β-Naphthoflavone protects mice from aristolochic acid-l-induced acute kidney injury in a CYP1A dependent mechanism
文献类型:期刊论文
作者 | Ying XIAO2; Xiang XUE2; Yuanfeng WU2; GuozhengXIN2; Yong QIAN1; Tianpei XIE1; Likun GONG2![]() ![]() |
刊名 | Acta Pharmacologica Sinica
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出版日期 | 2009 |
卷号 | 30期号:11页码:1559 |
关键词 | aristolochic acid kidney injury beta-naphthoflavone biotransformation CYP1A |
ISSN号 | 1671-4083 |
英文摘要 | Aim: The role of CYP1A in the protection of aristolochic acid (AA)l-induced nephrotoxicity has been suggested. In the present study we investigated the effects of P-naphthoflavone (BNF), a non-carcinogen CYP1A inducer, on Aal-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 Aal-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 Aal-induced kidney toxicity primarily through CYP1A induction. |
语种 | 英语 |
源URL | [http://119.78.100.183/handle/2S10ELR8/293710] ![]() |
专题 | 中国科学院上海药物研究所 |
作者单位 | 1.Shanghai TenGen Biomedical Co Ltd, China 2.中国科学院上海药物研究所 |
推荐引用方式 GB/T 7714 | Ying XIAO,Xiang XUE,Yuanfeng WU,et al. β-Naphthoflavone protects mice from aristolochic acid-l-induced acute kidney injury in a CYP1A dependent mechanism[J]. Acta Pharmacologica Sinica,2009,30(11):1559. |
APA | Ying XIAO.,Xiang XUE.,Yuanfeng WU.,GuozhengXIN.,Yong QIAN.,...&Jin REN.(2009).β-Naphthoflavone protects mice from aristolochic acid-l-induced acute kidney injury in a CYP1A dependent mechanism.Acta Pharmacologica Sinica,30(11),1559. |
MLA | Ying XIAO,et al."β-Naphthoflavone protects mice from aristolochic acid-l-induced acute kidney injury in a CYP1A dependent mechanism".Acta Pharmacologica Sinica 30.11(2009):1559. |
入库方式: OAI收割
来源:上海药物研究所
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