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Acta Pharmacol Sin ; 30(11): 1559-65, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19890363

ABSTRACT

AIM: The role of CYP1A in the protection of aristolochic acid (AA)I-induced nephrotoxicity has been suggested. In the present study we investigated the effects of beta-naphthoflavone (BNF), a non-carcinogen CYP1A inducer, on AAI-induced kidney injury. METHODS: Mice were pretreated with 80 mg/kg BNF by daily intraperitoneal injection (ip) for 3 days followed by a single ip of 10 mg/kg AAI. AAI and its major metabolites in blood, liver and kidney, the expression of CYP1A1 and CYP1A2 in microsomes of liver and kidney, as well as the nephrotoxicity were evaluated. RESULTS: BNF pretreatment prevented AAI-induced renal damage by facilitating the disposal of AAI in liver. BNF pretreatment induced the expression of CYP1A1 in both liver and kidney; but the induction of CYP1A2 was only observed in liver. CONCLUSION: BNF prevents AAI-induced kidney toxicity primarily through CYP1A induction.


Subject(s)
Aristolochic Acids/toxicity , Kidney Diseases/prevention & control , beta-Naphthoflavone/pharmacology , Acute Disease , Animals , Aristolochic Acids/metabolism , Cytochrome P-450 CYP1A1/drug effects , Cytochrome P-450 CYP1A1/metabolism , Cytochrome P-450 CYP1A2/drug effects , Cytochrome P-450 CYP1A2/metabolism , Enzyme Induction/drug effects , Injections, Intraperitoneal , Kidney/drug effects , Kidney/metabolism , Kidney Diseases/chemically induced , Male , Mice , Mice, Inbred C57BL , Microsomes/drug effects , Microsomes/metabolism , Microsomes, Liver/drug effects , Microsomes, Liver/metabolism
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