The effect of resveratrol on pharmacokinetics of aripiprazole in vivo and in vitro.

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Citation

Zhan YY, Liang BQ, Li XY, Gu EM, Dai DP, Cai JP, Hu GX

The effect of resveratrol on pharmacokinetics of aripiprazole in vivo and in vitro.

Xenobiotica. 2016;46(5):439-44. doi: 10.3109/00498254.2015.1088175. Epub 2015 Sep 22.

PubMed ID
26391142 [ View in PubMed
]
Abstract

1. The objective of this study were to investigate the effect of orally administered resveratrol on the pharmacokinetics of aripiprazole (APZ) in rat, and the inhibitory effects of resveratrol on APZ dehydrogenation activity in liver microsomes and human cytochrome P450 3A4 and 2D6. 2. Twenty-five healthy male Sprague-Dawley rats were randomly divided into five groups: A (control group), B (multiple dose of 200 mg/kg resveratrol), C (multiple dose of 100 mg/kg resveratrol), D (a single dose of 200 mg/kg resveratrol) and E (a single dose of 100 mg/kg resveratrol). A single dose of 3 mg/kg APZ administered orally 30 min after administration of resveratrol. In addition, CYP2D6*1, CYP3A4*1, human and rat liver microsomes were performed to determine the effect of resveratrol on the metabolism of APZ in vitro. 3. The multiple dose of 200 or 100 mg/kg resveratrol significantly increased the AUC and Cmax of APZ. The resveratrol also obviously decreased the CL, but without any significant difference on t1/2 in vivo. On the other hand, resveratrol showed inhibitory effect on CYP3A4*1, CYP2D6*1, human and rat microsomes, the IC50 of resveratrol was 6.771, 87.87, 45.11 and 35.59 mumol l(-1), respectively. 4. Those results indicated more attention should be paid when APZ was administrated combined with resveratrol.

DrugBank Data that Cites this Article

Drug Enzymes
DrugEnzymeKindOrganismPharmacological ActionActions
ResveratrolCytochrome P450 2B6ProteinHumans
No
Inhibitor
Details
ResveratrolCytochrome P450 2C9ProteinHumans
Unknown
Inhibitor
Details
ResveratrolCytochrome P450 2D6ProteinHumans
No
Inhibitor
Details