Jia Yumeng, Wang Lei
Department of Nutrition and Food Hygiene, School of Public Health, Capital Medical University, Beijing, China.
Department of Nutrition and Food Hygiene, School of Public Health, Beijing Key Laboratory of Environment and Aging, Capital Medical University, Beijing, China.
J Cardiovasc Transl Res. 2025 Jul 24. doi: 10.1007/s12265-025-10670-7.
Cardiometabolic diseases (CMD) encompass a cluster of cardiovascular disorders primarily driven by metabolic dysregulation, such as obesity-associated cardiomyopathy, hypertensive heart disease, and diabetic cardiomyopathy. The pathogenesis of CMD is closely linked to chronic inflammation, myocardial hypertrophy, and mitochondrial energy metabolism dysfunction. Recently, the succinate-GPR91 pathway, a critical hub for metabolic regulation, has gained attention for its role in CMD. In addition to its function as an intermediate in the TCA cycle, succinate also exerts a range of pathophysiological effects by acting as a signaling molecule through the activation of its receptor, GPR91.Studies indicate that in metabolic disorders such as obesity, hypertension, diabetes,and atherosclerosis, abnormal activation of the succinate-GPR91 axis exacerbates inflammation, accelerates myocardial hypertrophy, and induces mitochondrial dysfunction, contributing to cardiovascular damage. Targeting the succinate-GPR91 pathway may offer novel CMD therapies. This article reviews succinate's role in inflammation, hypertrophy, mitochondrial dysfunction, and other diseases, offering insights for CMD research and treatment.
心脏代谢疾病(CMD)包括一系列主要由代谢失调驱动的心血管疾病,如肥胖相关性心肌病、高血压性心脏病和糖尿病性心肌病。CMD的发病机制与慢性炎症、心肌肥大和线粒体能量代谢功能障碍密切相关。最近,琥珀酸 - GPR91途径作为代谢调节的关键枢纽,因其在CMD中的作用而受到关注。除了作为三羧酸循环中的中间体发挥作用外,琥珀酸还通过激活其受体GPR91作为信号分子发挥一系列病理生理作用。研究表明,在肥胖、高血压、糖尿病和动脉粥样硬化等代谢紊乱中,琥珀酸 - GPR91轴的异常激活会加剧炎症、加速心肌肥大并诱导线粒体功能障碍,导致心血管损伤。靶向琥珀酸 - GPR91途径可能提供新的CMD治疗方法。本文综述了琥珀酸在炎症、肥大、线粒体功能障碍和其他疾病中的作用,为CMD的研究和治疗提供见解。