期刊文献+

神经病理性痛大鼠背根神经节TRESK mRNA表达的变化 被引量:8

Changes in TRESK mRNA expression in dorsal root ganglion in a rat model of neuropathic pain
原文传递
导出
摘要 目的 探讨神经病理性痛大鼠背根神经节(DRG) 孔钾离子通道TRESK mRNA表达的变化.方法 雄性SD大鼠32只,体重22、0~250 g,采用随机数字表法,将大鼠随机分为2组(n=16):假手术组(S组)和神经病理性痛组(NP组).采用坐骨神经分支选择性损伤法制备神经病理性痛模型.S组仅暴露神经,不结扎.于术前1 d和术后1、3、5、7、14 d取8只大鼠,测定左后肢机械缩足反应阈值(MWT)和热缩足潜伏期(TWL).于术前1 d和术后14 d痛阈测定结束后取L4,5术侧DRG,采用RT-PCR法测定TRESK mRNA的表达.结果 与S组比较,NP组MWT明显降低,DRG TRESK mRNA表达明显下调(P〈0.05或0.01),TWL差异无统计学意义(P〉0.05).结论 神经病理性痛大鼠DRG TRESK mRNA表达下调,该变化可能与神经病理性痛的形成有关. Objective To evaluate the changes in the expression of diplopore potassium ion channel TRESK mRNA in dorsal root ganlion (DRG) in rats with neuropathic pain (NP) .Methods Thirty-two male SD rats weighing 220-250 g were randomly divided into 2 groups ( n = 16 each) : group sham operation (group S) and group NP. NP was induced by ligation and severance of left tibial and common fibular nerves according to the technique described by Decosterd. Eight rats in each group were sacrificed 1 day before and 14 day after operation and their L4,5 DRGs in the operated side were isolated for determination of TRESK mRNA expression by RT-PCR. In the remaining 8 rats in each group paw withdrawal threshold to mechanical stimuli ( MWT) and paw withdrawal latency to a thermal nociceptive stimulus (TWL) were measured at 1 day before (baseline) and 1, 3, 5, 7, 14 day after operation. Results MWT was significantly lower in group NP than in group S. The TRESK mRNA expression in L4,5 DRGs in the operated side was significantly decreased after operation as compared with the baseline before operation in group NP and was significantly lower in group NP than in group S. Conclusion The development and maintenance of NP may be closely related with down-regulation of TRESK mRNA.
出处 《中华麻醉学杂志》 CAS CSCD 北大核心 2011年第2期183-185,共3页 Chinese Journal of Anesthesiology
关键词 神经痛 神经节 钾通道 Neuralgia Ganglia,spinal Potassium channels
  • 相关文献

参考文献14

  • 1Baumann TK,Chaudhary P,Martenson ME.Background potassium channel block and TRPV1 activation contribute to proton depolarization of sensory neurons from humans with neuropathic pain.Eur J Neurosci,2004,19(5):1343-1351. 被引量:1
  • 2Kang D,Mariash E,Kim D.Functional expression of TRESK-2,a new member of the tandem-pore K^+ channel family.J Biol Chem,2004,279(27):28063-28070. 被引量:1
  • 3Kang D,Kim D.TREK-2(K2P 10.1)and TRESK(K2P 18.1) are major background K+ channels in dorsal root ganglion neurons.Am J Physiol Cell Physiol,2006,291(1):C138-C146. 被引量:1
  • 4Enyedi P,Czirják G.Molecular background of leak K^+ currents:two-pore domain potassium channels.Physiol Rev,2010,90(2):559-605. 被引量:1
  • 5Lafreniere RG,Cader MZ,Poulin JF,et al.A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.Nat Med,2010,16 (10):1157-1160. 被引量:1
  • 6Decosterd I,Woolf CJ.Spared nerve injury:an animal model of persistent peripheral neuropathic pain.Pain,2000,87(2):149-158. 被引量:1
  • 7Chaplan SR,Bach FW,Pogrel JW,et al.Quantitative assessment of tactile allodynia in the rat paw.J Neurosci Methods,1994,53(1):55-63. 被引量:1
  • 8Hargreaves K,Dubner R,Brown F,et al.A new and sensitive method for measuring thermal nociception in cutaneous hyperalgesia.Pain,1998,32(1):77-88. 被引量:1
  • 9Czirják G,Enyedi P.TRESK background K^+ channel is inhibited by phosphorylation via two distinct pathways.J Biol Chem,2010,285 (19):14549-14557. 被引量:1
  • 10Czirják G,Enyedi P.Targeting of calcineurin to an NFAT-like docking site is required for the calcium-dependent activation of the background K^+ channel,TRESK.J Biol Chem,2006,281 (21):14677-14682. 被引量:1

同被引文献51

  • 1Enyedi P,Czirjak G.Molecular background of leak K+ currents:twopore domain potassium channels.Physiol Rev,2010,90 (2):559-605. 被引量:1
  • 2Kang D,Mariash E,Kim D.Functional expression of TRESK-2,a new member of the tandem-pore K+ channel family.J Biol Chem,2004,279 (27):28063-28070. 被引量:1
  • 3Kang D,Kim D.TREK-2(K2P 10.1) and TRESK(K2P 18.1) are major background K + channels in dorsal root ganglion neurons.Am J Physiol Cell Physiol,2006,291 (1):138-146. 被引量:1
  • 4Halfon P,Bourlière M,Pénaranda G,et al.Real-time PCR assays for hepatitis C virus (HCV) RNA quantitation are adequate for clinical management of patients with chronic HCV infection.J Clin Microbiol,2006,44(7):2507-2511. 被引量:1
  • 5Durham HD,Lochmuller H,Jani A,et al.Toxicity of replication-defective adenoviral recombinants in dissociated cultures of nervous tissue.Exp Neurol,1996,140(1):14-20. 被引量:1
  • 6Dragomira M,Andreja AR.Adenoviral vectors-How to use them in cancer gene therapy? Vir Res,2006,119(2):121-133. 被引量:1
  • 7Cohen A, Sagron R, Somech E, et al. Pain-associated signals, acidosis and lysophosphatidic acid, modulate the neuronal K2p 2.1 channe[J]. Mol Cell Neurosci,2009,40(3) :382-389. 被引量:1
  • 8Czirjek G, Enyedi P. Targeting of calcineurin to an NFAT-like docking site is required for the calcium-dependent activation of the background K+ channel, TRESK [ J]. J Biol Chem, 2006, 281 (21) :14677-14682. 被引量:1
  • 9Lafrenire RG, Cader MZ, Poulin JF, et al. A dominant-nega- tive mutation in the TRESK potassium cbannel is linked to familial migraine with aura [ J]. Nat Med, 2010, 16 (10) : 1157-1160. 被引量:1
  • 10Zhou J, Yang CX, Zhong JY, et al. Intrathecal TRESK gene recombinant adenovirus attenuates Spared nerve injury-induced neuropatbic pain in rats[J]. Neuroreport, 2013,24(3) : 131-136. 被引量:1

引证文献8

二级引证文献11

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