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普罗布考和抗氧化维生素可挽救吸烟小鼠缺血诱导的新生血管形成:内皮祖细胞的潜在作用。

Probucol and antioxidant vitamins rescue ischemia-induced neovascularization in mice exposed to cigarette smoke: potential role of endothelial progenitor cells.

机构信息

Department of Cardiovascular Research, Centre Hospitalier de l'Université de Montréal, Montréal, Québec H2L 4M1, Canada.

出版信息

Atherosclerosis. 2010 Feb;208(2):342-9. doi: 10.1016/j.atherosclerosis.2009.08.007. Epub 2009 Aug 13.

Abstract

OBJECTIVE

Cigarette smoking is associated with impaired neovascularization in response to ischemia. Potential mechanisms include increased generation of reactive oxygen species (ROS) and a reduction in the function of endothelial progenitor cells (EPCs). Here we tested the hypothesis that antioxidant therapies could stimulate EPC function and improve ischemia-induced neovascularization following cigarette smoke exposure.

METHODS AND RESULTS

C57Bl/6 mice exposed to cigarette smoke (MES) were fed a normal diet (controls) or a diet supplemented with probucol (0.5%) or a combination of vitamin C (25 g/l in drinking water) and vitamin E (0.1% in normal chow). After two weeks of treatment, hindlimb ischemia was surgically induced by femoral artery removal. Exposure to cigarette smoke was associated with a significant reduction of blood flow recuperation and vessel density in ischemic muscles. However, a complete rescue of neovascularization was demonstrated in MES treated with probucol or antioxidant vitamins. We found that antioxidant therapy in MES is associated with a significant reduction of oxidative stress levels both in the plasma and in ischemic muscles. Moreover, EPCs exposed to cigarette smoke extracts in vitro showed a significant impairment of their angiogenic activities (migration, adhesion, homing into ischemic tissues) that was completely rescued by probucol and antioxidant vitamins.

CONCLUSIONS

Probucol and antioxidant vitamins rescue cigarette smoke-dependent impairment of ischemia-induced neovascularization. The mechanisms involve beneficial effects on oxidative stress levels in ischemic tissues together with an improvement of EPC functional activities. Antioxidant therapy could constitute a novel therapeutic strategy to promote vessel growth and reduce tissue ischemia in atherosclerotic diseases.

摘要

目的

吸烟与缺血后血管新生受损有关。潜在的机制包括活性氧(ROS)生成增加和内皮祖细胞(EPC)功能降低。在这里,我们检验了抗氧化治疗可以刺激 EPC 功能并改善吸烟暴露后缺血诱导的血管新生的假说。

方法和结果

暴露于香烟烟雾(MES)的 C57Bl/6 小鼠给予正常饮食(对照组)或补充普罗布考(0.5%)或维生素 C(饮用水中 25g/L)和维生素 E(正常饲料中 0.1%)的饮食。治疗两周后,通过股动脉切除术诱导后肢缺血。香烟烟雾暴露与缺血肌肉中的血流恢复和血管密度显著降低有关。然而,MES 用普罗布考或抗氧化维生素治疗完全挽救了血管新生。我们发现,MES 中的抗氧化治疗与血浆和缺血肌肉中氧化应激水平的显著降低有关。此外,体外暴露于香烟烟雾提取物的 EPC 显示其血管生成活性(迁移、黏附、归巢至缺血组织)显著受损,普罗布考和抗氧化维生素完全挽救了这一损伤。

结论

普罗布考和抗氧化维生素可挽救吸烟依赖性缺血诱导的血管新生受损。其机制涉及对缺血组织中氧化应激水平的有益影响,以及 EPC 功能活性的改善。抗氧化治疗可能是促进血管生长和减少动脉粥样硬化疾病中组织缺血的一种新的治疗策略。

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