期刊文献+

β-榄香烯对CCI模型大鼠疼痛行为学及背根神经节ERK5蛋白的影响 被引量:1

The efects of β-elemene on pain behavior and ERK5 protein in dorsal root ganglia of CCI rats
下载PDF
导出
摘要 目的观察β-榄香烯对慢性坐骨神经挤压损伤(CCI)模型大鼠疼痛行为学及背根神经节ERKS蛋白表达的影响。方法SD大鼠32只,建立CCI模型,随机分为造模组、假手术组、文拉法辛组和β-榄香烯组(n=8),对各组大鼠进行机械缩足阈值(PMWT)测定,用免疫组化法测定大鼠背根神经节中ERK5蛋白的表达情况。结果与术前1d比较,术后2d各CCI手术组的PMWT明显降低(P<0.01),说明CCI模型造模成功;与术后2d比较,β-榄香烯组和文拉法辛组术后14~28d的PMWT绝对值明显增加(P<0.05);与模型组比较,β-榄香烯组大鼠背根神经节ERK5的免疫反应积分降低,差异具有显著性(P<0.05)。结论β-榄香烯可上调CCI模型大鼠机械痛阈值,并且抑制模型大鼠背根神经节ERK5蛋白的表达从而对神经病理性疼痛起到干预作用。 Objective To investigate the effect ofβ-elemene on pain behavior and ERK5 Epression of dorsal root ganglion(DRG)in CCI rats.Methods After establishment of CCI models,,thirty-two SD rats were randomly divided into 4 groups(n=8):sham group,model group,venlafaxine group andβ-elemene group.Each rat was tested with PMWT,and ERK5 albumen expression in DRG were detected by immunohistochemistry assay.Results Compared to 1d before CCI operation,the thresholds of PMWT of every CCI operation group were significantly decreased at 2d after CCI operation(P<0.01),which indicated the successful establishment of CCI rats model.Compared to 2d after CCI operation,the PMWT thresholds were significantly increased from 14d to 28d after CCI operation inβ-elemene group and venlafaxine group(P<0.05)Compared with the model group,the integral of immune response of ERKS albumen ofDRG inβ-elemene group was significantly reduced(P<0.05).Conclusionβ-elemene can intervene neuropathic pain by up-regulating the PMWT thresholds and reducing DRG BDNF expression in CCI rats.
作者 龚敏操 陈眉 张丽娟 Gong Minchao
出处 《浙江临床医学》 2020年第10期1414-1416,共3页 Zhejiang Clinical Medical Journal
基金 浙江省医药卫生科技计划项目(2017KY510)。
关键词 Β-榄香烯 神经病理性疼痛 背根神经节 ERK5 β-elemene Neuropathic pain Dorsal root ganglion ERK5
  • 相关文献

参考文献3

二级参考文献31

  • 1杨建平,蒋豪.大鼠蛛网膜下腔埋管并长期留置操作的改进[J].中华麻醉学杂志,1993,13(2):110-112. 被引量:123
  • 2徐淑云,卞如濂,陈修.药理实验方法学[M].3版.北京:人民卫生出版社,2002:1346-1347
  • 3Old EA, Malcangio M. Chemokine mediated neuron-glia communication and aberrant signalling in neuropathic pain states. Curt" Opin Pharmacol,2012, 12:67-73.
  • 4Obata K, Katsura H, Mizushima T, et al. Roles of extracellular signal-regulated protein kinases 5 in spinal rnicroglia and primary sensory neurons for neuropathic pain. J Neurochem, 200"7, 102: 1569-1584.
  • 5Kim SH, Chung JM. An experimental model for peripheral neuropathy produced by segmental spinal nerve |igation in the rat. Pain, 1992, 50:355-363.
  • 6Chaplan SR, Bach FW, Pogtel JW, et al. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods, 1994, 53: 5553.
  • 7Hargreaves K, Dubner R, Brown F, et al. A new and sensitive method for measuring thermal nociception in cutaneous hyperalgesia. Pain, 1988, 32:77-88.
  • 8Jha MK, Jeon S, Suk K. Glia as a link between neuroinflammation and neuropathic pain. Immune Netw, 2012, 12.41 -47.
  • 9Milligan ED, Watkins LR. Pathological and protective roles of glia in chronic pain. Nat Rev Neurosci, 2009,10:23-36.
  • 10Mika J, Zychowska M, Popiolek-Barczyk K, et al. Importance of glial activation in neuropathic pain. Eur J Pharmacol,2013, 13: 171-174.

共引文献20

同被引文献38

引证文献1

二级引证文献1

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