Peripheral Nervous System Pharmacology 1 Flashcards

1
Q

What receptors doe the sympathetic and parasympathetic systems use to act on the kidney? What is their respective effects?

A

D1 activation causes vasodilation and increased blood flow/GFR
B1 activation stimulates renin release from the kidney

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2
Q

What receptors doe the sympathetic and parasympathetic systems use to act on the bladder? What is their respective effects?

A

M3 activation causes contraction of bladder detrusor and relaxation of trigone (urination)

B2 activation relaxes detrusor
a1 activation constricts trigone and sphincter (urinary retention)

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3
Q

What receptors doe the sympathetic and parasympathetic systems use to act on the penis? What is their respective effects?

A

M3 activation causes relaxation of vessels via action of ACh which causes NO release

a1 activation causes contraction of seminal vesicles, prostitc capsule and vas deferens in ejaculation

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4
Q

What receptors doe the sympathetic and parasympathetic systems use to act on the uterus? What is their respective effects?

A

B2 activation relaxes the uterus

in pregnancy
M3 activation contracts uterus and
a1 activation contracts uterus

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5
Q

What are the typical receptors activated by bodily secretions?

A

M3 activation causes watery secretion (salivary, nasopharyngeal, pulmonary, GI and eccrine sweat

a1 activation stimulates apocrine sweat glands; viscous salivary secretions

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6
Q

What are the effects of receptors (which?) on the body’s metabolism?

A

a2 activation causes a decrease in insulin release

B2 activation promotes glycogenolysis and gluconeogenesis in liver; glycogenolysis and K+ uptake in skeletal muscles and increase in insulin release

B3 activation stimulates lipolysis in adipocytes

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7
Q

Which bodies sites have primarily sympathetic activity as the predominant tone?

A

arterioles, veins (vasculature)- adrenergic

sweat glands - cholinergic

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8
Q

Describe the two classes of cholinergic drugs that are used to modulate Acetylcholine activity.

A

cholinomimetic drugs (mimic ACh activity): agonists at M and N receptors and blocking AChE

cholinolytic drugs (inhibit ACh activity): antagonists at M and N receptors, and one that reactivates AChE

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9
Q

Contrast the shape of nicotine and muscarine receptors and the effect on Acetylcholine on both.

A

nicotinic and muscarinic receptors are both cholinergic receptors in that they respond to Acetylcholine but they are specific to nicotine and muscarine respectively (shows some specificity)

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10
Q

Carbachol (Miostat)

A

agonist at muscarinic receptors with significant Nn activity

used in obtaining mitosis and reducing IOP elevation

precautions: widespread side effects on cholinergic receptors: bradycardia, asthma, hyperthyroidism (already sensitive to catecholamines) peptic ulcer, urinary tract obstruction and parkinsonism

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11
Q

Methacholine

A

agonist at muscarinic receptors with slight nicotinic activity

used in diagnosis of airway hyperactivity, administered by inhalation via nebulizer, very resistant to ACh degradation

precautions with widespread muscarinic activation

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12
Q

Bethanechol (Urecholine)

A

muscarinic agonist with no nicotinic activity

used post op for promoting GI and urinary bladder motility or atony of urinary bladder or stomach

not susceptible to AChE activation; precautions with increasing body wide muscarinic activity

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13
Q

Pilocarpine (Piloptic)

A

muscarinic agonist

particularly active on sweat, salivary glands and eyes (esp for xerstomia caused by Sjorgren’s syndrome); causes miosis and second line tx for open or closed angle glaucoma by causing cilia muscle to contract

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