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甲基黄嘌呤引起小肠分泌。

Methylxanthine induced small intestinal secretion.

作者信息

Brady P G, Bayless T M

出版信息

Johns Hopkins Med J. 1975 Jun;136(6):251-3.

PMID:167215
Abstract

Methylxanthines, being potent phosphodiesterase inhibitors, produce increased intestinal cyclic AMP levels and would be predicted to produce increased net intestinal fluid secretion. Their effect when presented to the intestinal lumen, which would be analogous to human ingestion, had not been previously determined. Isolated loops of rat jejunum were perfused with solutions of caffeine and theophylline in vivo. There was a decrease in net fluid absorption in both neonatal and mature animals exposed to theophylline. Mature animals exposed to caffeine developed a prompt secretory response, comparable to thax induced by cholera toxin. The data indicate that methylxanthines are potent intestinal secretagogues when administered intraluminally and suggest that secretory stimulation could be important in the gastrointestinal symptomatology elicited in man by these compounds.

摘要

甲基黄嘌呤作为强效磷酸二酯酶抑制剂,可使肠道环磷酸腺苷(cAMP)水平升高,预计会导致肠道净液分泌增加。此前尚未确定它们在肠腔内的作用效果,而这类似于人体摄入后的情况。在体内用咖啡因和茶碱溶液灌注大鼠空肠的分离肠袢。暴露于茶碱的新生动物和成年动物的净液体吸收均减少。暴露于咖啡因的成年动物出现了迅速的分泌反应,类似于霍乱毒素诱导的反应。数据表明,甲基黄嘌呤经肠腔内给药时是强效肠道促分泌剂,提示分泌刺激在这些化合物引起的人类胃肠道症状中可能起重要作用。

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