School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Department of Radiology, Shanghai East Hospital, Tongji University, Shanghai, China.
Front Endocrinol (Lausanne). 2024 Nov 4;15:1490143. doi: 10.3389/fendo.2024.1490143. eCollection 2024.
Obesity significantly contributes to the progression of cardiovascular diseases (CVDs) and elevates the risk of cardiovascular mortality. Atherosclerosis, the primary pathogenic process underlying CVDs, initiates with vascular endothelial dysfunction, serving as the cornerstone of vascular lesions. Adipokines, bioactive molecules secreted by adipose tissue that regulate metabolic and endocrine functions, play a pivotal role in modulating endothelial function during atherosclerosis. This review comprehensively examines the distinct roles of various adipokines in regulating endothelial function in atherosclerosis. We categorize these adipokines into two main groups: protective adipokines, including adiponectin, FGF21, CTRP9, PGRN, Omentin, and Vaspin, and detrimental adipokines such as leptin, Chemerin, Resistin, FABP4, among others. Targeting specific adipokines holds promise for novel clinical interventions in the management of atherosclerosis-related CVDs, thereby providing a theoretical foundation for cardiovascular disease treatment strategies.
肥胖显著促进心血管疾病(CVDs)的进展,并增加心血管死亡率的风险。动脉粥样硬化是 CVDs 的主要发病机制,始于血管内皮功能障碍,是血管病变的基石。脂肪细胞因子是脂肪组织分泌的生物活性分子,调节代谢和内分泌功能,在动脉粥样硬化过程中调节内皮功能方面发挥着关键作用。本综述全面研究了各种脂肪细胞因子在调节动脉粥样硬化内皮功能中的不同作用。我们将这些脂肪细胞因子分为两大类:保护性脂肪细胞因子,包括脂联素、FGF21、CTRP9、PGRN、网膜素和 Vaspin,以及有害脂肪细胞因子,如瘦素、Chemerin、抵抗素、FABP4 等。针对特定的脂肪细胞因子为管理与动脉粥样硬化相关的 CVD 的新型临床干预提供了可能,为心血管疾病治疗策略提供了理论基础。