Central Nervous System Flashcards

(48 cards)

1
Q

Gray matter

A

Contains the cell bodies of neurons

Cortex and deep grey matter

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2
Q

White matter

A

Contains myelinated axons

Below the cortex and running along tracts in the brain

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3
Q

Diencephalon

A

The posterior part of the forebrain
Contains hypothalamus, thalamus, epithalamus, ventral thalamus and third ventricle
Relay and processing center

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4
Q

3 things that make up the basal ganglia (and 3 functions)

A

Caudate nucleus
Putamen
Globis palladis
These supply inhibitory stimuli to skeletal muscles, coordinate skeletal muscle contractions, and block unwanted muscle contractions

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5
Q

4 lobes of the cerebrum and what are they responsible for

A

Frontal: controls movement, behavior, emotions, higher intellectual functions
Parietal: integrates sensory inputs like touch and controls language (ability to understand words)
Temporal: hearing, smelling, memory and expression (ability to express words)
Occipital: vision

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6
Q

Thalamus

A

Important for integrating sensory stimuli (like pain and touch) and determinant of conciousness

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7
Q

Gray and white matter in brain vs spinal chord

A

In the spinal chord the gray matter is internal and the white matter is external
In the brain the gray is on the outside and the white is on the inside

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8
Q

Hypothalamus

A

Connects many different parts of the brain and regulates many body functions like appetite, thirst and temperature
Controls the pituitary by secreting factors that regulate hormonal release

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9
Q

Functions of each part of the brainstem

A

Midbrain: visual, auditory reflex centers
Medulla oblongata: cardiac, vasomotor, respiratory centers
Pons: contains bundles of axons carrying info to and from the brain

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10
Q

Cerebellum

A

Coordinated voluntary movement
Controls ability to stand upright without falling over
Controls muscle toone

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11
Q

3 inputs to the cerebellum

A
  1. Sensory info carried by the spinal chord
  2. Vestibular organ in the inner ear
  3. Motor impulses from cerebral cortex
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12
Q

What type of neurons synapse in the dorsal versus anterior horn of the spinal chord?

A

Dorsal: sensory neurons
Anterior: motor neurons (lower motor neurons)

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13
Q

3 layers of the meninges

A
  1. Dura: outer layer
  2. Arachnoidae: middle layer
  3. Pia: innermost layer
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14
Q

Another word for neuronal cell body

A

Perikaryon

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15
Q

4 types of glial cells

A

Astrocytes: support cells
Oligodendrocytes: wrap around axons and form myelin sheaths
Microglia: resident macrophages
Ependymal cells: line ventricles and make CSF

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16
Q

Dysgraphic disorders

A

Incomplete fusion of the neural tube and defective formation of meninges, calvaria, or vertebras

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17
Q

Malformations in

  1. Ancephaly
  2. Meningocele
  3. Spina bifida
  4. Myelomeningocele
A
  1. No brain
  2. Vertebrae doesn’t form and meninges protrude through bony defect
  3. No vertebral arches, resulting in exposure of meninges or spinal cord to outside
  4. Same as 2, but along with a bit of the spinal cord protruding
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18
Q

Epidural Hematomas

A

Between skull and dura
Rupture of middle meningeal artery (fracture related)
Tight space, so hematoma takes hours to develop and its localized
Coma can result; lethal if unrecognized because arterial bleeding will continue

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19
Q

Subdural hematomas

A
Between dura and arachnoid
Caused by blunt trauma
Ruptured bridging veins
Venous bleeding occurs slowly, so may be asymptomatic
Can produce headache, coma, death
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20
Q

Subarachnoid hemorrhages

A

Located between arachnoid and pia

Caused by traumatic contusion of the brain and/or the rupture of congenital aneurysms (in the circle of Willis)

21
Q

Intracerebral hemorrhages

A

Rupture of intracerebral vessels
Common complication of head trauma, gunshot wounds
Nontraumatic forms include stroke
Common with poor clotting, so blood spreads easily

22
Q

Stroke

A

Sudden persistent loss of brain function from a vascular cause
Risk factors include hypertension, smoking, diabetes, high cholesterol

23
Q

Global ischemia

A

If many vessels are narrowed they can develop small infarcts, which over time can lead to dementia
Hypoperfusion from cardiac arrest or peripheral bleeding
Watershed infarcts (systemic hypotension lowers the perfusion from both sides and the area in the border zone becomes hypoxic)
Laminar necrosis from hypoperfusion

24
Q

Cerebral infarct

A

Caused by thrombotic occlusion, thromboemboli
Pale or hemorrhagic infarct (reperfusion)
Surrounding brain tissue: edematous
Fluid filled cavity
Never heals (damage is permanent)
Clinical presentation depends on site of occlusion
Acute stroke can kill
MCA stokes result in contralateral hemiplegia and sensory loss, global aphasia in the dominant hemisphere

25
Intracerebral hemorrhage
``` Most caused by arterial hypertension Others from vascular malformations Basal ganglia, cerebellum and pons Well-circumscribed Clinical features often severe, high mortality ```
26
Multiple Sclerosis
Demyelinating, chronic disease (presumed autoimmune) Women > men Most common neurological disease in young adults Mediated by helper lymphocytes, macrophages, and B cells/plasma cells Exacerbation and remission episodes Sensory and motor abnormalities Unpredictable course
27
Oligoclonal T cells
Oligoclona proliferations of sensitized T cells is considered to be the basis of MS lesions Macrophages also found in the lesions
28
2 possible courses for MS
Relapsing remitting type: works well with therapy (beta interferons, etc), during remission function returns to normal, dampens down symptoms of inflammation Chronic: permanent due to neurodegeneration
29
What is found in early vs late lesions in MS
Early: contain demyelinated axons surrounded by lymphocytes and foamy macrophages Late: demyelinated axons and astrocytes
30
Wernicke-Korsakoff syndrome (deficiency in, symptoms)
``` Vitamine B1 (thiamine) deficiency W part is more acute (abnormal eye movements) and K part is more chronic (loses short term memory) ```
31
Vitamin B12 deficiency
Leads to loss of sensation and motor function with uncoordinated movements plus psychiatric symptoms Leads to subacute combined degeneration of the ascending tracts of the spinal cord
32
Pellagra | deficiency in, symptoms
Nicotinic acid deficiency | Dermatitis, diarrhea, delirium/dementia
33
Myelopathy vs neuropathy
M: damage to spinal cord N: damage to peripheral nerves Both can be a direct effect of alcoholism
34
Alzheimers Disease
Sporadic neurodegenerative disease Genes increase levels of beta-amyloid and apoE4 Atrophy greatest in frontal and temporal lobes Dementia Requires nursing care, death due to physical deterioration or infection Can see histological changes in cortex, neuritic plaques, neurofibrillary tangles
35
Parkinson's Disease
Subcortical neurodegenerative disorder Decreased number of dopaminergic neurons in the substantial nigra (appears pale) Disturbances of movement, TRAP Depression, dementia common Presence of Lewy bodies (with alpha synuclein)
36
TRAP
Tremor, rigidity, brady or akinesia, postural instability | In Parkinson's disease
37
Huntington's Disease
Autosomal dominant, familial Gene is huntingtin gene on chromosome 4 with CAG trinucleotide repeat expansion Disease only occurs when the repeats exceed a threshold Involuntary, gyrating movements, progressive dementia Atrophy of cortex, caudate, putamen Loss of neurons and reactive gliosis
38
Amyotrophic Lateral Sclerosis
Neurodegenerative disease, most sporadic 10% have mutations in copper-zinc superoxide dismutase (SOD1) gene Loss of motor neurons in cortex, brainstem and spinal cord and of corticospinal tracts in spinal cord Weakness and wasting of muscles, fasciculations, slurred speech Incurable and progressive disease
39
Epilepsy (2 types)
Generalized: discharges all over the brain - leads to aura, tonic clonic seizures and post ictal drowsiness, can be controlled Focal: one spot that can be detected - many causes - drugs or surgery
40
One differences between malignant tumors in the CNS and malignant tumors everywhere else
Malignant tumors in the CNS do NOT metastasize, they just grow rapidly
41
Astrocytomas
Solid cerebral tumors in adults, cystic cerebellar tumors in children Well-differentiated astrocytes Progress into lesions Cannot distringuish from glioblastoma multiforme
42
Glioblastoma Multiform
Most common CNS tumor Lateral hemispheres Gross appearance: parts are necrotic/yellow, hemorrhagic/red, or white, irregularly shaped, poor demarcations, butterfly appearance Cells are very atypical
43
Oligodendrogliomas
Cerebral hemispheres Well circumscribed, partially cystic, calcified Well-differentiated Possible progression to GBM
44
Ependymomas
Children: ventricles, adults: spinal cord Ependymoma or filum terminale Tumor cells line papillary structures or form rosettes
45
Medulloblastoma
Cerebellum Childhood Cells are primitive neuroectodermal cells Cells may enter CSF and metastasize to other sites in the CNS Poor prognosis
46
Meningiomas
Arise from meninges and are dural based Mostly benign Most located near midline, base of brain, along spinal cord Cause epileptic seizures or motor deficits Excellent prognosis - surgery is curative unless malignant or in unreachable location
47
Neurofibromatosis type 1 vs 2
1: produces multiple peripheral neurofibromas 2: produces acoustic schwannomas as well as multiple meningiomas
48
3 most common cancers to metastasize to brain
Lung Breast Melanoma