PHRM 845 Exam 3 Roche Flashcards

1
Q

What composes the Hindbrain?

A
  • medulla

- pons, cerebellum

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2
Q

What composes the midbrain?

A

-substantia nigra

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3
Q

What composes the forebrain?

A
  • cerebral cortex
  • basal ganglia
  • limbic system
  • diencephalon
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4
Q

medulla (autonomic functions)

A
  • includes centers for controlling respiration, cardiac functionm vasomotor responses, and reflexes
  • part of the reticular system and brain stem
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5
Q

pons “bridge”

A
  • relays signals from the forebrain to the cerebellum

- part of the brain stem

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6
Q

cerebellum

A
  • governs motor coordination for producing smooth movements

- undergoes neurodegeneration in spinocerebellar ataxias

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7
Q

SN pars compacta

A
  • provides input to the basal ganglia, supplies dopamine to the striatum
  • involved in voluntary motor control
  • undergoes neurodegeneration in PD
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8
Q

SN pars reticulata

A

-output function, relays signals from the basal ganglia to the thalamus

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9
Q

cortex (cerebrum)

A

-involved in processing and interpreting info (decision making, higher level functions)

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10
Q

basal ganglia

A

voluntary motor control, some cognitive functions

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11
Q

limbic system

A
  • emotions (amygdala)

- memory (hippocampus)

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12
Q

diencephalon

A
  • thalamus: relay station to and from cortex

- hypothalamus: regulates internal homeostasis, emotions, hormonal control and direct neural regulation

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13
Q

How are “decisions” made in the brain

A

the senses receive info about the environment, which is passed through the thalamus to the cortex and back. this is called a cortico-thalamic loop

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14
Q

efferent neuron tracks

A

transmit signals from the cortex to the periphery

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15
Q

afferent neuron tracks

A

transmit signals from the periphery to the cortex

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16
Q

meninges

A

layers of membranes that surround the brain

  • dura (outer layer below skull)
  • arachnoid: middle
  • pia: inner layer
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17
Q

What artery does blood enter the brain through?

18
Q

astrocytes

A
  • provide neurons with growth factors, antioxidants
  • remove excess glutamate (excitotoxic neurotransmitter)
  • support the blood-brain barrier
19
Q

oligodendrocytes

A

-produce myelin sheath that insulates axons

20
Q

microglia

A
  • provide growth factors
  • clear debris by phagocytosis
  • role in neuroinflammation
21
Q

how is neurotransmission triggered

A

-electrical depolarization of the neuron by an influx of Na ions that changes the charge polarity of the membrane

22
Q

EPSP

A

excitatory postsynaptic potential

-works when an excitatory neurotransmitter acts on an ionotropic receptor, allowing Na ions to cross the membrane

23
Q

IPSP

A

inhibitory postsynaptic potential

  • induces hyperpolarization by allowing Cl ions to cross the membrane
  • they can decrease the magnitude of a subsequent EPSP
24
Q

GABA

A
  • major inhibitory neurotransmitter in the brain
  • depresses neuronal excitability by increasing the flux of Cl ions into the neuron
  • there are A and B receptors
  • drugs affecting GABA are generally CNS depressants and include: sedative hypnotics, anticonvulsants, anxiolytics
25
glycine
- inhibitory neurotransmitter released by interneurons in the spinal cord - like GABA, induces hyperpolarization by allowing the inward flow of Cl ions - antagonized by toxic alkaloid strychnine
26
glutamate
- major excitatory aa neurotransmitter in the brain - excess glutamate can cause neuronal damage by allowing excessive Ca influx into the neuron - metabotropic (GPCRs) or ionotropic (NMDA and AMPA)
27
acetylcholine
- both muscarinic and nicotinic receptors | - an example is a cholinesterase inhibitor
28
dopamine
- drug targets include D1-D5 receptors and dopamine transporter - DA neurons arise from the ventral tegmental area and the SN - drugs that interact with DA pathways include: antipsychotics and D2/D3 and D1 receptor agonists for PD
29
norepinephrine
- drug targets include the a and b adrenergic receptors (GPCRs) and the norepinephrine transporter - NE axons arise from the locus coeruleus in the brain stem - NET inhibitors are used to treat depression
30
serotonin, 5-HT
- drug targets are serotonin receptors and serotonin transporter - 5-HT axons arise from a group of cell bodies in the brainstem called raphe nuclei - serotonin systems are involved in sleep, vigilancem mood, and sexual function - drugs include: 5-HT2a antagonsits as atypical antipsychotics, 5-HT1D agonists for migraine, SERT uptake inhibitors for depression, 5-HT2A agonists are hallucinogenic
31
multiple sclerosis
-immune-mediated inflam disorder involving destruction of the myelin sheath that surrounds neuronal axons
32
sclerosis
scars that accumulate in the white matter of MS patients
33
Genes linked to MS encode what immune related proteins?
- MHC (HLA)-DR15/DR6 - interleukin-2a receptor - interleukin-7a receptor
34
relapsing-remitting MS
- involves relapses of neurological dysfunction lasting weeks or months and affecting the brain, optic nerves and/or spinal cord. - multifocal areas of damage are revealed by magnetic resonanace imaging, generally in white matter - initial symptoms disappear, but less remission with each relapse - most cases of RRMS eventually enter a phase of SPMS
35
Secondary progressive MS
- characterized by less inflammation than RRMS | - involves slowly progressive neurological decline and CNS damage with little remission
36
Primary progressive MS
- resembles SPMS at the initial stage of the disease | - mean age of onset is later then RRMS
37
Clinically isolated syndrome (CIS)
- initial episode of neurologic symptoms lasting more than 24hrs - involves inflammation and demyelination in the optic nerve, cerebrum, cerebellum, brainstem or spinal cord - most cases progress to MS
38
Marburg variant of MS
- aggressive form of MS involving a high degree of inflammation - may resemble a brain tumor in a brain scan
39
Autoimmune phase
- antigens released from CNS are presented to B and T cells in lymph nodes. - B and T cells w/high affinity receptors for these antigens are expanded and migrate to CNS sites where they-reencounter and are activated by their target ligands - activated B and T cells then carry out immune functions at the CNS sites
40
Degenerative phase
- CNS damage is triggered by activated B and T cells or by other insults such as infection or stroke - antigens released from damaged sites in the CNS further prime immune cells in the periphery, thus completing a vicious cycle