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黄连对大鼠灌胃黄芩后黄酮类成分药代动力学的影响。

Influence of coptis Chinensis on pharmacokinetics of flavonoids after oral administration of radix Scutellariae in rats.

机构信息

Laboratory of Pharmacokinetics, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

出版信息

Biopharm Drug Dispos. 2009 Oct;30(7):398-410. doi: 10.1002/bdd.674.

Abstract

Radix Scutellariae (RS) and Coptis Chinensis (CC) are the most popular components in traditional Chinese medicine prescriptions. Flavonoids are the main effective ingredients in RS and berberine is the main effective ingredient in CC. The aim of this study was to determine the influence of CC on the pharmacokinetics of flavonoids following the administration of RS in rats and to investigate the effects of CC on the pharmacokinetic mechanism. Rats were administered RS or RS+CC by intragastric gavage (i.g.). Plasma concentrations of baicalin (baicalein 7-glucuronide) and wogonoside (wogonin 7-glucuronide) were measured by HPLC. Pharmacokinetic parameters were calculated from the plasma concentration time curve. The effect of CC on the metabolism of flavonoids in RS by rat intestinal flora was studied using rat fecal suspensions after ig administration of CC. The effect of berberine on the bi-directional transport of baicalein and baicalin was studied in Caco-2 monolayer models. The effect of CC on the metabolism of baicalein and baicalin by the liver was studied using rat liver microsomes after i.g. administration of CC. Compared to RS alone, RS+CC decreased AUC and C(max) of baicalin and wogonoside. CC decreased the hydrolyzation of baicalin and wogonoside by intestinal flora. Berberine decreased the amount of baicalein transported to the basolateral side and the amount of baicalin which appeared at the basolateral side. The results showed that CC may decrease the bioavailability of baicalin and wogonoside in RS and the mechanism was related to CC decreasing the transport of flavonoid aglycones from the mucosa side to the serosal side and the hydrolyzation of flavonoids by inhibiting intestinal flora.

摘要

黄芩(RS)和黄连(CC)是中药方剂中最常用的两种成分。黄酮类化合物是 RS 的主要有效成分,小檗碱是 CC 的主要有效成分。本研究旨在确定 CC 对大鼠给予 RS 后黄酮类化合物药代动力学的影响,并探讨 CC 对药代动力学机制的影响。大鼠通过灌胃(i.g.)给予 RS 或 RS+CC。采用 HPLC 法测定血浆中黄芩苷(黄芩素 7-葡萄糖醛酸苷)和汉黄芩苷(汉黄芩素 7-葡萄糖醛酸苷)的浓度。根据血浆浓度-时间曲线计算药代动力学参数。通过大鼠灌胃给予 CC 后粪便混悬液研究 CC 对 RS 中黄酮类化合物在大鼠肠道菌群中代谢的影响。采用 Caco-2 单层模型研究小檗碱对黄芩素和黄芩苷双向转运的影响。通过大鼠灌胃给予 CC 后肝微粒体研究 CC 对黄芩素和黄芩苷代谢的影响。与单独给予 RS 相比,RS+CC 降低了黄芩苷和汉黄芩苷的 AUC 和 Cmax。CC 降低了肠道菌群对黄芩苷和汉黄芩苷的水解作用。小檗碱降低了黄芩素转运到基底外侧的量和出现在基底外侧的黄芩苷的量。结果表明,CC 可能降低 RS 中黄芩苷和汉黄芩苷的生物利用度,其机制与 CC 降低黄酮类苷元从粘膜侧向浆膜侧的转运以及通过抑制肠道菌群水解黄酮类有关。

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