Institute of Toxicology, School of Public Health, Shandong University, 44 Wenhua West Road, Jinan, 250012, Shandong, China.
Department of Pharmacy, Qilu Hospital of Shandong University, 107 Wenhua West Road, Jinan, 250012, Shandong, China.
Cell Mol Life Sci. 2018 Sep;75(17):3143-3157. doi: 10.1007/s00018-018-2852-6. Epub 2018 Jun 11.
Alcoholic liver disease (ALD) remains to be a worldwide health problem. It is generally accepted that oxidative stress plays critical roles in the pathogenesis of ALD, and antioxidant therapy represents a logical strategy for the prevention and treatment of ALD. Nuclear factor erythroid-derived 2-like 2 (NFE2L2 or Nrf-2) is essential for the antioxidant responsive element (ARE)-mediated induction of endogenous antioxidant enzymes such as heme oxygenase 1 (HO-1) and glutamate-cysteine ligase [GCL, the rate-limiting enzyme in the synthesis of glutathione (GSH)]. Activation of Nrf-2 pathway by genetic manipulation or pharmacological agents has been demonstrated to provide protection against ALD, which suggests that targeting Nrf-2 may be a promising approach for the prevention and treatment of ALD. Herein, we review the relevant literature about the potential hepatoprotective roles of Nrf-2 activation against ALD.
酒精性肝病(ALD)仍然是一个全球性的健康问题。一般认为,氧化应激在ALD 的发病机制中起着关键作用,抗氧化治疗代表了预防和治疗 ALD 的一种合理策略。核因子红细胞衍生 2 样 2(NFE2L2 或 Nrf-2)是抗氧化反应元件(ARE)介导的内源性抗氧化酶如血红素加氧酶 1(HO-1)和谷胱甘肽合成中谷氨酰半胱氨酸连接酶[GCL,限速酶]诱导所必需的。遗传操作或药理制剂激活 Nrf-2 途径已被证明可提供对 ALD 的保护,这表明针对 Nrf-2 可能是预防和治疗 ALD 的一种有前途的方法。在此,我们综述了关于 Nrf-2 激活对抗 ALD 的潜在肝保护作用的相关文献。