2014 Fiscal Year Final Research Report
Development Mechanism and Physiological Roles of Brown Fat Regulating Energy Expenditure
Project/Area Number |
22228001
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Research Category |
Grant-in-Aid for Scientific Research (S)
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Allocation Type | Single-year Grants |
Research Field |
Food science
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Research Institution | Kyoto University |
Principal Investigator |
KAWADA Teruo 京都大学, (連合)農学研究科(研究院), 教授 (10177701)
|
Co-Investigator(Kenkyū-buntansha) |
TAKAHASHI Nobuyuki 東京農業大学, 応用生物科学部, 准教授 (50370135)
GOTO Tsuyoshi 京都大学, 農学研究科, 准教授 (10550311)
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Co-Investigator(Renkei-kenkyūsha) |
SAITO Masayuki 北海道大学, 名誉教授 (80036441)
MATSUDA Hideo 大阪大学, 情報科学研究科, 教授 (50183950)
MATSUDA Tetsuya 京都大学, 情報学研究科, 教授 (00209561)
AMRI Ez-Zoubir フランス科学研究機構
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Project Period (FY) |
2010-04-01 – 2015-03-31
|
Keywords | 肥満 / エネルギー代謝 / 脂肪細胞 / 褐色脂肪 / メタボリック症候群 |
Outline of Final Research Achievements |
It was revealed that brown adipose tissue (BAT) presents in human adult and it function as the organ acting consumption of extra energy depot in adult. The loss or less of BAT correlates closely with the onset of diabetes and obesity, hence it is recently recognized the importance of classical brown adipocyte and non-classical adipocyte (Beige cell) in human health. In this study, we elucidated about the following points. (1) The transgenic mouse expressing the specific fluoresce protein in BAT were developed. The mouse used to analysis of expression and function of classical brown adipocyte and non-classical adipocyte (Beige cell) by food factors and others in vivo. (2) The molecular analysis of differentiation and functional suppression of BAT were conducted. (3) The systematic analysis of food components to intensify BAT development and function was conducted. These results suggest the key to the success of solution of obesity disease and metabolic syndrome.
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Free Research Field |
食品機能学
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