Metabolic Regulation in Acute Respiratory Distress Syndrome: Implications for Inflammation and Oxidative Stress.

IF 2.7 3区 医学 Q2 RESPIRATORY SYSTEM
Lixia Yue, Yihe Yan
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Abstract

Acute respiratory distress syndrome (ARDS) is a severe and life-threatening pulmonary condition characterized by intense inflammation and disrupted oxygen exchange, which can lead to multiorgan failure. Recent findings have established ARDS as a systemic inflammatory disorder involving complex interactions between lung injury, systemic inflammation, and oxidative stress. This review examines the pivotal role of metabolic disturbances in the pathogenesis of ARDS, emphasizing their influence on inflammatory responses and oxidative stress. Common metabolic abnormalities in ARDS patients, including disruptions in carbohydrate, amino acid, and lipid metabolism, contribute significantly to the disease's severity. These metabolic dysfunctions interplay with systemic inflammation and oxidative stress, further exacerbating lung injury and worsening patient outcomes. By analyzing the regulatory mechanisms of various metabolites implicated in ARDS, we underscore the potential of targeting metabolic pathways as a therapeutic approach. Such interventions could help attenuate inflammation and oxidative stress, presenting a promising strategy for ARDS treatment. Additionally, we review potential drugs that modulate metabolic pathways, providing valuable insights into the etiology of ARDS and potential therapeutic directions. This comprehensive analysis enhances our understanding of ARDS and highlights the importance of metabolic regulation in the development of effective treatment strategies. Key findings from this review demonstrate that metabolic disturbances, particularly those affecting carbohydrate, amino acid, and lipid metabolism, play critical roles in amplifying inflammation and oxidative stress, underscoring the potential of metabolic-targeted therapies to improve patient outcomes.

急性呼吸窘迫综合征的代谢调节:对炎症和氧化应激的影响。
急性呼吸窘迫综合征(ARDS)是一种严重的危及生命的肺部疾病,其特征是剧烈的炎症和氧气交换中断,可导致多器官衰竭。最近的研究结果表明,ARDS是一种系统性炎症性疾病,涉及肺损伤、全身炎症和氧化应激之间的复杂相互作用。本文综述了代谢紊乱在ARDS发病机制中的关键作用,强调了它们对炎症反应和氧化应激的影响。ARDS患者常见的代谢异常,包括碳水化合物、氨基酸和脂质代谢的中断,对疾病的严重程度有重要影响。这些代谢功能障碍与全身炎症和氧化应激相互作用,进一步加剧肺损伤和患者预后恶化。通过分析与ARDS相关的各种代谢物的调节机制,我们强调了靶向代谢途径作为治疗方法的潜力。这些干预措施可以帮助减轻炎症和氧化应激,为ARDS治疗提供了一个有希望的策略。此外,我们回顾了调节代谢途径的潜在药物,为ARDS的病因和潜在的治疗方向提供了有价值的见解。这项综合分析增强了我们对ARDS的理解,并强调了代谢调节在制定有效治疗策略中的重要性。本综述的主要发现表明,代谢紊乱,特别是影响碳水化合物、氨基酸和脂质代谢的代谢紊乱,在放大炎症和氧化应激中起着关键作用,强调了代谢靶向治疗改善患者预后的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
10.70%
发文量
372
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal of therapeutics and pharmacology focusing on concise rapid reporting of clinical studies and reviews in COPD. Special focus will be given to the pathophysiological processes underlying the disease, intervention programs, patient focused education, and self management protocols. This journal is directed at specialists and healthcare professionals
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