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十二指肠溃疡原半胱胺和丙腈可降低大鼠十二指肠对酸的中和作用。

Duodenal ulcerogens cysteamine and propionitrile decrease duodenal neutralization of acid in the rat.

作者信息

Adler R S, Gallagher G T, Szabo S

出版信息

Dig Dis Sci. 1983 Aug;28(8):716-23. doi: 10.1007/BF01312562.

Abstract

Neutralization of acid was evaluated in rat proximal duodenal segments isolated from biliary and pancreatic secretions. Duodenal ulcerogenic doses of cysteamine produced a significant decrease in acid disposal 0.5-2 hr after treatment. Oral or subcutaneous administration of the duodenal ulcerogen was effective. The potent ulcerogen cysteamine produced a more pronounced decrease than propionitrile (a weak duodenal ulcerogen). The failure of ethanolamine, a nonulcerogenic structural analog of cysteamine to significantly alter acid disposal suggests that the effect is not due to the toxic properties of the duodenal ulcerogen. The results reinforce the concept that the duodenum is able to dispose of significant quantities of acid. The decrease in acid-handling may contribute to duodenal susceptibility to acid after treatment with ulcerogens and possibly reflects pathophysiologic changes early in duodenal ulceration.

摘要

在从胆汁和胰液分泌中分离出的大鼠近端十二指肠段中评估酸的中和作用。十二指肠溃疡致剂量的半胱胺在治疗后0.5 - 2小时使酸处理能力显著降低。十二指肠溃疡原经口服或皮下给药均有效。强效溃疡原半胱胺比丙腈(一种弱十二指肠溃疡原)产生更明显的降低。半胱胺的非溃疡ogenic结构类似物乙醇胺未能显著改变酸处理,这表明该作用不是由于十二指肠溃疡原的毒性特性。结果强化了十二指肠能够处理大量酸的概念。酸处理能力的降低可能导致十二指肠在用溃疡原治疗后对酸的易感性增加,并且可能反映十二指肠溃疡早期的病理生理变化。

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