a very common feature of temporal lobe epilepsy (complex partial seizures or limbic epilepsy). It is found in approximately 50–75%
[120]
Mesial Temporal Lobe Epilepsy - StatPearls - NCBI Bookshelf - NIH
Most cases of MTLE are sporadic in occurrence, although familial forms are not uncommon.[5] · Hippocampal sclerosis (HS) is the most common histopathological ...
[121]
The Role of Hippocampal Mossy Fiber Sprouting in Epilepsy - PMC
Sep 26, 2019 · Sprouted mossy fibers serve as “spark plugs” that reliably activate (ie, detonate) recurrent excitatory networks within the dentate gyrus.
[122]
Mossy Fiber Sprouting in the Dentate Gyrus - NCBI - NIH
Thus, two hypotheses (recurrent excitation and zinc-induced collapse of inhibition) contend that mossy fiber sprouting is epileptogenic. In contrast, Sloviter ...Missing: unmyelinated | Show results with:unmyelinated
[123]
CA3-Driven Hippocampal-Entorhinal Loop Controls Rather ... - NIH
Acute models with chronic properties. Human temporal lobe epilepsy is associated with hippocampal sclerosis in which dentate hilus, CA3, and CA1 neurons are ...
[124]
CA3-Released Entorhinal Seizures Disclose Dentate Gyrus ...
We have investigated the propagation of epileptiform discharges induced by 4-aminopyridine (4-AP, 50 μM) in adult mouse hippocampus-entorhinal cortex slices ...
[125]
Circuit-based interventions in the dentate gyrus rescue epilepsy ...
Jul 30, 2019 · In the systemic pilocarpine mouse model of temporal lobe epilepsy, the epileptic dentate gyrus excessively recruits granule cells in behavioural ...
[126]
Massively augmented hippocampal dentate granule cell activation ...
Feb 20, 2017 · Pilocarpine-induced status epilepticus (SE) model of epilepsy. Mice aged 6 weeks were injected with scopolamine (1 mg/kg), and 30 min later ...
[127]
Abnormal dentate gyrus network circuitry in temporal lobe epilepsy
Jul 2, 2012 · We attributed the immediate granule cell hyperexcitability that we observed after prolonged perforant pathway stimulation to the extensive loss ...
[128]
Deficits in Behavioral and Neuronal Pattern Separation in Temporal ...
Nov 17, 2021 · In temporal lobe epilepsy, the ability of the dentate gyrus to limit excitatory cortical input to the hippocampus breaks down, leading to ...
[129]
Selective alterations of neurons and circuits related to early memory ...
In this review, we will discuss mainly the alterations of the granule cell neurons of the dentate gyrus and the atrophy of CA1 pyramidal neurons that occur in ...
[130]
Entorhinal cortex dysfunction in Alzheimer's disease - PMC - NIH
Feb 1, 2023 · This review will focus on recent findings on EC dysfunction in AD, and discuss the potential pathways for mitigating AD progression by protecting the EC.Histological Alterations In... · Figure 1. Putative Time... · Dysfunction Of Ec Neuronal...
[131]
Beta Amyloid-Induced Depression of Hippocampal Long-Term ...
Nov 28, 2012 · Alzheimer's disease (AD) is characterized by accumulation of amyloid-β peptide (Aβ) in the brain regions that subserve memory and cognition.
[132]
Neuron Number in the Entorhinal Cortex and CA1 in Preclinical ...
In the entorhinal cortex, in particular, marked cell loss was found even in very mild AD cases (CDR 0.5, mild cognitive impairment [MCI]). This study sought to ...
[133]
Entorhinal Tau Pathology, Episodic Memory Decline, and ... - NIH
Our data are consistent with neuropathological studies and further suggest that entorhinal tau pathology underlies memory decline in old age even without Aβ.
[134]
Clinical Correlates of the PET-based Braak Staging Framework in ...
Memory dysfunction was observed starting at Braak stage II and worsening across groups with higher Braak stages (36). Executive function, language, or ...
[135]
Specific Hippocampal Volume Reductions in Individuals at Risk for ...
We found hippocampal volume reductions of 14% for the MCI and 22% for the DAT group compared to the NL group. Utilizing regression analyses and after accounting ...
[136]
Late‐life cognitive decline is associated with hippocampal volume ...
Jan 8, 2020 · In particular, hippocampal volume accounted for 5.4% of the variation in the decline rate of global cognition and up to 6.4% in individual ...INTRODUCTION · METHODS · RESULTS · DISCUSSION
[137]
Network-specific mechanisms may explain the paradoxical effects of ...
Apr 8, 2013 · A common notion of the mechanism by which the antiepileptic drugs (AEDs) carbamazepine and phenytoin act is that they block sodium channels by binding ...
[138]
Carbamazepine Reduces Sharp Wave-Ripple Complexes and ... - NIH
Jun 15, 2021 · Our results demonstrate that CBZ reduced SPW-Rs at therapeutically relevant concentrations (IC 50 = 37 μM) and altered the core characteristics of ripples.
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Carbamazepine-resistance in the epileptic dentate gyrus of human ...
Altered patterns of dynorphin immunoreactivity suggest mossy fiber reorganization in human hippocampal epilepsy. ,. J Neurosci. ,. 1990. , vol. 10. (pg. 267. -.
[140]
Neuropathologic changes and amyloid-related imaging ... - NIH
Nov 1, 2025 · Neuropathology studies have reported inconsistent evidence of Aβ clearance following aducanumab, likely reflecting cumulative dose variability.
[141]
Plaque-Associated Oligomeric Amyloid-Beta Drives Early ... - Frontiers
In this work, we report an early decline in spatial memory, along with hippocampal synaptic changes, in an amyloidogenic APP/PS1 transgenic model.
[142]
A comparative study of the effects of Aducanumab and scanning ...
Apr 9, 2021 · Aducanumab analog, SUS, and the combination therapy all effectively reduce amyloid plaques in the hippocampus of APP23 mice. In APP23 mice, ...Missing: perforant | Show results with:perforant
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Visual-spatial memory may be enhanced with theta burst deep brain ...
Apr 21, 2015 · Visual-spatial memory may be enhanced with theta burst deep brain stimulation of the fornix: a preliminary investigation with four cases.Missing: MCI | Show results with:MCI
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Directional DBS of the Fornix in Alzheimer's Disease Achieves Long ...
Mar 31, 2022 · The dDBS stimulation in the fornix seems to be a safe treatment for patients in the first stage of AD. Effects on cognition seem to be mild to moderate.
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CA3 synaptic silencing attenuates kainic acid induced seizures and ...
Feb 10, 2016 · TrkB Signaling Influences Gene Expression in Cortistatin-Expressing Interneurons · Optogenetic Activation of β-Endorphin Terminals in the ...
[146]
Optogenetics for controlling seizure circuits for translational ...
Optogenetic stimulation of PV interneurons in the CA3 region of the hippocampus led to excitatory GABAergic transmission and an increase in seizure activity ( ...
[147]
Seizure suppression by high frequency optogenetic stimulation ...
This study shows that optical stimulation at high frequency targeting an excitatory opsin has potential therapeutic application for fast control of an ...
[148]
Boosting Neurogenesis as a Strategy in Treating Alzheimer's Disease
... CRISPR/Cas9 now enable precise gene manipulation of neurogenesis ... Hippocampal neurogenesis confers stress resilience by inhibiting the ventral dentate gyrus.
[149]
Stem cell and CRISPR/Cas9 gene editing technology in Alzheimer's ...
The key findings suggest that gene-edited iPSCs can reduce abnormal Aβ and tau protein accumulation in AD models, improve cognitive function, and provide a ...
[150]
CRISPR/Cas9 and iPSC-Based Therapeutic Approaches in ...
Preclinical studies in animal models of AD reported that gene therapy could lower Aβ deposition and enhance cognitive function, alongside a reduction in ...