2013 Fiscal Year Final Research Report
Potential mechanisms and therapeutic strategies of sarcopenia
Project/Area Number |
22390143
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
General internal medicine (including Psychosomatic medicine)
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Research Institution | Nagoya University |
Principal Investigator |
KUZUYA Masafumi 名古屋大学, 医学(系)研究科(研究院), 教授 (10283441)
|
Co-Investigator(Renkei-kenkyūsha) |
CHENG Xian Wu 名古屋大学, 医学系研究科, 特任准教授 (30378228)
|
Project Period (FY) |
2010-04-01 – 2014-03-31
|
Keywords | 老化 / サルコペニア / 動物 |
Research Abstract |
To examine the effect of bone marrow stem cells as well as exercise on the age-associated skeletal muscle atrophy and weakness (sarcopenia), senescence-accelerated-prone mouse (SAMP10) were transplanted with bone marrow of wild-type (C57BL/6) at 8 weeks of age. Control non-transplant and transplant SMAP10 were randomly assigned to 2 groups with or without exercise training (from 25 weeks of age). At 40 weeks of age, muscle weight, endurance capacity, and the tissue biochemical analysis were carried out. These studies provide the evidences that the bone marrow-derived stem cells differentiate into skeletal muscle cells. Bone marrow transplantation of wild type mice improves the age-associated skeletal muscle atrophy and weakness (sarcopenia), suggesting that aging of bone marrow cells may contribute to the cause of sarcopenia of SAMP10. In addition, exercise can prevent sarcopenia through the prevention of muscle protein degradation and mitochondrial activation in SAMP10.
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Research Products
(7 results)