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醋托芬可预防霍乱毒素诱导的人空肠水和电解质分泌。

Acetorphan prevents cholera-toxin-induced water and electrolyte secretion in the human jejunum.

作者信息

Hinterleitner T A, Petritsch W, Dimsity G, Berard H, Lecomte J M, Krejs G J

机构信息

Department of Internal Medicine, Karl Franzens University, Graz, Austria.

出版信息

Eur J Gastroenterol Hepatol. 1997 Sep;9(9):887-91. doi: 10.1097/00042737-199709000-00012.

Abstract

OBJECTIVES

Acetorphan is an orally administered inhibitor of enkephalinase in the wall of the digestive tract. It prevents inactivation of endogenous opioid peptides released by submucosal and myenteric neurons. The aim of this study was to examine the effect of acetorphan on jejunal water and electrolyte transport in healthy volunteers under basal conditions and in a state of intestinal secretion induced by a bacterial enterotoxin.

DESIGN

Ten volunteers in two groups were studied in an open trial. For the experimental design an intestinal perfusion technique was used.

METHODS

Cholera toxin was used to induce intestinal secretion in a model employing segmental perfusion of the human proximal jejunum. Acetorphan was given orally prior to intrajejunal administration of cholera toxin; its effect on intestinal transport was measured over a period of four hours after exposure to cholera toxin. Serum levels of methylthioether of thiorphan as the main metabolite were measured throughout three experiments to assure sufficient drug absorption.

RESULTS

Acetorphan had no influence on basal water and electrolyte absorption (133 vs. 140 ml/30 cm x h). In a control group with cholera toxin alone, significant water secretion was induced (131 ml/30 cm x h). Acetorphan completely prevented this secretion by leaving an absorption rate of 27 ml/30 cm x h. Intestinal electrolyte transport was also significantly changed towards absorption by acetorphan.

CONCLUSION

Acetorphan can prevent jejunal water and electrolyte secretion induced by cholera toxin. Enkephalins may thus protect the small intestine from enterotoxin-induced secretion.

摘要

目的

醋托芬是一种消化道壁内脑啡肽酶的口服抑制剂。它可防止黏膜下和肌间神经释放的内源性阿片肽失活。本研究的目的是在基础条件下以及在细菌肠毒素诱导的肠道分泌状态下,研究醋托芬对健康志愿者空肠水和电解质转运的影响。

设计

在一项开放试验中对两组共10名志愿者进行了研究。实验设计采用肠道灌注技术。

方法

在人体近端空肠节段灌注模型中,使用霍乱毒素诱导肠道分泌。在空肠内给予霍乱毒素之前口服醋托芬;在接触霍乱毒素后的4小时内测量其对肠道转运的影响。在整个三个实验过程中测量主要代谢产物硫喷妥的甲硫醚血清水平,以确保药物充分吸收。

结果

醋托芬对基础水和电解质吸收无影响(133对140毫升/30厘米×小时)。在仅使用霍乱毒素的对照组中,诱导出显著的水分泌(131毫升/30厘米×小时)。醋托芬通过使吸收速率达到27毫升/30厘米×小时,完全阻止了这种分泌。醋托芬还使肠道电解质转运显著转向吸收。

结论

醋托芬可预防霍乱毒素诱导的空肠水和电解质分泌。因此,脑啡肽可能保护小肠免受肠毒素诱导的分泌。

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