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腺病毒介导的基质细胞衍生因子-1对心肌梗死大鼠心脏功能的影响
引用本文:王杨,张娟,唐俊明,杨建业,王家宁,孔霞,郭凌郧,郑飞,黄永章.腺病毒介导的基质细胞衍生因子-1对心肌梗死大鼠心脏功能的影响[J].第四军医大学学报,2009(15):1375-1378.
作者姓名:王杨  张娟  唐俊明  杨建业  王家宁  孔霞  郭凌郧  郑飞  黄永章
作者单位:郧阳医学院附属人民医院临床医学研究所;郧阳医学院国际药护学院;郧阳医学院生理学教研室;
基金项目:国家自然科学基金(30700306); 湖北省卫生厅重点项目(JX3B29); 湖北省自然科学基金(2005ABA079); 湖北省教育厅重点项目B类(B200624006)
摘    要:目的:探索腺病毒介导的基质细胞衍生因子-1对心肌梗死心脏功能的影响.方法:采用成年SD大鼠,经左冠状动脉前降支结扎建立急性心肌梗死模型.术后1h,将1×10^10 PFU Adv—SDF-1分6个点注射到心肌梗死部位及其周边区域.移植后4wk测定心脏功能,随后取材、连续冰冻切片,观察CD133和CD31的表达以及心肌组织形态学.结果:注射在心肌梗死部位的Adv—SDF-1高表达,促进了CD133和CD31阳性细胞迁移到心肌梗死部位,增加了心肌梗死部位毛细血管的密度(Ad—SDF-1组与模型组和Ad—LacZ组相比:32±4vs15±2,16±3,P〈0.05),保护并促进了心肌再生,从而缩小梗死区域面积,心室壁的厚度和弹性增加;心室胶原含量减少Ad—SDF-1组与模型组和Ad—LacZ组相比:(41±3)%vs(78±8)%,(76±7)%,P〈0.05],延缓心室重构而改善心脏的收缩和舒张功能.结论:SDF-1过表达通过促进血管新生改善心肌的血供,达到改善心脏功能的目的.

关 键 词:人基质细胞衍生因子-1  腺病毒科  心肌梗塞  新生血管化  病理性

Effect of adenovirus-mediated stromal cell-derived-factor-1 alpha gene transfer on heart function in myocardial infarction of rats
WANG Yang,ZHANG Juan,TANG Jun-Ming,YANG Jian-Ye,WANG Jia-Ning,KONG Xia,GUO Ling-Yun,ZHENG Fei,HUANG Yong-ZhangInstitute of Clinical Medicine,People's Hospital.Effect of adenovirus-mediated stromal cell-derived-factor-1 alpha gene transfer on heart function in myocardial infarction of rats[J].Journal of the Fourth Military Medical University,2009(15):1375-1378.
Authors:WANG Yang    ZHANG Juan  TANG Jun-Ming  YANG Jian-Ye  WANG Jia-Ning  KONG Xia  GUO Ling-Yun  ZHENG Fei  HUANG Yong-ZhangInstitute of Clinical Medicine  People's Hospital
Institution:WANG Yang1,2,3,ZHANG Juan1,TANG Jun-Ming1,YANG Jian-Ye1,WANG Jia-Ning1,KONG Xia1,GUO Ling-Yun1,ZHENG Fei1,HUANG Yong-Zhang11Institute of Clinical Medicine,People's Hospital,2Institute of Pharmacy and Nursing,3Department of Physiology,Yunyang Medical College,Shiyan 442000,China
Abstract:AIM: To explore the effect of adenovirus-mediated stromal cell-derived-factor-1 ( Adv-SDF-1 ) alpha on angiogenesis and heart function of myocardial infarction in rats. METHODS: The animal model of myocardial infarction (MI) was established by occluding the rat left anterior descending arteries (LAD). 1 × 10^10 PFU Adv-SDF-1 or 1 × 10^10 PFU Ad-LacZ was immediately injected into the infarcted myocardium, and 200 μL cell-free PBS was injected into the infarcted region or the myocardial wall in control and sham group, respectively. Four weeks after injection, cardiac function was analyzed. Heart tissues were taken after the measurement of hemodynamics. Histological and morphometric measurement was performed by image analysis system and expressions of CD133 and CD31 were detected by immunofluorescent histochemistry. RESULTS: Significantly higher expression of Adv-SDF-1 was observed in the Adv-SDF-1 injected MI areas, which promoted CD133 and CD31 positive cells migrating into the infarcted hearts, enhanced the density of blood vessels, and contributed to the protection and regeneration of myocardium. Decreased infarct size, reduced collagen contents and thicker left ventricle wall were observed in Adv-SDF-1 group. These changes of structure in the infarcted hearts improved the systolic and diastolic function of the heart. CONCLUSION: The high expression
of SDF-1 improves cardiac structure and function of MI through angiogenesis.
Keywords:hSDF-1  adenoviridae  myocardial infarction  neovascularization  pathologic  
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