Hyperglycemia prevents the suppressive effect of hyperinsulinemia on plasma adiponectin levels in healthy humans

被引:23
作者
Blumer, Regje M. E. [1 ]
van der Crabben, Saskia N. [1 ]
Stegenga, Michiel E. [2 ]
Tanck, Michael W. [3 ]
Ackermans, Mariette T. [4 ]
Endert, Erik [4 ]
van der Poll, Tom [2 ]
Sauerwein, Hans P. [1 ]
机构
[1] Acad Med Ctr, Dept Endocrinol & Metab, NL-1100 DD Amsterdam, Netherlands
[2] Acad Med Ctr, Ctr Expt & Mol Med, NL-1100 DD Amsterdam, Netherlands
[3] Acad Med Ctr, Dept Clin Epidemiol & Biostat, NL-1100 DD Amsterdam, Netherlands
[4] Acad Med Ctr, Lab Endocrinol & Radiochem, Dept Clin Chem, NL-1100 DD Amsterdam, Netherlands
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2008年 / 295卷 / 03期
关键词
hypoadiponectinemia; glucose metabolism; type; 2; diabetes;
D O I
10.1152/ajpendo.90288.2008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adiponectin is a fat-derived hormone with insulin-sensitizing properties. In patients with type 2 diabetes plasma adiponectin levels are decreased. Since these patients are characterized by high plasma insulin and glucose concentrations, hyperinsulinemia and hyperglycemia could be responsible for the downregulation of adiponectin. Insulin decreases adiponectin levels in humans. The effect of hyperglycemia is unknown. To determine the selective effects of insulin, glucose, or their combination on plasma adiponectin, clamps were performed in six healthy males on four occasions in a crossover design: 1) lower insulinemic-euglycemic clamp (100 pmol/l insulin, 5 mmol/l glucose) (reference clamp); 2) hyperinsulinemic-euglycemic clamp (400 pmol/l insulin, 5 mmol/l glucose); 3) lower insulinemic-hyperglycemic clamp (100 pmol/l insulin, 12 mmol/l glucose); and 4) hyperinsulinemic-hyperglycemic clamp (400 pmol/l insulin, 12 mmol/ l glucose). Adiponectin concentrations and high-molecular-weight (HMW)-to-total adiponectin ratio were measured at the start and end of the 6-h clamps. After the 6-h study period, total plasma adiponectin levels were significantly (P = 0.045) decreased by 0.63 mu g/ml in the lower insulinemic-euglycemic clamp (clamp 1). In both euglycemic groups (clamps 1 and 2) adiponectin concentrations significantly declined (P = 0.016) over time by 0.56 mu g/ml, whereas there was no change in both hyperglycemic groups (clamps 3 and 4) (P = 0.420). In none of the clamps did the ratio of HMW to total adiponectin change. We conclude that insulin suppresses plasma adiponectin levels already at a plasma insulin concentration of 100 pmol/l. Hyperglycemia prevents the suppressive effect of insulin. This suggests that, in contrast to glucose, insulin could be involved in the downregulation of plasma adiponectin in insulin-resistant patients.
引用
收藏
页码:E613 / E617
页数:5
相关论文
共 37 条
[1]   Discrimination between obesity and insulin resistance in the relationship with adiponectin [J].
Abbasi, F ;
Chu, JW ;
Lamendola, C ;
McLaughlin, T ;
Hayden, J ;
Reaven, GM ;
Reaven, PD .
DIABETES, 2004, 53 (03) :585-590
[2]   Adipose tissue as an endocrine organ [J].
Ahima, RS ;
Flier, JS .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2000, 11 (08) :327-332
[4]   Selective downregulation of the high-molecular weight form of adiponectin in hyperinsulinemia and in type 2 diabetes - Differential regulation from nondiabetic subjects [J].
Basu, Rita ;
Pajvani, Utpal B. ;
Rizza, Robert A. ;
Scherer, Philipp E. .
DIABETES, 2007, 56 (08) :2174-2177
[5]  
Blümer RME, 2008, AIDS, V22, P227, DOI 10.1097/QAD.0b013e3282f33557
[6]   Adiponectin and glucose production in patients infected with Plasmodium falciparum [J].
Blümer, RME ;
van Thien, H ;
Ruiter, AFC ;
Weverling, GJ ;
Thuan, DV ;
Endert, E ;
Kager, PA ;
Sauerwein, HP .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2005, 54 (01) :60-66
[7]   Two compartments for insulin-stimulated exocytosis in 3T3-L1 adipocytes defined by endogenous ACRP30 and GLUT4 [J].
Bogan, JS ;
Lodish, HF .
JOURNAL OF CELL BIOLOGY, 1999, 146 (03) :609-620
[8]   Insulin and endothelin in the acute regulation of adiponectin in vivo in humans [J].
Brame, LA ;
Considine, RV ;
Yamauchi, M ;
Baron, AD ;
Mather, KJ .
OBESITY RESEARCH, 2005, 13 (03) :582-588
[9]   Endogenous glucose production is inhibited by the adipose-derived protein Acrp30 [J].
Combs, TP ;
Berg, AH ;
Obici, S ;
Scherer, PE ;
Rossetti, L .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (12) :1875-1881
[10]   Differential responses of visceral and subcutaneous fat depots to nutrients [J].
Einstein, FH ;
Atzmon, G ;
Yang, XM ;
Ma, XH ;
Rincon, M ;
Rudin, E ;
Muzumdar, R ;
Barzilai, N .
DIABETES, 2005, 54 (03) :672-678