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Increased oxidative stress precedes the onset of high-fat diet-induced insulin resistance and obesity

フォーマット:
論文
責任表示:
Matsuzawa-Nagata, Naoto ; Takamura, Toshinari ; Ando, Hitoshi ; Nakamura, Seiji ; Kurita, Seiichiro ; Misu, Hirofumi ; Ota, Tsuguhito ; Yokoyama, Masayoshi ; Honda, Masao ; Miyamoto, Ken-ichi ; Kaneko, Shuichi
言語:
英語
出版情報:
Elsevier, 2008-08-01
著者名:
Matsuzawa-Nagata, Naoto
Takamura, Toshinari
Ando, Hitoshi
Nakamura, Seiji
Kurita, Seiichiro
Misu, Hirofumi
Ota, Tsuguhito
Yokoyama, Masayoshi
Honda, Masao
Miyamoto, Ken-ichi
Kaneko, Shuichi
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掲載情報:
Metabolism: Clinical and Experimental
ISSN:
0026-0495  CiNii Research  Webcat Plus  JAIRO
巻:
57
通号:
8
開始ページ:
1071
終了ページ:
1077
バージョン:
author
概要:
金沢大学医薬保健研究域医学系<br />Insulin resistance is a key pathophysiological feature of metabolic syndrome. However, the initial events triggering the development of insulin resistance and its causal relations with dysregulation of glucose and fatty acids metabolism remain unclear. We investigated biological pathways that have the potential to induce insulin resistance in mice fed a high-fat diet (HFD). We demonstrate that the pathways for reactive oxygen species (ROS) production and oxidative stress are coordinately up-regulated in both the liver and adipose tissue of mice fed an HFD before the onset of insulin resistance through discrete mechanism. In the liver, an HFD up-regulated genes involved in sterol regulatory element binding protein 1c-related fatty acid synthesis and peroxisome proliferator-activated receptor α-related fatty acid oxidation. In the adipose tissue, however, the HFD down-regulated genes involved in fatty acid synthesis and up-regulated nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex. Furthermore, increased ROS production preceded the elevation of tumor necrosis factor-α and free fatty acids in the plasma and liver. The ROS may be an initial key event triggering HFD-induced insulin resistance. © 2008 Elsevier Inc. All rights reserved. 続きを見る
URL:
http://hdl.handle.net/2297/11570
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