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オクヤマ ミチヒロ
Michihiro Okuyama
奥山 倫弘 所属 川崎医科大学 医学部 臨床医学 心臓血管外科学 職種 講師 |
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| 言語種別 | 英語 |
| 発表タイトル | Vasohibin-2 exacerbates development of angiotensin II-induced thoracic aortic aneurysms independent of VEGF |
| 会議名 | ESC Congress 2017 |
| 学会区分 | 国際学会及び海外の学会 |
| 発表形式 | ポスター掲示 |
| 講演区分 | 一般 |
| 発表者・共同発表者 | Michihiro Okuyama, Haruhito A Uchida, Ryoko Umebayashi, Yuki Kakio, Hidemi Takeuchi, Katsuyuki Tanabe, Yasufumi Sato, Jun Wada |
| 発表年月日 | 2017/08/29 |
| 国名 | スペイン |
| 開催地 (都市, 国名) |
Barcelona |
| 開催期間 | 2017/08/26~2017/08/30 |
| 学会抄録 | European Heart Journal 38(suppl_1),ehx493, P5398 2017 |
| 概要 | Chronic angiotensin II (AngII) infusion promotes both thoracic (TAAs) and abdominal aortic aneurysms (AAAs) in mice. Previous studies showed that vascular endothelial growth factor (VEGF) enhanced AngII-induced AAA formation, and VEGF significantly increased Angll-induced AAA diameter in hypercholesterolemic mice. Meanwhile, vasohibin-1 (VASH1) is induced by VEGF and inhibits angiogenesis under various pathologic conditions. In contrast, a VASH1 homolog, vasohibin-2 (VASH2) promotes angiogenesis at the sprouting front of neovascularization. Therefore, we hypothesized that exogenous VASH2 influences AngII-induced TAAs in normocholesterolemic mice.
Exogenous VASH2 administration expands AngII-induced TAAs in vivo. VASH2 may accelerate MMP-2 activation. VASH2-induced cell apoptosis may influence AngII-induced TAA formation independent of VEGF. |