Bach1 as a therapeutic target for ischemic cardiovascular diseases
Project/Area Number |
23590381
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Human genetics
|
Research Institution | Hiroshima University |
Principal Investigator |
ISHIDA Takafumi 広島大学, 医歯薬保健学研究院(医), 講師 (40346482)
|
Co-Investigator(Kenkyū-buntansha) |
ISHIDA Mari 広島大学, 大学院医歯薬保健学研究院, 講師 (30359898)
|
Project Period (FY) |
2011 – 2013
|
Project Status |
Completed (Fiscal Year 2013)
|
Budget Amount *help |
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2011: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
|
Keywords | 心血管疾患 / RNA干渉 / 酸化ストレス / 酸化ストレス応答 / 虚血 |
Research Abstract |
Bach1 is a stress-responsive transcriptional factor that orchestrates the expression levels of cytoprotective factors, including heme-oxygenase (HO)-1. In the present study, we investigated the effect of suppression of Bach1 expression on cardiac remodeling after myocardial infarction and limb ischemia in mice. Adverse cardiac remodeling and fibrosis after myocardial infarction was significantly attenuated in Bach1-deficient mice. Intramuscular administration of siRNA against Bach1 accelerated blood flow perfusion and capillary density in a hindlimb ischemia model. These results suggest that Bach1 expression can be a therapeutic target in ischemic cardiovascular diseases.
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Report
(4 results)
Research Products
(14 results)
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[Journal Article] Reorganization of damaged chromatin by the exchange of histone variant H2A.Z-2.2014
Author(s)
Nishibuchi I, Suzuki H, Kinomura A, Sun J, Liu N-A, Horikoshi Y, Shima H, Kusakabe M, Harata M, Fukagawa T, Ikura T, Ishida T, Nagata Y and Tashiro S
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Journal Title
Int. J Radiation Oncol Biol Phys.
Volume: 89/90
Related Report
Peer Reviewed
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[Journal Article] Species differences of macrophage very low-density-lipoprotein (VLDL) receptor protein expression2011
Author(s)
Takahashi S, Ito T, Zenimaru Y, Suzuki J, Miyamori I, Takahashi M, Ishida T, Hirata K, Yamamoto TT, Iwasaki T, Hattori H, Shiomi M
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Journal Title
Biochem Biophys Res Commun
Volume: 407
Pages: 656-662
Related Report
Peer Reviewed
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[Journal Article] Species differences of macrophage very low-density-lipoprotein (VLDL) receptor protein expression.2011
Author(s)
Takahashi S, Ito T, Zenimaru Y, Suzuki J, Miyamori I, Takahashi M, Takahashi M, Ishida T, Ishida T, Hirata K, Yamamoto TT, Iwasaki T, Hattori H, Shiomi M
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Journal Title
Biochem Biophys Res Commun.
Volume: 407
Pages: 652-662
Related Report
Peer Reviewed
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[Journal Article] Reorganization of Damaged Chromatin by the Exchange of Histone Variant H2A.Z-2
Author(s)
Nishibuchi I, Suzuki H, Kinomura A, Sun J, Liu N-A, Horikoshi Y, Shima H, Kusakabe M, Harata M, Fukagawa T, Ikura T, Ishida T, Nagata Y, Tashiro S
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Journal Title
Int Journal Radiation Oncol Biol Phys
Volume: (in press)
Related Report
Peer Reviewed
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