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地方性肾病病因学中的“嫌疑犯”:马兜铃酸与真菌毒素。

«Suspects» in etiology of endemic nephropathy: aristolochic acid versus mycotoxins.

机构信息

Department of Microbiology, Faculty of Pharmacy and Biochemistry, University of Zagreb, Schrottova 39, HR-10000 Zagreb, Croatia.

出版信息

Toxins (Basel). 2010 Jun;2(6):1414-27. doi: 10.3390/toxins2061414. Epub 2010 Jun 11.

Abstract

Despite many hypotheses that have been challenged, the etiology of endemic nephropathy (EN) is still unknown. At present, the implications of aristolochic acid (AA) and mycotoxins (ochratoxin A-OTA and citrinin-CIT) are under debate. AA-theory is based on renal pathohistological similarities between Chinese herbs nephropathy (CHN) and EN, findings of AA-DNA adducts in EN and in patients with urinary tract tumors (UTT), as well as the domination of A:T®T:A transversions in the p53 mutational spectrum of UTT patients, which corresponds with findings of such mutations in AA-treated rats. However, exposure pathways of EN residents to AA are unclear. Experimental studies attempting to deduce whether nephrotoxins OTA and CIT appear at higher frequencies or levels (or both) in the food and blood or urine of EN residents support the mycotoxin theory. Also, some molecular studies revealed the presence of OTA-DNA adducts in the renal tissue of EN and UTT patients. In this review, data supporting or arguing against AA and mycotoxin theory are presented and discussed.

摘要

尽管有许多假说受到了挑战,但地方性肾病(EN)的病因仍然未知。目前,马兜铃酸(AA)和霉菌毒素(赭曲霉毒素 A-OTA 和桔青霉素-CIT)的影响正在讨论之中。AA 理论基于中草药肾病(CHN)和 EN 之间的肾组织病理学相似性、EN 和尿路肿瘤(UTT)患者中 AA-DNA 加合物的发现,以及 UTT 患者 p53 突变谱中 A:T®T:A 颠换的主导地位,这与 AA 处理的大鼠中发现的此类突变相符。然而,EN 居民接触 AA 的途径尚不清楚。试图推断食物和血液或尿液中 OTA 和 CIT 等肾毒素是否在 EN 居民中出现更高频率或水平(或两者兼而有之)的实验研究支持霉菌毒素理论。此外,一些分子研究揭示了 EN 和 UTT 患者肾组织中 OTA-DNA 加合物的存在。在这篇综述中,提出并讨论了支持或反对 AA 和霉菌毒素理论的数据。

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