2007 Fiscal Year Final Research Report Summary
Functional study on muscle nucleotide metabolism and AMP-activated protein kinase
| Project/Area Number |
18590309
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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 |
Pathological medical chemistry
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| Research Institution | National Cardiovascular Center Research Institute |
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Principal Investigator |
MORISAKI Takayuki National Cardiovascular Center Research Institute, National Cardiovascular Center Research Institute, Department of Bioscience, Director (30174410)
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| Co-Investigator(Kenkyū-buntansha) |
MORISAKI Hiroko National Cardiovascular Center Research Institute, Department of Bioscience, Laboratory Chief (40311451)
HIDAKA Kyoko National Cardiovascular Center Research Institute, Department of Bioscience, Laboratory Chief (00216681)
CHENG Jidong National Cardiovascular Center Research Institute, Department of Bioscience, Laboratory Chief (40399605)
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| Project Period (FY) |
2006 – 2007
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| Keywords | AMP / AMPK / nucleotide metabolism / genetically modified animal / skeletal muscle function / metabolic disorder / phosphorylation |
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| Research Abstract |
Adenine nucleotide metabolism has many functions including maintenance of ATP, regulation of DNA or RNA synthesis and production of cAMP or adenosine. AMPD, which catalyzes AMP to IMP, is thought to play an important role in this metabolism, though detailed function of AMPD in vivo has not been well understood. In this study, we studied gene knock-out mice for each AMPD gene or combined AMPD genes. First, we investigated those model mice for skeletal muscle function, since we successfully established skeletal muscle AMPD deficiency as seen in patients with myoadenylate deaminase deficiency. In skeletal muscle, AMPD deficiency did not cause dramatic changes in ATP/AMP ratio or AMPK phophorylation status. However, AMPD2 gene defect caused dramatic changes of glucose and lipid metabolism in liver through changes of AMPK phosphorylation status. These studies revealed the functional relevance of AMPD in mabolism and further studies are awaited.
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[Journal Article] Remote reperfusion lung injury is associated with AMP deaminase 3 activation and attenuated by inosine monophosphate.2007
Author(s)
Li P, Ogino K, Hoshikawa Y, Morisaki H, Cheng J, Toyama K, Morisaki T, Hashimoto K, Ninomiya H, Tomikura-Shimoyama Y, Igawa O, Shigemasa C, Hisatome I
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Journal Title
Circulation Journal 71巻
Pages: 591-596
Description
「研究成果報告書概要(和文)」より
Peer Reviewed
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[Journal Article] Remote reperfusion lung injury is associated with AMP deaminase 3 activation and attenuated by inosine monophosphate.2007
Author(s)
Li P, Ogino K, Hoshikawa Y, Morisaki H, Cheng J, Toyama K, Morisaki T, Hashimoto K, Ninomiya H, Tomikura-Shimoyama Y, Igawa O, Shigemasa C, Hisatome I.
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Journal Title
Circulation Journal 71
Pages: 591-596
Description
「研究成果報告書概要(欧文)」より
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