Department of Pediatric Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Institute for Health and Sport, Victoria University, St Albans, VIC 3021, Australia.
Biomolecules. 2023 Oct 27;13(11):1586. doi: 10.3390/biom13111586.
Oxidative stress is increasingly recognized as a central player in a range of gastrointestinal (GI) disorders, as well as complications stemming from therapeutic interventions. This article presents an overview of the mechanisms of oxidative stress in GI conditions and highlights a link between oxidative insult and disruption to the enteric nervous system (ENS), which controls GI functions. The dysfunction of the ENS is characteristic of a spectrum of disorders, including neurointestinal diseases and conditions such as inflammatory bowel disease (IBD), diabetic gastroparesis, and chemotherapy-induced GI side effects. Neurons in the ENS, while essential for normal gut function, appear particularly vulnerable to oxidative damage. Mechanistically, oxidative stress in enteric neurons can result from intrinsic nitrosative injury, mitochondrial dysfunction, or inflammation-related pathways. Although antioxidant-based therapies have shown limited efficacy, recognizing the multifaceted role of oxidative stress in GI diseases offers a promising avenue for future interventions. This comprehensive review summarizes the literature to date implicating oxidative stress as a critical player in the pathophysiology of GI disorders, with a focus on its role in ENS injury and dysfunction, and highlights opportunities for the development of targeted therapeutics for these diseases.
氧化应激被越来越多地认为是一系列胃肠道 (GI) 疾病以及治疗干预引起的并发症的核心因素。本文概述了 GI 疾病中氧化应激的机制,并强调了氧化损伤与控制胃肠道功能的肠神经系统 (ENS) 功能障碍之间的联系。ENS 功能障碍是一系列疾病的特征,包括神经胃肠病和炎症性肠病 (IBD)、糖尿病性胃轻瘫和化疗引起的胃肠道副作用等病症。ENS 中的神经元对于正常的肠道功能至关重要,但它们似乎特别容易受到氧化损伤。从机制上讲,肠神经元中的氧化应激可能源于内在的硝化损伤、线粒体功能障碍或炎症相关途径。尽管基于抗氧化剂的治疗方法显示出有限的疗效,但认识到氧化应激在 GI 疾病中的多方面作用为未来的干预措施提供了一个有前途的途径。这篇全面的综述总结了迄今为止将氧化应激作为 GI 疾病病理生理学中关键因素的文献,重点介绍了其在 ENS 损伤和功能障碍中的作用,并强调了针对这些疾病开发靶向治疗的机会。