1.4 Cholinergic Pharmacology II Flashcards

1
Q

Cholinoceptor blocking drugs are divided into _________ antagonists and ________ antagonists

A

muscarinic, nicotinic

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2
Q

antimuscarinics: ________ compounds used for effects in eye or CNS, and ________ amines selectively produce peripheral effects

A

tertiary - eye or CNS

quaternary - peripheral

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3
Q

prototypic anticholinergic drug is _______, which causes reversible blockade

A

atropine

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4
Q

Muscarinic antagonist effect on eye:

  • blockade by topical atropine results in ________
  • paralysis of _______ muscle (cycloplegia)
  • contraindicated in ________
A

mydriasis (dilation)

ciliary

acute glaucoma

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5
Q

Muscarinic antagonist effects on cardiovascular system:

-atropine produces _________

A

tachycardia

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6
Q

M antagonist effect on respiratory system:

  • ________ and reduction of secretion
  • not as useful as beta-adrenceptor stimulants in treatment of asthma
A

bronchodilation

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7
Q

M antagonist effect on GI tract:

  • _______ motility and secretion
  • can be useful as preoperative adjuvant before abdominal surgery
A

reduces

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8
Q

M antagonist effect on GU tract

-can produce urinary _________

A

retention

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9
Q

M antagonist effect on sweat glands

  • suppresses _________ sweating
  • body temp can be _______
A

thermoregulatory

elevated

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10
Q

tolterodine is an M2 selective antagonist, which treats urinary ________

A

urgency and frequency

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11
Q

reversal of cholinergic poisoning requires a ______ drug, and large doses of _______ may be needed

A

tertiary (not quaternary)

atropine

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12
Q
  • dry mouth, mydriasis, tachycardia, flushed skin, delirium
  • can be treated with physostigmine or symptom management
  • contraindications in glaucoma and prostatic hyperplasia
A

atropine poisoning (adverse effects of cholinoceptor blocking drugs)

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13
Q
  • block actions of acetylcholine and other agonists at nicotinic receptors
  • receptors located on PNS and SNS autonomic ganglia
  • non selectivity produces limiting side effect profiles
  • all synthetic amines, originally developed for HTN
A

ganglion blocking drugs

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14
Q

______ readily enters the CNS –> sedation, tremor, choreiform movements, mental aberrations

A

mecamylamine

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15
Q

Ganglion blocking drugs in eye:

  • ciliary muscle ______
  • moderate _______ of pupil
A

cycloplegia

dilation

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16
Q

Ganglion blocking drugs in cardiovascular:

  • ________ in blood pressure
  • orthostatic hypotension
  • moderate _______
A

decrease

tachycardia

17
Q

Ganglion blockers in GI tract:

-_______ secretion and motility, since tone is PNS

A

reduced

18
Q

Ganglion blockers in GU system:

  • urinary ________
  • sexual function impaired
A

retention

19
Q
atropine
scopolamine
homatropine
pirenzipine
tropicamide
tolterodine
dicylclomine
fesoteridine
mepenzolate
solifenacin
oxybutynin
darifenacin
trospium
A

anticholinergics (M antagonists)

tertiary amines

20
Q
atropine methyl nitrate
methscopolamine
ipatropium
propantheline
glycopyrrolate
A

anticholinergics - quaternary amines (lack central effects)

21
Q

hexamethonium
trimethaphan
mecamylamine

A

ganglion blocking drugs

22
Q

pralidoxime (2-PAM)

A

cholinesterase regenerator