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佛波酯对青蛙皮肤抗利尿激素水渗透性反应的影响。

Phorbol ester effect on the hydrosmotic response to vasopressin in frog skin.

作者信息

Casavola V, Iacovelli L, Svelto M

出版信息

Pflugers Arch. 1987 Mar;408(3):318-20. doi: 10.1007/BF02181476.

Abstract

Serosal preincubation of frog skin with tetradecanoyl phorbol acetate, TPA, an activator of protein kinase C, inhibits the hydrosmotic response elicited by vasopressin (AVP) but not that induced by 8br-cAMP. This proves that serosal TPA primarily influences a pre-cAMP step. The TPA-induced inhibition of AVP response appears to be related to TPA-induced prostaglandin synthesis. The pretreatment with naproxen, in fact, prevents the inhibition induced by serosal TPA on the AVP response. On the contrary, mucosal TPA produces a more marked inhibition of the response to AVP and significantly diminishes the water flow induced by 8br-cAMP; this suggests that mucosal TPA interferes mainly with a post-cAMP step. Furthermore, naproxen is unable to completely prevent the inhibition induced by mucosal TPA on AVP response thus indicating that mucosal TPA may also activate a prostaglandin-independent mechanism able to inhibit one of the last steps of the hydrosmotic response to AVP.

摘要

用蛋白激酶C激活剂十四酰佛波醇乙酸酯(TPA)对蛙皮进行浆膜预孵育,可抑制血管加压素(AVP)引发的渗透反应,但不抑制8-溴-cAMP诱导的反应。这证明浆膜TPA主要影响cAMP前的步骤。TPA诱导的对AVP反应的抑制似乎与TPA诱导的前列腺素合成有关。事实上,用萘普生预处理可防止浆膜TPA对AVP反应的抑制。相反,黏膜TPA对AVP反应产生更显著的抑制,并显著减少8-溴-cAMP诱导的水流量;这表明黏膜TPA主要干扰cAMP后的步骤。此外,萘普生无法完全阻止黏膜TPA对AVP反应的抑制,因此表明黏膜TPA也可能激活一种不依赖前列腺素的机制,该机制能够抑制对AVP渗透反应的最后步骤之一。

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