Koistinen H A, Vidal H, Karonen S L, Dusserre E, Vallier P, Koivisto V A, Ebeling P
Department of Medicine, Helsinki University Central Hospital, Helsinki, Finland.
Arterioscler Thromb Vasc Biol. 2001 Jun;21(6):1034-9. doi: 10.1161/01.atv.21.6.1034.
We studied the effect of an oral fat load on plasma acylation stimulating protein (ASP) concentrations in 9 lean healthy (age 59+/-2 years, body mass index [BMI] 23.2+/-0.4 kg/m(2); both mean+/-SEM), 9 obese nondiabetic (58+/-2 years, BMI 29.4+/-0.5 kg/m(2)), and 12 type 2 diabetic (60+/-2 years, BMI 29.6+/-1.0 kg/m(2)) men. Because ASP is a cleavage product of complement protein C3 (C3adesArg) and its secretion is regulated by insulin, we also examined the subcutaneous adipose tissue expression of C3 mRNA before and after a 240-minute euglycemic hyperinsulinemic clamp in a subgroup of these men. Plasma ASP concentration and adipose tissue C3 mRNA expression were higher in the obese groups than in the lean men. Plasma ASP concentration did not change significantly after the fat load. Fasting plasma ASP concentration and C3 mRNA expression were correlated negatively with insulin sensitivity and positively with the magnitude of postprandial lipemia in nondiabetic but not in type 2 diabetic men. The expression of C3 mRNA was not regulated by insulin. These data suggest that ASP is associated with whole-body glucose and lipid metabolism in nondiabetic individuals, whereas metabolic disturbances in diabetes may overcome the regulatory role of ASP in lipid and glucose metabolism.
我们研究了口服脂肪负荷对9名健康瘦男性(年龄59±2岁,体重指数[BMI]23.2±0.4kg/m²;均为平均值±标准误)、9名肥胖非糖尿病男性(58±2岁,BMI 29.4±0.5kg/m²)和12名2型糖尿病男性(60±2岁,BMI 29.6±1.0kg/m²)血浆酰化刺激蛋白(ASP)浓度的影响。由于ASP是补体蛋白C3(C3adesArg)的裂解产物,其分泌受胰岛素调节,我们还在这些男性的一个亚组中,检测了在240分钟正常血糖高胰岛素钳夹前后皮下脂肪组织中C3 mRNA的表达。肥胖组的血浆ASP浓度和脂肪组织C3 mRNA表达高于瘦男性。脂肪负荷后血浆ASP浓度无显著变化。在非糖尿病男性中,空腹血浆ASP浓度和C3 mRNA表达与胰岛素敏感性呈负相关,与餐后血脂水平呈正相关,但在2型糖尿病男性中并非如此。C3 mRNA的表达不受胰岛素调节。这些数据表明,ASP与非糖尿病个体的全身葡萄糖和脂质代谢相关,而糖尿病中的代谢紊乱可能会克服ASP在脂质和葡萄糖代谢中的调节作用。