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尾核内微量注射一氧化氮前体和供体对大鼠痛行为的影响

Effects of administration of L-arginine and sodium nitroprusside into caudate nucleus on pain behavior of rats
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摘要 目的观察大鼠尾核内一氧化氮(NO)对动物痛阈(痛行为)的影响.方法以钾离子透入引起大鼠甩尾的电流强度(mA)作为痛反应指标,尾核内微量注射L-精氨酸(L-Arg)、D-精氨酸(D-Arg)、硝普钠(SNP)和血红蛋白(Hb)等,观察0~30min内大鼠痛阈的变化.结果大鼠尾核内微量注射NO的前体L-Arg和供体SNP引起明显的痛敏效应,与对照组比较有显著性差异(P〈0.01或P〈0.05).微量注射D-Arg、Hb及SNP和Hb的混合液后大鼠痛阈变化30min内与对照组比较无显著性差异(P〈0.05).结论中枢神经系统内NO水平升高具有明显的痛敏效应,提示大鼠脑内NO在痛觉调制的复杂过程中发挥着重要作用. Objective: To observe the effect of nitric oxide (NO) on the pain threshold of rats. Methods:The potassium iontophoresis induced tail-flick was used to measure the pain threshold (PT). The changes were observed by micro-injecting L-arginine(L-Arg), D-arginine(D-Arg), sodium nitroprusside (SNP) and hemoglobin ( tab} into rat caudate nucleus in 30 minuts. Results: The significant hyperalgesic effects were observed by micro-injecting L-Arg and SNP into candate nucleus of rats. There were significant differences in the treatment groups ( P 〈 0.01, P 〈 0.05 ), while the PT of rats showed no changes by micro-injecting D-Arg, lib and the mixed liquid which included SNP and Hb. There were no significant differences in the changes of pain threshold compared with those of NS group in 30 minutes ( P 〈 0.05). Conclusion:An increase of NO in central nervous system (CNS) produces hyperalgesia, and NO in the brain may be involved in pain modulation.
出处 《泰山医学院学报》 CAS 2006年第1期7-9,共3页 Journal of Taishan Medical College
基金 山东省科技厅资助项目 2001BB1CDA1 山东省中医药管理局资助项目 2001-82
关键词 尾核 一氧化氮 痛阈 L-精氨酸 硝普钠 caudate nucleus nitric oxide pain modulation L-arginine sodium nitroprusside
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参考文献6

  • 1白波,刘文彦,宋朝佑.中枢神经系统一氧化氮对大鼠的痛觉调制作用[J].中国神经科学杂志,2000,16(1):52-55. 被引量:12
  • 2Haley JE.Gases as neurotransmitters[J].Essays Biochem,1998,33:79-91.
  • 3林雪梅,王泉云,朱琳,杨邦祥,刘斌.福尔马林致痛对大鼠行为学及脊髓NO、Fos的影响[J].四川大学学报(医学版),2003,34(3):523-526. 被引量:22
  • 4Cizkova D,Lukacova N,Marsala M,et al.Neuropathic pain is associated with alterations of nitric oxide synthase immunoreactivity and catalytic activity in dorsal root ganglia and spinal dorsal horn[J].Brain Res Bull,2002,58(2):161-71.
  • 5ZhangXT.Neurophysiology Basis Of Acupuncture analgesia[J].Sci Sin,1978,4:465-475.
  • 6Papapetropoulos A,Go CY,Murad F,et al.Mechanisms of tolerence to sodium nitroprusside in rat cultured aortic smoon muscle cells[J].Br J Pharmacol,1996,117:147-155.

二级参考文献12

  • 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
  • 2Malmberg AB, Yaksh TL. Spinal nitric oxide synthesis inhibition blocks NMDA-induced thermal hyperalgesia and produces antinociception in the formalin test in rats. Pain,1993; 54(3):291.
  • 3Abbott FV, Franklin KB, Westbrook RF. The formalin test;scoring properties of the first and second phases of the pain response in rats. Pain, 1995, 060(1) :91.
  • 4Zhou HJ, Li HD, Li XC, et al. Intrathecal injection of corticotropin inhibited nitric-oxide synthase-positive neuron increase in rat spinal cord after formalin-induced hyperalgesia.Zhongguo Yao Li Xue Bao, 1999;20(8):737.
  • 5Okuda K, Sakurada C, Takahashi M, et al. Characterization of nociceptive responses and spinal releases of nitric oxide metabolites and glutamate evoked by different concentrations of formalin in rats. Pain, 2001;92(1-2):107.
  • 6Hao S, Takahata O, Iwasaki H. Intrathecal endomorphin-1 produces antinociceptive activities modulated by alpha 2-adrenoceptors in the rat tail flick, tail pressure and formalin tests. Life Scl, 2000; 66(15):PL195.
  • 7Chen J, Koyama N. Differential activation of spinal dorsal horn units by subcutaneous formalin injection in the cat: an electrophysiological study. Exp Brain Res, 19981 118(1):14.
  • 8Vetter G, Oeisslinger G, Tegeder I. Release of glutamate,nitric oxide and prostaglandin E2 and metabolic activity in the spinal cord of rats following peripheral nociceptive stimulation.Pain, 2001; 92(1-2):213.
  • 9Peunova N, Enikolopov O. Amplification of calcium-induced gene transcription by nitric oxide in neuronal cells. Nature,1993; 364(6436) :450.
  • 10Roche AK, Cook M, Wilcox GL, et al. A nitric oxide synthesis inhibitor (L-NAME) reduces licking behavior and Fos-labeling in the spinal cord of rats during formalin-induced inflammation. Pain, 1996; 66(2-3);331.

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