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首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Pharmacokinetic interaction of astragaloside IV with atractylenolide i and prim-O-glucosylcimifugin in male Sprague Dawley rats
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Pharmacokinetic interaction of astragaloside IV with atractylenolide i and prim-O-glucosylcimifugin in male Sprague Dawley rats

机译:黄芪甲苷IV与白术烯内酯i和prim-O-葡糖基cimifugin在雄性Sprague Dawley大鼠中的药代动力学相互作用

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摘要

Astragaloside IV, atractylenolide I, and prim-O-glucosylcimifugin are main medicinal components of the traditional Chinese medicine prescription Yu-ping-feng which is composed of three herbs: Astragalus membranaceus, Atractylodes macrocephala, and Saposhnikovia divaricata. This study is aimed to assess the influence of atractylenolide I and prim-O-glucosylcimifugin on the pharmacokinetic profile of astragaloside IV so as to investigate the pharmacokinetic mechanisms of the Yu-ping-feng prescription. Fifteen Sprague Dawley rats were randomized to three groups; astragaloside IV, astragaloside IV plus atractylenolide I, and a combination of astragaloside IV, atractylenolide I, and prim-O-glucosylcimifugin were respectively administered to rats of these three groups via intragastric gavage. Serum samples were collected at different times after drug administration, and serum concentrations of astragaloside IV and atractylenolide I were simultaneously detected using HPLC-electrospray ionization-MS. Compared with administration of astragaloside IV alone, concentrations of astragaloside IV in the serum were significantly increased when it was given in combination with atractylenolide I or atractylenolide I+prim-O-glucosylcimifugin, with higher values for Cmax (p = 0.019 and p = 0.033 compared with astragaloside IV + atractylenolide I and astragaloside IV + atractylenolide I + prim-O-glucosylcimifugin groups, respectively) and AUC (p = 0.0052 and p = 0.0047 compared with astragaloside IV + atractylenolide I and astragaloside IV + atractylenolide I + prim-O-glucosylcimifugin groups, respectively). Improvement in mean oral C max and mean systemic serum exposure because of the pharmacokinetic interaction between astragaloside IV and atractylenolide I might explain the rationale for the use of multiple herbs in Yu-ping-feng and of combinations of A.membranaceus and A. macrocephala.
机译:黄芪甲苷IV,白术烯内酯I和prim-O-葡萄糖基cimifugin是中药处方玉屏风的主要药物成分,玉屏风由三种草药组成:黄芪,白术和Saposhnikovia divaricata。本研究旨在评估白术内酯I和prim-O-葡萄糖基cimifugin对黄芪甲苷IV药代动力学的影响,以探讨玉屏风方剂的药代动力学机制。将15只Sprague Dawley大鼠随机分为三组;每组15只。通过胃内灌胃法分别给这三组大鼠分别施用黄芪甲苷IV,黄芪甲苷IV加白术烯内酯I,以及黄芪甲苷IV,白术烯内酯I和prim-O-葡糖基cimifugin的组合。在给药后的不同时间收集血清样品,并使用HPLC-电喷雾电离-MS同时检测黄芪甲苷IV和白术烯内酯I的血清浓度。与单独使用黄芪甲苷IV相比,当与白术烯内酯I或白术内酯I + prim-O-葡糖基嘧啶核苷联用时,血清中黄芪甲苷IV的浓度显着增加,Cmax值较高(p = 0.019,p = 0.033分别与黄芪甲苷IV +白术烯内酯I和黄芪甲苷IV +白术烯内酯I + prim-O-葡萄糖基cimifugin组相比)和AUC(与黄芪甲苷IV +白术烯内酯I和黄芪甲苷IV +白术内酯I + prim-O相比,p = 0.0052和p = 0.0047 -葡糖基cimifugin基团)。由于黄芪甲苷IV和白术烯内酯I之间的药代动力学相互作用,平均口服C max和平均全身血清暴露的改善可能解释了在玉屏风中使用多种草药以及A.memranaceus和A.macrocephala的组合的基本原理。

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