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127 Cards in this Set

  • Front
  • Back
Brainstem nuclei associated with CN V
Spinal and principle sensory nucleus of V
Mesencephalic V
Motor nucleus of V
Brainstem nuclei associated with X
Nucleus ambiguus
Dorsal motor nucleus of X
Spinal nucleus of V (skin and outer ear)
Nucleus solitarius
Brainstem nuclei associated with VII
Facial nucleus
Superior salivatory nucleus
Nucleus solitarius
Spinal nucleus of V
Reticular formation (3, where?)
Located medially throughout
1. Autonomic functions: BP, heart rate, respiration
2. Descending pathways for motor and pain
3. Neurotransmitters
Branchial motor nuclei of brainstem (4)
Motor nucleus of V
Facial nucleus
Nucleus ambiguus (IX, X)
Spinal accesory XI
Inferior olivary nucleus
Lateral in rostral medulla
Cell bodies that relay coordination info b/w cortex and cerebellum via inferior cerebellar peduncle
Inferior cerebellar peduncles
Dorsolaterally in rostral medulla
Mostly comprised of olivocerebellar fibers
Posterior spinocerebellar
Cuneocerebellar
Vestibulocerebellar
Where is major motor decussation?
Caudal medulla
Pyrimidal fibers cross to form corticospinal tracts
Where is major sensory decussation?
Dorsal column pathway crosses in caudal medulla to form medial lemniscus
Hypoglossal nucleus (where, action, in lesion?)
Most of medulla in midline
Innervates tongue
When lesioned, tongue deviates to side of lesion (weak side)
Nucleus ambiguus (where, action, in lesion?)
In medulla lateral and ventral to somatic motor nuclei
Branchial motor nucleus for IX and X- swallowing and speech
Lesion - hoarseness and difficulty swallowing
Dorsal motor nucleus of X (what type of innervations?)
Medial ventral in medulla
Parasympathetic visceral motor for vagus traveling to ab and thorax
Spinal nucleus and descending tract of V
Medulla to mid pons up to principal nucleus of V, lateral
Spinal nucleus of V receives pain afferents and tract carries pain afferents before synapsing
Nucleus solitarius
Meduall thru caudal pons, medial
Principal visceral afferent nucleus of brainstem
Taste - VII, IX, X
Carotid - IX
Vagus - X
Vestibular nucleus
Mid medulla - mid pons laterally
Vestibular division of VIII terminates here after first synapsing in vestibular ganglion outside of brainstem
Cochlear nucleus
Mid medulla to mid pons laterally
Cochlear (auditory) of VII synapse in spiral ganglion outside brainstem then go into cochlear nuclei
Pontine nuclei
Transmit info from cerebral cortex to cerebellum
How is auditory info distributed in CNS?
Spiral ganglion -> Cochlear nucleus -> decussates -> ascends in lateral lemniscus -> medial geniculate -> auditory cortex
CN VI nucleus
Caudal pons medial
LMN that innervate lateral rectus
Parapontine reticular formation (lateral gaze center)
Pons, adjacent to CN VI nuclei
Causes VI to move lateral rectus
Uses MLF to CN III nucleus to move medial rectus
Mediates horizontal gaze, responds to change in head position
Facial motor nucleus (upper vs lower)
Caudal pons
Innervate facial muscles
Upper part receives bilateral CB input, lower receives only contralateral
Principle sensory nucleus of V (where, what kind of sensation?, tract)
Rostral pons
For general sensation
Primary cell bodies are located in trigeminal ganglion
Fibers leave main nucleus of V thru trigeminothalamic pathway to thalamus
Motor nucleus of V
Rostral pons
Supply muscles of mastication
CN IV nucleus (unique feature?)
Midbrain
To superior oblique
Only CN to exit dorsally
Locus coeruleus
Medulla - Pons junction near floor of 4th ventricle
Noradrenergic neurons to all CNS
Superior cerebellar peduncle decussation
In medial midbrain
Has to cross because is carrying info from body from cerebellum, so crosses for cortex
CN III nucleus
Midbrain
Motor to all 4 ocular muscles
If lesioned, eye deviates laterally
Edinger-Westphal nucleus
Midbrain
Parasympathetic preganglionic cells
To ipsilateral ciliary ganglion for pupillary constriction in light reflex
Fibers travel w/ CN III
What is contained in the cerebral peduncles? (3)
Midbrain
Fibers that originate in cerebral cortex and form:
Corticospinal/pyramidal tract
Corticobulbar tract
Corticopontine fibers of cortico-ponto-cerebellar tract
Mesencephalic nucleus of V
Midbrain
Primary sensory cell bodies (only type of this in CNS)
Proprioception for mastication
Substantia nigra (4)
Midbrain
Separates cerebral peduncles from tegmentum
Major source of dopaminergic input to striatum
Damaged in Parkinson's
Superior and Inferior colliculus (where?)
Dorsal midbrain (tectum)
Inferior - from lateral lemniscus auditory
Superior - from retina
Flow of CSF in ventricles
Lateral -> foramens of Munro -> 3rd -> aqueduct of Sylvius -> 4th -> subarachnoid space medially by foramen of Magendie laterally by the 2 foramens of Luschka
What level does the spinal cord end at? (for LP?)
L1-2
L4 for LP
Hydrocephalus (communicating vs non)
Failure to absorb CSF, swelling of ventricles
Communicating -> ventricles still communicate w/ lumbar CSF
Non-communicating -> don't due to block
Types of glia
Astrocytes
Oligodendrocytes
Microglia
Scwhann (peripheral)
Astrocytes
Synaptogenesis
Metabolic support
Signaling
Form glial scars
Microglia
Phagocytosis
Surveillance
Cervical and lumbar enlargements
Cervical: C5-T1
Lumbar: L3-S2
Clarke's nucleus
Relay info to cerebellum
T1-L2/3
Intermediolateral cell column
Preganglionic sympathetic neurons
T1-L2/2
Accessory nucleus (function, where)
Motor neurons for trap and SCM
Medullary -> C5
One general feature of secondary and tertiary neurons
2 - decussate
3 - cell body in thalamus
Dorsal column pathway: modality, route, location
Vibratory, touch, joint position
Dorsal funiculus
1 - DRG -> fasciculus cuneatus or gracilis
2 - nucleus C or G -> decussate to ML
3 - thalamus -> S1
Gracilis vs Cuneatus
Gracilis - medial T6 and below
Cuneatus - lateral T5 and above
Dorsal column pathway somatotopic organization
Sacral enter first so are most medial
Headless man with feet medially
Spinothalamic tract: modality, route, location
Pain and temp
Anterior funiculus
1 - DRG -> ipsilateral Lissauer's for 2 levels ->
2 - Dorsal horn -> ducussate in ventral white commisure
3 - thalamus -> S1
Spinothalamic tract: somatotopic organization
Headless man with feet pointing laterally
Corticospinal tract: modality and route
Voluntary motor
Lateral funiculus
1 - cortex -> decussate in caudal medulla
2 - motor neurons in ventral horn
Corticospinal tract: somatotopic organization
Headless man with feet laterally
Clonus
Rapid beating of an extremity when one of its muscles it placed under rapid and sustained tension
UMN lesion signs (5)
Babinski
Spastic paralysis
Increased stretch reflexes
Clonus
Mild atrophy
LMN lesion signs
Segmental distribution of deficit

Decreased stretch reflexes
Flaccid paralysis
Pronounced atrophy
Fasciculations as signs of atrophy
C4
Clavicle
L1
Inguinal crease
L5
Lateral calf
Biceps
C5
Triceps
C7
Gastroc
S1-2
Brown-Sequard syndrome
Hemisection of spinal cord
Ipsilateral loss of position and vibration and UMN
Contralateral loss of pain and temp
Syringomyelia (3)
Suspended sensory loss due to damage of spinothalamic fibers as they cross in ventral white commisure
LMN due to damage to anterior horn cells
Pain and temp normal above and below lesions
Amyotrophic lateral sclerosis
Signs: combined UMN and LMN, with LMN predominating
Corticospinal tract and ventral horn cells lesion
Normal sensory pathways
Tabes Dorsalis
Predominant posterior column findings
Loss of position and vibratory
Romberg sign
Subacute combined degeneration
B12 deficiency -> present w/ pernicious anemia
Posterior columns and corticospinal tract
Loss of pos/vib sense w/ UMN
Anterior spinal artery syndrome
Occlusion of artery causes lesion in ventral cord
Affects corticospinal and spinothalamic tracts below lesion
Anterograde transport and neuropathy
Away from cell body
Sustains muscle
Vincristine and vinblastine disrupt MT organization and so cause neuropathy
Wallerian degeneration (3)
Dying-forward - degeneration from point of injury peripherally
Chromatolysis
Regeneration is possible
Segmental demyelination (5, histologic feature?)
Axon is intact
No chromatolysis
Remyelination can occur
Rapid recovery
Onion bulbs
Distal axonal degeneration (6, most common cause?)
Metabolic damage
Most distal degenerates first and procedes back to cell body
Stocking-glove distribution
Chromatolysis
Slow recovery
Usually toxic/metabolic neuropathies
Distal vs proximal weakness are associated with which types of degeneration?
Distal - axonal
Proximal - demyelinating
Clinical signs of axonal neuropathy (5)
Stocking glove
Slow and chronic
Loss of reflexes distally
Muscle wasting distally
Low amplitude Compound muscle action potentials (CMAP)
Guillian-Barre Syndrome
Autoimmune against peripheral myelin occuring after GI or respiratory infection
Primarily motor
Rapidly progressive
Areflexia and ataxia
Conduction block in NCSs
Ach receptor at NMJ properties
Ionotropic
Binding of Ach opens Na+ channel
Receptor has main immunogenic region which is near the Ach binding site
Myasthenia Gravis: pathophysiology
Auto-Ab to main immunogenic region of AchR ->
Increased nAChR turnover
Blocking of Ach binding sites
Reduced EPP
Myasthenia Gravis: clinical features (common muscles affected 4)
MUSCLE WEAKNESS
Fatiguable weakness to striated muscle
OCULAR, Diplopia, ptosis
Slurred speech
Myasthenia Gravis: treatment
AChase inhibitors - pyridostigmine
Autoimmune
Thymectomy - for patients w/ thymoma
Corticosteroids
Lambert Eaton Myasthenic Syndrome: pathophys
PRE-SYNAPTIC
Ab to presynaptic voltage gated calcium channel ->
Reduced Ca influx ->
Reduced Ach release into synapse
Lambert Eaton Myasthenic Syndrome: clinical features (3)
Paraneoplastic - associated w/ SCLC
Slowly progressive proximal muscle weakness in hips and shoulders
Repetitive stimulation can alleviate weakness, releases more calcium
Lambert Eaton Myasthenic Syndrome: treatment
Search for tumor
Immunosuppresives - prednisone
Mechanism of spinal cord injury (7)
Injury ->
Swelling longitudinally ->
Damaged axons ->
Glial cells form glial scar blocks regeneration ->
Release of glutamate ->
Excitotoxicity and cell death ->
Depletion of growth factors to neurons and more cell death
Spinal cord regeneration: neuronal survival (3)
Swelling increases damage -> Methylprednisone
Glutamate causes excitotoxicity -> block AMPA-R
Supply growth factors
Spinal cord regeneration: inhibitors
Inhibitors in myelin prevent sprouting -> block/kill oligodendrocytes
Features suggestive of myopathy (4)
Proximal distribution of weakness
Symmetric weakness
Normal muscles (no atrophy)
Normal deep tendon reflexes
Polymyositis: clinical features and treatment (pathophys, onset)
Primary inflammatory myositis
T-cell mediated autoimmune disease -> muscle fiber damage
Adult onset
Proximal weakness
Responds to immunosuppresives
Dermatomyositis: clinical features and treatment
Primary inflammatory myositis
Ab to endothelial cells -> vascular injury -> ischemic muscle damage
Childhood or adult onset
Rash early feature
Inclusion-body myositis: clinical features and treatment
Primary inflammatory myositis
Adult onset
Quadriceps weakness
No response to immunosuppresives
Metabolic myopathies present with . . .
Exercise intolerance
Muscle atrophy vs degeneration
Atrophy - response of muscle to damage to anterior horn cell, shrinking of fiber, can return to normal if renervated
Degeneration- breakdown of muscle fiber -> elevated CK
Duchenne muscular dystrophy
Muscle breakdown and degeneration -> macrophages
Inflammatory myopathies
Characterized by lymphocytes in muscle
Re-innervation of a muscle fiber
Converts muscle to whatever type (slow or fast) the new axon is -> type grouping
If re-innervation fails -> grouped atrophy
Periaqueductal gray
Sounds cerebral aqueduct in midbrain
Perception of pain?
Tectum+ tegmentum
Tectum - dorsal to periaqueductal gray in midbrain, contains white and gray matter
Tegmentum - inferior to central grey in midbrain (present at all levels), nuclei for III, IV, red, decussation of SCBP
How do cranial nerves exit brainstem?
Somatic (3,4,6,12)- ventromedially
Branchial - (5, 7, 9, 10, 11) - laterally
IV - dorsally
Loss of pain and temp on opp sides of face and body suggests . . .
Lesion in upper outer quadrant of brainstem affecting:
spinothalamic + spinal descending V
Cranial nerve lesion and brainstem localization
Midbrain - III - IV
Pons - V-VIII
Medulla - IX - XII
Quadrant of brainstem and localization of disease
Medial - corticospinal and medial lemniscus
Lateral - spinothalamic
Damage to long circumferential vessels of medulla
Loss of pain and temp in ipsilateral face and contralateral body
Damage to paramedian penetrating artery affects . .
Laterally exiting nerves like VI
Lateral brainstem syndromes (4) (which lateral cranial nerves?)
Spinothalamic - controlateral loss of pain and temp in body
Descending V - ipsilateral loss of pain and temp in face
Lateral cranial nerves - ambiguus, facial, trigeminal
NO BODY WEAKNESS
Medial brainstem syndromes (3)
Corticospinal - contralateral hemiparesis
Medial lemniscus - contralateral loss of position and vibratory
Medially exiting cranial nerves - XII, VI, III
Lateral medullary infarct (Wallenberg) (5)
Contralateral loss of pain and temp (spinothalamic)
Ipsi loss of pain and temp in face (desc V)
Hoarseness, deviated uvula to strong side(ambiguus)
Ipsilateral Horner (sympathetics)
Ipsilateral ataxia (ICBP)
Medial medullary infarct (Hughlings Jackson) (3)
Contralateral hemiparesis (CST)
Ipsilateral tongue paralysis (to weak side) (XII)
Contralateral loss of pos. and vib (ML)
Lateral pontine syndrome (5)
Contra pain and temp loss (ST)
Ipsi pain and temp face loss (V)
Ipsi paralysis of face, LMN type (VII)
Ipsi loss of facial sensation and paralysis of mastication muscles (V)
Ipsilateral ataxia (MCBP)
Medial pontine syndrome (2)
Contralateral hemiparesis (CST)
Ipsilateral paralysis of eye abduction (VI)
Medial midbrain syndrome (Weber) (2)
Contralateral hemiparesis (CST)
Ipsilateral III palsy
Acoustic neuroma (3)
Lesion extrinsic to stem
Begins w/ cranial nerves signs: VIII (vestibular before cochlear) then V and VII
Late occurrence of long tract signs (ataxia from MCBP and hemiparesis)
Basilar artery occlusion (5)
Benign tumor
Bilateral hemiparesis (both CST)
Bilateral sensory loss (ascending systems)
Variable CN signs
Reticular system: coma if involved, locked-in if spared
How is cerebellum related to cortex and body (ispi vs contralateral)?
Contralateral to cortex and ipsilateral to body
Cerebellar input
Motor cortex
Cortico pontine
MCBP
Vestibular via ICBP
Spinocerebellar to vermis
Vestibular cerebellar and spinocerebellar input
Vestibular - via ICBP to flocculonodular lobule
Spinocerebella - from trunk and legs to vermis and paravermis
Cerebellar output (4 step pathway)
Cerebellar cortex ->
Deep cerebellar nuclei -> SCBP
VL thalamus
Motor cortex
Cerebellar cortex cells
3 layers
Internal granular
Purkinje
Molecular
Cerebellar cortex circuit
Input ->
Synapse on internal granule cells from mossy fibers ->
Axons to molecular layer ->
Synapse on Purkinje cells
-> Output to deep nuclei of cerebellum
Cerebellar areas
Vestibulocerebellum (flocculonodular)
Spinocerebellum (vermis) - from olives, spinocerebellar
Neocerebellum (most of cerebellum) - input from cortex to pontine, output back to cortex via VL
4 signs of cerebellar disease
Incoordination (ataxia)
Equilibrium + gait - wide base walk
Nystagmus
Hypotonia - decreased resistance to passive movement
Flocculonodular syndrome (2)
Balance and oculomotor control
Spinal cerebellum - midline tumors
Truncal + leg incoordination
Chronic alcoholics
Lateral syndrome (Cerebellar degneration)
Acute - cerebellar hemorrhage/infarct, anoxia, heat stroke
Subacute - alcoholics, paraneoplastic, tumors, MS
Chronic - spinocerebellar degen, metabolic disease
SCBP
Output from CB
MCBP
Cortico-pontine-cerebellar fibers
ICBP
Spinocerebellar, vestibulocerebellar
Hemispheric syndrome (symptoms, unilateral vs bilateral)
Ataxia, dysmetria, intention tremor, dysdiadochokinesis
Unilateral - tumor, vascular
Bilateral - cerebellar degneneration
Vergence
Eyes are aligned for binocular vision: converge for near and diverge for far
Horizontal vs vertical double vision: caused by?
Horizontal - VI palsy
Vertical - IV palsy
Vertical eye movements
Mediated by MLF of midbrain
Internuclear ophthalmoplegia
Interruption in axons of MLF lead to weakness of adduction of ipsilateral eye