Shimomura Iichiro
Department of Medicine and Pathophysiology, Graduate School of Frontier Bioscience, Graduate School of Medicine, Osaka University, Suita 565-0871.
Rinsho Byori. 2003 Nov;51(11):1090-5.
The adipose tissue produces and secretes many bioactive substances, which we conceptualized as Adipocytokines (Nature Medicine 1996). Adiponectin is a novel adipocytokine, which we identified by screening the adipose-specific genes from human fat. Adiponectin is a secreted protein, the concentration of which reaches as high as 5-15 micrograms/ml in human plasma. Adiponectin mRNA is expressed exclusively in adipose tissues. The adiponectin mRNAs and its plasma levels are reduced in obesity, type 2 diabetes and atherosclerosis. Hyperinsulinemic euglycemic clamp studies in humans and monkeys, and several recent studies from others revealed that adiponectin is an insulin-sensitizing hormone. Furthermore, adiponectin exhibited anti-atherogenic moieties, decreasing the attachment of monocytes to endothelial cells through inhibiting the expression levels of adhesion molecules. It reduced the lipid accumulation in macrophages through reducing the expression of scavenger receptor, and inhibited the cytokine-stimulated proliferation of smooth muscle cells. The genetic mutation of the adiponectin gene accompanying hypoadiponectinemia was strongly associated with the incidence of type 2 diabetes and atherosclerosis in Japanese subjects. Hypoadiponectinemia was the strongest predictor for the development of type 2 diabetes in humans. Adiponectin knockout mice exhibited diet-induced diabetes and severer atherosclerotic response by vascular injury. Adiponectin supplement reversed the insulin resistance syndrome including diabetes and atherosclerotic change in the knockout mice. We conclude that "Hypoadiponectinemia" stands upstream of the pathophysiology of metabolic syndrome, hence, can be a direct target of drug intervention to tackle life style-related disease rampant in developed countries.
脂肪组织产生并分泌多种生物活性物质,我们将其概念化为脂肪细胞因子(《自然医学》,1996年)。脂联素是一种新型脂肪细胞因子,我们通过筛选人类脂肪中的脂肪特异性基因而鉴定出它。脂联素是一种分泌蛋白,在人体血浆中的浓度高达5 - 15微克/毫升。脂联素mRNA仅在脂肪组织中表达。在肥胖症、2型糖尿病和动脉粥样硬化患者中,脂联素mRNA及其血浆水平均降低。对人类和猴子进行的高胰岛素正常血糖钳夹研究以及其他一些近期研究表明,脂联素是一种胰岛素增敏激素。此外,脂联素具有抗动脉粥样硬化作用,通过抑制黏附分子的表达水平来减少单核细胞与内皮细胞的黏附。它通过降低清道夫受体的表达来减少巨噬细胞中的脂质积累,并抑制细胞因子刺激的平滑肌细胞增殖。在日本受试者中,伴随低脂联素血症的脂联素基因突变与2型糖尿病和动脉粥样硬化的发病率密切相关。低脂联素血症是人类患2型糖尿病的最强预测指标。脂联素基因敲除小鼠表现出饮食诱导的糖尿病以及血管损伤后更严重的动脉粥样硬化反应。补充脂联素可逆转基因敲除小鼠的胰岛素抵抗综合征,包括糖尿病和动脉粥样硬化改变。我们得出结论,“低脂联素血症”处于代谢综合征病理生理学的上游,因此,它可以成为药物干预的直接靶点,以应对发达国家普遍存在的与生活方式相关的疾病。