Diet-induced insulin resistance in mice lacking adiponectin/ACRP30

被引:0
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作者
Norikazu Maeda
Iichiro Shimomura
Ken Kishida
Hitoshi Nishizawa
Morihiro Matsuda
Hiroyuki Nagaretani
Naoki Furuyama
Hidehiko Kondo
Masahiko Takahashi
Yukio Arita
Ryutaro Komuro
Noriyuki Ouchi
Shinji Kihara
Yoshihiro Tochino
Keiichi Okutomi
Masato Horie
Satoshi Takeda
Toshifumi Aoyama
Tohru Funahashi
Yuji Matsuzawa
机构
[1] Graduate School of Medicine,Department of Internal Medicine and Molecular Science
[2] Osaka University,Department of Aging Biochemistry
[3] Otsuka GEN Research Institute,Department of Organismal Biosystems, Graduate School of Frontier Bioscience, Department of Medicine and Pathophysiology, Graduate School of Medicine
[4] Otsuka Pharmaceutical Co. Ltd.,undefined
[5] School of Medicine,undefined
[6] Shinshu University,undefined
[7] Osaka University,undefined
来源
Nature Medicine | 2002年 / 8卷
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摘要
Here we investigated the biological functions of adiponectin/ACRP30, a fat-derived hormone, by disrupting the gene that encodes it in mice. Adiponectin/ACRP30-knockout (KO) mice showed delayed clearance of free fatty acid in plasma, low levels of fatty-acid transport protein 1 (FATP-1) mRNA in muscle, high levels of tumor necrosis factor-α (TNF-α) mRNA in adipose tissue and high plasma TNF-α concentrations. The KO mice exhibited severe diet-induced insulin resistance with reduced insulin-receptor substrate 1 (IRS-1)-associated phosphatidylinositol 3 kinase (PI3-kinase) activity in muscle. Viral mediated adiponectin/ACRP30 expression in KO mice reversed the reduction of FATP-1 mRNA, the increase of adipose TNF-α mRNA and the diet-induced insulin resistance. In cultured myocytes, TNF-α decreased FATP-1 mRNA, IRS-1-associated PI3-kinase activity and glucose uptake, whereas adiponectin increased these parameters. Our results indicate that adiponectin/ACRP30 deficiency and high TNF-α levels in KO mice reduced muscle FATP-1 mRNA and IRS-1-mediated insulin signaling, resulting in severe diet-induced insulin resistance.
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页码:731 / 737
页数:6
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