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High-Resolution Metabolomics Study of Occupational Exposure to Trichloroethylene

机译:职业接触三氯乙烯的高分辨率代谢组学研究

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Introduction: Trichloroethylene (TCE) is a common water contaminant and continues to be used in the workplaces of many developing countries. It causes kidney cancer and possibly non-Hodgkin lymphoma and liver cancer. However, the underlying pathophysiology of TCE-induced cancer is not well understood. To evaluate biological responses to TCE, we conducted a cross-sectional molecular epidemiology study of workers exposed to TCE and unexposed controls and applied non-targeted metabolomics analysis. Methods: We studied 80 healthy workers that used TCE and 95 comparable unexposed controls in Guangdong, China. The TCE-exposed workers had a median 8-hour time weighted average personal air exposure of 12 ppm (range: 0.4 to 230 ppm), with almost all workers having exposure under the current U.S. OSHA Permissible Exposure Limit of 100 ppm. Metabolomics analysis of plasma samples was conducted by ultra-high resolution mass spectrometry Results: Metabolic features associated with TCE exposure included known TCE metabolites and additional unidentified chlorinated compounds. TCE exposure was also associated with multiple alterations in endogenous metabolism, including changes in purine catabolism and decreases in sulphur amino acid and bile acid biosynthesis pathways. Specific metabolite associations with TCE exposure included uric acid, glutamine, cystine, methylthioadenosine, taurine and chenodeoxycholic acid, consistent with immunosuppressive, hepatotoxic and nephrotoxic effects that have been related to TCE. There were also correlations between multiple metabolites and additional exposure, immunologic, and nephrotoxic biomarkers that had been measured previously. Conclusion: Untargeted high-resolution metabolomics correlated occupational exposure to TCE with internal dose and metabolic responses, providing new insights into molecular mechanisms of TCE-related disease.
机译:简介:三氯乙烯(TCE)是一种常见的水污染物,并在许多发展中国家的工作场所中继续使用。它会导致肾癌,并可能引起非霍奇金淋巴瘤和肝癌。但是,TCE诱导的癌症的潜在病理生理学还不清楚。为了评估对TCE的生物学反应,我们对暴露于TCE和未暴露的对照的工人进行了横断面分子流行病学研究,并应用了非靶向代谢组学分析。方法:我们在中国广东省研究了80名使用TCE的健康工人和95名可比较的未暴露对照。暴露于TCE的工人的中位数8小时时间加权平均个人空气暴露为12 ppm(范围:0.4至230 ppm),几乎所有工人的暴露程度都低于现行的美国OSHA允许暴露极限100 ppm。通过超高分辨率质谱对血浆样品进行代谢组学分析结果:与TCE暴露相关的代谢特征包括已知的TCE代谢物和其他未确定的氯化化合物。 TCE暴露还与内源性代谢的多种变化有关,包括嘌呤分解代谢的变化以及硫氨基酸和胆汁酸生物合成途径的减少。与TCE接触的特定代谢产物包括尿酸,谷氨酰胺,胱氨酸,甲硫腺苷,牛磺酸和鹅脱氧胆酸,与TCE相关的免疫抑制,肝毒性和肾毒性作用一致。多种代谢产物与先前已测定的其他暴露,免疫和肾毒性生物标志物之间也存在相关性。结论:无针对性的高分辨率代谢组学将职业接触三氯乙烯与内部剂量和代谢反应相关,从而为三氯乙烯相关疾病的分子机制提供了新见解。

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