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A study of the sympathomimetic action of guanethidine on the isolated anococcygeus muscle of the rat.

机译:胍乙啶对大鼠离体无球囊肌的拟交感神经作用的研究。

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摘要

Guanethidine, acting on the rat isolated anococcygeus, causes adrenergic neurone blockade (slowly terminated by washing), noradrenaline potentiation and, with higher concentrations, spasm (both rapidly terminated by washing). 2 The spasm is an indirect sympathomimetic action, for it is sensitive to phentolamine and reserpine and shows tachyphylaxis. 3 The concentration of cocaine equieffective with the spasmogenic concentration of guanethidine as an inhibitor of noradrenaline uptake caused much less spasm. Moreover, it did not enhance noradrenaline efflux from anococcygeus loaded with (-)-[3H]-noradrenaline, as guanethidine did. 4 The spasm induced by guanethidine in excess of cocaine is due to guanethidine-evoked noradrenaline release.
机译:胍乙啶作用于大鼠离体的无囊球菌,引起肾上腺素能神经元阻滞(通过冲洗缓慢终止),去甲肾上腺素增强,以及更高浓度的痉挛(两者均通过冲洗迅速终止)。 2痉挛是一种间接拟交感神经作用,因为它对苯妥拉明和利血平敏感,并表现出速激肽作用。 3可卡因浓度与痉挛浓度胍乙啶(去甲肾上腺素摄取抑制剂)等效,引起的痉挛少得多。而且,它没有像胍乙啶那样增强载有(-)-[3H]-去甲肾上腺素的无球藻的去甲肾上腺素外排。 4胍乙啶过量可卡因引起的痉挛是由于胍乙啶引起的去甲肾上腺素释放。

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