期刊文献+

对SNI和CCI两种大鼠神经病理性疼痛模型的实验观察 被引量:8

Experimental observation of SNI and CCI two kinds of rat neuropathic pain models
下载PDF
导出
摘要 目的观察并比较大鼠坐骨神经分支选择性损伤(SNI)和慢性坐骨神经压迫损伤(CCI)两种神经病理性模型引起疼痛的效果。方法 Wistar大鼠30只,随机分为3组:Sham组(n=10)、SNI组(n=10)和CCI组(n=10)。Sham组仅暴露坐骨神经后缝合皮肤,分别制作SNI模型和CCI模型,于术前及术后28d内测定大鼠术侧机械疼痛阈值,并于术后第14天和第28天行Western Blotting检测大鼠背根神经节(DRG)内疼痛相关基因三磷酸环化水解酶1(GCH1)的表达变化。结果 Sham组大鼠术后未见疼痛敏感症状,SNI组和CCI组大鼠疼痛阈值于术后第1天较Sham组显著降低(P<0.05),SNI组疼痛阈值直至术后第28天都维持在较低水平,而CCI组痛阈值于术后第3天起才趋于稳定,术后21d开始痛敏症状有所缓解。Western Blotting检测显示,术后第14天SNI组和CCI组GCH1表达均高于Sham组(P<0.05),术后第28天CCI组GCH1表达有所降低,与SNI组出现显著性差异(P<0.05)。结论相比传统CCI模型,SNI模型是一种更敏感、更稳定的神经病理性疼痛模型。 Objective To observe and compare the efficacy of 2 neuropathic pain models: spared nerve injury model (SNI) and chronic constriction injury of sciatic nerve model (CCI).Methods 30 Wistar rats were dividedrandomly into 3 groups : sham group (n= 10), SNI group (n= 10), and CCI group (n= 10 ). In the sham group, the sciatic nerves of rats were just surgically exposed,and the SNI model and CCI model were operated on the rightposterior limb. The mechanical withdrawal threshold (MWT) were tested from the lth day preoperative to the 28th day postoperative,and GTP cyclohydrolase 1 (GCH1), which is a kind of pain-related gene, in dorsal root gan-glion was measured by Western blotting on the 14th and 28th days postoperative.Results The rats in sham group did not appear hyperalgia. MWT in both SNI group and CCI group were obviously declined on the lth day postoper-ative compared with Sham group (P〈0.05). MWT of SNI rats keeped a low level to the 28th day postoperative, but MWT in CCI group rose again from the 21th day postoperative. The results of Western blotting showed that,onthe 14th day after the operation, the expression of GCH1 in both SNI and CCI group increased compared with sham group (P〈0.05) ,but on the 28th day it decreased in CCI group,and there were statistical differences comparedwith SNI group (P〈0.05). Conclusion Compared with CCI model,SNI model is a more sensitive and stable neuropathic pain model.
出处 《济宁医学院学报》 2013年第1期22-24,27,共4页 Journal of Jining Medical University
基金 山东省教育厅高校科技计划资助课题(J11LF19)
关键词 神经病理性疼痛 大鼠 动物模型 GCH1 Neuropathic pain Rat Animal model GCH1
  • 相关文献

参考文献13

  • 1Decosterd I, Woolf CJ. Spared nerve injury: an animal model of persistent peripheral neuropathic pain[J]. Pain, 2000,87 (2) :149-158.
  • 2Bennett GJ ,Xie YK. A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man [J]. Pain, 1988,33 ( 1 ) : 87-107.
  • 3Tegeder I,Costigan M, Griffin RS, et al. GTP eyelohydrolase and tetrahydrobiopterin regulate pain sensitivity and persist- ence[J]. Nat Med, 2006,12 ( 11 ) : 1269-1277.
  • 4Zhang L,Rao F,Zhang K,et al. Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1)governing nitric oxide,autonomic activity, and cardiovascular risk[J]. J Clin Invest,2007,117(9) :2658-2671.
  • 5Kealey C, Roche S, Claffey E, et al. Linkage and candidate gene analysis of 14q22-24 in bipolar disorder support for GCHI as a novel susceptibility gene[J]. Am J Med Genet B Neuropsychiatr Genet, 2005,136B(1) : 75-80.
  • 6Chaplan SR,Bach FW, Pogrel JW, et al. Quantitative assess- ment of tactile allodynia in the rat paw[J]. Journal of neuro- science methods, 1994,53 (1) : 55-63.
  • 7Siniscalco D,Fuccio C,Giordano C,et al. Role of reactive oxy- gen species and spinal cord apoptotic genes in the develop- ment of neuropathic pain[J]. Pharmacol Res,2007,55(2): 158-166.
  • 8Kramar EA,Lin B,Lin CY,et al. A novel mechanism for the facilitation of theta-induced long-term potentiation by brain- derived neurotrophic factor [J]. J Neurosci, 2004, 24 ( 22 )5151-5161.
  • 9Boettger MK, Till S, Chen MX, et al. Calcium-activated po- tassium channel SKl-and IKl-like immunoreactivity in in- jured human sensory neurones and its regulation by neuro- trophic factors[J]. Brain, 2002,125(Pt 2) :252-263.
  • 10王红,冯泽国,徐龙河,周晓巍,张宏.坐骨神经慢性挤压伤模型大鼠行为学及形态学变化[J].中国组织工程研究与临床康复,2007,11(23):4590-4593. 被引量:10

二级参考文献33

  • 1刘甬民,姚尚龙,宋文阁,刘东,王月兰,曾涟.不同神经病理性疼痛模型下钠通道αⅢmRNA表达的改变[J].临床麻醉学杂志,2005,21(5):344-346. 被引量:2
  • 2Jarvis MF, Boyce-Rustay JM. Neuropathic pain: models and mechanisms[J].Curr Pharm Des, 2009, 15 (15): 1711-1716.
  • 3Decosterd I, Woolf CJ. Spared nerve injury: an animal model of persistent peripheral neuropathie paln[J]. Pain, 2000, 87 (2) :149-158.
  • 4Bennett GJ,Xie YK. A Peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man[J]. Pain,1988,38:87-107.
  • 5Kawakami M,Weinstein JN,Spratt KF,et al. Experimen- tal lumbar radiculopathy. Immunohistochemical and quan- titative demonstrations of pain induced by lumbar nerve root irritation of the rat[J]. Spine, 1994, 19 (16) : 1780- 1794.
  • 6Chaplan SR, Bach FW, Pogrel JW, et al. Quantitative assess- ment of tactile a[lodynia in the rat paw[J]. Neurosei Meth- ods,1994,53(1):55-63.
  • 7Dixon WJ. Efficient analysis of experimental observation[J]. Ann Rev Pharmacol Toxicol, 1980,20 : 441-462.
  • 8Hargreaves K,Dubner R,Brown F, et al. A new and sensitive method for measuring thermal nociception in cutaneous hy- peralgesia[J]. Pain, 1988,32 (1) : 77-88.
  • 9Forerun H J, Fukuto JM, Miller T, et al. The chemistry of cell signaling by reactive oxygen and nitrogen species and 4 hydroxynonenal[J]. Arch Biochem Biophys, 2008,477 (2) : 183-195.
  • 10Varija D, Kumar KP, Reddy KP, et al. Prolonged constric tion of sciatic nerve affecting oxidative stressors and an- tioxidant enzymes in rat[J]. Indian J Med Res, 2009,129 (5):587.

共引文献17

同被引文献38

引证文献8

二级引证文献31

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