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Herbal medicine Yin Zhi Huang induces CYP3A4-mediated sulfoxidation and CYP2C19-dependent hydroxylation of omeprazole

  
@article{APS5911,
	author = {Lan Fan and Guo Wang and Lian-sheng Wang and Yao Chen and Wei Zhang and Yuan-fei Huang and Rui-xue Huang and Dong-li Hu and Dan Wang and Hong-hao Zhou},
	title = {Herbal medicine Yin Zhi Huang induces CYP3A4-mediated sulfoxidation and CYP2C19-dependent hydroxylation of omeprazole},
	journal = {Acta Pharmacologica Sinica},
	volume = {28},
	number = {10},
	year = {2016},
	keywords = {},
	abstract = {Aim: To explore the potential interactions between Yin Zhi Huang (YZH) and omeprazole, a substrate of CYP3A4 and CYP2C19.
Methods: Eighteen healthy volunteers, including 6 CYP2C19*1/*1, 6 CYP2C19*1/*2 or *3 and 6 CYP2C19*2/*2 were enrolled in a 2-phase, randomized, crossover clinical trial. In each phase, the volunteers received either placebo or 10 mL YZH oral liquid, 3 times daily for 14 d. Then all the patients took a 20 mg omeprazole capsule orally. Blood samples were collected up to 12 h after omeprazole administration. Plasma concentrations of omeprazole and its metabolites were quantified by HPLC with UV detection.
Results: After 14 d of treatment of YZH, plasma omeprazole significantly decreased and those of omeprazole sulfone and 5-hydroxyomeprazole significantly increased. The ratios of the area under the plasma concentration-time curves from time 0 to infinity (AUC(0-infinity) of omeprazole to 5-hydroxyomprazole and those of omeprazole to omeprazole sulfone decreased by 64.80%plusminus12.51% (P=0.001) and 63.31%plusminus18.45% (P=0.004) in CYP2C19*1/*1, 57.98%plusminus14.80% (P=0.002) and 54.87%plusminus18.42% (P =0.003) in CYP2C19*1/*2 or *3, and 37.74%plusminus16.07% (P=0.004) and 45.16%plusminus15.54% (P=0.003) in CYP2C19*2/*2, respectively. The decrease of the AUC(0-infinity) ratio of omeprazole to 5-hydroxyomprazole in CYP2C19*1/*1 and CYP2C19*1/*2 or *3 was greater than those in CYP2C19*2/*2 (P=0.047 and P=0.009).
Conclusion: YZH induces both CYP3A4-catalyzed sulfoxidation and CYP2C19-dependent hydroxylation of omeprazole leading to decreases in plasma omeprazole concentrations.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/5911}
}