Gauvreau D, Villeneuve N, Deshaies Y, Cianflone K
Centre de recherche de l'institut universitaire de cardiologie et de pneumologie de Québec (CRIUCPQ), chemin Sainte-Foy, pavillon Marguerite-D'Youville, Québec (QC), Canada.
Ann Endocrinol (Paris). 2011 Jun;72(3):224-31. doi: 10.1016/j.ando.2010.02.025. Epub 2011 May 17.
Today, cardiovascular diseases (CVD) remain the principal cause of death in industrialized countries and are linked to obesity and metabolic syndrome. Metabolic syndrome is characterized by changes in arterial blood pressure, glucose metabolism, lipid and lipoprotein profiles in addition to inflammation. Adipose tissue produces many cytokines and secretory factors termed adipokines. Intra-abdominal (visceral) adipose tissue in particular, rather than peripheral, appears to be associated with global cardiometabolic risk. The present article summarizes information on five recently discovered adipokines: vaspin, visfatin, apelin, acylation stimulating protein (ASP) and retinol-binding protein 4 (RBP4) and their potential beneficial or deleterious roles in obesity and atherosclerosis. Vaspin may have antiatherogenic effects through its potential insulin-sensitizing properties. Similarly, visfatin has been suggested to enhance insulin sensitivity, but its potential role in plaque destabilization may counteract this. Apelin, via inhibition of food intake, and increases in physical activity and body temperature, may promote weight loss, resulting in a beneficial antiatherogenic effect. Further, favourable effects on vasodilatation and blood pressure add to this positive effect. Considering its increased levels in subjects with demonstrated atherosclerosis, RBP4 may constitute a biomarker. Lastly, ASP, often increased in obesity and metabolic disorders, may be contributing to efficient lipid storage, and decreasing or blocking ASP may provide a potential antiobesity target. Adipokines may further contribute to obesity-atherosclerosis relationships, the full understanding of which will require further research.
如今,心血管疾病(CVD)仍是工业化国家的主要死因,且与肥胖和代谢综合征相关。代谢综合征的特征是除炎症外,动脉血压、葡萄糖代谢、脂质和脂蛋白谱发生变化。脂肪组织会产生许多细胞因子和被称为脂肪因子的分泌因子。尤其是腹内(内脏)脂肪组织,而非外周脂肪组织,似乎与整体心脏代谢风险相关。本文总结了关于最近发现的五种脂肪因子的信息:内脏脂肪素、内脂素、Apelin、酰化刺激蛋白(ASP)和视黄醇结合蛋白4(RBP4),以及它们在肥胖和动脉粥样硬化中潜在的有益或有害作用。内脏脂肪素可能通过其潜在的胰岛素增敏特性产生抗动脉粥样硬化作用。同样,有人认为内脂素可增强胰岛素敏感性,但其在斑块不稳定中的潜在作用可能会抵消这一作用。Apelin通过抑制食物摄入、增加身体活动和体温,可能促进体重减轻,从而产生有益的抗动脉粥样硬化作用。此外,其对血管舒张和血压的有利影响进一步增强了这种积极作用。鉴于其在已证实患有动脉粥样硬化的受试者中水平升高,RBP4可能构成一种生物标志物。最后,ASP在肥胖和代谢紊乱中通常会升高,可能有助于高效的脂质储存,减少或阻断ASP可能提供一个潜在的抗肥胖靶点。脂肪因子可能进一步影响肥胖与动脉粥样硬化的关系,对此的全面理解仍需进一步研究。