Department of Emergency Medical, General Hospital of Ningxia Medical University, Yinchuan, Ningxia, China.
Ningxia Key Laboratory of Clinical and Pathogenic Microbiology, General Hospital of Ningxia Medical University, Yinchuan, China.
Front Immunol. 2024 Oct 31;15:1487576. doi: 10.3389/fimmu.2024.1487576. eCollection 2024.
Sepsis represents a severe condition characterized by organ dysfunction resulting from a dysregulated host response to infection. Among the organs affected, the kidneys are particularly vulnerable, with significant functional impairment that markedly elevates mortality rates. Previous researches have highlighted that both inflammatory response dysregulation and metabolic reprogramming are crucial in the onset and progression of sepsis associated acute kidney injury (SA-AKI), making these processes potential targets for innovative therapies. This study aims to elucidate the pathophysiological mechanisms of renal injury in sepsis by perspective of inflammatory response dysregulation, with particular emphasis on pyroptosis, necroptosis, autophagy, and ferroptosis. Furthermore, it will incorporate insights into metabolic reprogramming to provide a detailed analysis of the mechanisms driving SA-AKI and explore potential targeted therapeutic strategies, providing solid theoretical framework for the development of targeted therapies for SA-AKI.
脓毒症是一种严重的病症,其特征是由于宿主对感染的反应失调而导致器官功能障碍。在受影响的器官中,肾脏特别脆弱,功能明显受损,死亡率显著升高。先前的研究强调,炎症反应失调和代谢重编程在脓毒症相关急性肾损伤 (SA-AKI) 的发生和进展中至关重要,使这些过程成为创新治疗的潜在靶点。本研究旨在从炎症反应失调的角度阐明脓毒症肾损伤的病理生理机制,特别关注细胞焦亡、坏死性凋亡、自噬和铁死亡。此外,它还将纳入代谢重编程的见解,以详细分析驱动 SA-AKI 的机制,并探索潜在的靶向治疗策略,为 SA-AKI 的靶向治疗提供坚实的理论框架。