马兜铃酸i致小鼠肾毒性的性别差异及雌二醇的影响。

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Toxicology and applied pharmacology Pub Date : 2025-03-01 Epub Date: 2025-01-26 DOI:10.1016/j.taap.2025.117240
Qianru Wang , Jiuwen Hou , Fan Shui , Jia Tang , Jianjun Du , Cheng Chen , Wenjing Zhang , Maggie Shiliu Tu , Chunhui Li , Qibing Mei
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引用次数: 0

摘要

马兜铃酸I (AAI)是马兜铃酸中最重要的成分,几乎存在于所有马兜铃草本植物中,已被证明具有显著的肾毒性。本研究通过单次注射AAI建立AAI小鼠急性肾毒性模型。观察到雌鼠和雄鼠对AAI肾毒性的敏感性存在差异,即使在较低剂量下,雄鼠也表现出肾毒性作用。雌二醇(E2)给药后,雄性小鼠血清肌酐和尿素氮水平下降。采用UPLC-MS/MS法测定AAI及其代谢物马兜铃内酰胺I (ALI)的药代动力学和肾组织分布。结果发现,雌性小鼠血浆中AAI的半衰期较长,而雄性小鼠肾组织中ALI的含量远高于雌性小鼠。E2可以延长AAI的半衰期,降低雄性小鼠肾脏中ALI的水平。提出的机制可能涉及E2降低肾脏燕麦转运蛋白活性,导致肾小管中ALI浓度降低。这种减少可能减轻其对上皮细胞的毒性作用,减少其有害代谢物的产生,从而减轻aai诱导的肾毒性。
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Sex differences in aristolochic acid I-induced nephrotoxicity in mice and the effect of estradiol
Aristolochic acid I (AAI), the most prominent component of aristolochic acids and found in nearly all aristolochic herbs, has been demonstrated significant nephrotoxicity. In this study, an acute nephrotoxicity model of AAI mice was established by a single dose injection of AAI. It was observed that there are differences of the sensitivity to AAI nephrotoxicity in female and male mice, with male mice exhibiting nephrotoxic effects even at lower doses. After the administration of estradiol (E2), serum levels of creatinine and urea nitrogen in male mice were observed to decrease. We used UPLC-MS/MS to determine the pharmacokinetics and renal tissue distribution of AAI and its metabolite aristololactam I (ALI). It was found that AAI had a longer plasma half-life in female mice, while the content of ALI in renal tissue of male mice was much higher than that in female. The administration of E2 was found to extend the half-life of AAI and reduce the levels of ALI in the kidneys of male mice. The proposed mechanism may involve the reduction of renal OATs transporter activity by E2, leading to decreased concentrations of ALI in the renal tubules. This reduction may mitigate its toxic effects on epithelial cells and diminish the production of its harmful metabolites, thereby alleviating AAI-induced nephrotoxicity.
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来源期刊
CiteScore
6.80
自引率
2.60%
发文量
309
审稿时长
32 days
期刊介绍: Toxicology and Applied Pharmacology publishes original scientific research of relevance to animals or humans pertaining to the action of chemicals, drugs, or chemically-defined natural products. Regular articles address mechanistic approaches to physiological, pharmacologic, biochemical, cellular, or molecular understanding of toxicologic/pathologic lesions and to methods used to describe these responses. Safety Science articles address outstanding state-of-the-art preclinical and human translational characterization of drug and chemical safety employing cutting-edge science. Highly significant Regulatory Safety Science articles will also be considered in this category. Papers concerned with alternatives to the use of experimental animals are encouraged. Short articles report on high impact studies of broad interest to readers of TAAP that would benefit from rapid publication. These articles should contain no more than a combined total of four figures and tables. Authors should include in their cover letter the justification for consideration of their manuscript as a short article.
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