The fat-derived hormone adiponectin reverses insulin resistance associated with both lipoatrophy and obesity

被引:3910
作者
Yamauchi, T
Kamon, J
Waki, H
Terauchi, Y
Kubota, N
Hara, K
Mori, Y
Ide, T
Murakami, K
Tsuboyama-Kasaoka, N
Ezaki, O
Akanuma, Y
Gavrilova, O
Vinson, C
Reitman, ML
Kagechika, H
Shudo, K
Yoda, M
Nakano, Y
Tobe, K
Nagai, R
Kimura, S
Tomita, M
Froguel, P
Kadowaki, T [1 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Internal Med, Tokyo, Japan
[2] Pasteur Inst Lille, CNRS, Inst Biol, Lille, France
[3] Natl Inst Hlth & Nutr, Div Clin Nutr, Tokyo 162, Japan
[4] Asahi Life Fdn, Inst Diabet Care & Res, Tokyo, Japan
[5] NIDDKD, Diabet Branch, NIH, Bethesda, MD 20892 USA
[6] NCI, Lab Metab, NIH, Bethesda, MD 20892 USA
[7] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Physiol Chem, Tokyo, Japan
基金
英国医学研究理事会;
关键词
D O I
10.1038/90984
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adiponectin is an adipocyte-derived hormone. Recent genome-wide scans have mapped a susceptibility locus for type 2 diabetes and metabolic syndrome to chromosome 3q27, where the gene encoding adiponectin is located. Here we show that decreased expression of adiponectin correlates with insulin resistance in mouse models of altered insulin sensitivity. Adiponectin decreases insulin resistance by decreasing triglyceride content in muscle and liver in obese mice. This effect results from increased expression of molecules involved in both fatty-acid combustion and energy dissipation in muscle. Moreover, insulin resistance in lipoatrophic mice was completely reversed by the combination of physiological doses of adiponectin and leptin, but only partially by either adiponectin or leptin alone. We conclude that decreased adiponectin is implicated in the development of insulin resistance in mouse models of both obesity and lipoatrophy. These data also indicate that the replenishment of adiponectin might provide a novel treatment modality for insulin resistance and type 2 diabetes.
引用
收藏
页码:941 / 946
页数:6
相关论文
共 37 条
[1]   Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity [J].
Arita, Y ;
Kihara, S ;
Ouchi, N ;
Takahashi, M ;
Maeda, K ;
Miyagawa, J ;
Hotta, K ;
Shimomura, I ;
Nakamura, T ;
Miyaoka, K ;
Kuriyama, H ;
Nishida, M ;
Yamashita, S ;
Okubo, K ;
Matsubara, K ;
Muraguchi, M ;
Ohmoto, Y ;
Funahashi, T ;
Matsuzawa, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (01) :79-83
[2]  
Ebisawa M, 1999, CHEM PHARM BULL, V47, P1778
[3]   C1q - how many functions? How many receptors? [J].
Eggleton, P ;
Reid, KBM ;
Tenner, AJ .
TRENDS IN CELL BIOLOGY, 1998, 8 (11) :428-431
[4]   Obesity in the new millennium [J].
Friedman, JM .
NATURE, 2000, 404 (6778) :632-634
[5]   Proteolytic cleavage product of 30-kDa adipocyte complement-related protein increases fatty acid oxidation in muscle and causes weight loss in mice [J].
Fruebis, J ;
Tsao, TS ;
Javorschi, S ;
Ebbets-Reed, D ;
Erickson, MRS ;
Yen, FT ;
Bihain, BE ;
Lodish, HF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (04) :2005-2010
[6]   Surgical implantation of adipose tissue reverses diabetes in lipoatrophic mice [J].
Gavrilova, O ;
Marcus-Samuels, B ;
Graham, D ;
Kim, JK ;
Shulman, GI ;
Castle, AL ;
Vinson, C ;
Eckhaus, M ;
Reitman, ML .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (03) :271-278
[7]   The role of TNFα and TNF receptors in obesity and insulin resistance [J].
Hotamisligil, GS .
JOURNAL OF INTERNAL MEDICINE, 1999, 245 (06) :621-625
[8]   AdipoQ is a novel adipose-specific gene dysregulated in obesity [J].
Hu, E ;
Liang, P ;
Spiegelman, BM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (18) :10697-10703
[9]  
Kahn CR, 1996, ANNU REV MED, V47, P509
[10]   Peroxisome proliferator-activated receptors γ and α mediate in vivo regulation of uncoupling protein (UCP-1, UCP-2, UCP-3) gene expression [J].
Kelly, LJ ;
Vicario, PP ;
Thompson, GM ;
Candelore, MR ;
Doebber, TW ;
Ventre, J ;
Wu, MS ;
Meurer, R ;
Forrest, MJ ;
Conner, MW ;
Cascieri, MA ;
Moller, DE .
ENDOCRINOLOGY, 1998, 139 (12) :4920-4927