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“转非氯增加细胞外游离脂肪酸积累和从头脂肪生成,导致 McArdle-RH7777 细胞发生肝脂肪变性”。

"Trans-nonachlor increases extracellular free fatty acid accumulation and de novo lipogenesis to produce hepatic steatosis in McArdle-RH7777 cells".

机构信息

Mississippi State University College of Veterinary Medicine, Department of Basic Sciences, Mississippi State, MS 39762, United States.

Mississippi State University College of Veterinary Medicine, Department of Basic Sciences, Mississippi State, MS 39762, United States.

出版信息

Toxicol In Vitro. 2018 Aug;50:285-292. doi: 10.1016/j.tiv.2018.04.003. Epub 2018 Apr 11.

Abstract

Recent studies suggest there may be an environmental exposure component to the development and progression of non-alcoholic fatty liver disease (NAFLD) involving the organochlorine (OC) pesticides or their metabolites. However, the roles of OC compounds in the development of NAFLD has not been fully elucidated. Therefore, the current study was designed to determine if exposure to trans-nonachlor, a prevalent OC compound, could promote hepatocyte lipid accumulation and determine potential pro-steatotic mechanisms. McArdle-RH7777 (McA) hepatoma cells were incubated with trans-nonachlor for 24 h then neutral lipid accumulation was determined by Oil Red O staining. Exposure to trans-nonachlor produced a concentration dependent increase in neutral lipid accumulation. Trans-nonachlor also increased extracellular free fatty acid-induced neutral lipid accumulation which appears to be due at least in part to increased free fatty acid accumulation as evident by increased accumulation of Bodipy labeled dodecanoic acid. Additionally, C-acetate incorporation into total cellular lipids was increased by trans-nonachlor implicating increased de novo lipogenesis (DNL) as a potential mediator of trans-nonachlor-induced neutral lipid accumulation. Taken together, the present data indicate exposure to trans-nonachlor has a direct, pro-steatotic effect on hepatocytes to increase lipid accumulation through the combinatorial actions of extracellular free fatty acid accumulation and increased DNL.

摘要

最近的研究表明,非酒精性脂肪性肝病(NAFLD)的发生和进展可能与有机氯(OC)农药或其代谢物的环境暴露因素有关。然而,OC 化合物在 NAFLD 发展中的作用尚未完全阐明。因此,本研究旨在确定暴露于反式-十氯酮(一种常见的 OC 化合物)是否会促进肝细胞脂质积累,并确定潜在的促脂肪生成机制。将 McArdle-RH7777(McA)肝癌细胞与反式-十氯酮孵育 24 小时,然后通过油红 O 染色测定中性脂质积累。反式-十氯酮的暴露会导致中性脂质积累呈浓度依赖性增加。反式-十氯酮还增加了细胞外游离脂肪酸诱导的中性脂质积累,这似乎至少部分是由于游离脂肪酸积累增加所致,这可通过 Bodipy 标记的十二烷酸的积累明显看出。此外,反式-十氯酮增加了 C-乙酸盐掺入总细胞脂质,表明增加从头脂肪生成(DNL)可能是反式-十氯酮诱导中性脂质积累的潜在介导物。总之,目前的数据表明,暴露于反式-十氯酮对肝细胞具有直接的促脂肪生成作用,通过细胞外游离脂肪酸积累和增加的 DNL 的协同作用增加脂质积累。

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