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洛哌丁胺对脱氧胆酸诱导的肠道分泌的抑制作用。

Inhibition by loperamide of deoxycholic acid induced intestinal secretion.

作者信息

Farack U M, Loeschke K

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1984 Mar;325(3):286-9. doi: 10.1007/BF00495957.

Abstract

The effect of loperamide on deoxycholic acid (DOC)-induced secretion was studied in ligated loops of the rat jejunum and colon in vivo. In controls, loperamide slightly augmented fluid absorption. 3 mmol DOC caused net fluid secretion. Loperamide reduced this secretion in the colon and reversed it to absorption in the jejunum. Na-K-ATPase specific activity and cAMP levels were measured in the jejunum, and [14C]erythritol clearance as an index of mucosal permeability in the colon. In the jejunum this opiate analogue affected neither basal or DOC-depressed Na-K-ATPase, nor mucosal cAMP. In the colon it reduced a large increase of the erythritol clearance caused by DOC. It is suggested that loperamide interferes with DOC-induced intestinal secretion in part by lowering mucosal permeability.

摘要

在大鼠空肠和结肠体内结扎肠袢中研究了洛哌丁胺对脱氧胆酸(DOC)诱导的分泌的影响。在对照组中,洛哌丁胺略微增强了液体吸收。3 mmol DOC引起净液体分泌。洛哌丁胺减少了结肠中的这种分泌,并使空肠中的分泌逆转至吸收。在空肠中测量了钠钾ATP酶比活性和cAMP水平,并在结肠中测量了[14C]赤藓糖醇清除率作为粘膜通透性的指标。在空肠中,这种阿片类药物类似物既不影响基础或DOC抑制的钠钾ATP酶,也不影响粘膜cAMP。在结肠中,它减少了DOC引起的赤藓糖醇清除率的大幅增加。提示洛哌丁胺部分通过降低粘膜通透性来干扰DOC诱导的肠道分泌。

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