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三聚氰胺潜在毒性机制的研究进展:基于计算机的研究。

Insight into potential toxicity mechanisms of melamine: an in silico study.

机构信息

School of Life Sciences and Technology, Tongji University, 1239 Siping Road, Shanghai 200092, PR China.

出版信息

Toxicology. 2011 May 10;283(2-3):96-100. doi: 10.1016/j.tox.2011.02.009. Epub 2011 Mar 3.

DOI:10.1016/j.tox.2011.02.009
PMID:21376774
Abstract

The toxicity of melamine has attracted much attention since the outbreak of nephrolithiasis among children ingesting melamine-contaminated infant formula in China. However, there is little knowledge about the molecular mechanisms underlying the melamine-induced toxicity. In this paper, a ligand-protein docking method (INVDOCK) was applied to predict the toxicity-related target proteins for melamine and its metabolite, cyanuric acid. As a result, 23 and 35 proteins were finally identified as the potential target proteins for melamine and cyanuric acid, respectively. Through an enrichment analysis, it was found that nephrotoxicity and lung toxicity might be the most significant toxicities induced by melamine and cyanuric acid. Four target proteins (glutathione peroxidase 1, beta-hexosaminidase subunit beta, L-lactate dehydrogenase and lysozyme C) may be related to the molecular basis of the nephrotoxicity induced by melamine except for known kidney crystals formation. After mapping all these toxicity-related target proteins onto cellular pathways, it was indicated that the toxicities of melamine and cyanuric acid might also be caused by breaking down redox balance, perturbing the arginine and proline metabolism and damaging the homeostasis of energy production system. To further explore the mechanisms underlying the toxicities of melamine and cyanuric acid, a biological signal cascades network constructed by some of the toxicity-related target proteins was discussed.

摘要

三聚氰胺的毒性自中国发生婴幼儿食用受三聚氰胺污染的配方奶粉引发肾结石事件以来引起了广泛关注。然而,人们对三聚氰胺引起毒性的分子机制知之甚少。本文应用配体-蛋白对接方法(INVDOCK)预测三聚氰胺及其代谢物三聚氰酸的毒性相关靶蛋白。结果最终分别确定了 23 种和 35 种蛋白为三聚氰胺和三聚氰酸的潜在靶蛋白。通过富集分析发现,三聚氰胺和三聚氰酸可能引起的主要毒性为肾毒性和肺毒性。除了已知的肾脏结晶形成外,有 4 种靶蛋白(谷胱甘肽过氧化物酶 1、β-己糖胺酶亚基β、L-乳酸脱氢酶和溶菌酶 C)可能与三聚氰胺引起的肾毒性的分子基础有关。将所有这些毒性相关靶蛋白映射到细胞途径上后,表明三聚氰胺和三聚氰酸的毒性也可能是由于打破了氧化还原平衡、扰乱了精氨酸和脯氨酸代谢以及破坏了能量产生系统的内稳态引起的。为了进一步探讨三聚氰胺和三聚氰酸毒性的机制,讨论了由一些毒性相关靶蛋白构建的生物信号级联网络。

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