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脊髓ERK1/2的激活参与福尔马林所致家兔胆囊痛的形成 被引量:2

Activation of ERK1/2 in spinal cord contributes to the development of acute gallbladder pain caused by formalin in rabbits
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摘要 Objective To investigate the role of activated ERK1/2 in spinal cord in the development of gallbladder pain in rabbit. Methods Rabbits were divided into consisted of eight groups: nave group, surgery group, saline group, formalin group, U0126 100 μg/kg group,200 μg/kg group,400 μg/kg group and DMSO( menstruum )group, with six animals in each. The relationship between the activation of pERK1/2 in spinal cord and nociceptive behaviors, as well as the effect of U0126, which was the inhibitor of MEK1/2(upstream protein of ERK1/2 ) on gallbladder pain in rabbits were observed by Western blot and behavior test. Results There was a significant increase of pERK1/2 expression in spinal cord, as well as the increase of behaviors of gasping cheek and licking abdomen in 30 minutes after injection of 0.5ml formalin into gallbladder. The duration of behaviors were respective 23.17±1.47 and 23.00±1.41(P<0.01)in the rabbits with gallbladder pain. Administration of U0126(100 μg/kg^400 μg/kg, intravenous injection, 10 min before administration of formalin) dose-dependently attenuated nociceptive behaviors in rabbits with gallbladder pain caused by formalin. The most effective dose was 400 μg/kg . It decreased the nociceptive behaviors of grasping cheek and licking abdomen to 7.17±1.17 and 9.00±1.4(P<0.01).But it could not restrain these nociceptive behaviors completely. Conclusion It has suggested that activated ERK1/2 in spinal cord partly participates in the development of acute inflammative gallbladder pain caused by formalin in rabbits. Objective To investigate the role of activated ERK1/2 in spinal cord in the development of gallbladder pain in rabbit. Methods Rabbits were divided into consisted of eight groups: naive group, surgery group, saline group, formalin group, U0126 100 μg/kg group,200 μ/kg group,400 μ/kg group and DMSO( menstruum )group, with six animals in each. The relationship between the activation of pERK1/2 in spinal cord and nociceptive behaviors, as well as the effect of U0126, which was the inhibitor of MEK1/2( upstream protein of ERK1/2 ) on gallbladder pain in rabbits were observed by Western blot and behavior test. Results There was a significant increase of pERK1/2 expression in spinal cord, as well as the increase of behaviors of gasping cheek and licking abdomen in 30 minutes after injection of 0. 5ml formalin into gallbladder. The duration of behaviors were respective 23.17 ± 1.47 and 23.00 ± 1.41 (P 〈 0. 01 ) in the rabbits with gallbladder pain, Administration of U0126( 100 μg/kg -400 μg/kg, intravenous injection, 10 min before administration of formalin) dose-dependently attenuated nociceptive behaviors in rabbits with gallbladder pain caused by formalin. The most effective dose was 400μg/kg . It decreased the nociceptive behaviors of grasping cheek and licking abdomen to 7. 17 ± 1.17 and 9.00 ± 1.4(P 〈 0. 01 ). But it could not restrain these nociceptive behaviors completely. Conclusion It has suggested that activated ERK1/2 in spinal cord partly participates in the development of acute inflammative gallbladder pain caused by formalin in rabbits.
出处 《国际麻醉学与复苏杂志》 CAS 2006年第3期155-157,共3页 International Journal of Anesthesiology and Resuscitation
基金 江苏省研究生创新计划工程资(项目编号:XM04-69)
关键词 gallbladder pain RABBIT spinal cord PERK1/2 U0126 gallbladder pain rabbit spinal cord pERK1/2 U0126
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参考文献12

  • 1Impey S, Obrietan K, Storm DR. Making new connections: role of ERK/MAPK kinase signalling in neuronal plasticity. Neuron, 1999,23( 1 ) :11-14.
  • 2Mazzucchelli C , Brambilla R. Ras-related and MAPK signaling inneuronal plasticity and memory formation, Cell. Mol. Life Sci, 2000, 57(4.):604-611.
  • 3Ji R , Baba H, Brenner GJ, et al. Nociceptive-specificactivation of ERK in spinal neurons contributes to pain hypersensitivity, Nature Neurosci, 1999,2(12) :1114-1119.
  • 4Karim F , Wang C, C, ereau RW. Metabotropic glutamate receptor subtypes 1 and 5 are activators of extracellular signal-regulated kinase signaling required for inflammatory pain in mice, J. Neurosci, 2001,21 ( 11 ) :3771-3779.
  • 5张立丰,张励才,曾因明.胆囊痛牵涉区的定位[J].中国疼痛医学杂志,2003,9(1):19-22. 被引量:8
  • 6Cervero F. Sensory innervation of the vicera: peripheral basis of visceral pain. Phsiol Rev, 1994, 74(1) :95-138.
  • 7Martin SE, Pilkington DM, Longhurst JC. Coronary vascular responses to chemical stimulation of abdominal viscera organs. Am J Physiol, 1989,256(3Pt2) :H735-744.
  • 8张立丰,张励才.胆囊痛神经传导的基础研究[J].国外医学(麻醉学与复苏分册),2002,23(2):103-105. 被引量:3
  • 9Gioia M , Galbiati S, Rigamonti L, et al. Extracellular signal-regulated kinases I and 2 phosphorylated neurons in the tele- anddiencephalons of rat after visceral pain stimulation: an immunocytochemical study, Neurosci.Lett, 2001, 308(3) :177-180.
  • 10Galan A , Lopez-Garcia JA, Cervero F, et al, Activation of spinal extracellular signaling-regulated kinase-1 and -2 by Bingham, intraplantar carrageenan in rodents, Neurosci. Lett, 2002, 322(1):37-40.

二级参考文献19

  • 1[1]Ammons WS, Blair RW, Foreman RD. Responses of primate T1-T5 spinothalamic neurons to gallbladder distension. Am J Physiol, 1984, Dec;247(6 Pt 2): R995~1002.
  • 2[2]Cervero F. Afferent activity evoked by natural stimulation of the biliary system in the ferret. Pain, 1982, 13: 137~151.
  • 3[3]Ness TJ, Gebhart GF.Colorectal distension as a noxious visceral stimulus: physiologic and pharmacologic characterization of pseudoaffective reflexes in the rat.Brain Res, 1988, 31;450(1~2): 153~169.
  • 4[4]Cervero F. Sensory innervation of the viscera: peripheral basis of visceral pain.Physiol Rev. 1994 Jan;74(1): 95~138. Review. No abstract available.
  • 5[5]Crousillat J, Ranieri F. Splanchnic gallbladder mechanoreceptors (author's transl). Exp Brain Res, 1980,40: 146~153.
  • 6[6]Tseng LJ, Tsai CC, Mo LR, et al.Palliative percutaneous transhepatic gallbladder drainage of gallbladder empyema before laparoscopic cholecystectomy.Hepatogastroenterology, 2000, 47: 932~936.
  • 7[7]Thornell E. Effects of raised intraluminal pressure on gallbladder function and hepatic bile outflow in the cat.Scand J Gastroenterol, 1981,16: 873~877.
  • 8[8]Malatjalian DA. Pathology of inflammatory bowel disease in colorectal mucosal biopsies.Dig Dis Sci, 1987, 32(12 Suppl): 5S~15S.
  • 9[9]Joshi SK, Gebhart GF.Visceral pain.Curr Rev Pain, 2000,4: 499~506.
  • 10[10]Miampamba M, Chery-Croze S, Gorry F,et al. Inflammation of the colonic wall induced by formalin as a model of acute visceral pain.Pain, 1994, 57: 327~334.

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