neurotransmitters + pharm Flashcards

1
Q

acetylcholine site of snythesis

A

nucleus basalis of Meynert

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2
Q

Where and with what enzyme is acetylcholine formed?

A

Formed in the nerve terminal using choline acetyltransferase.

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3
Q

ACh in Alzheimers?

A

Decreased ACh in Alzheimers

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4
Q

Molecule dopamine is synthesized from

A

tyrosine

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5
Q

fluoxetine

A

SSRI

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6
Q

paroxetine

A

SSRI

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7
Q

sertraline

A

SSRI

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8
Q

citalopram

A

SSRI

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9
Q

venlafaxine

A

SNRI

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10
Q

duloxatine

A

SNRI

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11
Q

amitriptyline

A

TCA

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12
Q

nortrytriptyline

A

TCA

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13
Q

imipramine

A

TCA

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14
Q

desipramine

A

TCA

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15
Q

clomipramine

A

TCA

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16
Q

amoxapine

A

TCA

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17
Q

doxepin

A

TCA

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18
Q

amoxapine

A

TCA

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19
Q

tranylcypromine

A

MAOI

20
Q

phenelzine

A

MAOI

21
Q

isocarboxazid

A

MAOI

22
Q

selegiline

A

MAOI

23
Q

bupropion

A

atypical - increases NE and dopamine via unknown mechanism

24
Q

mirtazapine

A

atypical - alpha-2 antagonist (increased release of NE and 5-HT) and potent 5-ht2 receptor antagonist

25
Q

trazodone

A

atypical - blocks 5HT2 and alpha-1 adrenergic receptors

26
Q

bromocriptine

A

ergot, dopamine agonist

27
Q

pramipexole

A

dopamine agonist non-ergot

28
Q

ropinirole

A

dopamine agonist (non-ergot)

29
Q

amantadine MOA

A

increases dopamine and may increase dopamine release, also used as an antiviral against influenza A

30
Q

amantadine toxicity

A

ataxia

31
Q

ataxia is toxicity of what parkinsons drug

A

amantadine

32
Q

selegiline

A

selectively inhibits MOA-B which preferentially metabolizes dopamine over NE and serotonin (5 HT) (increases bioavailability of dopamine)
(prevents dopamine breakdown)

33
Q

clinical use of selegiline

A

adjunctive agent to L-dopa for parkinsons

34
Q

selegiline toxicity

A

may enhance adverse effects of L-dopa

35
Q

COMT inhibitors

A

entacapone, tolcapone

36
Q

entacapone, tolcapone

A

COMT inhibitors
When administered in conjunction with dopaminergic agents such as L-DOPA, entacapone prevents COMT from metabolizing L-DOPA into 3-methoxy-4-hydroxy-L-phenylalanine (3-OMD) in the periphery, which does not easily cross the blood brain barrier (BBB).

37
Q

L-dopa must be co-administered with

A

carbidopa

38
Q

benztropine MOA

A

antimuscaranic, curbs excess cholinergic activity

39
Q

benztropine affects what symptoms

A

imrpoves muscle rigidity and tremor but has little effect on bradykinesia

40
Q

L-dopa MOA

A

increases amount of dopamine in brain, can cross BBB (unlike dopamine)

41
Q

L-dopa is converted to dopamine using which enzyme?

A

dopa decarboxylase in the CNS

42
Q

What is carbidopa

A

dopa decarboxylase in the periphery, used to increase bioavailability of l-dopa and to limit peripheral side effects

43
Q

clinical use of l-dopa and carbidopa?

A

parkinson’s disease

44
Q

l-dopa/carbidopa toxicity

A

arrythmias from increased peripheral formation of catecholamines. long-term use can lead to dyskinesia following administration, akinesia between doses

45
Q

name the drug that causes the following toxicity: arrythmias from increased peripheral formation of catecholamines. long-term use can lead to dyskinesia following administration, akinesia between doses

A

l-dopa/carbidopa