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三环类抗抑郁药作为交感神经节中毒蕈碱受体的拮抗剂。

Tricyclic antidepressant drugs as antagonists of muscarinic receptors in sympathetic ganglia.

作者信息

Weinstock M, Cohen D

出版信息

Eur J Pharmacol. 1976 Dec;40(2):321-8. doi: 10.1016/0014-2999(76)90069-8.

Abstract

Close arterial injection of McN-A-343 into the superior cervical ganglion of the cat resulted in contractions of the nictitating membrane. The ganglionic effects of McN-A-343 but not those of DMPP were antagonized in a dose-related manner by 2-10 mug of desipramine, imipramine, chlorimpramine, iprindole and viloxazine. No correlation was found between the dose of each drug which blocked the effects of McN-A-343 and that required to potentiate the responses of the nictitating membrane to intra-arterial administration of noradrenaline. It is concluded that clinically effective antidepressant agents can block muscarinic receptors in neural tissue, even if they do not do so in smooth muscle and gland cells.

摘要

向猫的颈上神经节近距离动脉注射 McN - A - 343 会导致瞬膜收缩。2 - 10微克的地昔帕明、丙咪嗪、氯丙咪嗪、茚满丙二胺和维洛沙嗪以剂量相关的方式拮抗 McN - A - 343 的神经节效应,但不拮抗 DMPP 的效应。在阻断 McN - A - 343 效应的每种药物剂量与增强瞬膜对动脉内注射去甲肾上腺素反应所需剂量之间未发现相关性。得出的结论是,临床有效的抗抑郁药可阻断神经组织中的毒蕈碱受体,即使它们在平滑肌和腺细胞中不这样做。

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