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前列腺素与肾素释放:III. PGE1、E2、F2α和D2对兔肾皮质切片肾素释放的影响

Prostaglandins and renin release: III. Effects of PGE1, E2 F2 alpha and D2 on renin release from rabbit renal cortical slices.

作者信息

Whorton A R, Lazar J D, Smigel M D, Oates J A

出版信息

Prostaglandins. 1981 Sep;22(3):455-68. doi: 10.1016/0090-6980(81)90106-4.

Abstract

We have investigated the direct effects of prostaglandins E1, E2, F2 alpha and D2 on renin release from rabbit renal cortical slices. Prostaglandin E1 (PGE1) was the most potent stimulant of renin release, while PGE2 was 20-30 fold less active. PGF2 alpha was found not to be an inhibitor of renin release as reported by others, but rather a weak agonist. PGD2 up to a concentration of 10 microgram/ml had no activity in this system. That the stimulation of renin release by PGE1 is a direct effect is supported by the finding that PGE1-induced release is not blocked by L-propranolol or by delta 5,8,11,14-eicosatetraynoic acid (ETYA), a prostaglandin synthesis inhibitor. The fatty acid precursor of PGE1, delta 8,11,14-eicosatrienoic acid, also stimulated renin release, an effect which was blocked by ETYA. In addition to the above findings, ethanol, a compound frequently used to dissolve prostaglandins, was shown to inhibit renin release.

摘要

我们研究了前列腺素E1、E2、F2α和D2对兔肾皮质切片肾素释放的直接影响。前列腺素E1(PGE1)是肾素释放最有效的刺激物,而PGE2的活性则低20 - 30倍。与其他人报道的不同,我们发现PGF2α不是肾素释放的抑制剂,而是一种弱激动剂。在该系统中,浓度高达10微克/毫升的PGD2没有活性。PGE1诱导的释放不受L - 普萘洛尔或前列腺素合成抑制剂δ5,8,11,14 - 二十碳四烯酸(ETYA)的阻断,这一发现支持了PGE1对肾素释放的刺激是一种直接作用的观点。PGE1的脂肪酸前体δ8,11,14 - 二十碳三烯酸也能刺激肾素释放,这一作用被ETYA阻断。除上述发现外,常用于溶解前列腺素的化合物乙醇被证明能抑制肾素释放。

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