Insulin decreases human adiponectin plasma levels

被引:100
作者
Möhlig, M
Wegewitz, U
Osterhoff, M
Isken, F
Ristow, M
Pfeiffer, AFH
Spranger, J
机构
[1] Free Univ Berlin, Benjamin Franklin Med Ctr, Dept Endocrinol Diabet & Nutr, D-12200 Berlin, Germany
[2] German Inst Human Nutr Potsdam, Dept Clin Nutr, Bergholz Rehbrucke, Germany
关键词
adiponectin; insulin resistance; atherosclerosis; diabetes; insulin; cytokine; obesity;
D O I
10.1055/s-2002-38248
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin resistance and hyperinsulinemia are known atherosclerosis risk factors. The association between adiponectin plasma levels and obesity, insulinemia, and atherosclerosis has been shown. Thus, adiponectin may be a link between hyperinsulinemia and vascular disease. In vitro data demonstrated a reduction of adiponectin expression by insulin. However, it is still unclear whether insulin regulates adiponectinemia in vivo in humans. Five healthy male volunteers were studied. Circulating adiponectin levels were determined before and during hyperinsulinemic euglycemic clamp. Adiponectin was measured by radioimmunoassay. Hyperinsulinemia (85.0 +/- 33.2 at baseline vs. 482.8 +/- 64.4pmol/l during steady state; p < 0.01) was achieved using a euglycemic hyperinsulinemic clamp, keeping blood glucose levels basically unchanged during the intervention (4.6 +/- 0.14 vs. 4.37 +/- 0.15 mmol/l, respectively; ns). We found a significant decrease of adiponectin plasma levels during the steady state of hyperinsulinemic euglycemic clamp (26.7 +/- 3.5 mug/ml) compared to baseline levels (30.4 +/- 5 mug/ml; p < 0.05). Hyperinsulinemia caused a significant decrease of adiponectin plasma levels under euglycemic conditions. Considering existing data about adiponectin dependent effects, hypoadiponectinemia might at least partly be a link between hyperinsulinemia and vascular disease in metabolic syndrome.
引用
收藏
页码:655 / 658
页数:4
相关论文
共 31 条
[11]  
KUBOTA N, 2002, J BIOL CHEM, V24, P24
[12]   Adiponectin and development of type 2 diabetes in the Pima Indian population [J].
Lindsay, RS ;
Funahashi, T ;
Hanson, RL ;
Matsuzawa, Y ;
Tanaka, S ;
Tataranni, PA ;
Knowler, WC ;
Krakoff, J .
LANCET, 2002, 360 (9326) :57-58
[13]   Increased β-oxidation but no insulin resistance or glucose intolerance in mice lacking adiponectin [J].
Ma, K ;
Cabrero, A ;
Saha, PK ;
Kojima, H ;
Li, L ;
Chang, BHJ ;
Paul, A ;
Chan, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (38) :34658-34661
[14]   CDNA cloning and expression of a novel adipose specific collagen-like factor, apM1 (Adipose most abundant gene transcript 1) [J].
Maeda, K ;
Okubo, K ;
Shimomura, I ;
Funahashi, T ;
Matsuzawa, Y ;
Matsubara, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 221 (02) :286-289
[15]  
MAEDA N, 2002, NAT MED, V17, P17
[16]  
MATSUDA M, 2002, J BIOL CHEM, V22, P22
[17]   A haplotype at the adiponectin locus is associated with obesity and other features of the insulin resistance syndrome [J].
Menzaghi, C ;
Ercolino, T ;
Di Paola, R ;
Berg, AH ;
Warram, JH ;
Scherer, PE ;
Trischitta, V ;
Doria, A .
DIABETES, 2002, 51 (07) :2306-2312
[18]   Genome-wide search for type 2 diabetes in Japanese affected sib-pails confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate loci on 7p and 11p [J].
Mori, Y ;
Otabe, S ;
Dina, C ;
Yasuda, K ;
Populaire, C ;
Lecoeur, C ;
Vatin, V ;
Durand, E ;
Hara, K ;
Okada, T ;
Tobe, K ;
Boutin, P ;
Kadowaki, T ;
Froguel, P .
DIABETES, 2002, 51 (04) :1247-1255
[19]  
Nakano Y, 1996, J BIOCHEM-TOKYO, V120, P803
[20]   Androgens decrease plasma adiponectin, an insulin-sensitizing adipocyte-derived protein [J].
Nishizawa, H ;
Shimomura, H ;
Kishida, K ;
Maeda, N ;
Kuriyama, H ;
Nagaretani, H ;
Matsuda, M ;
Kondo, H ;
Furuyama, N ;
Kihara, S ;
Nakamura, T ;
Tochino, Y ;
Funahashi, T ;
Matsuzawa, Y .
DIABETES, 2002, 51 (09) :2734-2741