Everolimus-eluting stents improve vascular response in a diabetic animal model.
Everolimus-eluting stents improve vascular response in a diabetic animal model.
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DOI:
10.1161/circinterventions.113.001023
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发表时间:
2014-08
期刊:
影响因子:
--
通讯作者:
Finn AV
中科院分区:
文献类型:
--
作者:
Habib A;Karmali V;John MC;Polavarapu R;Nakazawa G;Pachura K;Davis T;Kolodgie FD;Virmani R;Finn AV
Pre-clinical evaluation of the vascular response of drug eluting stents (DES) is limited especially in the setting of diabetes mellitus (DM) preventing the evaluation of changes in DES design and eluted drugs until after clinical use. Cultured human aortic endothelial cells (HAEC) were used to assess the differences between sirolimus (SRL) and its analog, everolimus (EVL), in the setting of hyperglycemia on various cellular functions necessary for endothelial recovery. A diabetic rabbit model of iliac artery stenting was used to compare histologic and morphometric characteristics of the vascular response to everolimus-eluting (EES), sirolimus-eluting (SES) and bare metal stent (BMS) placement. Under hyperglycemic conditions, SRL impaired HAEC endothelial barrier function, migration and proliferation to a greater degree compared with EVL. In our in vivo model of diabetes, endothelialization at 28 days was significantly lower and endothelial integrity was impaired in SES when compared to both EES and BMS. Neointimal area, uncovered struts and fibrin deposition was significantly higher in SES when compared to EES and BMS. Use of EES results in improved vascular response in our pre-clinical models of diabetes.