Examination of calcification of anastomotic site by suppression of RAGE expression
| Project/Area Number |
15K10237
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Cardiovascular surgery
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| Research Institution | University of Yamanashi |
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Principal Investigator |
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| Project Period (FY) |
2015-04-01 – 2019-03-31
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| Project Status |
Completed (Fiscal Year 2018)
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| Budget Amount *help |
¥3,250,000 (Direct Cost: ¥2,500,000、Indirect Cost: ¥750,000)
Fiscal Year 2017: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2016: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2015: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
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| Keywords | ＡＧＥ / RAGE / 内膜肥厚 |
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| Outline of Final Research Achievements |
Intimal hyperplasia is one of the most important reasons of graft occlusion.We have aimed to prevent from intimal hyperplasia to keep the graft patency. We think that the signaling of calcification would lead to further graft patency. The advanced glycation end-product (AGE) increased the proliferation of vascular smooth muscle cells. It was considered to be one of the causes of intimal thickening at the anastomosis. In the group to which AGE was administered, transformation was induced and calcification was promoted as compared with the control group.
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| Academic Significance and Societal Importance of the Research Achievements |
動脈硬化症に対するバイパス術の患者は増加傾向にある。静脈グラフトを使用したバイパス閉塞は、吻合部での血管内膜肥厚が主たる原因と考えられ、10年の間に約60％は閉塞すると報告されている。この内膜肥厚の原因として、血管平滑筋の遊走能、増殖能の亢進、細胞外基質の堆積、アポトーシス抑制によるものが主な原因とされている。。さらに臨床検体を検討すると、吻合部で石灰化をきたしていることが確認され、血管壁の石灰化もグラフト閉塞の一つの要因と考えられた。今回そのメカニズムの検討を行った。
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Report
(5 results)
Research Products
(3 results)
