Project/Area Number |
24591100
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Circulatory organs internal medicine
|
Research Institution | Fukushima Medical University |
Principal Investigator |
|
Co-Investigator(Kenkyū-buntansha) |
OIKAWA Masayoshi 福島県立医科大学, 医学部, 助教 (30457775)
SUZUKI Satoshi 福島県立医科大学, 医学部, 助教 (60536944)
|
Co-Investigator(Renkei-kenkyūsha) |
ISHIGAMI Akihito 地方独立行政法人東京都健康長寿医療センター, 東京都健康長寿医療センター研究所, 研究部長 (50270658)
|
Project Period (FY) |
2012-04-01 – 2015-03-31
|
Project Status |
Completed (Fiscal Year 2014)
|
Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2012: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
|
Keywords | SMP30 / doxorubcin / oxidative stress / signal transduction / heart failure / ROS / NADPH / 加齢 / 心不全 / 酸化ストレス / ドキソルビシン / アポトーシス / 遺伝子操作マウス |
Outline of Final Research Achievements |
Doxorubicin was administerd to wild type mice, SMP30 knockout mice, and transgenic mice with cardiac specific overexpression of SMP30. We demonstrated that SMP30 has a cardio-protective role by anti-oxidative and anti-apoptotic effects in doxorubicin-induced cardiotoxicity. Anti-aging gene, SMP30, can be a new therapeutic target to prevent heart failure.
|