Inhibitory effect of celecoxib on agomelatine metabolism in vitro and in vivo

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 o...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Drug design, development and therapy development and therapy, 2018-01, Vol.12, p.513-519
Hauptverfasser: He, Jiayang, Fang, Ping, Zheng, Xiang, Wang, Chenchen, Liu, Tenghui, Zhang, Bowen, Wen, Jian, Xu, Ren-Ai
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung: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.
ISSN:1177-8881
1177-8881
DOI:10.2147/DDDT.S160316