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Peroxisome Proliferator-Activated Receptor and Retinoic X Receptor in Alcoholic Liver Disease

机译:酒精性肝病中过氧化物酶体增殖物激活受体和维甲酸X受体

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摘要

A growing number of new studies demonstrate that nuclear receptors are involved in the development of alcoholic liver disease (ALD). Ethanol metabolism and RXR/PPAR functions are tightly interconnected in the liver. Several ethanol metabolizing enzymes are potently regulated by RXR and PPARα after alcohol consumption. The increased ethanol metabolism, in turn, leads to alteration of the redox balance of the cells and impairment of RXR/PPAR functions by direct and indirect effects of acetaldehyde, resulting in deranged lipid metabolism, oxidative stress, and release of proinflammatory cytokines. The use of animal models played a crucial role in understanding the molecular mechanisms of ALD. In this paper we summarize the reciprocal interactions between ethanol metabolism and RXR/PPAR functions. In conclusion, RXR and PPAR play a central role in the onset and perpetuation of the mechanisms underling all steps of the clinical progression in ALD.
机译:越来越多的新研究表明,核受体与酒精性肝病(ALD)的发展有关。乙醇代谢和RXR / PPAR功能在肝脏中紧密相连。饮酒后,几种乙醇代谢酶受到RXR和PPARα的有效调节。乙醇代谢增加,进而通过乙醛的直接和间接作用导致细胞氧化还原平衡的改变和RXR / PPAR功能的损害,从而导致脂质代谢紊乱,氧化应激和促炎细胞因子的释放。动物模型的使用在了解ALD的分子机制中起着至关重要的作用。在本文中,我们总结了乙醇代谢与RXR / PPAR功能之间的相互作用。总之,RXR和PPAR在ALD临床进展所有步骤背后的机制的发生和持久化中起着核心作用。

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