| Project/Area Number |
15K08594
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Applied pharmacology
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| Research Institution | Kanazawa University |
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Principal Investigator |
ANDO Hitoshi 金沢大学, 医学系, 教授 (50382875)
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| Co-Investigator(Renkei-kenkyūsha) |
USHIJIMA Kentaro 自治医科大学, 医学部, 講師 (70448843)
TAKAMURA Toshinari 金沢大学, 医学系, 教授 (00324111)
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| Project Period (FY) |
2015-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2017: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
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| Keywords | 体内時計 / 概日リズム / 時計遺伝子 / 生活習慣病 / 糖尿病 / 肥満 |
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| Outline of Final Research Achievements |
The results of studies using tissue-specific clock gene knock out mice etc. suggest that circadian clocks play a significant role in maintaining homeostasis of various physiological functions including glucose and lipid metabolisms. However, it remains to be seen what happens if circadian clocks (in particular, peripheral clocks) are disrupted in bodies with innately intact clocks. In this study, we've developed the models of systemic and peripheral tissues-specific disruption of circadian clocks by changing the light/dark cycle or feeding time, respectively, using normal mice. Consequently, decreased food intake without change in body weight was found in both the models, and impaired glucose tolerance was seen in the systemic model. These results suggest that both central and peripheral clocks play an important role in regulating metabolisms.
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