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淫羊藿总黄酮在骨质疏松大鼠体内的药动学行为

刘聪燕 高霞 陈彦 黄萌萌 瞿鼎

中成药2017,Vol.39Issue(8):1595-1600,6.
中成药2017,Vol.39Issue(8):1595-1600,6.DOI:10.3969/j.issn.1001-1528.2017.08.010

淫羊藿总黄酮在骨质疏松大鼠体内的药动学行为

Pharmacokinetic behaviors of total flavonoids from Epimedii Folium in osteoporotic rats in vivo

刘聪燕 1高霞 1陈彦 1黄萌萌 1瞿鼎1

作者信息

  • 1. 南京中医药大学附属中西医结合医院,江苏省中医药研究院中药组分与微生态研究中心,江苏南京210028
  • 折叠

摘要

Abstract

AIM To investigate the pharmacokinetic behaviors of total flavonoids from Epimedii Folium in osteoporotic rats in vivo.METHODS Twelve rats were divided into model group and sham group,after which the osteoporotic rat model was established by removing bilateral ovaries.After intragastric administration with total flavonoids (500 mg/kg),HPLC-DAD was applied to detecting the plasma concentrations of total flavonoids' prototype glycosides (epimedin A,epimedin B,epimedin C,icariin) and their metabolites (sagittatoside A,sagittatoside B,2"-O-rhamnosylicariside Ⅱ,baohuoside Ⅰ,icaritin) at thirteen time points (0.083,0.25,0.5,0.75,1,2,3,4,6,8,12,24 and 48 h),then the plasma concentration-time curves were drawn,followed by the calculation of pharmacokinetic parameters.RESULTS Doubled peaks were observed in the plasma concentration-time curves of total flavonoids' prototype glycosides and their metabolites in both groups.Compared with the sham group,the integrated AUC and Cmax in the model group were significantly decreased (P < 0.01),as well as the prolonged t1/2 (P < 0.01).CONCLUSION The in vivo absorption and metabolism of total flavonoids from Epimedii Folium are much slower in the state of osteoporosis,thus affects the efficacy.

关键词

淫羊藿/总黄酮/药动学行为/骨质疏松大鼠

Key words

Epimedii Folium/total flavonoids/pharmacokinetic behaviors/osteoporotic rats

分类

医药卫生

引用本文复制引用

刘聪燕,高霞,陈彦,黄萌萌,瞿鼎..淫羊藿总黄酮在骨质疏松大鼠体内的药动学行为[J].中成药,2017,39(8):1595-1600,6.

基金项目

国家自然科学基金(81173557) (81173557)

中成药

OA北大核心CSCDCSTPCD

1001-1528

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