He Jiayang, Fang Ping, Zheng Xiang, Wang Chenchen, Liu Tenghui, Zhang Bowen, Wen Jian, Xu Ren-Ai
Department of Pharmacy, The First Hospital of Jiaxing, Jiaxing, Zhejiang, China.
Department of Pharmacology, School of Pharmacy of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Drug Des Devel Ther. 2018 Mar 9;12:513-519. doi: 10.2147/DDDT.S160316. eCollection 2018.
The aim of this study was to study the effect of celecoxib on agomelatine metabolism in vitro and in vivo.
Ten healthy male Sprague-Dawley rats were randomly divided into 2 groups: Group A (control group) and Group B (30 mg/kg celecoxib). Then a single dose of 20 mg/kg agomelatine was administered orally 30 min after administration of celecoxib. In an in vitro study, celecoxib with a series of concentrations was added to an incubation mixture containing recombinant human CYP2C9, human or rat liver microsomes to determine the half-maximal inhibitory concentration on the metabolism of agomelatine. Moreover, a mechanism study was performed to determine the inhibitory effect of celecoxib on CYP2C9.
The results showed that a single dose of 30 mg/kg celecoxib significantly increased the area under the concentration-time curve and maximum concentration of agomelatine. In addition, celecoxib inhibited the metabolism of agomelatine in the in vitro studies, which was determined to be by a competitive mechanism on CYP2C9. Those results indicated that celecoxib has an inhibitory effect on the metabolism of agomelatine both in vivo and in vitro.
Thus, more attention should be paid when celecoxib is administered combined with agomelatine.
本研究旨在探讨塞来昔布在体外和体内对阿戈美拉汀代谢的影响。
将10只健康雄性Sprague-Dawley大鼠随机分为2组:A组(对照组)和B组(30mg/kg塞来昔布)。在给予塞来昔布30分钟后,口服单剂量20mg/kg阿戈美拉汀。在体外研究中,将一系列浓度的塞来昔布添加到含有重组人CYP2C9、人或大鼠肝微粒体的孵育混合物中,以确定对阿戈美拉汀代谢的半数最大抑制浓度。此外,进行了机制研究以确定塞来昔布对CYP2C9的抑制作用。
结果显示,单剂量30mg/kg塞来昔布显著增加了阿戈美拉汀的浓度-时间曲线下面积和最大浓度。此外,在体外研究中塞来昔布抑制了阿戈美拉汀的代谢,确定其通过对CYP2C9的竞争性机制发挥作用。这些结果表明,塞来昔布在体内和体外均对阿戈美拉汀的代谢有抑制作用。
因此,塞来昔布与阿戈美拉汀联合使用时应更加注意。