基础医学与临床 ›› 2009, Vol. 29 ›› Issue (1): 29-32.

• 研究论文 • 上一篇    下一篇

VEGF降低家兔脑缺血再灌注损伤与caspase-3表达的关系

杨冀萍 刘新峰 刘怀军 张仁良 殷勤 李芸   

  1. 河北医科大学第二医院医学影像科 南京军区总医院神经内科 河北医科大学第二医院医学影像科 南京军区总医院神经内科 南京军区总医院神经内科 南京军区总医院神经内科
  • 收稿日期:2007-06-26 修回日期:2008-08-11 出版日期:2009-01-25 发布日期:2009-01-25
  • 通讯作者: 刘新峰

Relationship between VEGF decreases cerebral ischemia/reperfusion injury and the expression of caspase-3 in rabbits

Ji-ping YANG, Xin-feng LIU, Huai-jun LIU, Ren-liang ZHANG, Qin YIN, Yun LI   

  1. Dept. of Medicine Imaging, the Second Hospital, Hebei Medical University Dept. of Neueology, Jinling Hospital, Nanjing University School of Medicine Dept. of Medicine Imaging, the Second Hospital, Hebei Medical University Dept. of Neueology, Jinling Hospital, Nanjing University School of Medicine Dept. of Neueology, Jinling Hospital, Nanjing University School of Medicine Dept. of Neueology, Jinling Hospital, Nanjing University School of Medicine
  • Received:2007-06-26 Revised:2008-08-11 Online:2009-01-25 Published:2009-01-25
  • Contact: Xin-feng LIU,

摘要: 目的 探讨血管内皮生长因子(VEGF)治疗家兔局灶性脑缺血/再灌注损伤与半胱氨酸蛋白酶-3(caspase-3)表达的关系。 方法 复制兔局灶性脑缺血/再灌注模型,分别在缺血2 h,再灌注0、1和3 h应用微量进样器将VEGF立体定向导入梗死灶周,于再灌注3 d观察神经功能、梗死体积、水肿体积、灶周凋亡数和caspase-3表达。 结果 缺血/再灌注0和1 h时,灶周给予VEGF,梗死体积分别较对照组下降23.3%、17.9%,相应的水肿体积、灶周凋亡率及caspase-3表达明显下降(P均<0.01),神经功能恢复较好,用药越早越明显;再灌注3 h后给药,则无明显作用。梗死体积下降与caspase-3表达下降明显相关(P<0.05)。 结论 VEGF可能通过抑制caspase-3的表达减少脑缺血/再灌注损伤细胞凋亡的发生。

Abstract: Objective To study the relationship between VEGF decreases focal cerebral ischemia/reperfusion injury in rabbits and the expression of cysteinyl aspirate-specific proteinase-3 (caspase-3) protein. Methods Focal cerebral ischemia/reperfusion model in rabbit was induced. The VEGF was administered at 0, 1 and 3 h after reperfusion respectively. Infarct and edema volumes, neurological deficit score, apoptotic cells, and expression of caspase-3 were assessed at 3 d after reperfusion. Results VEGF reduced infarct volumes compared with controls by 23.3% and 17.9% when administered VEGF at 0 and 1 h after reperfusion. Edema volumes, apoptotic cells and expression of caspase-3 in the perifocal regions were significantly lower than that in control group when administered VEGF within 1h after reperfusion (P<0.01). There was no difference when administered VEGF at 3h after reperfusion. Infarct volumes were correlated significantly with expression of caspase-3 in the perifocal regions (P<0.05). Conclusions The effect of VEGF on the expression of caspase-3 is related with the neuroprotective time window. The VEGF can reduce the incidence of neuronal apoptosis during the cerebral ischemia/reperfusion injury by reducing the expression of caspase-3 protein.