OPC-28326, a selective femoral arterial vasodilator, augments ischemia induced angiogenesis

被引:5
作者
Sumi, Makoto
Sata, Masataka
Hashimoto, Ayako
Imaizumi, Takashi
Yanaga, Katsuhiko
Ohki, Takao
Mori, Toyoki
Nagai, Ryozo
机构
[1] Univ Tokyo, Grad Sch Med, Dept Cardiovasc Med, Bunkyo Ku, Tokyo 1138655, Japan
[2] Jikei Univ, Sch Med, Dept Surg, Tokyo 1058471, Japan
[3] Univ Tokyo, Grad Sch Med, Dept Adv Clin Sci & Therapeut, Bunkyo Ku, Tokyo 1138655, Japan
[4] Otsuka Pharmaceut Co Ltd, Res Inst Pharmacol & Therapeut Dev, Tokushima 7710192, Japan
关键词
angiogenesis; OPC-28326; ischemia; Akt; eNOS;
D O I
10.1016/j.biopha.2006.12.004
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
OPC-28326,4-(N-methyl-2-phenylethylamino)-1-(3,5-dimethyl-4-propionyl-aminobenzoyl) piperidine hydrochloride monohydrate, is a newly developed selective peripheral vasodilator and increases blood flow to lower extremities with alpha 2-adrenergic antagonist property. Here, we investigated the effect of OPC-28326 on ischemia-induced angiogenesis. OPC-28326 enhanced tube formation by human aortic endothelial cells (HAECs). Moreover, OPC-28326 enhanced the number of microvessels sprouting from aortic rings embedded in collagen gel. OPC-28326 markedly induced phosphorylation of endothelial nitric oxide synthase (eNOS) in HAECs via phosphatidylinositol-3 kinase PI3K/Akt (PI3K/ Akt) pathway. Next, the angiogenic effect of OPC-28326 was evaluated in a mouse hindlimb ischemia model. Blood flow recovery to the ischemic leg was significantly enhanced by OPC-28326. Furthermore, anti-CD31 immunostaining revealed that OPC-28326 increased capillary density in the ischemic muscle. However, OPC-28326 failed to promote blood flow recovery in ischemic hindlimb in eNOS-deficient mice. These results suggest that OPC-28326 promotes angiogenesis, which was associated with activation of eNOS via PI3K/Akt pathway. OPC-28326 might be promising to treat patients with ischemic vascular diseases. (C) 2006 Published by Elsevier Masson SAS.
引用
收藏
页码:209 / 215
页数:7
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