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赭曲霉毒素A:分子相互作用、毒性机制及分子水平的预防

Ochratoxin A: Molecular Interactions, Mechanisms of Toxicity and Prevention at the Molecular Level.

作者信息

Kőszegi Tamás, Poór Miklós

机构信息

Department of Laboratory Medicine, University of Pécs, H-7624 Pécs, Hungary.

János Szentágothai Research Center, Lab-on-a-chip Research Group, H-7624 Pécs, Hungary.

出版信息

Toxins (Basel). 2016 Apr 15;8(4):111. doi: 10.3390/toxins8040111.

Abstract

Ochratoxin A (OTA) is a widely-spread mycotoxin all over the world causing major health risks. The focus of the present review is on the molecular and cellular interactions of OTA. In order to get better insight into the mechanism of its toxicity and on the several attempts made for prevention or attenuation of its toxic action, a detailed description is given on chemistry and toxicokinetics of this mycotoxin. The mode of action of OTA is not clearly understood yet, and seems to be very complex. Inhibition of protein synthesis and energy production, induction of oxidative stress, DNA adduct formation, as well as apoptosis/necrosis and cell cycle arrest are possibly involved in its toxic action. Since OTA binds very strongly to human and animal albumin, a major emphasis is done regarding OTA-albumin interaction. Displacement of OTA from albumin by drugs and by natural flavonoids are discussed in detail, hypothesizing their potentially beneficial effect in order to prevent or attenuate the OTA-induced toxic consequences.

摘要

赭曲霉毒素A(OTA)是一种在全球广泛传播的霉菌毒素,会造成重大健康风险。本综述的重点是OTA的分子和细胞相互作用。为了更好地了解其毒性机制以及为预防或减轻其毒性作用所做的一些尝试,本文详细描述了这种霉菌毒素的化学性质和毒代动力学。OTA的作用方式尚未完全明确,似乎非常复杂。其毒性作用可能涉及蛋白质合成和能量产生的抑制、氧化应激的诱导、DNA加合物的形成以及细胞凋亡/坏死和细胞周期停滞。由于OTA与人及动物白蛋白结合非常紧密,因此重点讨论了OTA-白蛋白相互作用。详细讨论了药物和天然黄酮类化合物对OTA从白蛋白上的置换作用,并假设它们可能具有有益作用,以预防或减轻OTA诱导的毒性后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d663/4848637/042afd6acc33/toxins-08-00111-g001.jpg

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