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甘草提取物中甘草酸的胃肠道吸收特性

Gastrointestinal absorption characteristics of glycyrrhizin from glycyrrhiza extract.

作者信息

Wang Z, Nishioka M, Kurosaki Y, Nakayama T, Kimura T

机构信息

Faculty of Pharmaceutical Sciences, Okayama University, Japan.

出版信息

Biol Pharm Bull. 1995 Sep;18(9):1238-41. doi: 10.1248/bpb.18.1238.

Abstract

The differences in gastrointestinal absorption behaviors of glycyrrhizin (GZ) between pure GZ and GZ in glycyrrhiza extract (GE) (equivalent dose as GZ) were examined in rats. Similarly to the case of pure GZ, both GZ and glycyrrhetic acid (GA) were detected in the plasma after oral administration of GE. However, the plasma concentration-time curves of GZ and GA after GE oral administration were much lower than those of pure GZ, indicating the marked reduction in bioavailability of GZ and as GA after this administration. To identify the GE components affecting the absorption of GZ, GZ was removed from GE and the effect of the remaining components on the gastrointestinal absorption process of GZ was examined. The lipophilic components of GE reduced the gastric emptying rate and the absorption of GZ from the small intestine, while these effects were not observed in the hydrophilic components. In contrast, the bioavailability of GZ as GA was increased by the hydrophilic components, but not the lipophilic ones. At least some of the factors in GE altering the bioavailability of GZ were identified.

摘要

在大鼠中研究了甘草甜素(GZ)在纯GZ与甘草提取物(GE)中(与GZ等效剂量)胃肠道吸收行为的差异。与纯GZ的情况类似,口服GE后在血浆中检测到了GZ和甘草次酸(GA)。然而,口服GE后GZ和GA的血浆浓度-时间曲线远低于纯GZ的曲线,表明此次给药后GZ和GA的生物利用度显著降低。为了确定影响GZ吸收的GE成分,从GE中去除GZ,并研究了其余成分对GZ胃肠道吸收过程的影响。GE的亲脂性成分降低了胃排空率和GZ从小肠的吸收,而亲水性成分未观察到这些作用。相反,亲水性成分增加了GZ作为GA的生物利用度,而亲脂性成分则没有。确定了GE中至少一些改变GZ生物利用度的因素。

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