Role of resistin in diet-induced hepatic insulin resistance

被引:296
作者
Muse, ED
Obici, S
Bhanot, S
Monia, BP
McKay, RA
Rajala, MW
Scherer, PE
Rossetti, L
机构
[1] Albert Einstein Coll Med, Ctr Diabet Res & Training, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[4] ISIS Pharmaceut, Carlsbad, CA 92008 USA
[5] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10461 USA
关键词
D O I
10.1172/JCI200421270
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Resistin is an adipose-derived hormone postulated to link adiposity to insulin resistance. To determine whether resistin plays a causative role in the development of diet-induced insulin resistance, we lowered circulating resistin levels in mice by use of a specific antisense oligodeoxynucleotide (ASO) directed against resistin mRNA and assessed in vivo insulin action by the insulin-clamp technique. After 3 weeks on a high-fat (HF) diet, mice displayed severe insulin resistance associated with an approximately 80% increase in plasma resistin levels. In particular, the rate of endogenous glucose production (GP) increased more than twofold compared with that in mice fed a standard chow. Treatment with the resistin ASO for I week normalized the plasma resistin levels and completely reversed the hepatic insulin resistance. Importantly, in this group of mice, the acute infusion of purified recombinant mouse resistin, designed to acutely elevate the levels of circulating resistin up to those observed in the HF-fed mice, was sufficient to reconstitute hepatic insulin resistance. These results provide strong support for a physiological role of resistin in the development of hepatic insulin resistance in this model.
引用
收藏
页码:232 / 239
页数:8
相关论文
共 39 条
[1]   Correlation between serum resistin level and adiposity in obese individuals [J].
Azuma, K ;
Katsukawa, F ;
Oguchi, S ;
Murata, M ;
Yamazaki, H ;
Shimada, A ;
Saruta, T .
OBESITY RESEARCH, 2003, 11 (08) :997-1001
[2]   2'-O-(2-methoxy)ethyl-modified anti-intercellular adhesion molecule 1 (ICAM-1) oligonucleotides selectively increase the ICAM-1 mRNA level and inhibit formation of the ICAM-1 translation initiation complex in human umbilical vein endothelial cells [J].
Baker, BF ;
Lot, SS ;
Condon, TP ;
ChengFlournoy, S ;
Lesnik, EA ;
Sasmor, HM ;
Bennett, CF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (18) :11994-12000
[3]  
Barthel A, 2002, ENDOCRINOLOGY, V143, P3183, DOI 10.1210/endo.143.8.8792
[4]   The adipocyte-secreted protein Acrp30 enhances hepatic insulin action [J].
Berg, AH ;
Combs, TP ;
Du, XL ;
Brownlee, M ;
Scherer, PE .
NATURE MEDICINE, 2001, 7 (08) :947-953
[5]   Central role of the adipocyte in the metabolic syndrome [J].
Bergman, RN ;
Van Citters, GW ;
Mittelman, SD ;
Dea, MK ;
Hamilton-Wessler, M ;
Kim, SP ;
Ellmerer, M .
JOURNAL OF INVESTIGATIVE MEDICINE, 2001, 49 (01) :119-126
[6]   MECHANISMS OF FATTY ACID-INDUCED INHIBITION OF GLUCOSE-UPTAKE [J].
BODEN, G ;
CHEN, XH ;
RUIZ, J ;
WHITE, JV ;
ROSSETTI, L .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (06) :2438-2446
[7]   LOSS OF HEPATIC AUTOREGULATION AFTER CARBOHYDRATE OVERFEEDING IN NORMAL MAN [J].
CLORE, JN ;
HELM, ST ;
BLACKARD, WG .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (04) :1967-1972
[8]   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
[9]  
Combs TP, 2002, ENDOCRINOLOGY, V143, P998, DOI 10.1210/endo.143.3.8662
[10]   Serum resistin (FIZZ3) protein is increased in obese humans [J].
Degawa-Yamauchi, M ;
Bovenkerk, JE ;
Juliar, BE ;
Watson, W ;
Kerr, K ;
Jones, R ;
Zhu, QH ;
Considine, RV .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (11) :5452-5455