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Cerebrospinal fluid

Cerebrospinal fluid (CSF) is a clear, colorless, plasma-like liquid that bathes and surrounds the and , occupying the , central spinal canal, and subarachnoid spaces of the (CNS). It serves as a protective cushion, reducing the effective weight of the from approximately 1,500 grams to 50 grams through and shock absorption, while also facilitating transport, waste removal, and maintenance of intracranial . Produced primarily by the in the 's ventricles at a rate of about 400–600 mL per day, CSF is continuously renewed, with a total adult volume of around 125–150 mL that turns over 4–5 times in 24 hours. The of CSF is predominantly (99%), with the remaining 1% consisting of electrolytes, glucose, proteins, vitamins, and trace neurotransmitters, differing from in having higher concentrations of sodium (135–150 mmol/L), , and magnesium, but lower levels of (2.6–3.0 mmol/L), calcium, proteins (15–45 mg/dL), and glucose (2.8–4.4 mmol/L). This unique ionic profile helps maintain a stable chemical environment for the CNS despite fluctuations in composition. CSF production involves active secretion by epithelial cells through mechanisms like and transport, with minor contributions from ependymal cells and interstitial fluid. In terms of circulation, CSF flows from the lateral ventricles through the interventricular foramina (foramina of Monro) into the third ventricle, then via the cerebral aqueduct to the fourth ventricle, exiting through the foramina of Luschka and Magendie into the subarachnoid space surrounding the brain and spinal cord. It circulates downward around the spinal cord and upward over the cerebral hemispheres, where it is primarily reabsorbed into the venous system via arachnoid granulations (or villi) into the dural venous sinuses, with additional drainage through dural lymphatics and the glymphatic system for waste clearance. Normal CSF pressure ranges from 8–15 mm Hg in the lateral decubitus position, and disruptions in production, circulation, or absorption can lead to conditions like hydrocephalus or intracranial hypertension. Beyond protection and homeostasis, CSF plays roles in immune surveillance by transporting immunoglobulins and mononuclear cells, and it serves as a medium for delivering hormones, drugs, and diagnostic biomarkers via procedures like lumbar puncture.

Anatomy and Composition

Physical properties

Cerebrospinal fluid (CSF) in adults has a total volume of approximately 125 to 150 mL, with about 25 mL contained within the cerebral ventricles and the remaining volume distributed in the subarachnoid spaces surrounding the and . Under normal conditions, CSF is a clear, colorless that maintains due to its low cellular and protein content. The normal pressure of CSF, measured in the lateral decubitus position during , ranges from 6 to 25 cm H₂O, reflecting the balance between production and reabsorption that supports intracranial dynamics. The density of CSF is slightly higher than that of , ranging from 1.003 to 1.008 /cm³, which is influenced by its protein composition and contributes to its buoyant properties within the . Its viscosity at body temperature (approximately 37°C) is about 0.7 to 1.0 times that of water, behaving as a that facilitates smooth flow through narrow pathways without significant resistance. The pH of CSF is around 7.33, closely mirroring that of (7.35-7.45) due to free diffusion of across the blood-CSF barrier. CSF exhibits a high turnover rate, with the entire volume renewed approximately 3 to 4 times per day in young adults, driven by a daily production of 400 to 600 mL that ensures continuous refreshment and waste clearance.

Chemical composition

Cerebrospinal fluid (CSF) serves as an ultrafiltrate of , with its composition actively modified through selective transport mechanisms mediated by the . This process ensures that CSF maintains a distinct biochemical profile optimized for homeostasis, differing from in key solutes. The blood-CSF barrier, characterized by tight junctions in the , limits the of large molecules greater than approximately 500 , while permitting regulated passage of ions and small metabolites. As a result, CSF contains lower concentrations of proteins and certain compared to , contributing to its low viscosity and clarity. concentrations in CSF are as follows: sodium at 140-145 mEq/L, at 120-130 mEq/L, and at 2.7-3.9 mEq/L, with notably lower than the range of 3.5-5.0 mEq/L.
ComponentNormal CSF ConcentrationNotes/Comparison to Plasma
Total Protein15-45 mg/dLPredominantly (about 56-76% of total); ~1% of protein levels (: 6,000-8,000 mg/dL).
Glucose40-70 mg/dL60-80% of simultaneous glucose (: 70-110 mg/dL).
Lactate1-2 mmol/LDerived from cerebral ; elevated in pathological states.
White Blood Cells (WBC)<5 cells/μLPrimarily mononuclear; no red cells normally present.
Immunoglobulins, such as IgG (0.1-0.45 mg/dL), and neurotransmitters are present in only trace amounts, reflecting the barrier's selective permeability. The ionic milieu also influences CSF , typically 7.31-7.34, which is slightly more acidic than due to differences in and other buffers.

Circulation

Cerebrospinal fluid (CSF) is primarily produced by the located in the , , and of the . The fluid flows from the through the interventricular foramina of Monro into the , then passes via the to the . From the , CSF exits through the median foramen of Magendie and the paired lateral foramina of Luschka into the subarachnoid space surrounding the and . In this space, CSF circulates around the cerebral hemispheres, , , and , distributing nutrients and removing waste products. The bulk flow of CSF is propelled by arterial pulsations from the and pressure changes associated with , which facilitate its movement through the and subarachnoid space. These dynamics result in a complete turnover of the total CSF volume—approximately 125–150 mL in adults—every 6–8 hours, ensuring continuous renewal. Key reservoirs within the subarachnoid space, such as the (cerebellomedullary cistern), store larger volumes of CSF and aid in buffering flow variations between the cranial and spinal compartments. The spinal subarachnoid space accounts for about 30% of the total CSF volume, extending from the to the sacral region and contributing to the fluid's overall circulation around the . In pathological conditions like , where natural CSF pathways are obstructed, ventriculoperitoneal shunts are used to divert excess fluid from the ventricles to the , thereby mimicking the directional bulk flow to restore pressure balance.

Development and Production

Embryonic development

The development of cerebrospinal fluid (CSF) begins during early embryogenesis, closely tied to the formation of the . The , which forms the precursor to the and , closes by the end of week 4 of gestation, enclosing a initially filled with that transitions into primitive CSF. This , particularly of the caudal neuropore around days 26-28, establishes the foundational ventricular spaces. The , responsible for CSF production in later stages, arises from ependymal cells lining the roof around week 7, with initial invagination of mesenchymal cells into the ventricular spaces. By week 7, the (), (), and () have expanded, forming distinct cavities—the precursors to the lateral, third, and fourth ventricles, respectively—that become filled with CSF. Prior to full maturation, initial CSF is generated through across the primitive and subarachnoid spaces, which emerge around week 5 as cavities within the meningeal layers. CSF production by the nascent commences around the 9th week, contributing to the that support . This early CSF exerts hydrostatic pressure that drives expansion, promotes , and facilitates the initial stages of cortical folding or gyration by maintaining ventricular shape and providing mechanical support during rapid growth. Unlike adult CSF, the embryonic variant has a markedly higher protein concentration—up to 30 times greater in some vertebrates, with a complex profile rich in growth factors that actively influence and tissue differentiation. Disruptions in this process, such as in —a where the anterior neuropore fails to close—prevent development and the formation of associated ventricular cavities, thereby abolishing localized CSF production and circulation in the affected region. These embryonic events establish the foundational architecture that evolves into the adult CSF system.

Mechanisms of production

Cerebrospinal fluid (CSF) is primarily produced by the epithelial cells of the , specialized structures located in the lateral, third, and fourth ventricles of the , accounting for approximately 70-80% of total CSF volume through active secretion. These cells form a selective blood-CSF barrier via tight junctions, which prevent paracellular leakage and ensure unidirectional transport of ions and water from the bloodstream into the ventricular lumen. In adults, the production rate is about 0.3-0.4 mL/min, yielding roughly 500 mL per day, though only about 150 mL is present in the CSF spaces at any time due to continuous turnover. Minor contributions, estimated at 20-30%, arise from the ependymal lining of the ventricles and diffusion from brain interstitial fluid. The secretion process is an energy-dependent mechanism driven by ion transport across the polarized choroid plexus epithelium, where the apical (CSF-facing) membrane faces the ventricle and the basolateral membrane contacts the fenestrated capillaries. Central to this is the Na⁺/K⁺-ATPase pump, predominantly located on the apical membrane, which actively extrudes three Na⁺ ions into the CSF while importing two K⁺ ions, using ATP to maintain a low intracellular Na⁺ concentration and establish an electrochemical gradient. This gradient facilitates secondary active transport of other ions; for instance, the Na⁺-K⁺-2Cl⁻ cotransporter 1 (NKCC1) on the apical membrane enables Na⁺ influx coupled with K⁺ and Cl⁻, contributing to Cl⁻ accumulation and secretion into the CSF, with studies showing NKCC1 inhibition reduces CSF production by up to 50% in animal models. Water follows osmotically through aquaporin-1 (AQP1) water channels abundantly expressed on the apical membrane, though secretion can occur independently of AQP1, as evidenced by only a 20% reduction in AQP1 knockout mice. Bicarbonate (HCO₃⁻) secretion, essential for CSF pH regulation, involves enzymes (primarily CA II) in the , which catalyze the reaction CO₂ + H₂O ⇌ H⁺ + HCO₃⁻, allowing HCO₃⁻ to exit apically via exchangers like anion exchanger 2 (AE2) while H⁺ is extruded basolaterally. The overall ion transport creates a local osmotic without requiring a transepithelial hyperosmolarity, emphasizing active solute secretion as the driving force; for example, the NKCC1-mediated flux can be represented conceptually as Na⁺ + K⁺ + 2Cl⁻ influx, supporting net Cl⁻ secretion and osmotic water flow. This tightly regulated process ensures CSF differs from , with lower protein and higher Cl⁻ levels.

Physiology

Functions

Cerebrospinal fluid (CSF) provides mechanical protection to the (CNS) by offering support that significantly reduces the effective weight of the . The , which weighs approximately 1,500 grams in air, experiences a reduction to about 50 grams when immersed in CSF, achieving nearly a 97% decrease in weight and thereby minimizing mechanical stress on neural and blood vessels. This buoyancy also acts as a cushion, absorbing impacts and protecting delicate neural structures from during everyday movements or injuries. In maintaining , CSF facilitates the transport of essential nutrients such as glucose and oxygen to neural tissues, complementing the blood-brain barrier by distributing solutes that may lack specific transporters. It also removes products, including and , ensuring a stable extracellular environment critical for optimal neuronal function. These processes help preserve and support ongoing cellular within the CNS. CSF contributes to immune surveillance by circulating immune mediators like cytokines and antibodies throughout the CNS, enabling rapid response to pathogens or inflammation. Integral to this is the , a perivascular pathway that leverages CSF flow to clear soluble proteins such as amyloid-beta, thereby preventing accumulation that could contribute to neurodegenerative conditions. Additionally, CSF transports signaling molecules, including neurotransmitters and neurohormones, allowing their redistribution beyond localized release sites to influence distant neural circuits via volume transmission. It also buffers changes associated with neuronal activity through ion regulation across the , stabilizing the extracellular milieu to support consistent synaptic signaling. A key role of CSF lies in intracranial , where it adjusts volume within the to accommodate physiological fluctuations and prevent imbalances. This function is enhanced during , when glymphatic flow increases dramatically—up to several-fold—promoting efficient waste clearance and overall CNS .

Reabsorption

The reabsorption of cerebrospinal fluid (CSF) is a critical process for maintaining intracranial volume and preventing imbalances within the . Primarily, CSF is reabsorbed into the venous circulation through arachnoid granulations (also called arachnoid villi), which are specialized protrusions of the that extend into the , most notably the . These structures enable the bulk transfer of CSF from the subarachnoid space directly into the bloodstream, accounting for the majority of drainage under normal conditions. The mechanism at the arachnoid granulations involves pressure-dependent bulk flow, where CSF moves across the when subarachnoid exceeds venous . These granulations act as one-way valves, featuring slit-like openings that permit unidirectional passage while resisting flow, thus ensuring efficient clearance without contamination of the CSF by components. This flow is governed by principles analogous to , described by an adapted : J_v = K_f (\Delta P - \sigma \Delta \pi) Here, J_v represents the volume flux of CSF, K_f is the (filtration coefficient) of the granulation , \Delta P is the net hydrostatic across the barrier, \sigma is the for solutes, and \Delta \pi is the difference. The process is predominantly driven by hydrostatic forces, with minimal contribution from oncotic pressures due to the protein-poor of CSF. Complementing venous drainage, a substantial portion (30–50% in animal models) of CSF is reabsorbed via lymphatic pathways, which provide an alternative route for fluid and solute clearance. These include the nasal lymphatic route, where CSF exits through perineural spaces around olfactory nerves and the into nasal submucosal lymphatics, and spinal routes along cranial and spinal nerve sheaths to and lymph nodes. Aquaporins, particularly aquaporin-4 (AQP4) expressed on astrocytic endfeet and meningeal cells, facilitate in the glymphatic-lymphatic interface, enhancing the efficiency of this by supporting convective flow of CSF-derived fluid into peripheral lymphatics. In healthy adults, the rate equilibrates with CSF at approximately 500 mL per day, ensuring steady-state turnover despite a total CSF volume of only 125–150 mL. Disruption of these pathways, such as obstruction or fibrosis of arachnoid granulations, impairs and can result in , leading to ventricular enlargement and elevated . The arachnoid granulations exhibit a functional around 15 kDa, allowing small solutes to pass while restricting larger proteins, which further supports selective clearance during bulk flow.

Regulation

The regulation of cerebrospinal fluid (CSF) volume and composition involves a dynamic balance between and , ensuring stable (ICP) and within the . Autoregulation mechanisms maintain a relatively constant CSF volume of approximately 150 ml in adults, despite fluctuations in systemic , through adjustments in cerebral and CSF dynamics governed by the Monro-Kellie doctrine. This process is essential for protecting from changes, with rates typically matching reabsorption under normal conditions. Hormonal factors play a key role in modulating CSF production. , also known as antidiuretic hormone, decreases CSF production by reducing blood flow to the , with infusions leading to a 35% reduction in secretion rates in experimental models. Similarly, (ANP) binds to receptors on choroid plexus epithelial cells, elevating cyclic GMP levels and inhibiting ion transport, which slows CSF production. These hormones integrate systemic signals, such as osmolality and volume status, to fine-tune CSF secretion and prevent imbalances. Autonomic influences further regulate CSF dynamics by controlling choroid plexus blood flow. Sympathetic innervation exerts an inhibitory tone on the , reducing vascular and thereby modulating CSF rates during physiological or . Parasympathetic inputs may counteract this by promoting , contributing to overall autonomic balance in CSF circulation. Feedback mechanisms involving sensing help maintain equilibrium. Although CSF production is relatively insensitive to direct ICP changes, brainstem-mediated responses to pressure variations can influence aqueductal CSF flow and overall circulation, adjusting for minor perturbations through neural pathways. This integrates with broader to stabilize volume. CSF regulation exhibits diurnal variations, with rates showing circadian rhythms; studies indicate a nocturnal increase in , contributing to higher ICP at night compared to daytime minima. Aging impairs this , reducing CSF and turnover by approximately 50% in the elderly compared to young adults, due to decreased and altered . These changes underscore the adaptive yet age-sensitive nature of CSF regulatory processes.

Clinical Aspects

Intracranial pressure

() refers to the pressure exerted by the cerebrospinal fluid (CSF), brain tissue, and blood within the rigid . In healthy adults, normal ranges from 7 to 15 mmHg (equivalent to 10 to 20 cm H₂O) when measured in the . This range reflects the balanced production, circulation, and absorption of CSF, maintaining intracranial . is typically measured through , which assesses CSF opening pressure at the spinal level, or via an intraventricular inserted directly into the brain's for continuous monitoring. Posture significantly influences these readings, with pressures higher in the sitting position compared to due to gravitational effects on CSF distribution. The Monro-Kellie doctrine explains the physiological constraints on ICP, positing that the total volume of brain tissue, blood, and CSF within the skull remains constant, such that increases in one component must be compensated by decreases in others to avoid pressure elevation. For instance, CSF volume expansion is offset by reductions in intracranial blood volume through vascular adjustments. Elevated ICP exceeding 20 mmHg signals intracranial hypertension, which can impair cerebral perfusion and lead to neurological compromise. In severe cases, this manifests as Cushing's triad—systemic hypertension, bradycardia, and irregular respirations—indicating critical brainstem compression. Pseudotumor cerebri, or idiopathic intracranial hypertension, exemplifies elevated CSF pressure without identifiable mass lesions, often with opening pressures above 25 cm H₂O.

Pathological conditions

Cerebrospinal fluid (CSF) leaks occur either spontaneously or due to , leading to intracranial and characteristic orthostatic headaches that worsen upon upright positioning. Traumatic CSF leaks, often resulting from craniofacial injuries, account for approximately 80% of cases, while spontaneous leaks may arise from underlying disorders or idiopathic causes. These leaks disrupt the normal containment of CSF, potentially causing symptoms such as , , and , with post-traumatic incidence reported as uncommon but significant in severe . Hydrocephalus represents a pathological accumulation of CSF resulting from an imbalance between and , leading to and increased . It is classified into obstructive (non-communicating) hydrocephalus, where CSF flow is blocked within the —such as by or tumors—and communicating hydrocephalus, characterized by impaired at the arachnoid granulations due to post-hemorrhagic or inflammatory changes. This imbalance causes progressive enlargement of the brain's ventricles, compressing surrounding neural tissue and potentially leading to neurological deficits if untreated. Infectious and inflammatory conditions can profoundly alter CSF composition, reflecting underlying pathology. Bacterial meningitis typically presents with CSF pleocytosis, featuring a markedly elevated (WBC) count, predominantly polymorphonuclear leukocytes, alongside decreased glucose and increased protein levels. Similarly, Guillain-Barré syndrome is associated with albuminocytologic dissociation in CSF, characterized by elevated protein concentrations—often exceeding 100 mg/—despite a normal cell count, due to disruption of the blood-nerve barrier. These changes provide critical insights into the disease process, with high CSF protein in Guillain-Barré linked to more severe demyelinating subtypes. Froin's syndrome arises in the context of spinal subarachnoid blockages, such as from tumors or abscesses, resulting in stagnation of CSF below the obstruction and markedly elevated protein levels—often exceeding 500 mg/dL—due to impaired and local . This leads to xanthochromic, coagulable CSF with high fibrinogen content, distinguishing it from diffuse protein elevations. Complementing this, Queckenstedt's test historically assessed spinal CSF flow obstruction by measuring lumbar pressure changes during compression; a lack of pressure rise below the block indicates impaired transmission, confirming obstructive . These concepts highlight how localized CSF dynamics reveal underlying structural disruptions.

Diagnostic procedures

The primary method for obtaining cerebrospinal fluid (CSF) for diagnostic purposes is , a procedure in which a needle is inserted into the subarachnoid space, typically at the L3-L4 or L4-L5 intervertebral space, to access the CSF below the termination of the . This site is chosen to minimize the risk of , as the usually ends above L2 in adults. Contraindications include , , local at the puncture site, and signs of increased such as , as these increase the risk of complications like or herniation. During the procedure, a sterile, atraumatic needle (often 22-25 gauge) is advanced in the midline after , and CSF is collected in tubes for analysis, typically yielding 10-20 mL depending on the diagnostic needs. Opening pressure is measured using a manometer attached to the needle before significant fluid withdrawal, providing an estimate of in the range of 70-180 mm H₂O in adults when with legs extended. Alternative methods for CSF sampling are employed when lumbar puncture is contraindicated or technically challenging, such as in patients with spinal deformities or . Cisternal tap, or suboccipital puncture, involves needle insertion into the below the , offering access to CSF near the but carrying higher risks of brainstem injury and is rarely used outside specialized settings. Ventricular tap accesses CSF directly from the cerebral ventricles, often via an existing or during neurosurgical procedures, and is particularly useful in cases of or when ventricular pressure monitoring is required. For high-risk patients, imaging guidance enhances safety; or can direct needle placement during lumbar puncture, while computed tomography (CT) or (MRI) may be used pre-procedure to identify anatomical variants or contraindications. Once collected, CSF undergoes laboratory analysis to aid . Routine evaluation includes cell count and (normal <5 /μL, no red blood cells), protein concentration (15-45 mg/dL), and glucose level (40-70 mg/dL, approximately two-thirds of glucose), which help identify , , or hemorrhage. Microbiological cultures and Gram staining are performed to detect bacterial, fungal, or viral pathogens in suspected infections. Specialized tests, such as for , are crucial for diagnosing , where these bands are present in over 90% of cases but absent in , indicating intrathecal synthesis. A common complication of lumbar puncture is post-dural puncture headache, occurring in approximately 30% of cases due to persistent CSF leakage through the dural puncture site, leading to intracranial hypotension and postural symptoms. This typically manifests within 48 hours and resolves spontaneously in most patients, though severe cases may require an .

Therapeutic applications

Cerebrospinal fluid (CSF) serves as a critical pathway for targeted therapeutic interventions, particularly when systemic administration is limited by the blood-brain barrier, which restricts the passage of many hydrophilic and large-molecule drugs into the . Intrathecal delivery directly into the CSF circumvents this barrier, enabling higher local concentrations with reduced systemic exposure and side effects. This approach is widely used in , , and management. Intrathecal anesthesia involves injecting anesthetics into the CSF via spinal or epidural routes to provide localized relief during surgical procedures, particularly for lower operations. For instance, opioids or local anesthetics administered intrathecally block sensory and motor nerves by diffusing through the CSF to act on receptors. In , intrathecal delivers agents like directly into the CSF to treat malignancies affecting the , such as meningeal involvement in . The , a subcutaneous device connected to a ventricular , facilitates repeated intraventricular administration of such , improving access and reducing the need for repeated punctures while achieving prolonged remission in select cases. CSF shunting procedures divert excess fluid to alleviate , a condition characterized by impaired CSF flow and accumulation. Ventriculoperitoneal (VP) shunts, the most common type, route CSF from the brain's ventricles to the for absorption, demonstrating efficacy in over 75% of patients with idiopathic by improving gait, cognition, and continence. Ventriculoatrial (VA) shunts, an alternative, direct CSF to the venous system and are particularly useful in cases of recurrent VP shunt failures or abdominal complications. These shunts incorporate programmable valves to regulate flow and pressure, minimizing over-drainage risks. For autoimmune conditions like Guillain-Barré syndrome, liquorpheresis—filtration of CSF to remove elevated proteins and potential blocking factors—has shown therapeutic benefit by accelerating recovery in severe cases. This procedure involves repeated CSF withdrawal and filtration, reducing neurotoxic substances without relying on plasma exchange. Implantable intrathecal drug delivery systems, such as programmable pumps, provide continuous infusion of medications like for managing chronic and pain associated with injuries or . These pumps deliver low doses directly into the CSF, offering sustained relief while minimizing oral medication requirements and associated side effects. Despite these advantages, CSF interventions carry risks, including infections occurring in approximately 5-10% of shunt placements, often due to bacterial during .

Historical and Comparative Aspects

History

The recognition of cerebrospinal fluid (CSF) dates to ancient times, with (c. 460–370 BCE) describing a "water" surrounding the brain, particularly in cases of , as a protective or pathological element. In the CE, (c. 129–216 CE) observed an "excremental liquid" within the brain ventricles, which he believed was purged through nasal passages, and he identified the as a site potentially involved in fluid production based on animal dissections. These early accounts laid rudimentary groundwork, though they were intertwined with humoral theories of bodily spirits rather than a distinct physiological fluid. During the , advanced anatomical understanding in his 1543 work De Humani Corporis Fabrica, where he first illustrated the cerebral ventricles filled with an aqueous humor, rejecting Galen's gaseous spirit model and emphasizing the fluid's physical presence. In the 19th century, François Magendie identified the median aperture of the —now known as the foramen of Magendie—in 1825, demonstrating its role in allowing CSF to flow from the into the subarachnoid space. Magendie further characterized CSF's properties through animal experiments, likening its role to suspending the and . Key milestones in CSF circulation followed, with Ernst Key and Magnus Gustaf Retzius reporting in 1875 that CSF is reabsorbed via arachnoid granulations into , based on gelatin injection studies in cadavers that traced dye pathways. Heinrich Quincke introduced in 1891, a technique using a hollow needle to access CSF in the subarachnoid space for and sampling, revolutionizing diagnostic access. Circulation pathways, such as the foramina of Magendie and later Luschka (discovered 1855), were named after these pioneers to reflect their contributions to mapping CSF flow. The marked a toward viewing CSF production as an active secretory process primarily by the epithelium, with early proposals in the mid-1800s confirmed through physiological studies demonstrating ion transport and energy-dependent mechanisms by . A major modern advance came in 2012, when Maiken Nedergaard's team proposed the , revealing perivascular routes for CSF influx into brain parenchyma to facilitate interstitial fluid exchange and waste clearance during . In 2024, the was confirmed in living humans through MRI imaging of CSF flow during brain surgery.

In other animals

In mammals other than s, the cerebrospinal fluid (CSF) system closely mirrors the configuration, serving essential roles in mechanical cushioning, , and waste clearance while adapting to species-specific demands. For instance, in large cetaceans such as whales, the substantially increased —up to 9 kg in sperm whales—correlates with proportionally larger CSF volumes that enhance buoyancy support for the during deep dives and rapid movements. , particularly mice, are pivotal model organisms for investigating the , a CSF-mediated perivascular network that promotes interstitial fluid exchange and metabolic waste removal from the ; this pathway was first characterized in models, underscoring its evolutionary preservation across mammalian lineages. Across non-mammalian vertebrates, the remains a conserved structure for CSF production, reflecting deep evolutionary roots from early chordates, though the overall and barrier properties vary with phylogenetic position and . In fish, such as , CSF occupies the ventricles and facilitates neuroepithelial signaling and waste clearance during development, but the system lacks the extensive subarachnoid spaces of higher vertebrates, relying instead on simpler ventricular circulation and perineural fluid pathways around for analogous protective functions. Birds exhibit a comparable CSF circulation to mammals, with the forming a tight-junction-based blood-CSF barrier that regulates ionic balance, though adaptations for high-metabolic demands during flight may influence flow rates. Reptiles display notable variations in CSF reabsorption, where lymphatic vessels often predominate over arachnoid granulations seen in mammals; in species like the , spinal lymphatics and perineural routes provide primary drainage pathways, potentially aiding adaptation to terrestrial and aquatic transitions. In striking contrast, invertebrates such as fundamentally diverge from vertebrates by lacking a discrete CSF compartment altogether; their is immersed in within an open , which directly bathes neural tissues and serves integrated roles in nutrient delivery and without specialized barriers or enclosed .