Xu Wenping, Wang Lang, Chen Ruili, Liu Yi, Chen Wendong
Department of Anesthesiology, The First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan Province, 650032, China.
Naunyn Schmiedebergs Arch Pharmacol. 2025 May 15. doi: 10.1007/s00210-025-04261-1.
Intestinal ischemia-reperfusion injury (II/RI) is a critical acute condition characterized by complex pathological mechanisms, including various modes of cell death. Among these, pyroptosis has garnered significant attention in recent years. This review explores the characteristics, molecular mechanisms, and implications of pyroptosis in II/RI, with a focus on therapeutic strategies targeting the pyroptosis pathway. Key processes such as NOD-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome activation, caspase-1 activation, and gasdermin D (GSDMD)-mediated membrane pore formation are identified as central to pyroptosis. Compounds like MCC950, CY-09, metformin, and curcumin have shown promise in attenuating II/RI in preclinical studies by modulating these pathways. However, challenges remain in understanding non-canonical pyroptosis pathways, unraveling the exact mechanisms of GSDMD-induced pore formation, and translating these findings into clinical applications. Addressing these gaps will be crucial for developing innovative and effective treatments for II/RI.
肠缺血再灌注损伤(II/RI)是一种危急的急性病症,其特征在于复杂的病理机制,包括多种细胞死亡模式。其中,近年来焦亡受到了广泛关注。本综述探讨了焦亡在II/RI中的特征、分子机制及意义,重点关注针对焦亡途径的治疗策略。诸如含NOD样受体家族吡咯结构域蛋白3(NLRP3)炎性小体激活、半胱天冬酶-1激活以及gasdermin D(GSDMD)介导的膜孔形成等关键过程被确定为焦亡的核心。在临床前研究中,MCC950、CY-09、二甲双胍和姜黄素等化合物通过调节这些途径在减轻II/RI方面显示出前景。然而,在理解非经典焦亡途径、阐明GSDMD诱导孔形成的确切机制以及将这些发现转化为临床应用方面仍存在挑战。填补这些空白对于开发针对II/RI的创新有效治疗方法至关重要。