4.7 Article

Oxidative stress in the pathophysiology of type 2 diabetes and related complications: Current therapeutics strategies and future perspectives

期刊

FREE RADICAL BIOLOGY AND MEDICINE
卷 184, 期 -, 页码 114-134

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2022.03.019

关键词

Pancreatic beta-cells; Reactive oxygen species; Hyperglycemia; Insulin resistance; Oxidative stress; Antioxidant enzymes; Electron transport system

资金

  1. Science and Engineering Research Board (SERB)
  2. National Institutes of Health (NIH) [NS105473, AG060767, AG069333, AG066347, R41 AG060836, AG047812, AG042178]
  3. statutory body of Department of Science and Technology (DST) , Government of India [EEQ/2020/000188, TAR/2020/000430]

向作者/读者索取更多资源

Type 2 diabetes is a rapidly rising metabolic disorder characterized by insulin resistance and beta-cell dysfunction. High blood sugar levels lead to the production of reactive oxygen species (ROS) and oxidative stress, which contribute to the development and progression of the disease. Antioxidants can neutralize ROS and maintain bodily homeostasis. However, the efficacy of antioxidant therapies in preventing diabetes is conflicting in clinical evidence.
Type 2 diabetes (T2DM) is a persistent metabolic disorder rising rapidly worldwide. It is characterized by pancreatic insulin resistance and beta-cell dysfunction. Hyperglycemia induced reactive oxygen species (ROS) production and oxidative stress are correlated with the pathogenesis and progression of this metabolic disease. To counteract the harmful effects of ROS, endogenous antioxidants of the body or exogenous antioxidants neutralise it and maintain bodily homeostasis. Under hyperglycemic conditions, the imbalance between the cellular antioxidant system and ROS production results in oxidative stress, which subsequently results in the development of diabetes. These ROS are produced in the endoplasmic reticulum, phagocytic cells and peroxisomes, with the mitochondrial electron transport chain (ETC) playing a pivotal role. The exacerbated ROS production can directly cause structural and functional modifications in proteins, lipids and nucleic acids. It also modulates several intracellular signaling pathways that lead to insulin resistance and impairment of beta-cell function. In addition, the hyperglycemia-induced ROS production contributes to micro-and macro-vascular diabetic complications. Various in-vivo and in-vitro studies have demonstrated the anti-oxidative effects of natural products and their derived bioactive compounds. However, there is conflicting clinical evidence on the beneficial effects of these antioxidant therapies in diabetes prevention. This review article focused on the multifaceted role of oxidative stress caused by ROS overproduction in diabetes and related complications and possible antioxidative therapeutic strategies targeting ROS in this disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据