Center for Inflammation Research, VIB, Ghent, Belgium.
Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
EMBO Mol Med. 2018 Aug;10(8). doi: 10.15252/emmm.201708712.
Sepsis is a highly lethal and urgent unmet medical need. It is the result of a complex interplay of several pathways, including inflammation, immune activation, hypoxia, and metabolic reprogramming. Specifically, the regulation and the impact of the latter have become better understood in which the highly catabolic status during sepsis and its similarity with starvation responses appear to be essential in the poor prognosis in sepsis. It seems logical that new interventions based on the recognition of new therapeutic targets in the key metabolic pathways should be developed and may have a good chance to penetrate to the bedside. In this review, we concentrate on the pathological changes in metabolism, observed during sepsis, and the presumed underlying mechanisms, with a focus on the level of the organism and the interplay between different organ systems.
脓毒症是一种具有高度致命性且未满足医疗需求的疾病。它是由多种途径(包括炎症、免疫激活、缺氧和代谢重编程)复杂相互作用的结果。具体而言,在后一种途径的调控和影响方面,人们有了更好的理解,其中脓毒症期间高度分解代谢状态及其与饥饿反应的相似性似乎是脓毒症预后不良的关键。基于在关键代谢途径中识别新的治疗靶点而开发新的干预措施似乎是合理的,并且可能有很好的机会应用于临床。在这篇综述中,我们集中讨论了脓毒症期间观察到的代谢变化以及推测的潜在机制,重点是在机体水平和不同器官系统之间的相互作用。