Local insulin application on the carotid artery inhibits neointima formation

被引:4
|
作者
Chiang, Simon [1 ]
Breen, Danna M. [1 ]
Guo, June [1 ]
Mori, Yusaku [1 ,2 ]
Giacca, Adria [1 ,3 ,4 ]
机构
[1] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A8, Canada
[2] Showa Univ, Div Diabet Metab & Endocrinol, Shinagawa, Tokyo 1420064, Japan
[3] Univ Toronto, Dept Med, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A8, Canada
关键词
insulin; NPH; pluronic gel; neointima; angioplasty; restenosis; MUSCLE-CELL-MIGRATION; NITRIC-OXIDE SYNTHASE; DRUG-ELUTING STENT; TISSUE FACTOR EXPRESSION; LIPOPROTEIN-LIPASE MASS; GROWTH-FACTOR; ENDOTHELIAL-CELLS; PLATELET-AGGREGATION; CORONARY STENT; IN-VITRO;
D O I
10.1139/cjpp-2013-0038
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Anti-mitogenic agents currently used to prevent restenosis in drug-eluting stents delay re-endothelialization. Delayed re-endothelialization is now considered as the main cause of late stent thrombosis with drug-eluting stents, which emphasizes the need for new treatments. We have shown that systemic insulin treatment decreases neointimal growth and accelerates re-endothelialization after arterial injury in a rat model of restenosis. However, systemic insulin treatment cannot be given to non-diabetic individuals because of the risk of hypoglycemia. Thus, we investigated whether local insulin treatment is also effective in reducing neointimal growth after arterial injury. Rats were given local vehicle or local insulin delivered via Pluronic gel applied around the carotid artery immediately following balloon injury. Plasma glucose and systemic insulin levels were not affected by local insulin treatment. Insulin decreased intimal area at 28 days (P < 0.05) and also inhibited vascular smooth muscle cell migration by 60% at 4 days (P < 0.05). NPH (a longer-lasting insulin) also decreased neointimal area. These results indicate that local insulin treatment can lead to decreased restenosis, suggesting a protective vascular effect of insulin in vivo and that local insulin treatment, possibly via insulin-eluting stents, may be clinically relevant.
引用
收藏
页码:1086 / 1094
页数:9
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