Arroyave-Ospina Johanna C, Wu Zongmei, Geng Yana, Moshage Han
Department of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, 9713 GZ Groningen, The Netherlands.
Antioxidants (Basel). 2021 Jan 26;10(2):174. doi: 10.3390/antiox10020174.
Oxidative stress (OxS) is considered a major factor in the pathophysiology of inflammatory chronic liver diseases, including non-alcoholic liver disease (NAFLD). Chronic impairment of lipid metabolism is closely related to alterations of the oxidant/antioxidant balance, which affect metabolism-related organelles, leading to cellular lipotoxicity, lipid peroxidation, chronic endoplasmic reticulum (ER) stress, and mitochondrial dysfunction. Increased OxS also triggers hepatocytes stress pathways, leading to inflammation and fibrogenesis, contributing to the progression of non-alcoholic steatohepatitis (NASH). The antioxidant response, regulated by the Nrf2/ARE pathway, is a key component in this process and counteracts oxidative stress-induced damage, contributing to the restoration of normal lipid metabolism. Therefore, modulation of the antioxidant response emerges as an interesting target to prevent NAFLD development and progression. This review highlights the link between disturbed lipid metabolism and oxidative stress in the context of NAFLD. In addition, emerging potential therapies based on antioxidant effects and their likely molecular targets are discussed.
氧化应激(OxS)被认为是包括非酒精性肝病(NAFLD)在内的炎症性慢性肝病病理生理学中的一个主要因素。脂质代谢的慢性损害与氧化还原平衡的改变密切相关,氧化还原平衡的改变会影响与代谢相关的细胞器,导致细胞脂毒性、脂质过氧化、慢性内质网(ER)应激和线粒体功能障碍。氧化应激增加还会触发肝细胞应激途径,导致炎症和纤维化,促进非酒精性脂肪性肝炎(NASH)的进展。由Nrf2/ARE途径调节的抗氧化反应是这一过程的关键组成部分,可抵消氧化应激诱导的损伤,有助于恢复正常的脂质代谢。因此,调节抗氧化反应成为预防NAFLD发生和发展的一个有吸引力的靶点。本综述强调了在NAFLD背景下脂质代谢紊乱与氧化应激之间的联系。此外,还讨论了基于抗氧化作用及其可能的分子靶点的新兴潜在疗法。