期刊文献+

慢性痛大鼠背根神经元基因表达的研究 被引量:2

Study on Gene Expression of Neurons in Dorsal Root Ganglia of Rat with Neuropathic Pain
下载PDF
导出
摘要 目的研究与慢性痛相关基因的特异表达,比较大鼠背根神经节损伤神经元与正常神经元之间基因表达的差异,以寻找构成神经病性疼痛的内在因素。方法应用mRNA差异显示方法从损伤背根神经节中寻找特异表达的基因。结果损伤侧背根节中cDNA条带(25.75±4.7)明显多于对照侧(18.0±5.0)。反向杂交后进行亚克隆得到10个含插入片段的阳性质粒,并对其中4个进行测序。结论神经轴突损伤可导致胞体基因表达改变,其中某些可能与痛觉异常有关,也可能与细胞结构恢复及免疫功能改变有关。 Objective To study the specific expression gene related chronic pain and to investigate on intrinsic reason of neuropathic pain, gene expressions were compared between normal neurons and injured ones of DRGs from rats. Methods mRNA differential display was used in searching for specific expression gene from injured dorsal root ganglia neurons of chronic constriction injury (CCI) rats. Results It was found that cDNA bands were significantly increased in CCI DRGs (25.7 ± 5 4. 7) than in normal ones (18.0 ±5.0). 10 plasmas with inserted genes were obtained from subclones after inverse hybridization, and 4 of them were sequenced. Conclusions It has been proved that axon injury of the neuron can result in alteration in genes expression of the cell soma, some of which may be involved in allodynia, others may be related to cell's structure reconstruction or change in immunological functions.
出处 《中国神经免疫学和神经病学杂志》 CAS 2006年第3期144-149,共6页 Chinese Journal of Neuroimmunology and Neurology
基金 国家自然科学基金资助项目(39770247 39830150)
关键词 背根神经节 基因表达 慢性痛 MRNA差异显示 dorsal root ganglia gene expression neuropathic pain, mRNA differential display
  • 相关文献

参考文献12

  • 1Dyck PJ, Tomas PK, Griffin JW, et al. Peripheral neuropathy [M]. 3rd ed. Saunders:Philadelphia,1993.30-34, 82-94.
  • 2Ying JS, Richard TA. Pathways that elicit long-term changes in gene expression in nociceptive neurons following nerve injury:contributions to neuropathic pain[J]. Neurol Res, 2004, 26: 195-203.
  • 3谢益宽,肖文华,李惠清.神经损伤区新生离子通道与异常电活动的关系[J].中国科学(B辑),1991(12):1289-1294. 被引量:14
  • 4Lewin GR, Mendell LM. Nerve growth factor and nociception [J]. Trends Neurosci, 1993, 16:353-359.
  • 5Donnerer J, Schuligoi R, Stein C. Increased content and transport of substance P and calcitonin gene-related peptide in sensory nerve innervating inflamed tissue:evidence for a regulatory function of growth factor in vivo [J]. Neuroscience, 1992, 49:693-698.
  • 6Cho HJ, Kim SY, Park MJ,et al. Expression of mRNA for brain-derived neurotrophic factor in the dorsal root ganglion following peripheral inflammation [J].Brain Research, 1997, 749:358-362.
  • 7Bennett GJ, Xie YK. Peripheral mononeuropathy in rat that produces disorders of pain sensation like these seen in man [J]. Pain, 1988,33: 87-107.
  • 8萨姆布鲁克丁,佛里奇 EF,曼尼呵帝斯 T.分子克隆实验指南[M].第2版.北京:科学出版社,1992.304-311.
  • 9Zhang XL, Peng XQ, Jing YL, et al. Sialic acid contributes to generation of ectopic spontaneous discharges in rats with neuropathic pain [J]. Neurosci Lett,2003,346 : 65-68.
  • 10Peng XQ, Zhang XL, Fang Y, et al. Sialic acid contributes to hyperexcitability of dorsal root ganglion neurons in rats with peripheral nerve injury [J]. Brain Res, 2004,1026:185-193.

共引文献13

同被引文献27

引证文献2

二级引证文献7

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