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Differentiation between the actions of acetylcholine and tetramethylammonium on the isolated taenia of the guinea‐pig caecum by hemicholinium‐3
Author(s) -
MITCHELSON F.
Publication year - 1971
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.1971.tb07085.x
Subject(s) - acetylcholine , chemistry , acetylcholine receptor , stimulation , muscarinic acetylcholine receptor , endocrinology , edrophonium , medicine , cholinergic , atropine , pharmacology , receptor , biology , biochemistry , neostigmine
Summary1 Contractions of the isolated taenia of the guinea‐pig caecum produced by acetylcholine and TMA were examined in the presence of various antagonists and anticholinesterases. 2 Hemicholinium‐3 (HC‐3) (50–400 μg/ml) inhibited contractions or relaxations produced by TMA but not contractions produced by acetylcholine. The inhibition was rapid in onset and readily reversible. Contractions produced by transmural stimulation were unaffected by HC‐3 but responses produced by nicotine were inhibited. 3 Low concentrations of hyoscine and benzhexol inhibited responses to acetylcholine to a greater extent than those to TMA. 4 Morphine, raised concentrations of Mg ++ or reduced concentrations of Ca ++ inhibited contractions produced by TMA and by acetylcholine to a similar extent. 5 Edrophonium, in concentrations which preferentially inhibit acetylcholinesterase, increased contractions produced by acetylcholine and converted responses to nicotine or transmural stimulation into contractions or biphasic responses with a marked contraction phase but did not increase contractions produced by TMA. 6 Iso ‐OMPA, in concentrations which preferentially inhibit butyrylcholinesterase, had no effect on responses to acetylcholine, nicotine, transmural stimulation or TMA. 7 HC‐3 inhibited contractions produced by TMA in the presence of anticholinesterases but had little effect on contractions produced by acetylcholine. 8 These results suggest that TMA produces contractions by acting directly on receptors of the smooth muscle. An analysis of possible reasons for HC‐3 (in the concentrations used) acting as an antagonist of TMA but not of acetylcholine indicates that the findings do not necessarily contradict the interpretation that both agonists act on the same receptor.

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