期刊文献+

CGRP和NGF对局灶性脑缺血再灌注大鼠海马p53蛋白表达的影响 被引量:7

THE EFFECTS OF CALCITONIN GENE RELATED PEPTIDE AND NERVE GROWTH FACTOR ON THE EXPRESSION OF p53 PROTEIN DURING FOCAL CEREBRAL ISCHEMIA/REPERFUSION IN RATS
下载PDF
导出
摘要 为了探讨外源性降钙素基因相关肽(CGRP)和神经生长因子(NGF)对局灶性脑缺血再灌注大鼠海马p53蛋白表达的影响,用线栓法制备大鼠大脑中动脉阻塞模型,应用免疫组化和显微图像分析方法检测脑缺血再灌注后大鼠海马CA1区p53蛋白的表达。结果如下:假手术组海马CA1区未见p53阳性细胞,而脑缺血再灌注组阳性细胞明显增多。分别注射CGRP或NGF后海马CA1区p53阳性细胞平均灰度值均明显高于缺血再灌注组(P<0.05),二者联合应用时平均灰度值较单独应用高(P<0.05)。以上结果提示:CGRP和NGF下调缺血神经元p53蛋白的表达,二者合用作用更强,可能对缺血神经元的恢复有促进作用。 To study the effects of calcitonin gene related peptide (CGRP) and nerve growth factor (NGF) on the expression of p53 protein in hippocampus of rats with focal cerebral ischemia/reperfusion (I/R), middle cerebral artery occlusion (MCAO) was employed to make focal cerebral ischemia, the expression of p53 protein was detected with SABC immunohistochemical method and analyzed by using microimage analysis system. The results showed that the number of p53 protein-positive cells in hippocampus CA1 was obviously increased in focal cerebral I/R group, whereas p53 protein-positive neurons were not observed in sham group. The average gray densities of p53 protein-positive product in CGRP or NGF group were higher compared with I/R group( P<0.05 ). Furthermore, the gray density in CGRP & NGF group was even higher than that in CGRP or NGF group ( P <0.05). The present results indicate that CGRP and NGF downregulate the expression of p53 protein in ischemia neurons and they may cooperate with each other and promote the recovery of the ischemia neurons.
出处 《神经解剖学杂志》 CAS CSCD 北大核心 2005年第2期124-128,共5页 Chinese Journal of Neuroanatomy
基金 辽宁省自然科学基金(No. 619019)资助项目
关键词 局灶性脑缺血 大鼠 海马 P53蛋白 神经生长因子 降钙素基因相关肽 CGRP GF 基因表达 focal cerebral ischemia, calcitonin gene related peptide, nerve growth factor, p53, hippocampus, rat
  • 相关文献

参考文献18

  • 1丁爱石,王福庄,杨宏,陈正英,王良友.降钙素基因相关肽对缺氧时大鼠海马培养神经元c—fos表达的影响[J].神经科学,1997,4(3):110-114. 被引量:23
  • 2王福庄,刘振伟,要航,丁爱石,黄燕华.降钙素基因相关肽对缺氧时海马细胞内游离Ca^(2+)的影响[J].中国应用生理学杂志,1994,10(4):325-328. 被引量:26
  • 3张拥波,董为伟.大鼠局灶性脑缺血后CPP32和P53蛋白的表达[J].卒中与神经疾病,2002,9(3):131-133. 被引量:6
  • 4Yuen EC, Mobley WC. Therapeutic potential of neurotrophic factors for neurological disorders. Ann Neurol, 1996 ;40:346 -354.
  • 5Li Y, Chopp M, Zhang Z et al. p53-immunoreactive protein and p53 mRNA expression after transient middle cerebral artery occlusion in rats. Stroke, 1994 ;25:849 - 856.
  • 6Crumrine RC, Thomas AL, Morgan PF et al. Attenuation of p53expression protects against focal ischemic damage in transgenic mice. J Cereb Blood Flow Metab, 1994 ;4:887 -891.
  • 7Longa EZ, Weinstein PR, Carlson S et al. Reversible middle cerebral artery occlusion without craniectomy in rats. Stroke, 1989 ;20:84 -91.
  • 8Holland JP, Sydserff SG, Taylor WA et al. Caleitonin gene related peptide reduces brain injury in a rat model of focal cerebral ischemia. Stroke, 1994;25:2055 -2059.
  • 9Holtzman DM, Sheldon RA, Jaffe W et al. Nerve growth factor protects the neonatal brain against ischemic injury. Ann Neurol,1996 ;39:114 - 122.
  • 10Yamamoto S, Yoshimine T, Fujita T et al. Protective effect of NGF atelocollagen mini-pellet on the hippocampal delayed neuronal death in gerbils. Neurosci Lett, 1992; 141:161 - 165.

二级参考文献21

共引文献85

同被引文献115

引证文献7

二级引证文献46

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部