| Project/Area Number |
16500508
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Eating habits, studies on eating habits
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| Research Institution | Kyoto University |
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Principal Investigator |
YAMADA Yuichiro Kyoto University, Graduate School of Medicine, Associate Professor, 医学研究科, 助教授 (60283610)
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| Co-Investigator(Kenkyū-buntansha) |
FUSHIKI Tohru Kyoto University, Graduate School of Agriculture, Professor, 農学研究科, 教授 (20135544)
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| Project Period (FY) |
2004 – 2005
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| Project Status |
Completed (Fiscal Year 2005)
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| Budget Amount *help |
¥3,700,000 (Direct Cost: ¥3,700,000)
Fiscal Year 2005: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 2004: ¥2,000,000 (Direct Cost: ¥2,000,000)
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| Keywords | incretin / GIP / GLP-1 / diabetes / obesity / energy expenditure |
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| Research Abstract |
The hormonal factor(s) implicated as transmitters of signals from the gut to pancreatic β-cells is referred to incretin and gastric inhibitory polypeptide (GIP) is identified as one of the incretins. GIP is a gastrointestinal peptide hormone of 42 amino acids that is released from duodenal endocrine K-cells after absorption of glucose or fat and exerts its effects by binding to its specific receptor, the GIP receptors (GIPR). We have characterized mice with a targeted mutation of the GIPR gene and found that IRS-1(-/-)GIPR(-/-) mice exhibited both reduced adiposity and ameliorated insulin resistance, indicating GIP plays a crucial role in switching from fat oxidation to fat accumulation under the diminished insulin action as a potential target for secondary prevention of insulin resistance. Furthermore, bone histomorphometrical analyses revealed that bone formation parameters were significantly lower and that the number of osteoclasts was significantly increased, indicating that GIP receptor(-/-) mice have high-turnover osteoporosis. These results indicated that GIP has not only an insulinotropic role but also physiological roles on fat-accumulation into adipose tissues and calcium-accumulation into bone. We here propose a new acronym GIP for Gut-derived nutrient-Intake Polypeptide.
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