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欧洲越橘花色苷的研究。II. 花色苷在大鼠体内的药代动力学研究

Studies on Vaccinium myrtillus anthocyanosides. II. Aspects of anthocyanins pharmacokinetics in the rat.

作者信息

Lietti A, Forni G

出版信息

Arzneimittelforschung. 1976;26(5):832-5.

PMID:989354
Abstract

Vaccinium myrtillus anthocyanins adminstered by i.v. or i.p. route to the rat undergo a rapid body distribution and in part also are easily eliminated such as to fit a three-compartments pharmacokinetic model. The anthocyanins elimination occurs mostly through urine and bile. The slight difference between the amount of anthocyanins eliminated after i.v. and after i.p. application shows a modest liver extracion of these substances. Vaccinium myrtillus anthocyanins possess a greater affinity for some tissues, namely kidneys and skin rather than for plasma. This fact could explain the long-lasting activity of anthocyanins on capillary resistance which is still elevated when plasma levels of these substances are no more detectable.

摘要

通过静脉注射或腹腔注射途径给予大鼠的欧洲越橘花青素在体内迅速分布,部分也易于消除,符合三室药代动力学模型。花青素的消除主要通过尿液和胆汁进行。静脉注射和腹腔注射后花青素消除量的细微差异表明这些物质在肝脏中的摄取量适中。欧洲越橘花青素对某些组织,即肾脏和皮肤具有更大的亲和力,而不是对血浆。这一事实可以解释花青素对毛细血管阻力的持久作用,当这些物质的血浆水平不再可检测时,毛细血管阻力仍然升高。

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