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赭曲霉毒素A:加拿大西部一种重要的储藏期霉菌毒素。

Ochratoxin A: an important western Canadian storage mycotoxin.

作者信息

Marquardt R R, Frohlich A, Abramson D

机构信息

Department of Animal Science, University of Manitoba, Winnipeg, Canada.

出版信息

Can J Physiol Pharmacol. 1990 Jul;68(7):991-9. doi: 10.1139/y90-151.

Abstract

Ochratoxin A (OA) is a mycotoxin produced by certain species of storage fungi of the Penicillium and Aspergillus genera. Toxin production by these fungi is influenced by species and even strain of fungi, time and temperature of incubation, moisture content of substrate, and type of substrate. OA has been shown to occur in various grains, cereals and other plant products, animal feeds, meats, and human tissues in countries throughout the world. Of interest is the discovery of OA in a high percentage of blood from humans in Germany. OA is acutely toxic to many different animals and in addition to being a nephrotoxin, it is a hepatotoxin, a teratogen, a very potent carcinogen, possibly a mutagen, and an immunosuppressive agent. OA is rapidly absorbed throughout the entire gastrointestinal tract and distributes itself in the body as a two-compartment open model and has a particular high affinity for serum albumin. OA is hydrolyzed by the intestinal microflora into nontoxic compounds (7-carboxy-5-chloro-8-hydroxy-3,4-dihydro-3R-methylisocoumarin (O alpha) and phenylalanine). It is excreted as either OA, hydroxylated OA, or O alpha in both the urine and feces. OA appears to exert its toxic effect by promoting an increased level of lipid peroxidation, by inhibition of an amino acylation reaction, and possibly by conversion into metabolites that are capable of binding DNA. These in turn cause other secondary effects associated with OA. It would appear that this compound presents a true potential hazard for humans as its occurrence is wide spread and it is highly carcinogenic.

摘要

赭曲霉毒素A(OA)是由青霉属和曲霉属的某些贮藏真菌产生的一种霉菌毒素。这些真菌产生毒素受真菌的种类甚至菌株、培养时间和温度、底物的水分含量以及底物类型的影响。已表明OA在世界各地的国家中的各种谷物、谷类和其他植物产品、动物饲料、肉类及人体组织中存在。有意思的是在德国人的血液中有高比例的OA被发现。OA对许多不同动物具有急性毒性,并且除了是一种肾毒素外,它还是一种肝毒素、致畸剂、非常强效的致癌物、可能是诱变剂以及免疫抑制剂。OA在整个胃肠道中迅速被吸收,并以二室开放模型在体内分布,并且对血清白蛋白具有特别高的亲和力。OA被肠道微生物群水解成无毒化合物(7-羧基-5-氯-8-羟基-3,4-二氢-3R-甲基异香豆素(Oα)和苯丙氨酸)。它以OA、羟基化OA或Oα的形式在尿液和粪便中排泄。OA似乎通过促进脂质过氧化水平的升高、抑制氨基酰化反应以及可能通过转化为能够结合DNA的代谢物来发挥其毒性作用。这些反过来又会引起与OA相关的其他继发效应。由于这种化合物的存在广泛且具有高度致癌性,它似乎对人类构成了真正的潜在危害。

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