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Tissue amine levels and sympathetic blockade after guanethidine and bretylium

机译:胍乙啶和后的组织胺水平和交感神经阻滞

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摘要

A single dose of guanethidine produces a substantial, long-lasting depletion of tissue catecholamines in the rat, whereas a similar dose of bretylium has no effect. Both drugs produce block of the eserine-induced sympathetic pressor effect. Block by guanethidine is induced more rapidly than is amine depletion. When amine depletion is maximal, a noradrenaline infusion is capable of restoring the response to eserine, but no restoration of the response to eserine occurs after noradrenaline infusion into bretylium-treated rats. Catecholamine levels in isolated tissues are not reduced when complete block of sympathetic nerve stimulation has been produced by guanethidine. It is suggested that guanethidine possesses a primary bretylium-like, and a secondary reserpine-like, blocking action. Guanethidine produces a transient lowering of intestinal 5-hydroxytryptamine, and this coincides with increased intestinal motility.
机译:单一剂量的胍乙啶在大鼠中会大量持久地消耗组织中的儿茶酚胺,而类似剂量的不起作用。两种药物均能阻止色氨酸诱导的交感神经升压作用。胍乙胺的阻断作用比胺消耗更快。当胺消耗最大时,去甲肾上腺素输注能够恢复对色氨酸的反应,但是在去甲肾上腺素输注经肉芽孢素处理的大鼠中后,对色氨酸的响应没有恢复。当胍乙啶产生完全的交感神经刺激阻滞时,分离组织中的儿茶酚胺水平不会降低。提示胍乙啶具有主要的肉类,和次要的利血平类,阻断作用。胍乙啶可导致肠内5-羟色胺降低,这与肠蠕动增加有关。

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