Peripheral Nervous System Pharmacology 1 Flashcards
What receptors doe the sympathetic and parasympathetic systems use to act on the kidney? What is their respective effects?
D1 activation causes vasodilation and increased blood flow/GFR
B1 activation stimulates renin release from the kidney
What receptors doe the sympathetic and parasympathetic systems use to act on the bladder? What is their respective effects?
M3 activation causes contraction of bladder detrusor and relaxation of trigone (urination)
B2 activation relaxes detrusor
a1 activation constricts trigone and sphincter (urinary retention)
What receptors doe the sympathetic and parasympathetic systems use to act on the penis? What is their respective effects?
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
What receptors doe the sympathetic and parasympathetic systems use to act on the uterus? What is their respective effects?
B2 activation relaxes the uterus
in pregnancy
M3 activation contracts uterus and
a1 activation contracts uterus
What are the typical receptors activated by bodily secretions?
M3 activation causes watery secretion (salivary, nasopharyngeal, pulmonary, GI and eccrine sweat
a1 activation stimulates apocrine sweat glands; viscous salivary secretions
What are the effects of receptors (which?) on the body’s metabolism?
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
Which bodies sites have primarily sympathetic activity as the predominant tone?
arterioles, veins (vasculature)- adrenergic
sweat glands - cholinergic
Describe the two classes of cholinergic drugs that are used to modulate Acetylcholine activity.
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
Contrast the shape of nicotine and muscarine receptors and the effect on Acetylcholine on both.
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)
Carbachol (Miostat)
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
Methacholine
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
Bethanechol (Urecholine)
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
Pilocarpine (Piloptic)
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