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合成脑啡肽类似物FK 33 - 824对前列腺素E1诱导的肠道分泌的抑制作用。

Inhibition of PGE1 induced intestinal secretion by the synthetic enkephalin analogue FK 33-824.

作者信息

Lembeck F, Beubler E

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1979 Sep;308(3):261-4. doi: 10.1007/BF00501391.

Abstract
  1. The effects of the enkephalin analogue, FK 33-824 were compared with those of morphine and naloxone on the prostaglandin E1-induced increase in intestinal fluid volume and unanaesthetized and pithed rats. 2. FK 33-824 inhibits the prostaglandin E1-induced increase in intestinal fluid volume both in unanaesthetized and pithed rats. 3. Naloxone abolished the inhibitory effect of FK 33-824 in both experimental models. 4. It can be concluded from the experiments in pithed rats that the inhibitory effect of FK 33-824, like that of morphine, on prostaglandin E1-induced secretion is caused by a peripheral action. 5. It is assumed that endogenous enkephalins protect against prostaglandin-mediated loss of fluid into the gut lumen. This protective effect can be mimicked by an enkephalin analogue and blocked by naloxone.
摘要
  1. 将脑啡肽类似物FK 33 - 824与吗啡和纳洛酮对前列腺素E1诱导的未麻醉和脊髓切断大鼠肠液量增加的影响进行了比较。2. FK 33 - 824在未麻醉和脊髓切断的大鼠中均抑制前列腺素E1诱导的肠液量增加。3. 在两种实验模型中,纳洛酮均消除了FK 33 - 824的抑制作用。4. 从脊髓切断大鼠的实验可以得出结论,FK 33 - 824对前列腺素E1诱导的分泌的抑制作用,与吗啡一样,是由外周作用引起的。5. 据推测,内源性脑啡肽可防止前列腺素介导的液体进入肠腔的损失。脑啡肽类似物可模拟这种保护作用,而纳洛酮可阻断这种作用。

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