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软体动物平滑肌的药理学。

The pharmacology of a molluscan smooth muscle.

作者信息

TWAROG B M

出版信息

Br J Pharmacol Chemother. 1959 Sep;14(3):404-7. doi: 10.1111/j.1476-5381.1959.tb00266.x.

Abstract

The effects of a number of pharmacologically active substances on contraction and on membrane polarization of the anterior byssal retractor muscle of Mytilus edulis, L., have been studied. Tetramethylammonium bromide, trimethyl(4-oxopentyl)ammonium chloride and nicotine, like acetylcholine, produced depolarization and sustained contraction. Nicotine, on repeated application, lost acetylcholine-like activity and effectively blocked acetylcholine. In order of decreasing potency, methanthelinium, tubocurarine, benzoquinonium, tetraethylammonium, atropine, pentamethonium, and decamethonium blocked acetylcholine action. These agents did not show initial acetylcholine-like action and did not relax sustained contractions. Adrenaline, noradrenaline, tyramine, dibenamine, phentolamine, and lysergic acid diethylamide relaxed sustained contractions without reducing initial depolarization and tension development in response to acetylcholine or electrical stimuli. Adrenaline and noradrenaline often caused depolarization and contraction when first applied, and displayed relaxing action on subsequent application.

摘要

已对多种药理活性物质对紫贻贝前足丝牵缩肌收缩和膜极化的影响进行了研究。溴化四甲铵、氯化三甲基(4-氧代戊基)铵和尼古丁与乙酰胆碱一样,可产生去极化和持续收缩。尼古丁反复应用后,失去了乙酰胆碱样活性,并有效阻断了乙酰胆碱。按效力递减顺序,甲溴东莨菪碱、筒箭毒碱、苯喹铵、四乙铵、阿托品、五甲铵和十甲铵可阻断乙酰胆碱的作用。这些药物未表现出初始的乙酰胆碱样作用,也未使持续收缩松弛。肾上腺素、去甲肾上腺素、酪胺、二苯胺、酚妥拉明和麦角酸二乙胺可使持续收缩松弛,而不会降低对乙酰胆碱或电刺激的初始去极化和张力发展。肾上腺素和去甲肾上腺素首次应用时常引起去极化和收缩,随后应用则表现出松弛作用。

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