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Citation
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HERO ID
8091985
Reference Type
Journal Article
Title
Actions of quinine on the rat isolated rectum
Author(s)
Savage, AO; Akinlalu, CA
Year
1985
Is Peer Reviewed?
1
Journal
Archives Internationales de Pharmacodynamie et de Thérapie
ISSN:
0003-9780
Volume
276
Issue
1
Page Numbers
163-176
Language
English
PMID
4051636
URL
https://www.ncbi.nlm.nih.gov/pubmed/4051636
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Abstract
The actions of quinine on the rat isolated rectum was studied. Quinine (2.5 X 10(-5) - 2.5 X 10(-4) M) initiated rhythmic phasic contractions (RPC) which were prevented by verapamil, lanthanum, indomethacin or Ca2+-withdrawal, but were unaffected by tetrodotoxin, L-propranolol, phentolamine, or atropine. Higher quinine concentrations (2.5 X 10(-4) - 10(-3) M) relaxed the rat rectum and inhibited the RPC induced by lower concentrations. Exposure to high Ca2+-Tyrode solution (6 Ca2+-Tyrode) increased the baseline tone of the muscle. Under this condition, quinine (2.5 X 10(-4) - 10(-3) M), but not lower concentrations relaxed the muscle. Quinine (2.5 X 10(-5) - 10(-3) M) concentration-dependently inhibited KCl and acetylcholine-induced contractions, but more readily blocked KCl than acetylcholine-induced responses; the inhibitory effect of quinine against KCl, but not acetylcholine, was largely reversed by increasing the Ca2+ concentration of the Tyrode solution. It is concluded that quinine-induced RPC occurred independently of adrenergic or cholinergic mechanisms, and are likely to be due to enhanced Ca2+ influx into the rectum, while the relaxation encountered with higher concentrations may be due to inhibition by quinine of transmembranal Ca2+ influx. Evidence was obtained that quinine may preferentially inhibit Ca2+ influx through a pathway linked to high K+ depolarisation.
Keywords
Acetylcholine/pharmacology; Animals; Biological Transport/drug effects; Calcium/metabolism; Drug Interactions; Electric Stimulation; In Vitro Techniques; Indomethacin/pharmacology; Muscle, Smooth/drug effects/metabolism; Parasympathomimetics/pharmacology; Potassium Chloride/pharmacology; Quinine/pharmacology; Rats, Inbred Strains; Rectum/drug effects/metabolism; Sympathomimetics/pharmacology; Tetrodotoxin/pharmacology
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