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与半胱氨酸和谷胱甘肽反应将马兜铃酸 I 转化为马兜铃酸:生物学意义。

Conversion of aristolochic acid I into aristolic acid by reaction with cysteine and glutathione: biological implications.

机构信息

Department of Biological Sciences, Florida International University, 11200 Southwest 8th Street, Miami, FL 33199, United States.

出版信息

J Nat Prod. 2013 May 24;76(5):965-8. doi: 10.1021/np300822b. Epub 2013 Apr 24.

DOI:10.1021/np300822b
PMID:23614652
Abstract

Aristolochic acid I (AA-I), naturally occurring in Aristolochia plants, is a potent nephrotoxin and carcinogen. Here we report that AA-I suffers hydrogenolysis with loss of the nitro group by reaction with cysteine or glutathione to give aristolic acid. Since the reaction can proceed in aqueous solutions at pH 7.0 and 37 °C, it is inferred that it may also occur in biological systems and contribute to the nephrotoxic effects induced by AA-I.

摘要

马兜铃酸 I(AA-I)存在于马兜铃属植物中,是一种强效的肾毒素和致癌物。在这里,我们报告 AA-I 可与半胱氨酸或谷胱甘肽发生氢解反应,硝基基团脱落,生成马兜铃酸。由于该反应可在 pH 值为 7.0 和 37°C 的水溶液中进行,因此可以推断它也可能在生物体系中发生,并导致 AA-I 引起的肾毒性。

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Aristolochic Acids: Newly Identified Exposure Pathways of this Class of Environmental and Food-Borne Contaminants and its Potential Link to Chronic Kidney Diseases.马兜铃酸:这类环境及食源性污染物新发现的暴露途径及其与慢性肾脏病的潜在关联
Toxics. 2019 Mar 19;7(1):14. doi: 10.3390/toxics7010014.