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人及大鼠小肠组织体外前列腺素的释放及内毒素对大鼠体内的影响。

Release of prostaglandins by small intestinal tissue of man and rat in vitro and the effect of endotoxin in the rat in vivo.

作者信息

Peskar B M, Weiler H, Kröner E E, Peskar B A

出版信息

Prostaglandins. 1981;21 Suppl:9-14. doi: 10.1016/0090-6980(81)90111-8.

Abstract

Rat jejunal tissue in vitro synthesizes large amounts of prostaglandin (PG) D2 and smaller amounts of 6-keto-PGF1 alpha and PGE2, whereas human small intestinal mucosa synthesizes much smaller amounts of the three PG determined with about equal amounts of PGE2 and PGD2. Intraperitoneal administration of bacterial endotoxin to rats induce fluid accumulation in the small intestine and increases significantly the release of PGD2, PGE2 and 6-keto-PGF1 alpha into the small intestinal lumen in vivo. Endotoxin-induced stimulation of PG release is particularly pronounced for PGD2. Fluid accumulation and PG output are inhibited by indomethacin. It seems possible that the different total amounts of PG synthesized by small intestinal tissue of man and rat as well as the different pattern of PG released might contribute to species-specific responses of the gastrointestinal tract to various pathophysiological stimuli.

摘要

大鼠空肠组织在体外可合成大量前列腺素(PG)D2以及少量的6-酮-PGF1α和PGE2,而人小肠黏膜合成的这三种前列腺素量则少得多,且PGE2和PGD2的量大致相等。给大鼠腹腔注射细菌内毒素可导致小肠积液,并显著增加体内PGD2、PGE2和6-酮-PGF1α向小肠肠腔的释放。内毒素诱导的PG释放刺激对PGD2尤为明显。吲哚美辛可抑制液体蓄积和PG的产生。人与大鼠小肠组织合成的PG总量不同以及PG释放模式不同,这可能导致胃肠道对各种病理生理刺激产生种属特异性反应。

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