Plasma resistin concentration, hepatic fat content, and hepatic and peripheral insulin resistance in pioglitazone-treated type II diabetic patients

被引:122
作者
Bajaj, M [1 ]
Suraamornkul, S [1 ]
Hardies, LJ [1 ]
Pratipanawatr, T [1 ]
DeFronzo, RA [1 ]
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Med, Diabet Div, San Antonio, TX 78284 USA
关键词
pioglitazone; hepatic fat content; hepatic insulin resistance; resistin; type II diabetes mellitus;
D O I
10.1038/sj.ijo.0802625
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: To study the effect of pioglitazone (PIO) on plasma resistin concentration, endogenous glucose production (EGP), and hepatic fat content (HFC) in patients with type II diabetes (T2DM). Subjects: A total of 13 T2DM patients (age=51+/-2 y, BMI=29.7+/-1.1 kg/m(2), HbA(1c)=8.0+/-0.5%). Methods: HFC (magnetic resonance spectroscopy) and basal plasma resistin concentration were quantitated before and after PIO treatment (45 mg/day) for 16 weeks. Subjects received a 3 h euglycemic insulin (100 mU/m(2)/min) clamp with 3-[H-3] glucose to determine rates of EGP and tissue glucose disappearance (Rd) before and after PIO. Results: PIO reduced fasting plasma glucose (10.3+/-0.7 to 7.6+/-0.6 mmol/l, P<0.001) and HbA(1c) (8.0 +/- 0.4 to 6.8 +/- 0.3%, P<0.001) despite increased body weight (83.2+/-3.4 to 86.3+/-3.4 kg, P<0.001). PIO improved Rd (4.9 +/- 0.4 to 6.6 +/- 0.5 mg/kg/min, P<0.005) and reduced EGP (0.22+/-0.04 to 0.06+/-0.02 mg/kg/min, P<0.01) during the insulin clamp. Following PIO, HFC decreased from 21.1 +/- 3.5 to 11.2 +/- 2.1% (P<0.005), and plasma resistin decreased from 5.3+/-0.6 to 3.5+/-0.3 ng/ml (P<0.01). Plasma resistin concentration correlated positively with HFC before (r=0.58, P<0.05) and after (r=0.55, P<0.05) PIO treatment. Taken collectively, plasma resistin concentration, before and after PIO treatment, correlated positively with hepatic fat content (r=0.66, P<0.001) and EGP during the insulin clamp (r=0.41, P<0.05). However, the plasma resistin concentration did not correlate with whole body glucose disposal (Rd) during the insulin clamp either before (r=-0.18, P=NS) or after (r=-0.13, P=NS) PIO treatment. Conclusions: PIO treatment in T2DM causes a significant decrease in plasma resistin concentration. The decrease in plasma resistin is positively correlated with the decrease in hepatic fat content and improvement in hepatic insulin sensitivity.
引用
收藏
页码:783 / 789
页数:7
相关论文
共 35 条
[32]   The hormone resistin links obesity to diabetes [J].
Steppan, CM ;
Bailey, ST ;
Bhat, S ;
Brown, EJ ;
Banerjee, RR ;
Wright, CM ;
Patel, HR ;
Ahima, RS ;
Lazar, MA .
NATURE, 2001, 409 (6818) :307-312
[33]   A family of tissue-specific resistin-like molecules [J].
Steppan, CM ;
Brown, EJ ;
Wright, CM ;
Bhat, S ;
Banerjee, RR ;
Dai, CY ;
Enders, GH ;
Silberg, DG ;
Wen, XM ;
Wu, GD ;
Lazar, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :502-506
[34]   Adipose tissue resistin expression is severely suppressed in obesity and stimulated by peroxisome proliferator-activated receptor γ agonists [J].
Way, JM ;
Görgün, CZ ;
Tong, Q ;
Uysal, KT ;
Brown, KK ;
Harrington, WW ;
Oliver, WR ;
Willson, TM ;
Kliewer, SA ;
Hotamisligil, GS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (28) :25651-25653
[35]   Comparative studies of resistin expression and phylogenomics in human and mouse [J].
Yang, RZ ;
Huang, Q ;
Xu, AH ;
McLenithan, JC ;
Eison, JA ;
Shuldiner, AR ;
Alkan, S ;
Gong, DW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 310 (03) :927-935