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Physiology 3% exam weight

Central Nervous System

Part of the NEET PG study roadmap. Physiology topic physio-010 of Physiology.

Central Nervous System

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Central Nervous System — Key Facts for NEET PG

  • Reflex arc: Receptor → Sensory neuron → CNS integration center → Motor neuron → Effector
  • Spinal cord tracts: Dorsal columns (fine touch, vibration), Spinothalamic (pain, temperature), Corticospinal (voluntary movement)
  • Cerebral cortex: Frontal (motor, language), Parietal (somatosensory), Temporal (auditory, memory), Occipital (visual)
  • Basal ganglia: caudate + putamen (striatum), globus pallidus, substantia nigra — movement regulation
  • Exam tip: Dorsal columns decussate in medulla (internal arcuate fibers); Spinothalamic decussates at spinal cord level (2 segments above entry)

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Central Nervous System — NEET PG Study Guide

Neurons and Support Cells

Neurons:

  • Cell body (soma): Nissl bodies (RER), neurofibrils, lipofuscin
  • Dendrites: Receive signals, have dendritic spines
  • Axon hillock: Site of action potential initiation
  • Axon: Transmits signals, myelin sheath (oligodendrocytes in CNS, Schwann cells in PNS)

Neuroglial Cells:

Cell TypeLocationFunction
AstrocytesCNSBBB formation, metabolism, K⁺ buffering, water transport
OligodendrocytesCNSMyelination (each oligodendrocyte myelinates multiple axons)
MicrogliaCNSMacrophages of CNS (CD68+)
Ependymal cellsCNSLine ventricles and central canal, produce CSF
Schwann cellsPNSMyelination (each Schwann cell myelinates one axon segment)
Satellite cellsPNSSupport neuronal cell bodies in ganglia

Exam tip: Multiple sclerosis = demyelination of CNS axons (oligodendrocyte dysfunction); Guillain-Barré = demyelination of PNS (autoimmune against myelin proteins)

Spinal Cord Organization

Grey Matter (butterfly-shaped):

  • Ventral horn: Motor neurons (LMN to skeletal muscles)
  • Dorsal horn: Sensory relay (Lamina I–VI)
  • Lateral horn: Preganglionic autonomic neurons (T1–L2)
  • Central canal: Contains CSF

White Matter (surrounds grey matter):

  • Dorsal columns: Fasciculus cuneatus (C2+) and gracilis (lower body) — fine touch, vibration, proprioception
  • Lateral columns: Spinothalamic tract (pain, temperature)
  • Ventral columns: Corticospinal tract (motor)

Major Ascending Tracts

Dorsal Column-Medial Lemniscal Pathway (conscious proprioception, fine touch, vibration):

StepDetails
1st neuronPseudounipolar neuron in dorsal root ganglion
EntryEnters dorsal horn, ascends 1–2 levels
SynapseDorsal column nuclei (gracilis, cuneatus) in medulla
2nd neuronDecussates as internal arcuate fibers → medial lemniscus
SynapseVPL nucleus of thalamus
3rd neuronThalamocortical radiations → somatosensory cortex

Spinothalamic Tract (pain, temperature, crude touch):

StepDetails
1st neuronPseudounipolar neuron in dorsal root ganglion
EntryEnters dorsal horn, synapses (Lamina I, V)
DecussationCrosses at spinal cord level (2 segments above entry)
AscendingLateral spinothalamic tract (contralateral)
SynapseVPL nucleus of thalamus
3rd neuronThalamocortical radiations → sensory cortex

Exam tip: Brown-Séquard syndrome = hemisection of spinal cord → ipsilateral motor loss (corticospinal) + ipsilateral proprioception loss (dorsal columns) + contralateral pain/temperature loss (spinothalamic, 2 segments below lesion)

Major Descending Tracts

Corticospinal Tract (voluntary movement):

StepDetails
OriginMotor cortex (precentral gyrus, Brodmann area 4)
DescendingInternal capsule → cerebral peduncle → pons → medulla
DecussationPyramidal decussation (most fibers cross)
DestinationLateral corticospinal tract → LMN in ventral horn
FunctionFine voluntary movement, dexterity

Other Descending Tracts:

TractOriginFunction
RubrospinalRed nucleus (midbrain)Flexor muscle tone (replaced by corticospinal in humans)
VestibulospinalDeiters’ nucleus (pons)Postural tone, extensor muscles
ReticulospinalPontine/medullary reticular formationAutonomic functions, muscle tone
TectospinalSuperior colliculusHead and neck reflexes

Exam tip: Upper motor neuron signs (corticospinal lesion): Spasticity, hyperreflexia, clonus, Babinski sign; Lower motor neuron signs (ventral horn lesion): Flaccid paralysis, hyporeflexia, fasciculations, atrophy

Brainstem

Midbrain:

  • Superior colliculus: Visual reflexes
  • Inferior colliculus: Auditory processing
  • Cerebral peduncle: Corticospinal, corticopontine fibers
  • Red nucleus: Rubrospinal tract origin
  • Substantia nigra: Dopaminergic neurons (Parkinson disease)

Pons:

  • Respiratory centers: Apneustic, pneumotaxic
  • Pontine nuclei: Cerebellar connections
  • Superior olivary nucleus: Sound localization
  • Trigeminal nuclei: Face sensation

Medulla:

  • Respiratory centers: Medullary respiratory center (inspiratory, expiratory)
  • Cardiovascular center: Vasomotor center
  • Dorsal motor nucleus of X: Parasympathetic output
  • Nucleus tractus solitarius: Taste, visceral afferents
  • Olive: Cerebellar connections

Exam tip: Locked-in syndrome = ventral pontine lesion → quadriplegia, anarthria, consciousness preserved; Patient communicates via vertical eye movements (intact cortical function)

Cerebellum

Anatomy:

  • Archicerebellum (vestibulocerebellum): Flocculonodular lobe — vestibular function, balance
  • Paleocerebellum (spinocerebellum): Vermis — trunk and proximal muscle coordination
  • Neocerebellum ( cerebrocerebellum): Lateral hemispheres — planning and initiation of movement

Connections:

  • Inputs: climbing fibers (from inferior olive), mossy fibers (from many sources)
  • Outputs: Deep nuclei → thalamus → motor cortex (dentate, emboliform, globose, fastigial)

Cerebellar Lesions (ipsilateral):

SignDescription
AtaxiaWide-based gait, incoordination
DysmetriaPast-pointing (finger-nose test)
Intention tremorTremor worse at end of movement
DysdiadochokinesiaCannot perform rapid alternating movements
HypotoniaDecreased muscle tone
NystagmusOscillating eye movements

Exam tip: Midline cerebellar lesions (vermis) → truncal ataxia, no appendicular signs; Lateral hemispheric lesions → appendicular ataxia, dysmetria, intention tremor

Basal Ganglia

Components:

  • Striatum: Caudate nucleus + putamen (receives cortical inputs)
  • Globus pallidus (GP): Internal (GPi) and External (GPe) segments
  • Substantia nigra: Pars compacta (dopamine) + Pars reticulata (output)
  • Subthalamic nucleus: excitatory input to GPi

Direct and Indirect Pathways:

PathwayFrom StriatumEffect on ThalamusMovement
DirectInhibits GPiDisinhibitionFacilitates
IndirectInhibits GPeLess inhibition of STN → more excitation of GPiInhibits

Parkinson Disease (basal ganglia disorder):

  • Pathology: Loss of dopaminergic neurons in substantia nigra pars compacta
  • Features: Resting tremor, rigidity, bradykinesia, shuffling gait, masked facies, micrographia
  • Treatment: Levodopa (DOPA decarboxylase → dopamine), MAO-B inhibitors, COMT inhibitors, anticholinergics

Exam tip: Huntington disease = autosomal dominant CAG repeat in HTT gene → chorea, psychiatric symptoms, dementia; Caudate atrophy; Hemiballismus = lesion of subthalamic nucleus → wild flinging movements

Diencephalon

Thalamus:

  • VPL: Somatosensory (body)
  • VPM: Somatosensory (face)
  • MGN/LGN: Auditory (medial) and visual (lateral) geniculate bodies
  • Anterior nucleus: Papez circuit (memory)
  • Pulvinar: Visual association
  • Intralaminar nuclei: Reticular activating system

Hypothalamus:

  • Anterior (parasympathetic): Preoptic area — thermoregulation (cooling), osmoreceptors
  • Posterior (sympathetic): Mammillary bodies — thermoregulation (heating)
  • Lateral: Feeding center — lesions → anorexia
  • Ventromedial: Satiety center — lesions → hyperphagia/obesity
  • Arcuate: Release-inhibiting hormones, dopamine (prolactin-inhibiting)

Hypothalamic Hormones:

HormoneTargetFunction
TRHAnterior pituitary↑ TSH
CRHAnterior pituitary↑ ACTH
GnRHAnterior pituitary↑ FSH, LH
GHRHAnterior pituitary↑ GH
SomatostatinAnterior pituitary↓ GH
DopamineAnterior pituitary↓ Prolactin
OxytocinPosterior pituitaryUterine contraction, milk let-down
ADHPosterior pituitaryWater retention

Exam tip: Korsakoff syndrome = thiamine (B1) deficiency → mammillary body damage → anterograde amnesia, confabulation; Wernicke-Korsakoff from chronic alcoholism


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Central Nervous System — Comprehensive NEET PG Notes

Meninges and CSF

Meninges:

LayerFeatures
Dura materOuter layer; epidural space (potential), venous sinuses
Arachnoid materSpider-web projections; subarachnoid space (contains CSF and vessels)
Pia materDelicate, closely adherent to brain surface

Subarachnoid cisterna:

  • Lumbar cistern: Below L2 — site for lumbar puncture
  • Cisterna magna: Below cerebellum — cerebellar infarcts can be seen here

CSF Circulation:

  1. Produced by choroid plexus in ventricles (80%) and ependymal cells
  2. Lateral ventricles → foramen of Monro → 3rd ventricle → cerebral aqueduct → 4th ventricle
  3. 4th ventricle → foramina of Magendie (median) and Luschka (lateral) → subarachnoid space
  4. Arachnoid granulations → venous sinuses (superior sagittal) → venous circulation

CSF Properties:

  • Volume: ~150 mL
  • Pressure: 70–180 mmH₂O (lying), 200–250 mmH₂O (sitting)
  • Composition: Low protein, glucose 60–70% of plasma, few cells

Exam tip: Lumbar puncture — needle enters at L3–L4 (below conus medullaris at L1–L2); Contraindications: ↑ ICP (risk of herniation), coagulopathy, infection at puncture site; Queckenstedt maneuver — manual compression of jugular veins → ↑ ICP → ↑ CSF pressure (blocked if spinal block)

Blood-Brain Barrier

Structure:

  • Tight junctions between endothelial cells
  • Basement membrane (pericytes embedded)
  • Astrocyte end-feet (perivascular)

Functions:

  • Protects CNS from blood-borne toxins
  • Maintains stable environment for neuronal function
  • Selectively allows necessary substances

Areas Without BBB:

  • Circumventricular organs: Subfornical organ, area postrema (detects blood toxins, triggers vomiting)
  • Choroid plexus: Selective secretion

Exam tip: Multiple sclerosis — inflammatory demyelination; Progressive multifocal leukoencephalopathy (PML) — JC virus reactivation in immunocompromised; Autoimmune encephalitis — antibodies against neuronal surface antigens (NMDA-R, VGKC)

Limbic System

Components:

  • Hippocampus (Ammon’s horn): Declarative memory, spatial navigation
  • Amygdala: Emotional processing, fear conditioning
  • Fornix: Hippocampal connections
  • Parahippocampal gyrus: Memory encoding
  • Mammillary bodies: Part of Papez circuit
  • Anterior thalamic nucleus: Part of Papez circuit

Papez Circuit (memory): Hippocampus → Fornix → Mammillary bodies → Anterior thalamic nucleus → Cingulate gyrus → Parahippocampal gyrus → Hippocampus

Exam tip: Klüver-Bucy syndrome = bilateral amygdala lesions → hyperorality, hypersexuality, visual agnosia, placidity; Bilateral hippocampal damage → anterograde amnesia (cannot form new memories)

Cerebral Cortex Functions

Lobes and Functions:

LobeAreaFunction
FrontalBroca area (BA 44, 45)Speech production
FrontalPrefrontal cortexExecutive function, planning, personality
FrontalPrimary motor (BA 4)Voluntary movement
FrontalPremotor, supplementary motorMovement planning
ParietalPrimary somatosensory (BA 1, 2, 3)Somatic sensation
ParietalSomatosensory association (BA 5, 7)Spatial orientation
TemporalWernicke area (BA 22)Speech comprehension
TemporalPrimary auditory (BA 41, 42)Sound processing
TemporalHippocampusMemory
OccipitalPrimary visual (BA 17)Visual perception
OccipitalVisual association (BA 18, 19)Visual integration

Dominant Hemisphere (usually left):

  • Language (Broca and Wernicke areas)
  • Logical reasoning
  • Sequential processing

Non-dominant Hemisphere (usually right):

  • Spatial abilities
  • Music and art appreciation
  • Holistic processing

Exam tip: Broca aphasia = non-fluent speech, good comprehension, naming difficulty; Lesion: inferior frontal gyrus; Wernicke aphasia = fluent but meaningless speech, poor comprehension; Lesion: superior temporal gyrus

Cerebrospinal Fluid Disorders

Hydrocephalus:

TypeCauseFeatures
Obstructive (non-communicating)Block in ventricular systemAcute ↑ ICP, papilledema
CommunicatingBlock in subarachnoid spaceGradual onset, dementia
Normal pressureImpaired CSF absorptionDementia, gait disturbance, incontinence
Ex vacuoBrain atrophy (elderly)Ventricular enlargement without ↑ ICP

Intracranial Pressure:

  • Normal: 10–20 mmHg
  • Compensation: CSF displacement, venous compression
  • Cushing triad: Hypertension, bradycardia, irregular respirations (late sign of ↑ ICP)
  • Herniation types: Uncal (CN III, ipsilateral pupil), central (diencephalon), tonsillar (brainstem)

Spinal Cord Lesions

LevelSyndromeFeatures
C2–C3High cervicalQuadriplegia, respiratory failure, sensory loss below clavicle
C5–C6RadiculopathyDeltoid/biceps weakness, sensory loss in arm
T4ThoracicParaplegia, sensory loss below T4, bladder dysfunction
L1–L2Cauda equinaLower motor neuron signs, saddle anesthesia, bowel/bladder dysfunction
Conus medullarisConusEarly bladder symptoms, erectile dysfunction

Exam tip: Anterior cord syndrome = anterior spinal artery occlusion → loss of motor (corticospinal) and pain/temperature (spinothalamic), preserved dorsal column function; Brown-Séquard = hemisection → ipsilateral motor + proprioception loss, contralateral pain/temperature loss

Autonomic Nervous System

Parasympathetic (craniosacral):

  • Cholinergic throughout (ACh at all synapses)
  • Receptors: Nicotinic (ganglia), Muscarinic (end organs)
  • Functions: Rest and digest,瞳孔缩小,促进分泌,心率减慢

Sympathetic (thoracolumbar):

  • Pre-ganglionic: ACh (nicotinic receptors)
  • Post-ganglionic: Mostly norepinephrine (α, β receptors), sweat glands (ACh, muscarinic)
  • Functions: Fight or flight,瞳孔开大,心率加快,血压升高

Autonomic Receptors:

ReceptorLocationEffectBlockers
α1Vascular smooth muscleVasoconstrictionPrazosin
α2Presynaptic nerve terminals↓ NE releaseYohimbine
β1Heart↑ HR, ↑ contractilityMetoprolol
β2Bronchial, vascular smooth muscleBronchodilation, vasodilationPropranolol
M1–M5Parasympathetic end organsVariableAtropine

Exam tip: Autonomic dysreflexia = lesion above T6 → triggers below lesion → massive sympathetic discharge → hypertension, bradycardia; Triggered by bladder distension, bowel impaction; Shy-Drager syndrome = multiple system atrophy with autonomic failure

Sleep

Wakefulness:

  • Reticular activating system (RAS): Midbrain reticular formation projects to thalamus → cortex
  • Neurotransmitters: Acetylcholine, dopamine, norepinephrine, serotonin

NREM Sleep (stages 1–3):

  • Stage 1: Light sleep (theta waves), sleep spindles and K-complexes appear
  • Stage 2: True sleep onset, sleep spindles (12–14 Hz), K-complexes
  • Stage 3 (slow-wave): Delta waves (0.5–2 Hz), restoration, GH and prolactin release

REM Sleep:

  • Desynchronized EEG (like wakefulness)
  • PGO waves (ponto-geniculo-occipital)
  • Dreaming occurs here
  • Muscle atonia (via descending pathways)
  • Penile/clitoral erection (parasympathetic)

Sleep Cycles:

  • 4–5 cycles per night
  • Early: More N3
  • Late: More REM

Exam tip: Narcolepsy = loss of hypocretin/orexin neurons → daytime somnolence, cataplexy, hypnagogic hallucinations, sleep paralysis; ** REM sleep behavior disorder** = loss of muscle atonia → acting out dreams (often precedes Parkinson disease)

Practice Questions for NEET PG

  1. Trace the dorsal column-medial lemniscal pathway from periphery to cortex.
  2. Compare upper motor neuron and lower motor neuron lesions.
  3. A patient has resting tremor, rigidity, and bradykinesia. Where is the lesion?
  4. Describe the CSF circulation pathway.
  5. What is the role of the limbic system in memory?
  6. A patient has loss of pain and temperature sensation but preserved proprioception. Which tract is affected and why?
  7. Compare the direct and indirect pathways of the basal ganglia.

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