Li Yun-xia, Gong Xiao-hong, Li Yan, Zhang Ruo-qi, Yuan An, Zhao Meng-jie, Zeng Dai-wen, Peng Cheng
Pharmacy College, State Key Laboratory Breeding Base of Systematic Research, Development and Utilization of Chinese Medicine Resources, Chengdu University of Traditional Chinese Medicine, Chengdu, 610075, China.
Sichuan Academy of Medical Science & Sichuan Provincial People's Hospital, Chengdu, China.
Phytother Res. 2015 Aug;29(8):1259-64. doi: 10.1002/ptr.5369. Epub 2015 May 12.
Rhei Radix et Rhizoma was one of the commonly used traditional Chinese medicines, and the compatibility of Rhei Radix et Rhizoma and Aconiti Lateralis Radix Praeparata was the basic herb pair applied in many Chinese traditional prescription. Rhubarb anthraquinones were the main bioactive materials of Rhei Radix et Rhizoma. To elucidate the compatibility of Rhei Radix et Rhizoma and Aconiti Lateralis Radix Praeparata, the pharmacokinetics of rhubarb anthraquinones as the main marker constituents were investigated. In the present study, pharmacokinetic differences of rhubarb anthraquinones were detected after oral administration of extract of Rheum palmatum L. and compatibility with Aconitum carmichaelii Debx. After oral administration, no difference of peak time can be found for anthraquinones between rhubarb group and compatibility group. But Cmax and area under the curve of aloe-emodin, emodin and chrysophanol in compatibility group were significantly higher than that in rhubarb group. Although the Cmax of rhein in compatibility group was much lower than that in rhubarb group, the area under the curve value was similar in two groups. The clearance and t1/2 of rhubarb anthraquinone were also changed after compatibility. The change of pharmacokinetics characteristics of rhubarb anthraquinone after compatibility may be caused by the drug-drug interaction medicated by chemical reaction and cytochromes P450.
大黄是常用的传统中药之一,大黄与附子的配伍是许多中药传统方剂中应用的基本药对。大黄蒽醌是大黄的主要生物活性物质。为阐明大黄与附子的配伍关系,以大黄蒽醌为主要指标成分进行了药代动力学研究。本研究检测了口服掌叶大黄提取物及其与制川乌配伍后大黄蒽醌的药代动力学差异。口服给药后,大黄组与配伍组蒽醌的达峰时间无差异。但配伍组中芦荟大黄素、大黄素和大黄酚的Cmax和曲线下面积均显著高于大黄组。虽然配伍组中大黄酸的Cmax远低于大黄组,但两组的曲线下面积值相似。配伍后大黄蒽醌的清除率和t1/2也发生了变化。大黄蒽醌配伍后药代动力学特征的改变可能是由化学反应和细胞色素P450介导的药物相互作用引起的。