Cytochrome P450s(CYPs) widely distribute in the liver of aquatic organisms and play a key role in drug metabolism.CYPs catalyze the N-deethylation of Enrofloxacin(ENR) to Ciprofloxacin(CIP).However,there is limited information regarding the action of CYPs in ?sh.We evaluated the metabolism of ENR following oral administrated of baicalin(100 mg/kg) and glycyrrhizin(100 mg/kg) in crucian carp,Carassium auratus gibelio.We measured the enzymatic activity of cytochrome P450 1A(CYP1A) and 3A(CYP3A) in liver microsomes.In addition,we documented the pharmacokinetics of ENR by continuous blood sampling.The absorption of ENR decreased significantly over time and both Cmax and AUC also deceased.AUC and t1/2z decreased signficantly whereas CL inceased after oral administrated of baicalin and glycyrrhizin,suggesting that ENR elimination was accelerated.The Cmax CIP/Cmax ENR was 1.48% and 2.22% for the BL and GZ groups,respectively(control: 0.95%).The AUC0-t-CIP/AUC0-t-ENR was 2.16% and 1.76% for the BL and GZ groups,respectively(control: 1.7%).Thus,BL and GZ contributed to induce N-deethylation of ENR.Pretreatment with BL and GZ was associated with a significant(P0.05) incease in ethoxyresorufin-O-deethylation(EROD) and erythromycin-N-demethylation(ERND) activity,the specific probes for CYP1A and CYP3A,respectively.In summary,BL and GZ accelerated the elimination of ENR.Furthermore,production of the ENR metabolite was related to the induction of CYP1A and CYP3A enzymatic activity.
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