Uddin Md Jamal, Kim Ee Hyun, Hannan Md Abdul, Ha Hunjoo
Graduate School of Pharmaceutical Sciences, College of Pharmacy, Ewha Womans University, Seoul 03760, Korea.
ABEx Bio-Research Center, East Azampur, Dhaka 1230, Bangladesh.
Antioxidants (Basel). 2021 Feb 7;10(2):258. doi: 10.3390/antiox10020258.
The global burden of chronic kidney disease (CKD) intertwined with cardiovascular disease has become a major health problem. Oxidative stress (OS) plays an important role in the pathophysiology of CKD. The nuclear factor erythroid 2-related factor 2 (Nrf2)-antioxidant responsive element (ARE) antioxidant system plays a critical role in kidney protection by regulating antioxidants during OS. Heme oxygenase-1 (HO-1), one of the targets of Nrf2-ARE, plays an important role in regulating OS and is protective in a variety of human and animal models of kidney disease. Thus, activation of Nrf2-HO-1 signaling may offer a potential approach to the design of novel therapeutic agents for kidney diseases. In this review, we have discussed the association between OS and the pathogenesis of CKD. We propose Nrf2-HO-1 signaling-mediated cell survival systems be explored as pharmacological targets for the treatment of CKD and have reviewed the literature on the beneficial effects of small molecule natural products that may provide protection against CKD.
慢性肾脏病(CKD)与心血管疾病交织所带来的全球负担已成为一个主要的健康问题。氧化应激(OS)在CKD的病理生理学中起重要作用。核因子红细胞2相关因子2(Nrf2)-抗氧化反应元件(ARE)抗氧化系统在氧化应激期间通过调节抗氧化剂在肾脏保护中起关键作用。血红素加氧酶-1(HO-1)是Nrf2-ARE的靶点之一,在调节氧化应激中起重要作用,并且在多种人类和动物肾脏疾病模型中具有保护作用。因此,激活Nrf2-HO-1信号通路可能为设计新型肾脏疾病治疗药物提供一种潜在方法。在本综述中,我们讨论了氧化应激与CKD发病机制之间的关联。我们建议探索Nrf2-HO-1信号介导的细胞存活系统作为治疗CKD的药理学靶点,并综述了关于可能提供CKD保护作用的小分子天然产物有益作用的文献。