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Noradrenaline as a possible mediator of the actions of angiotensin on fluid transport by rat rejunum in vivo

机译:去甲肾上腺素可能是血管紧张素对大鼠体内大鼠肠腔流体转运的作用的可能介质

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摘要

1. Net fluid absorption and transmural potential difference were measured in the rat jejunum in vivo.2. Increased rates of net fluid transport were observed following infusions of angiotensin or noradrenaline. There was a small, but significant, fall in transmural p.d. associated with noradrenaline but not with angiotensin infusions.3. The α-adrenergic antagonists phentolamine and dihydroergotamine abolished both the angiotensin and the noradrenaline stimulations of transport and the noradrenaline-induced fall in p.d., whereas the β-adrenergic antagonist propranolol did not significantly affect these responses.4. Phentolamine did not alter the rise in p.d. following administration of the cholinergic agonist pilocarpine.5. The protein synthesis inhibitor cycloheximide abolished both the angiotensin and the noradrenaline-induced stimulation of fluid transport.6. Neither angiotensin nor noradrenaline significantly altered jejunal cyclic AMP levels.7. Bilateral nephrectomy had no apparent effect upon the increase in fluid transport following noradrenaline infusions.8. The noradrenaline-induced stimulation of transport was unaffected, and the fall in p.d. potentiated in rats pre-treated with reserpine, but a marked inhibition of transport was observed following angiotensin infusions.9. The results are consistent with the view that noradrenaline may mediate the actions of angiotensin upon intestinal fluid absorption in the rat.
机译:1.测量大鼠空肠体内的净液体吸收和透壁电位差。2。输注血管紧张素或去甲肾上腺素后观察到净液体转运速率增加。透壁壁厚p.d的下降很小但很明显。与去甲肾上腺素有关,但与血管紧张素输注无关; 3。 α-肾上腺素拮抗剂酚妥拉明和二氢麦角胺消除了血管紧张素和去甲肾上腺素对运输的刺激,并且去甲肾上腺素引起的p.d下降,而β-肾上腺素拮抗剂普萘洛尔没有显着影响这些反应。4。酚妥拉明并没有改变p.d.胆碱能激动剂毛果芸香碱给药后5。蛋白质合成抑制剂环己酰亚胺消除了血管紧张素和去甲肾上腺素引起的液体转运刺激。6。血管紧张素和去甲肾上腺素均未显着改变空肠循环AMP水平7。去甲肾上腺素输注后双侧肾切除术对输液量的增加没有明显影响。8。去甲肾上腺素诱导的运输刺激不受影响,并且下降。在用利血平预处理的大鼠中被增强,但是在血管紧张素输注后观察到转运的显着抑制。9。结果与以下观点一致:去甲肾上腺素可能介导血管紧张素对大鼠肠液吸收的作用。

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