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血管紧张素可刺激人体释放抗利尿激素。

Angiotensin stimulated AVP-release in humans.

作者信息

Uhlich E, Weber P, Eigler J, Gröschel-Stewart U

出版信息

Klin Wochenschr. 1975 Feb 15;53(4):177-80. doi: 10.1007/BF01466762.

Abstract

Release of arginine vasopressin (AVP) from rat neurohypophysis in in vitro studies is significantly augmented by the addition of angiotensin (A-II), and in in vivo studies in dogs renin and A-II were found to stimulate secretion of AVP. Both these results suggest the existence of a direct relationship between the salt regulating renin-angiotensin-aldosterone system and the water controlling AVP system. To evaluate whether such observations apply also in man a sensitive double antibody radioimmunoassay for AVP was developed [17, 18]. Basal plasma levels of AVP in recumbent humans without salt and fluid restriction at room temperature were 3.4 plus or minus 2.2 pg/ml, and 30 min after the onset of an A-II infusion at a concentration of 3-30 ng/min-kg, a significant increase of AVP was found. Maximum measurements were 2-5 times basal levels which returned to normal within 90 min. During the A-II infusion one also noted a 20 mm Hg rise in blood pressure, accompanied by a significant decrease in plasma renin activity. During the same period serum osmolality and serum sodium concentration did not change. Elevation of blood pressure by norepinephrine was not followed by any detectable change of plasma AVP levels, thus excluding a nonspecific blood pressure effect.

摘要

在体外研究中,添加血管紧张素(A-II)可显著增强大鼠神经垂体中精氨酸加压素(AVP)的释放,并且在犬类体内研究中发现肾素和A-II可刺激AVP的分泌。这两个结果均表明调节盐的肾素 - 血管紧张素 - 醛固酮系统与控制水的AVP系统之间存在直接关系。为了评估这些观察结果是否也适用于人类,开发了一种用于AVP的灵敏双抗体放射免疫测定法[17,18]。在室温下无盐和液体限制的卧位人类中,基础血浆AVP水平为3.4±2.2 pg/ml,在以3 - 30 ng/min-kg的浓度输注A-II开始后30分钟,发现AVP显著增加。最大测量值为基础水平的2 - 5倍,并在90分钟内恢复正常。在输注A-II期间,还注意到血压升高20 mmHg,同时血浆肾素活性显著降低。在此期间,血清渗透压和血清钠浓度没有变化。去甲肾上腺素引起的血压升高并未伴随血浆AVP水平的任何可检测变化,从而排除了非特异性血压效应。

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