Cave Matthew C, Clair Heather B, Hardesty Josiah E, Falkner K Cameron, Feng Wenke, Clark Barbara J, Sidey Jennifer, Shi Hongxue, Aqel Bashar A, McClain Craig J, Prough Russell A
Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, University of Louisville School of Medicine, Louisville, KY 40202, USA; Department of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY 40202, USA; Department of Pharmacology and Toxicology, University of Louisville School of Medicine, Louisville, KY 40202, USA; The Robley Rex Veterans Affairs Medical Center, Louisville, KY 40206, USA; The KentuckyOne Health Jewish Hospital Liver Transplant Program, Louisville, KY 40202, USA.
Department of Biochemistry and Molecular Genetics, University of Louisville School of Medicine, Louisville, KY 40202, USA.
Biochim Biophys Acta. 2016 Sep;1859(9):1083-1099. doi: 10.1016/j.bbagrm.2016.03.002. Epub 2016 Mar 4.
Nuclear receptors are transcription factors which sense changing environmental or hormonal signals and effect transcriptional changes to regulate core life functions including growth, development, and reproduction. To support this function, following ligand-activation by xenobiotics, members of subfamily 1 nuclear receptors (NR1s) may heterodimerize with the retinoid X receptor (RXR) to regulate transcription of genes involved in energy and xenobiotic metabolism and inflammation. Several of these receptors including the peroxisome proliferator-activated receptors (PPARs), the pregnane and xenobiotic receptor (PXR), the constitutive androstane receptor (CAR), the liver X receptor (LXR) and the farnesoid X receptor (FXR) are key regulators of the gut:liver:adipose axis and serve to coordinate metabolic responses across organ systems between the fed and fasting states. Nonalcoholic fatty liver disease (NAFLD) is the most common liver disease and may progress to cirrhosis and even hepatocellular carcinoma. NAFLD is associated with inappropriate nuclear receptor function and perturbations along the gut:liver:adipose axis including obesity, increased intestinal permeability with systemic inflammation, abnormal hepatic lipid metabolism, and insulin resistance. Environmental chemicals may compound the problem by directly interacting with nuclear receptors leading to metabolic confusion and the inability to differentiate fed from fasting conditions. This review focuses on the impact of nuclear receptors in the pathogenesis and treatment of NAFLD. Clinical trials including PIVENS and FLINT demonstrate that nuclear receptor targeted therapies may lead to the paradoxical dissociation of steatosis, inflammation, fibrosis, insulin resistance, dyslipidemia and obesity. Novel strategies currently under development (including tissue-specific ligands and dual receptor agonists) may be required to separate the beneficial effects of nuclear receptor activation from unwanted metabolic side effects. The impact of nuclear receptor crosstalk in NAFLD is likely to be profound, but requires further elucidation. This article is part of a Special Issue entitled: Xenobiotic nuclear receptors: New Tricks for An Old Dog, edited by Dr. Wen Xie.
核受体是一类转录因子,可感知不断变化的环境或激素信号,并引发转录变化以调节核心生命功能,包括生长、发育和繁殖。为支持这一功能,在受到外源性物质的配体激活后,1 亚家族核受体(NR1s)成员可能与视黄酸 X 受体(RXR)形成异二聚体,以调节参与能量、外源性物质代谢和炎症的基因转录。其中一些受体,包括过氧化物酶体增殖物激活受体(PPARs)、孕烷和外源性物质受体(PXR)、组成型雄甾烷受体(CAR)、肝脏 X 受体(LXR)和法尼醇 X 受体(FXR),是肠道:肝脏:脂肪轴的关键调节因子,有助于协调进食和禁食状态下各器官系统之间的代谢反应。非酒精性脂肪性肝病(NAFLD)是最常见的肝脏疾病,可能进展为肝硬化甚至肝细胞癌。NAFLD 与核受体功能异常以及肠道:肝脏:脂肪轴的紊乱有关,包括肥胖、肠道通透性增加伴全身炎症、肝脏脂质代谢异常和胰岛素抵抗。环境化学物质可能通过直接与核受体相互作用使问题更加复杂,导致代谢紊乱,无法区分进食和禁食状态。本综述重点关注核受体在 NAFLD 发病机制和治疗中的作用。包括 PIVENS 和 FLINT 在内的临床试验表明,靶向核受体的疗法可能导致脂肪变性、炎症、纤维化、胰岛素抵抗、血脂异常和肥胖的矛盾性分离。目前正在开发的新策略(包括组织特异性配体和双受体激动剂)可能需要将核受体激活的有益作用与不良代谢副作用区分开来。核受体相互作用在 NAFLD 中的影响可能很大,但需要进一步阐明。本文是名为“外源性核受体:老狗新把戏”的特刊的一部分,由谢雯博士编辑。