Fan Jiwen, Ren Meng, Adhikari Binay Kumar, Wang Haodong, He Yuquan
Department of Cardiology, China-Japan Union Hospital of Jilin University, Changchun, People's Republic of China.
Department of Medical Oncology, Jilin Provincial Cancer Hospital, Changchun, People's Republic of China.
J Inflamm Res. 2022 Jul 7;15:3847-3858. doi: 10.2147/JIR.S370483. eCollection 2022.
Cardiac fibrosis often has adverse cardiovascular effects, including heart failure, sudden death, and malignant arrhythmias. However, there is no targeted therapy for cardiac fibrosis. Inflammation is known to play a crucial role in the disorder, and the NLR pyrin domain-containing-3 (NLRP3) inflammasome is closely associated with innate immunity. Therefore, further understanding the pathophysiological role of the inflammasome in cardiac fibrosis may provide novel strategies for the prevention and treatment of the disorder. The aim of this review was to summarize the present knowledge of NLRP3 inflammasome-related mechanisms underlying cardiac fibrosis and to suggest potential targeted therapy that could be used to treat the condition.
心脏纤维化通常会产生不良的心血管影响,包括心力衰竭、猝死和恶性心律失常。然而,目前尚无针对心脏纤维化的靶向治疗方法。已知炎症在该疾病中起关键作用,且含NLR吡喃结构域3(NLRP3)炎性小体与固有免疫密切相关。因此,进一步了解炎性小体在心脏纤维化中的病理生理作用可能为该疾病的预防和治疗提供新策略。本综述的目的是总结目前关于NLRP3炎性小体相关机制在心脏纤维化中的认识,并提出可用于治疗该疾病的潜在靶向治疗方法。