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基于 PPARα/SREBP-1c/FAS/GPAT/AMPK 信号通路探讨邻苯二甲酸二丁酯对肝脏及肝细胞脂质代谢的影响。

Effects of dibutyl phthalate on lipid metabolism in liver and hepatocytes based on PPARα/SREBP-1c/FAS/GPAT/AMPK signal pathway.

机构信息

Department of Pharmacy, Hefei BOE Hospital, Hefei, PR China.

Institute of Intelligent Machines, Chinese Academy of Sciences, Hefei, 230031, China; Department of Biological Physics, University of Science and Technology of China, Hefei, 230026, China.

出版信息

Food Chem Toxicol. 2021 Mar;149:112029. doi: 10.1016/j.fct.2021.112029. Epub 2021 Jan 26.

Abstract

Phateacid esters (PAEs), such as dibutyl phthalate (DBP), have been widely used and human exposure results into serious toxic effects; such as the development of fatty liver disease. In the present study, SD rat models for in vivo study (normal and fatty liver model group) and hepatocytes for in vitro study (normal and abnormal lipid metabolism model group) were established to determine the effects of DBP on liver function and discover the possible mechanisms. Meanwhile, the peroxisome proliferator activated receptor (PPARα) blocker, GW6471, with the Adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK) activator, AICAR, were applied in vitro study to clarify the role of PPARα/SREBP-1c/FAS/GPAT/AMPK signal pathway in the process. Results suggested that DBP could activate PPARα signaling pathway and affected the protein expression of SREBP, FAS and GPAT to cause hyperlipidemia and abnormal liver function. DBP also could inhibit the phosphorylation and activation of AMPK to inhibit the decomposition and metabolism of lipids. Interestingly, the effects of DBP could be alleviated by GW6471 and AICAR. Our experimental results provide reliable evidence that DBP exposure could further induce liver lipid metabolism disorder and other hepatic toxicity through PPARα/SREBP-1c/FAS/GPAT/AMPK signal pathway.

摘要

邻苯二甲酸酯(PAEs),如邻苯二甲酸二丁酯(DBP),已被广泛使用,人类接触会导致严重的毒性作用;如脂肪肝疾病的发展。在本研究中,建立了 SD 大鼠体内研究(正常和脂肪肝模型组)和肝细胞体外研究(正常和异常脂质代谢模型组)模型,以确定 DBP 对肝功能的影响,并发现可能的机制。同时,应用过氧化物酶体增殖物激活受体(PPARα)抑制剂 GW6471 和腺苷 5'-单磷酸(AMP)激活蛋白激酶(AMPK)激活剂 AICAR 进行体外研究,以阐明 PPARα/SREBP-1c/FAS/GPAT/AMPK 信号通路在该过程中的作用。结果表明,DBP 可激活 PPARα 信号通路,并影响 SREBP、FAS 和 GPAT 的蛋白表达,导致高脂血症和肝功能异常。DBP 还可以抑制 AMPK 的磷酸化和激活,从而抑制脂质的分解和代谢。有趣的是,DBP 的作用可以被 GW6471 和 AICAR 缓解。我们的实验结果为 DBP 暴露通过 PPARα/SREBP-1c/FAS/GPAT/AMPK 信号通路进一步诱导肝脂质代谢紊乱和其他肝毒性提供了可靠的证据。

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