摘要
为进一步了解中枢神经系统中选择性易损伤的分子机制,采用大鼠短暂前脑缺血再灌流损伤动物模型,应用Northern杂交、原位杂交及免疫组织化学方法,检测了hsp70及bcl-2基因的表达及其组织学分布。发现易损伤的海马CA1区锥体细胞出现hsp70基因的诱导表达,BCL-2蛋白合成受抑制;而耐受缺血的海马CA3区锥体细胞则明显地持续表达BCL-2蛋白,却未见明显的hsp70基因表达。因此提示,hsp70基因的表达是神经元缺血的应激指征,也可能对神经元有保护作用;
In order to study the molecular mechanism of the selective vulnerability in central nervous system,the expression and distribution of hsp70 and BCL 2 gene were detected by using Northern blot analysis , in situ hybridization and histochemistry method in transient forebrain ischemia and reperfusion rats It was found that hsp70 gene expression occurred and the synthesis of BCL 2 protein was inhibited in hippocampalCA 1 region vulnerable to ischemia,while BCL 2 protein was stained strongly and the signals of hsp70 were not observed in CA 3 region resistant to ischemia The results indicate that the expression of hsp70 gene may be not only as a marker for neuron ischemia,but also play a protective role in the neuronal injury BCL 2, meanwhile, may have neuro protective effect on the ischemic neurons
出处
《中国应用生理学杂志》
CAS
CSCD
1997年第3期224-227,共4页
Chinese Journal of Applied Physiology
关键词
脑缺血
再灌流
海马结构
基因表达
cerebral ischemia and reperfusion
hippocampal formation
gene expression
selective vulnerability