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190 Cards in this Set

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Basics: Nissl Substance
Stairs RER within cell bodies and dendrites, but not axons.
Basics: Microglia
Mesodermally-derived CNS macrophages.
Basics: Meissner's Corpuscles
Group Aβ fibers; rapidly-adapting proprioception and dynamic fine touch; within glabrous skin.
Basics: Pacinian Corpuscles
Group Aβ fibers; rapidly-adapting vibration and pressure; within deep skin, ligaments, and joints.
Basics: Merkel Disks
Group Aβ fibers; slowly-adapting proprioception and static touch; within hair follicles.
CNS Pathology: Norepinephrine
High in anxiety, low in depression.
CNS Pathology: Dopamine
High in schizophrenia, low in Parkinson's, low in depression.
CNS Pathology: 5-HT
Low in anxiety, low in depression.
CNS Pathology: ACh
Low in Alzheimer's, low in Huntington's, low in REM sleep.
CNS Pathology: GABA
Low in anxiety, low in Huntington's.
Function: Anterior Hypothalamus.
Senses elevated body temperature ---> parasympathetic output for body cooling.
Function: Posterior Hypothalamus.
Senses decreased body temperature ---> sympathetic output for body heating.
Function: Lateral Hypothalamus.
"Hunger center." Lesion ---> anorexia. Inhibited by leptin.
Function: Ventromedial Hypothalamus.
"Satiety center." Lesion ---> hyperphagia/obesity. Stimulated by leptin.
Product: Supraoptic Nucleus of the Hypothalamus.
ADH and Oxytocin.
Product: Paraventricular Nucleus of the Hypothalamus.
ADH and Oxytocin.
Function: Septal Nucleus.
Pleasure/Gratification/Sexual urges.
Connections: Ventral Posterior Lateral Nucleus of the Thalamus.
Dorsal columns, anterolateral tracts, primary somatosensory cortex.
Connections: Ventral Posterior Medial Nucleus of the Thalamus.
Sensory nucleus of V, spinal nucleus of V, primary somatosensory cortex.
Connections: Ventral Anterior, Ventral Lateral Nuclei of the Thalamus.
Basal ganglia, primary motor cortex.
Direct Basal Ganglia Pathway.
Excitatory to cortex:

Striatum to GPi/SNpr (GABA); GPi/SNpr to VA/VL thalamus (GABA).
Indirect Basal Ganglia Pathway.
Inhibitory to cortex.

Striatum to GPe (GABA); GPe to STN (GABA); STN to GPi/SNpr (Glu); GPi/SNpr to VA/VL thalamus (GABA)
Nigrostriatal Pathway.
Substantia nigra pars compacta to striatum.

D1: excitatory to direct pathway (net excitation)
D2: inhibitory to indirect pathway (net excitation)
Classic symptoms: Parkinson's.
TRAPG:

Tremor
Rigidity
Akinesia (Bradykinesia)
Postural instability
Gait instability
Basics: Hemiballismus.
Sudden, wild flailing of 1 arm +/− leg. Associated with damage to contralateral STN.
Classic symptoms: Huntington's.
Chorea, athetosis; depression; progressive dementia.
Imaging: Huntington's.
Severely atrophied caudate, enlarged ventricles, defined sulci.
Basics: Huntington's.
Autosomal dominant CAG repeated disorder. Chromosome 4.
Define: Chorea.
Sudden, jerky, purposeless movements. Characteristic of basal ganglia lesion (e.g. Huntington’s disease).
Define: Athetosis.
Slow, writhing movements, especially of fingers. Characteristic of basal ganglia lesion (e.g. Huntington’s disease).
Basics: Dystonia.
Sustained, involuntary muscle contractions.
Basics: Essential Tremor.
AKA "postural tremor."

Action tremor (worsens when holding posture), autosomal
dominant. Essential tremor patients often self-medicate with alcohol, which ↓
tremor.
Treatment: Essential Tremor.
Treatment: β-blockers.
Basics: Resting Tremor.
Abates with purposeful movement, most noticeable distally. Seen in Parkinson’s.
Basics: Intention Tremor.
Slow, zigzag motion when pointing toward a target; associated with
cerebellar dysfunction.
Function: Dorsolateral Prefrontal Cortex.
Working memory.
Function: Orbitofrontal Cortex.
Social and emotional decision-making.
Function: Anterior Cingulate Cortex.
Motivation.
Motor/Sensory Homunculus
Legs and feet medially; arms, hands, face laterally.
Basics: Klüver-Bucy Syndrome.
Results from bilateral amygdala lesion.

Hyperorality, hypersexuality,
and disinhibited behavior.
Lesion: Mammillary Bodies (Bilateral) .
Wernicke-Korsakoff syndrome

Wernicke's: ataxia, confusion, ophthalmopegia.
Korsakoff's: amnesia, confabulation.
Lesion: PPRF.
Eyes deviate AWAY from the side of the lesion.
Lesion: Frontal Eye Fields.
Eyes deviate TOWARD the side of the lesion.
Lesion: Hippocampus.
Anterograde amnesia.
Lesion: Cerebellar Vermis.
Truncal ataxia and dysarthria.
Lesion: Cerebellar Hemisphere.
Intention tremor, limb ataxia.
Lesion: Right Parietal Lobe.
Contralateral hemineglect.
Basics: Central Pontine Myelinolysis.
Demyelinating disorder ssociated with rapid correction of hyponatremia. Acute paralysis, dysarthria, dysphagia, diplopia, and loss of consciousness. Recovery rare.
Lesion: Recurrent Laryngeal Nerve.
Loss of all laryngeal muscles except cricothyroid. Hoarseness
Basics: Broca's Aphasia.
Non-fluent with intact comprehension.
Basics: Wernicke’s Aphasia.
Fluent aphasia with impaired comprehension.
Basics: Global Aphasia.
Nonfluent aphasia with impaired comprehension (Broca's + Wernicke's).
Basics: Conduction Aphasia.
Poor repetition but fluent speech, intact
comprehension. Arcuate fasciculus lesion—connects
Broca’s, Wernicke’s areas.
Basics: Berry Aneurysm.
Occur at the bifurcations in the circle of Willis. Most common site is bifurcation of the anterior communicating artery. Rupture (most common complication) leads to hemorrhagic stroke/subarachnoid hemorrhage.
Basics: Charcot-Bouchard Microaneurysms.
Associated with chronic hypertension; affects
small vessels (e.g., in basal ganglia, thalamus).
Basics: Epidural Hematoma.
Rupture of middle meningeal artery (branch of maxillary artery), often 2° to fracture of temporal bone. Lucid interval. Rapid expansion under systemic arterial pressure →
transtentorial herniation, CN III palsy.

“Biconvex disk” on CT.
Basics: Subdural Hematoma.
Rupture of bridging veins. Slow venous bleeding with delayed onset of symptoms. Seen in elderly individuals, alcoholics, blunt trauma, shaken babies.

Crescent-shaped hemorrhage on CT.
Basics: Subarachnoid Hemorrhage.
Rupture of an aneurysm or an AVM. Patients complain of “worst headache of my life.”
Bloody or yellow spinal tap.
2–3 days afterward, there is a risk of vasospasm due to blood breakdown products, which
irritate vessels (treat with calcium channel blockers).
Basics: Transient Ischemic Attack (TIA).
Brief, reversible episode of neurologic dysfunction due
to focal ischemia. Typically, symptoms last for < 24 hours.
Basics: Stroke Imaging.
Bright on diffusion-weighted MRI in 3–30 minutes and remains bright for 10 days, dark on CT in ~ 24 hours.
Basics: Normal Pressure Hydrocephalus.
Does not result in ↑ subarachnoid space volume. Expansion of ventricles distorts the fibers of the corona radiata and leads to the clinical triad of
dementia, ataxia, and urinary incontinence.
Basics: Communicating Hydrocephalus.
↓ CSF absorption by arachnoid villi, which can lead to ↑ intracranial pressure, papilledema, and herniation
Basics: Obstructive Hydrocephalus.
Caused by a structural blockage of CSF circulation within the ventricular system.
"Hydrocephalus ex vacuo"
Appearance of ↑ CSF in atrophy (e.g., Alzheimer’s disease, advanced HIV). Intracranial pressure is normal; triad is not seen.
Common location: Vertebral Disc Herniation.
Between L5 and S1.
Modalities: Dorsal Columns.
Fine touch, conscious proprioception, two-point discrimination, stereognosis.
Modalities: Anterolateral (Spinothalamic) Tract.
Pain and temperature.
Sx: LMN Syndrome.
Flaccid paralysis, hyporeflexia, atrophy, fibrillations, fasciculations.
Sx: UMN Syndrome.
Rigid paralysis, hyperreflexia, spasticity, Babinski sign
Sx: Horner's syndrome.
Ptosis, miosis, anhidrosis.

Associated with lesion of spinal cord above T1.
Spinal Level: Biceps Reflex.
C5, C6 nerve roots.
Spinal Level: Triceps Reflex.
C7, C8 nerve roots.
Spinal Level: Patellar Reflex.
L3, L4 nerve roots.
Spinal Level: Achilles Reflex.
S1, S2 nerve roots.
Functions: Solitary Nucleus.
"Nucleus of Sensation and Taste" = IX, X, and VII

Taste from VII, IX, X
Visceral sensory from IX, X
Function: Nucleus Ambiguus.
Motor nucleus of 9, 10.

Preganglionic parasympathetics of X to the heart.
Function: Dorsal Motor Nucleus of X.
Preganglionic parasympathetics of X to lungs, gut.
CN XII Lesion.
Tongue deviates toward side of lesion
CN V Motor Lesion.
Jaw deviates toward side of lesion. Bilateral cortical input to lateral pterygoid muscle.
CN X Lesion.
Uvula deviates away from side of lesion. Weak side collapses and uvula points away.
CN XI Lesion.
Weakness turning head to contralateral side of lesion (SCM). Ipsilateral shoulder
droop (trapezius).
Cortical Facial Palsy.
Contralateral facial paralysis only in lower quadrant.
Peripheral Facial Palsy.
Ipsilateral paralysis of upper and lower face.
Basics: Wallenberg Syndrome.
Sx: ipsilateral loss of face pain/temp; contralateral loss of body pain/temp; ipsilateral Horner's syndrome; nausea/vertigo/nystagmus; dysarthria/dysphagia
Vessel: Wallenberg Syndrome.
Vertebral artery or PICA
Basics: Weber Syndrome.
Ipsilateral oculomotor palsy and contralateral body paresis
Vessels: Weber Syndrome.
PCA or basilar artery
Components: Limbic System.
Cingulate, hippocampus, amgydala, fornix, mammillary bodies.
Cerebellar Nuclei and Associated Regions.
Lateral to medial:

Dentate (lateral); interposed (intermediate); fastigial (vermis)

Interposed = emboliform and globose.
Cerebellum: "Climbing" vs. "Mossy" Fibers.
Climbing fibers: from contralateral inferior olivary nucleus to Purkinje cells.

Mossy fibers: All other inputs (dorsal spinocerebellar, vestibular, pontine, etc) to granule cells.
Basics: OVLT
"Organum vasculosum of the lamina terminalis"

Circumventricular organ sensitive to body tonicity; output to neurohypophysis for regulation of ADH secretion.
Basics: SFO
"Sub-fornical organ"

Circumventricular ogran sensitive to [AT2]; output to hypothalamus for regulation of thirst (and ADH output).
Lesion: Cerebral Hemisphere.
Intention tremor, limb ataxia; damage to the cerebellum results in ipsilateral deficits
Lesion: Mammillary Bodies.
Wernicke-Korsakoff syndrome.
Lesion: Anterior Spinal Artery.
Contralateral hemiparesis (lower extremities), medial lemniscus (↓ contralateral proprioception), ipsilateral paralysis of hypoglossal nerve
Lesion: PICA
Wallenberg syndrome

Contralateral body pain/temp, ipsilateral face pain/temp, vestibular nucleus lesion (vertigo/nystagmus/diplopia), ipsilateral Horner's (RVLT lesion), dysphagia, dysarthria
Lesion: AICA
Ipsilateral facial palsy, ipsilateral deafness, loss of ipsilateral pain/temp, ipsilateral limbgait ataxia
Lesion: Posterior Cerebral Artery
Contralateral homonymous hemianopia with macular sparing (supplies occipital cortex)
Lesion: Middle Cerebral Artery
Contralateral face and arm paralysis and sensory loss, aphasia (dominant sphere),
left-sided neglect.
Lesion: Anterior Cerebral Artery.
Motor and sensory deficits to contralateral leg and trunk.
Infarct: Basilar Artery
"Locked-in" syndrome.
General Outcome: Anterior Circulation Stroke
General sensory and motor dysfunction, aphasia.
General Outcome: Posterior Circulation Stroke
Cranial nerve deficits (vertigo, visual deficits), coma, cerebellar deficits (ataxia).
Basics: Area Postrema
Circumventricular organ within 4th ventricular; chemoreceptor trigger zone for nausea/vomiting reflex; only bilateral CVO
# of Spinal Nerves
31 Total

8 Cervical
12 Thoracic
5 Lumbar
5 Sacral
1 Coccygeal
Pathway: Dorsal Columns.
Peripheral receptor ---> medial DREZ ---> ipsilateral fasciculus gracilis/cuneatus ---> nucleus gracilis/cuneatus (synapse) ---> decussate as internal arcuate fibers ---> ascend as medial lemniscus ---> ventral posterior lateral thalamus (synapse) ---> primary somatosensory cortex (synapse)
Pathway: Anterolateral (Spinothalamic) Tract.
Peripheral fibers ---> lateral DREZ ---> ipsilateral anterolateral spinal funiculus (synapse) ---> decussate within 2 spinal levels ---> ascend to ventral posterior lateral thalamus (synapse) ---> primary somatosensory cortex
Pathway: Dorsal Spinocerebellar Tract.
Peripheral receptor ---> medial DREZ ---> Column of Clarke nuclei ---> ipsilateral dorsolateral funiculus ---> ipsilateral cerebellum (via ICP)
Pathway: Corticospinal tract.
Primary motor cortex ---> corona radiata ---> internal capsule (posterior limb) ---> cerebral peduncles ---> decussation in medullary pyramids ---> lateral and anterior spinal funiculi ---> synapse on α and γ motor neurons.
Lesion: Horner's syndrome.
Spinal lesion above T1.
Sensory/Motor/Both: CN I
Sensory
Sensory/Motor/Both: CN II
Sensory
Sensory/Motor/Both: CN III
Motor
Sensory/Motor/Both: CN IV
Motor
Sensory/Motor/Both: CN V
Both
Sensory/Motor/Both: CN VI
Motor
Sensory/Motor/Both: CN VII
Both
Sensory/Motor/Both: CN VIII
Sensory
Sensory/Motor/Both: CN IX
Both
Sensory/Motor/Both: CN X
Both
Sensory/Motor/Both: CN XI
Motor
Sensory/Motor/Both: CN XII
Motor
Cranial Nerve Nuclei: Midbrain
III, IV
Cranial Nerve Nuclei: Pons
V, VI, VII, VIII
Cranial Nerve Nuclei: Medulla
IX, X, XI, XII
Afferent/Efferent: Corneal Reflex
Afferent: V1
Efferent: VII
Afferent/Efferent: Lacrimal Reflex
Afferent: V1
Efferent: VII
Afferent/Efferent: Jaw Jerk Reflex
Afferent: V3
Efferent: V3
Afferent/Efferent: Pupillary Reflex
Afferent: II
Efferent: III
Afferent/Efferent: Gag Reflex
Afferent: IX
Efferent: IX, X
Cranial Foramen: CN I
Cribiform plate of the ethmoid bone.
Cranial Foramen: CN II
Optic canal.
Cranial Foramen: CN III
Superior orbital fissure.
Cranial Foramen: CN IV
Superior orbital fissure.
Cranial Foramen: CN V1
Superior orbital fissure.
Cranial Foramen: CN VI
Superior orbital fissure.
Cranial Foramen: CN V2
Foramen rotundum.
Cranial Foramen: CN V3
Foramen ovale.
Cranial Foramen: CN VIII
Internal acoustic meatus.
Cranial Foramen: CN VIII
Internal acoustic meatus.
Cranial Foramen: CN IX
Jugular foramen.
Cranial Foramen: CN X
Jugular foramen.
Cranial Foramen: CN XI
Jugular foramen.
Cranial Foramen: CN XII
Hypoglossal canal.
Nerves that Pass Through the Cavernous Sinus
CN III, IV, V1, V2, VI
Sx: Cavernous Sinus Syndrome
Ophthalmoplegia and sensory loss within the distribution of V1 and V2 (ophthalmic and maxillary)
Functions: Muscles of Mastication
Jaw opening: Lateral pterygoid

Jaw closing: Medial pterygoid, masseter, temporalis
Function: Otolith Organs
Linear acceleration and gravity.
Function: Semicircular Canals.
Angular acceleration.
Mechanism: Semicircular Canals.
Endolymph displaces hair cell stereocilia enclosed within cupulas, contained within ampulas at the base of the canals.
Mechanism: Otolith Organs.
Endolymph displaces hair cell stereocilia embedded within calcium carbonate matrix.
Structure/Tonotopy of Basilar Membrane.
Base: Narrow, elastic; sensitive to high frequencies.

Apex: Wide, compliant; sensitive to low frequencies.
Function: Outer Cochlear Hair Cells.
Modulate sensitivity of basilar membrane to different frequencies.
Pathway: Sound ---> Hair Cells.
Tympanic membrane ---> malleus ---> incus ---> stapes ---> oval window ---> basilar membrane/tectorial membrane ---> hair cells.
Composition: Endolymph.
Very high [K+]
Composition: Perilymph
Very high [Na+]
Ocular Tunics and Components
Fibrous: Sclera, cornea
Vascular: Choroid, iris, ciliary body
Neural: Retina
Pathway: Aqueous Humor
Secreted in posterior chamber by ciliary bodies ---> passes between iris and lens into anterior chamber ---> drained by canal of Schlemm into ophthalmic veins
Basics: Glaucoma.
Impaired flow of aqueous humor →↑intraocular pressure → optic disk atrophy with cupping.
Wide-Angle Glaucoma.
Obstructed outflow through canal of Schlemm; much more common; painless/"silent"
Closed-Angle Glaucoma
Obstruction of flow between iris and cornea → pressure buildup
behind iris. Very painful, ↓ vision, rock-hard eye, frontal headache.

Do not give epinephrine!
Presentation: CN III damage
damage—eye looks down and out; ptosis, pupillary dilation, loss of accommodation.
Presentation: CN IV Palsy.
Diplopia with a defective
downward gaze (patients adjust by tilting head toward side of the lesion).
Presentation: CN VI Palsy.
Medially directed eyes.
Presentation: Unilateral MLF Lesion
"Internuclear ophthalmoplegia": Ipsilateral medial rectus palsy on attempted lateral gaze with contralateral nystagmus.

Convergence intact!
Findings: Caloric Test
Cold water: Ipsilateral deviation
Warm water: Contralateral deviation.
Charcot's Triad (Multiple Sclerosis)
Dysarthria, intention tremor, and nystagmus.
Classic findings: MS
Charcot's triad (dysarthria, intention tremor, nystagmus), unilateral optic neuritis, hemiparesis,
Course: MS
Relapsing and remitting inflammation and neurodegeneration.
Epidemiology: MS
Most commonly: white women in their 20s and 30s
Lab Findings: MS
Oligoclonal bands; MRI with periventricular plaques.
Treatment: MS
β-interferon, mitoxantrone, natalizumab.
Toxicity: Opioids
Respiratory depression, nausea/vomiting, constipation, miosis, pruritis

Additive CNS depression with other drugs.
Antidote: Opioid Overdose
Naltrexone.
Mechanism: Tramadol
Very weak opioid agonist; also inhibits serotonin and NE reuptake
Use: Tramadol
Chronic pain
Toxicity: Tramadol
Respiratory depression, nausea/vomiting, constipation, miosis, pruritis
Opioid Receptor Signaling
K+ channel activation, Ca2+ inactivation ---> hyperpolarization, inhibited transmitter release
Mechanism: Phenytoin
↑ Na+ channel inactivation
Mechanism: Carbamazepine
↑ Na+ channel
inactivation
Mechanism: Lamotrigine
Blocks voltage-gated
Na+ channels
Mechanism: Gabapentin
Primarily inhibits Ca2+ channels

GABA analogue with NO GABA receptor activity
Mechanism: Topiramte
Blocks Na+ channels, ↑ GABA action
Mechanism: Phenobartbital
Facilitate GABA-A action by ↑ duration of Cl− channels
Mechanism: Valproate
↑ Na+ channel inactivation, ↑ GABA concentration
Mechanism: Ethosuximide
Blocks thalamic T-type Ca2+ channels
Clinical Use: Phenytoin
Tonic-clonic seizures.
Clinical Use: Phenobarbital
Anxiety, seizures, insomnia
Clinical Use: Benzodiazepines
Anxiety, spasticity, status epilepticus
Tx: Benzodiazepine Overdose
Flumazenil, competitive GABA antagonist