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苯基双胍及其他脒衍生物与5-羟色胺相关的药理特性。

Pharmacological properties of phenyldiguanide and other amidine derivatives in relation to those of 5-hydroxytryptamine.

作者信息

FASTIER F N, McDOWALL M A, WAAL H

出版信息

Br J Pharmacol Chemother. 1959 Dec;14(4):527-35. doi: 10.1111/j.1476-5381.1959.tb00960.x.

Abstract

Cats in which the coronary and allied chemoreflexes could not be obtained with small intravenous doses of 5-hydroxytryptamine were insensitive also to phenyldiguanide. In cats which responded to phenyldiguanide with reflex falls of blood pressure and heart rate, abolished by vagotomy, the effects of graded doses (5 to 150 mug./kg.) of phenyldiguanide bore a striking resemblance to those produced initially by 5-hydroxytryptamine in somewhat smaller doses. Differences in the cardiovascular responses to the two drugs are attributed to additional (non-reflex) actions of 5-hydroxytryptamine. The reflex actions of both drugs were blocked reversibly also by 2-naphthylguanidine (500 mug.). Certain other drugs (bufotenine, procaine, S-decylisothiourea) antagonized the depressor action of phenyldiguanide as well as the reflex depressor action of 5-hydroxytryptamine. Like 5-hydroxytryptamine, phenyldiguanide and certain other amidine derivatives caused pain when applied to the base of blisters in human subjects. Unlike 5-hydroxytryptamine, phenyldiguanide did not constrict perfused rat blood vessels or increase the tone of the rat fundal strip preparation of Vane (1957). Phenyldiguanide did not affect the sensitivity of these smooth muscle preparations to 5-hydroxytryptamine, but other amidine derivatives proved to be moderately strong antagonists of the vasoconstrictor actions of 5-hydroxytryptamine and of adrenaline. Unlike 5-hydroxytryptamine, phenyldiguanide did not produce gastric haemorrhage in the mouse. Phenyldiguanide did not prolong chloral hydrate sleeping time in mice by the same mechanism as did 5-hydroxytryptamine. Phenyldiguanide was not highly toxic to mice (LD50 being 240 mg./kg.). It is concluded that phenyldiguanide and certain other amidine derivatives act on sensory receptors which respond to 5-hydroxytryptamine, but that they show little pharmacological resemblance to 5-hydroxytryptamine in other respects.

摘要

用小剂量静脉注射5-羟色胺无法引发冠状动脉及相关化学反射的猫,对苯基双胍也不敏感。在对苯基双胍有反应,出现血压和心率反射性下降且迷走神经切断可消除这种反应的猫中,不同剂量(5至150微克/千克)的苯基双胍产生的效应,与最初用稍小剂量5-羟色胺产生的效应极为相似。两种药物心血管反应的差异归因于5-羟色胺的额外(非反射性)作用。两种药物的反射作用也均可被2-萘基胍(500微克)可逆性阻断。某些其他药物(蟾蜍色胺、普鲁卡因、S-癸基异硫脲)可拮抗苯基双胍的降压作用以及5-羟色胺的反射性降压作用。与5-羟色胺一样,苯基双胍和某些其他脒衍生物应用于人体水泡底部时会引起疼痛。与5-羟色胺不同,苯基双胍不会使灌注的大鼠血管收缩,也不会增加Vane(1957年)制备的大鼠胃底条的张力。苯基双胍不影响这些平滑肌制剂对5-羟色胺的敏感性,但其他脒衍生物被证明是5-羟色胺和肾上腺素血管收缩作用的中度强效拮抗剂。与5-羟色胺不同,苯基双胍不会在小鼠中引起胃出血。苯基双胍不会像5-羟色胺那样通过相同机制延长小鼠水合氯醛睡眠时间。苯基双胍对小鼠的毒性不高(半数致死量为240毫克/千克)。得出的结论是,苯基双胍和某些其他脒衍生物作用于对5-羟色胺有反应的感觉受体,但在其他方面它们与5-羟色胺几乎没有药理学相似性。

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