几种甲肾上腺素解药的药理学研究。

P Mouillé, H Dabiré, M Andrejak, H Schmitt
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引用次数: 0

摘要

六种α -肾上腺素受体阻滞剂已经在狗和大鼠身上进行了研究。170 150和170 153被发现是这些药剂中最有效的。在低剂量(0.1微克/千克)下,它们逆转了对低剂量肾上腺素(0.1微克/千克和0.3微克/千克)的升压反应,抑制了对高剂量肾上腺素的反应。他们降低了对去甲肾上腺素的升压反应。此外,在狗170 150增加心动过速引起的刺激心脏神经。该化合物可防止和逆转可乐定对心脏神经刺激的抑制作用。170 153没有增加心神经刺激引起的心动过速,但它阻止并逆转了可乐定对这种刺激的抑制作用。结果表明,170 150和170 153是有效的α -肾上腺素受体阻断剂,可同时作用于突触前和突触后α -肾上腺素受体,是一种有趣的药理工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Pharmacologic study of several alpha-adrenolytics].

Six alpha-adrenoceptor blocking agents have been investigated in dogs and rats. 170 150 and 170 153 have been found the most potent of these agents. At low doses (0,1 microgram/kg) they reversed the pressor response to low doses of adrenaline (0,1 and 0,3 microgram/kg) and suppressed the response to high doses of adrenaline. They reduced the pressor response to noradrenaline. In addition, in dogs 170 150 increased the tachycardia caused by stimulation of the cardiac nerve. The compound prevented and reversed the inhibition caused by clonidine on the effects of cardiac nerve stimulation. 170 153 did not increase the tachycardia caused by cardiac nerve stimulation, but it prevented and reversed the inhibitory effects of clonidine on this stimulation. The results show that 170 150 and 170 153 are potent alpha-adrenoceptor blocking agents acting on both pre and post-synaptic alpha-adrenoceptors which could be interesting pharmacological tools.

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