Development of new treatment strategy in peripheral artery disease using apoA-I mimetic peptide
Project/Area Number |
26860591
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Cardiovascular medicine
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Research Institution | Fukuoka University |
Principal Investigator |
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Project Period (FY) |
2014-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
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Budget Amount *help |
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2015: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2014: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
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Keywords | ApoA-I模倣ペプチド / 下肢虚血 / 血管新生 / NO / HDL / FAMP / アポA-I模倣ペプチド / NO |
Outline of Final Research Achievements |
It is unclear whether an apoA-I mimetic peptide can promote neovascularization in vivo. Here, we investigated the effect of FAMP on endothelial nitric oxide synthase (eNOS) activation and angiogenesis in a murine hindlimb ischemia model. As a result, FAMP promoted recovery from hindlimb ischemia through a nitric oxide (NO)-related pathway by activation of a PI3K / Akt pathway. FAMP may become a new therapeutic agent for the future clinical treatment of peripheral artery disease (PAD).
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Report
(4 results)
Research Products
(4 results)
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[Journal Article] Newly developed apolipoprotein A-I mimetic peptide promotes macrophage reverse cholesterol transport in vivo.2015
Author(s)
Shimizu T, Tanigawa H, Miura S, Kuwano T, Takata K, Suematsu Y, Imaizumi S, Yahiro E, Zhang B, Uehara Y, Saku K.
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Journal Title
Int J Cardiol.
Volume: 192
Pages: 82-88
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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