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血管活性肠肽(VIP)和前列腺素E1(PGE1)通过不同机制激活大鼠肠上皮细胞膜中的腺苷酸环化酶。

VIP and PGE1 activate adenylate cyclase in rat intestinal epithelial cell membranes via different mechanisms.

作者信息

Beubler E

出版信息

Eur J Pharmacol. 1981 Aug 27;74(1):67-72. doi: 10.1016/0014-2999(81)90324-1.

Abstract

The effect of vasoactive intestinal polypeptide (VIP) and of prostaglandin E1 (PGE1) alone and in combination was tested in an adenylate cyclase (AC) preparation from rat intestinal epithelial cell membranes. AC activity increased linearly with time up to 15 min in the absence or presence of VIP or PGE1, respectively. NaF, VIP and PGE1 concentration-dependently stimulated AC activity. The dose-response curve of VIP in the presence of PGE1 was shifted to the left and the maximal effect of VIP was significantly enhanced. The dose-response curve obtained experimentally was significantly different from theoretical additive dose-response curve, indicating that PGE1 potentiates the effect of VIP on AC activity. The possible mechanisms of potentiation are discussed. The results suggest that VIP and PGE1 activate AC via two different but not entirely independent mechanisms.

摘要

分别在大鼠肠上皮细胞膜的腺苷酸环化酶(AC)制剂中测试了血管活性肠肽(VIP)、前列腺素E1(PGE1)单独及联合使用的效果。在不存在或存在VIP或PGE1的情况下,AC活性分别在15分钟内随时间呈线性增加。NaF、VIP和PGE1浓度依赖性地刺激AC活性。在PGE1存在的情况下,VIP的剂量反应曲线向左移动,且VIP的最大效应显著增强。实验获得的剂量反应曲线与理论相加剂量反应曲线显著不同,表明PGE1增强了VIP对AC活性的作用。讨论了增强作用的可能机制。结果表明,VIP和PGE1通过两种不同但并非完全独立的机制激活AC。

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