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PHARMACOLOGICAL ACTIONS OF PURE MUSCARINE CHLORIDE
Author(s) -
FRASER P. J.
Publication year - 1957
Publication title -
british journal of pharmacology and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0366-0826
DOI - 10.1111/j.1476-5381.1957.tb01361.x
Subject(s) - muscarine , chemistry , acetylcholine , atropine , muscarinic acetylcholine receptor , bronchoconstriction , cholinesterase , endocrinology , bronchodilatation , medicine , pharmacology , biochemistry , biology , receptor , salbutamol , asthma
The action of chromatographically pure crystalline muscarine chloride, prepared from Amanita muscaria , has been compared with acetylcholine chloride (ACh) on a number of different organs from a variety of species. Muscarine caused spasm in vivo and in vitro of muscles of the gut, uterus, urinary bladder, and bronchus. It also caused contraction of the horse ureter and carotid artery chain in vitro and slowed the isolated auricles of the guinea‐pig and rabbit, and the frog heart. Muscarine caused a drop in blood pressure, although in vitro it produced either constriction or dilatation of the blood vessels of the rabbit ear. All these actions resembled those of acetylcholine, though muscarine was usually more potent. Muscarine effects were readily prevented by atropine sulphate. It had a slight action on the frog rectus abdominis muscle, causing a contracture at high concentrations. Muscarine was destroyed neither by pepsin nor by boiling at any p H. It was inactive by mouth in a monkey in a quantity many times that which would cause poisoning by ingestion of Amanita muscaria in the human being. Muscarine neither inhibited nor was hydrolysed by either true‐ or pseudo‐cholinesterase. Muscarine chloride did not cause paralysis of the neuromuscular junctions of the rat diaphragm or of the cat gastrocnemius.