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[丙谷胺利胆作用机制的研究]

[A study on the mechanism of the choleretic effect of proglumide].

作者信息

Chen Y

机构信息

PUMC Hospital, CAMS and PUMC, Beijing.

出版信息

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1993 Dec;15(6):393-8.

PMID:7915971
Abstract

It has been found in this laboratory that proglumide (PGM) can increase hepatic bile flow in humans and in several species of animals, and lower gallstone formation in experimental animals. In order to further investigate the mechanisms of this choleretic effect of PGM, studies with isolated rat liver cells and plasma membranes were performed. The results indicated that PGM could increase the activity of membrane Na+, K(+)-ATPase significantly. On the other hand, PGM decreased the net uptake of 14C-glycocholic acid by rat liver cells. These data suggest that the choleretic effect of PGM is likely to be mediated through the enhancement of membrane Na+, K(+)-ATPase activity (which would in turn increase water and electrolyte output), rather than by affecting bile acid uptake by liver cells. It was also observed that PGM could reverse the inhibitory effect of somatostatin on the activity of membrane Na+, K(+)-ATPase. These results provide some clues for the elucidation of the mechanisms of the inhibitory effect of PGM on gallstone formation in experimental animals.

摘要

本实验室发现,丙谷胺(PGM)可增加人体及多种动物的肝胆汁流量,并降低实验动物的胆结石形成率。为进一步研究PGM利胆作用的机制,我们对分离的大鼠肝细胞和质膜进行了研究。结果表明,PGM可显著提高膜Na +,K(+)-ATP酶的活性。另一方面,PGM降低了大鼠肝细胞对14C-甘氨胆酸的净摄取。这些数据表明,PGM的利胆作用可能是通过增强膜Na +,K(+)-ATP酶的活性(进而增加水和电解质的排出)来介导的,而不是通过影响肝细胞对胆汁酸的摄取。还观察到,PGM可逆转生长抑素对膜Na +,K(+)-ATP酶活性的抑制作用。这些结果为阐明PGM对实验动物胆结石形成抑制作用的机制提供了一些线索。

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