Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry & Biomedical Science, Queen's University of Belfast, Belfast, United Kingdom.
Department of Chemistry, King's College London, London, United Kingdom.
Front Endocrinol (Lausanne). 2021 Feb 18;11:621938. doi: 10.3389/fendo.2020.621938. eCollection 2020.
Lipids can undergo modification as a result of interaction with reactive oxygen species (ROS). For example, lipid peroxidation results in the production of a wide variety of highly reactive aldehyde species which can drive a range of disease-relevant responses in cells and tissues. Such lipid aldehydes react with nucleophilic groups on macromolecules including phospholipids, nucleic acids, and proteins which, in turn, leads to the formation of reversible or irreversible adducts known as advanced lipoxidation end products (ALEs). In the setting of diabetes, lipid peroxidation and ALE formation has been implicated in the pathogenesis of macro- and microvascular complications. As the most common diabetic complication, retinopathy is one of the leading causes of vision loss and blindness worldwide. Herein, we discuss diabetic retinopathy (DR) as a disease entity and review the current knowledge and experimental data supporting a role for lipid peroxidation and ALE formation in the onset and development of this condition. Potential therapeutic approaches to prevent lipid peroxidation and lipoxidation reactions in the diabetic retina are also considered, including the use of antioxidants, lipid aldehyde scavenging agents and pharmacological and gene therapy approaches for boosting endogenous aldehyde detoxification systems. It is concluded that further research in this area could lead to new strategies to halt the progression of DR before irreversible retinal damage and sight-threatening complications occur.
脂质可以与活性氧(ROS)相互作用而发生修饰。例如,脂质过氧化导致产生各种高度反应性的醛类物质,这些物质可以在细胞和组织中引发一系列与疾病相关的反应。这些脂质醛与包括磷脂、核酸和蛋白质在内的大分子上的亲核基团反应,进而导致形成可逆或不可逆的加合物,称为晚期糖基化终产物(ALEs)。在糖尿病的情况下,脂质过氧化和 ALE 的形成与大血管和微血管并发症的发病机制有关。作为最常见的糖尿病并发症,糖尿病性视网膜病变是全球视力丧失和失明的主要原因之一。本文讨论了糖尿病性视网膜病变(DR)作为一种疾病实体,并综述了目前支持脂质过氧化和 ALE 形成在该疾病的发生和发展中起作用的知识和实验数据。还考虑了预防糖尿病视网膜中脂质过氧化和脂质氧化反应的潜在治疗方法,包括使用抗氧化剂、脂质醛清除剂以及药理学和基因治疗方法来增强内源性醛解毒系统。结论是,在这一领域的进一步研究可能会导致在不可逆的视网膜损伤和威胁视力的并发症发生之前阻止 DR 进展的新策略。