期刊文献+

内吗啡肽-1对神经源性疼痛镇痛作用的实验研究 被引量:1

The analgesic effect of endomorphin-1 on neuropathic pain
下载PDF
导出
摘要 目的 :观察内吗啡肽 1(endomorphin 1,EM 1)对神经源性疼痛动物的镇痛作用。方法 :用大鼠单侧坐骨神经部分结扎制成神经源性疼痛动物模型 ,采用钾离子透入法和辐射热 缩腿法两种测痛方法 ,观察腹腔注射EM 1(5 0 μg/kg)的作用。 结果 :EM 1对神经源性疼痛急性期和慢性期的痛阈均有提高作用 ,并且EM 1的作用可被纳络酮逆转。结论 :EM 1对神经源性疼痛急性期和慢性期的痛觉过敏均有镇痛作用。 Objective:To observe the analgesic effect of endomorphine 1(EM 1) on neuropathic pain model.Methods:The experiment was performed in rats which right sciatic nerve was partly crushed by K\++ iontophoresis and leg withdrawal to radiant heat to observe the analgesic effect of intraperitoneal injection(IP) of EM 1(50 μg/kg).Results:EM 1 could decrease the hyperalgesia in neuropathic pain model.The analgesic effect of EM 1 could be reversed by naloxone.Conclusions:EM 1 has analgesic effect on neuropathic pain model by IP EM 1.
出处 《蚌埠医学院学报》 CAS 2002年第6期478-480,共3页 Journal of Bengbu Medical College
关键词 内啡肽类 镇痛 Μ-阿片受体 大鼠 神经源性疼痛模型 endorphins analgesia μ opioid receptor rats,neuropathic pain model
  • 相关文献

参考文献13

  • 1Zadina JE;Hackler L;Ge LJ.A potent and selective endogenous against for theμ-opioid receptor[J],1997(6624).
  • 2Hackler L;Zadina JE;Ge LJ.Isolation of relatively large amounts of endomorphin- 1 and endomorphin-2 from human brain cortex[J],1997(18).
  • 3Przewlocka B;Mika J;Labuz D.Spinal analgesic action of endomorphins in acute, inflammatory and neuropathic pain in rats[J],1999(2/3).
  • 4Ronai AZ;Timar J;Mako E.Diprotin A, an inhibitor of dipeptidyl aminopeptidase Ⅳ(EC 3.4.14.5) produces naloxone- reversible analgesia in rats[J],1999(02).
  • 5Shane R;Wilk S;Bodnar RJ.Modulation of endomorphin-2 induced analgesia by dipeptidyl peptidase Ⅳ[J],1999(02).
  • 6Martin-Schild S;Gerall AA;Kastin AJ.Differential distribution of endomorphin 1 and endomorphin 2 like immunoreactivities in the CNS of the rodent[J],1999(04).
  • 7Martin-Schild S;Zadina JE;Gerall AA.Localization of endomorphin-2-like immunoreactivity in the rat medulla and spinal cord[J],1997(10).
  • 8Pierce TL;Grahck MD;Wcssendorf MW.Immunoreactivity for endomorphin-2 occurs in primary afferents in rats and monkey[J],1998(09).
  • 9Goldberg IE;Rossi GC;Letchworth SR.Pharmacological characterization of endomorphin-1 and endomorphin-2 in mouse brain[J],1998(02).
  • 10Seltzer Z;Dubner R;Shir Y.A novel behavioral model neuropathic pain disorders in rats by partial sciatic nerve injury[J],1990(02).

同被引文献12

  • 1Zadina JE,Hackler L,Ge LJ,et al.A potent and selective endogenous agonist for the μ-opiate receptor[J].Nature,1997,386(6 624):499~502.
  • 2Hackler L,Zadina JE,Ge LJ,et al.Isolation of relatively large amounts of endomorphin-1 and endomorphin-2 from human brain cortex[J].Petides,1997,18(10):1 635~1 639.
  • 3Rialas CM,Fimiani C,Bilfinger TV,et al.Endomorphin 1 and 2 inhibit human vascular sympathetic norepinephrine release:Lack of interaction with μ-opiate receptor subtype[J].Acta Pharmacol Sin,1998,19(5):403~407.
  • 4Hayar A,Guyenet PG.Pre and postsynaptic inhibitory actions of methionine-enkephalin on identified bulbospinal neurons of the rat RVL[J].J Neurophysiol,1998,80(4):2 003~2 014.
  • 5Czapla MA,Champion HC,Kadowitz PJ.Ncciccpcia ancndogcnculigand for the ORLI receptor has vasodilator activity in the hindquarters vascular bed of the rat[J].Peptides,1997,18(6):793~795.
  • 6Champion HC,Zadina JE,Kactin AJ,et al.The endogenous μopioid agonists endomorphin 1 and 2 have novel hypotensive activity in the rabbit[J].Biochem Biophys Res Commun,1997,235(3):567~570.
  • 7Champion HC,Zadina JE,Kactin AJ,et al.Endomorphin 1 and 2 have vasodepressor activity in the anesthetized mouse[J].Peptides,1998,19(5):925~929.
  • 8Champion HC,Bivalacqua TJ,Lambert DG,et al.Endomorphin 1 and 2,the endogenous μ-opioid agonists,produce biphasic changes in systemic arterial pressure in the cat[J].Life Sci,1998,63(9):PL131~136.
  • 9Kwok EH,Dun NJ.Endomorphins decrease heart rate and blood pressure possibly by activating vagal afferents in anesthetized rats[J].Brain Res,1998,803(1-2):204~207.
  • 10Czapla MA,Champion HC,Zadina JE,et al.Endomorphin 1 and 2,endogenous mu-opioid agonists,decrease systemic arterial pressure in the rat[J].Life Sci,1998,62(13):PL175~179.

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