重组人粒细胞集落刺激因子对缺血缺氧性脑损伤新生大鼠凋亡诱导因子表达的影响
[Abstract]:Aim: to study the effect of recombinant human granulocyte colony stimulating factor (rhGCSF) on the expression of apoptosis-inducing factor in neonatal SD rats. Methods: Thirty-six 7-day-old SD rats were randomly divided into sham-operated group (group A), cerebral ischemia-reperfusion group (group B) and drug therapy group (group C) with 12 rats in each group. The cerebral artery occlusion reperfusion model of rats was established by Longa thread occlusion. Rats in group C were perfused with drugs at 2 hours and 24 hours after cerebral ischemia, and the other two groups were given the same amount of 0.9% sodium chloride injection. At the end of the experiment, the nerve function of the rats was evaluated by the standard Longa scoring method at 24 h, and the phosphorylated c-jun amino-terminal kinases in the tissues of the rats were assessed by immunohistochemical method. Extracellular signal regulated protein kinase (ESRK) was detected by phosphorylation and in situ terminal transferase (TTC) staining was used to detect the volume of cerebral infarction. The expression of apoptosis-related genes and the level of apoptosis were evaluated. Results A large number of apoptotic cells were found in group B _ (2) after 24 hours of perfusion, and the nuclei were brown, mainly distributed in ischemic brain tissue. The degree of cerebral infarction in group C was less than that in group B (P0.01). Conclusion: recombinant human granulocyte colony stimulating factor can protect newborn SD rat neurons from ischemic hypoxic brain injury. This glycoprotein is related to the expression of apoptosis-related genes.
【作者单位】: 上海交通大学医学院附属第九人民医院儿科;
【基金】:上海市高校选拔优秀青年教师专项基金(ZZjdyx12114)
【分类号】:R742
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