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蛋白质合成抑制剂对大鼠空肠在体情况下血管紧张素刺激及血管紧张素抑制的液体转运的影响。

Effects of protein synthesis inhibitors on angiotensin-stimulated and angiotensin-inhibited fluid transport by rat jejunum in vivo.

作者信息

Bolton J E, Munday K A, Parsons B J

出版信息

J Endocrinol. 1977 Aug;74(2):213-21. doi: 10.1677/joe.0.0740213.

Abstract

A study has been made of the effects of protein synthesis inhibitors on the responses of rat jejunum in vivo to intravenous infusions of angiotensin. Actinomycin D, an inhibitor of the transcription stage of protein synthesis, was without effect on the stimulation of fluid transport which follows the infusion of low doses of angiotensin. Cycloheximide, an inhibitor of the translation stage of protein synthesis, blocked the stimulatory response to angiotensin, but was without effect on the inhibitory response to high doses of the hormone. It is concluded that low (physiological) doses of angiotensin stimulate fluid transport by a mechanism involving protein synthesis at a stage later than transcription whereas high doses of the hormone inhibit fluid transport by a process which does not require protein synthesis.

摘要

一项关于蛋白质合成抑制剂对大鼠空肠在体内对静脉输注血管紧张素反应影响的研究。放线菌素D是蛋白质合成转录阶段的抑制剂,对低剂量血管紧张素输注后刺激液体转运没有影响。环己酰亚胺是蛋白质合成翻译阶段的抑制剂,它阻断了对血管紧张素的刺激反应,但对高剂量该激素的抑制反应没有影响。得出的结论是,低(生理)剂量的血管紧张素通过一种涉及转录后期蛋白质合成的机制刺激液体转运,而高剂量的该激素通过一个不需要蛋白质合成的过程抑制液体转运。

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