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5-羟色胺诱导家禽直肠双相反应的机制。

Mechanism of 5-hydroxytryptamine-induced biphasic responses of fowl rectum.

作者信息

Mishra S K, Raviprakash V

出版信息

Arch Int Pharmacodyn Ther. 1983 Sep;265(1):29-35.

PMID:6651403
Abstract

The present study investigated the mechanism of the biphasic action of 5-hydroxytryptamine (5-HT) on isolated fowl rectum. 5-HT (2.6 X 10(-6) M) very often produced a biphasic response i.e., an initial relaxation followed by contraction. Tetrodotoxin completely abolished the relaxatory component and partially inhibited the contraction. On the Remak's nerve denervated preparation (in which the non-adrenergic inhibitory and non-cholinergic excitatory neural elements are eliminated), 5-HT produced only contraction. Lysergic acid diethylamide or methysergide completely blocked the contractile component and significantly inhibited the relaxation. Caffeine, given alone, reduced the relaxation without affecting the contraction caused by 5-HT. Atropine, mepyramine, propranolol, pentolinium or indomethacin did not alter the biphasic responses to 5-HT. Thus, it is concluded that the 5-HT-induced relaxation is mediated by non-adrenergic inhibitory neurons, while the contractions of the fowl rectum are partly due to a direct myogenic action and partly mediated by an indirect stimulation of non-cholinergic excitatory neurons.

摘要

本研究探讨了5-羟色胺(5-HT)对离体鸡直肠双相作用的机制。5-HT(2.6×10⁻⁶ M)常常产生双相反应,即先是松弛,随后是收缩。河豚毒素完全消除了松弛成分,并部分抑制了收缩。在雷马克神经去神经支配的标本中(其中非肾上腺素能抑制性和非胆碱能兴奋性神经成分被消除),5-HT仅产生收缩。麦角酸二乙胺或甲基麦角新碱完全阻断了收缩成分,并显著抑制了松弛。单独给予咖啡因可减少松弛,但不影响5-HT引起的收缩。阿托品、美吡拉敏、普萘洛尔、潘托铵或吲哚美辛均未改变对5-HT的双相反应。因此,得出结论:5-HT诱导的松弛是由非肾上腺素能抑制性神经元介导的,而鸡直肠的收缩部分归因于直接的肌源性作用,部分由非胆碱能兴奋性神经元的间接刺激介导。

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