期刊文献+

切口痛大鼠脊髓背角GluR1-AMPA受体和GluR2-AMPA受体胞浆至胞膜转运的变化 被引量:4

Changes in trafficking of GluRl-containing AMPA receptor and GluR2-containing AMPA receptor from cytoplasm to cell membrane in spinal dorsal horn in a rat model of incisional pain
原文传递
导出
摘要 目的探讨切口痛大鼠脊髓背角含谷氨酸受体1亚基的使君子酸(GluR1-AMPA)受体和含谷氨酸受体2亚基的使君子酸(GluR2-AMPA)受体胞浆至胞膜转运的变化。方法成年雄性清洁级sD大鼠32只,体重280~300g,6~8周龄,采用随机数表法,将其随机分为2组:正常对照组(C组,n=8)和切口痛组(I组,n=24)。I组大鼠制作右足底切口痛模型。I组于术后3h、1d和3d时取8只大鼠,测定累计痛评分(CPS)和机械缩足阈值(PWT)。然后处死大鼠,取L3-6节段脊髓背角,采用Western blot法检测胞浆和胞膜GluR1和GhtR2亚基的表达,采用免疫共沉淀技术检测脊髓背角Stargazin与GluR1或GluR2亚基的共表达。结果与C组比较,I组CPS评分升高,冈汀降低,脊髓背角胞浆GluR1亚基表达下调,脊髓背角胞膜GluR1表达及Stargazin与GluR1共表达上调(P〈0.05或0.01),脊髓背角胞浆和胞膜GluR2及Stargazin与GluR2共表达差异无统计学意义(p〉0.05)。结论切口痛大鼠脊髓背角GluR1-AMPA受体从胞浆转运至胞膜,而GluR2一AMPA受体不发生胞浆至胞膜的转运。 Objective To investigate the changes in traMcking of GluRl-containing AMPA (GluR1-AM- PA) receptor and GluR2-AMPA receptor from cytoplasm to cell membrane in the spinal cord dorsal ham in a rat model of incisional pain.Methods Thirty-two adult male SD rats aged 6-8 weeks weighing 280-300 g were randomly divided into 2 groups: control group (group C, n = 8) and incisional pain group (group I, n = 24). An 1 cm long incision was made in the plantar surface of right hindpaw according to Brennan et al. in group I. Cumula- tive pain score (CPS) and paw-withdrawal threshold to von Frey stimuli (PWT) were measured at 3 h and day 1 and 3 after incision (TL2,3). The animals were sacrificed after pain behavior assessment. Their lumbar segments of the spinal cord ( L3~ ) were removed. The expression of GluR1 and GluR2 in cell membrane and Cytoplasm in spinal cord dorsal ham was determined by Western blot analysis. The co-expression of Stargazing with GluR1 and GluR2 in the spinal cord dorsal horn was examined by co-immuno-precipitation. Results The CPS was increased and PWT decreased; the GluR1 expression in cytoplasm was decreased while the expression of GluR1 in cell membrane and the co-expression of Stargazing with GluR1 were up-regulated in group I as compared with group C. There was no significant change in the expression of GluR2 in cytoplasm and cell membrane and the co-expression of Stargazing with GluR2 in group I as compared with group C. Conclusion GluR1-AMPA receptor transfers from cytoplasm to cell membrane but GluP,2-AMPA receptor does not in rats with incisional pain.
出处 《中华麻醉学杂志》 CAS CSCD 北大核心 2012年第4期433-436,共4页 Chinese Journal of Anesthesiology
基金 国家自然科学基金(30801073,81171055) 北京市自然科学基金(7112054) 教育部新世纪优秀人才支持计划(NCET-10-0014)
关键词 疼痛 受体 AMPA 脊髓 蛋白转运 Pain Receptors, AMPA Spinal cord Protein transport
  • 相关文献

同被引文献59

  • 1薛旸,李海峰,徐凌云.小胶质细胞与炎症介导的神经系统退行性病变[J].生命科学,2007,19(1):43-46. 被引量:5
  • 2Wolf SA, Steiner B, Akpinarli A, et al.CD4-Positive T lymphocytes provide a neuroimmunological link in the control of adult hippocampal neurogenesis[J].J Immunol, 2009, 182: 3979-3984.
  • 3Lalancette-Hebert M,Growing G, Simard A, et al.Selective ablation of proliferating microglial cells exacerbates ischemie injury in the brain[J]. J NeurolSci, 2007, 27:259-260.
  • 4KimBJ, KimMJ, ParkJM, et al.Reduced neurogenesis after suppressed inflammation by minocycline in transient cerebral ischemia in rat[J].J Neurol Sci, 2009, 279: 70-75.
  • 5BernardinoL, AgasseF, SilvaB, et al.Tumor necrosis factor-alpha modulates survival, proliferation, and neuronal differentiation in neonatal subventrieular zone cell eultures[J].Stem cells, 2008, 26: 2361-2371.
  • 6Ma D, Jin S, Li E,et al. The neurotoxic effect of astrocytes activated with toll-like receptor ligands[J].JNeuroimmunol, 2013, 15,254 (1-2) : 8-10.
  • 7Ekdahl CT, Claasen JH, Bonde S, et al. Inflammation is detrimental for neurogenesis in adult brain[J]. ProeNatlAcadSciUSA, 2003, 100: 13632-13637.
  • 8Strassburger M, Braun H, Reymann KG.Anti-inflammatory treatment with the p38 mitogen-activated protein kinase inhibitor SB239063 is neuroprotective, decreases the number of activated mieroglia and facilitates neurogenesis in oxygen- glucose-deprived hippoeampal slice cultures[J].Eur J Pharmacol, 2008, 592: 55-61.
  • 9Takeuchi H, Mizoguchi H, Doi Y, et al. Blockade of gap junction hemichannel suppresses disease progression in mouse models of amyotrophic lateral sclerosis and Alzheimer's disease[J]. PLoS One, 6, e21108 (2011).
  • 10Welser-Alves JV, Milner R. Microglia are the major source of TNF-α and TGF-β1 in postnatal glial cultures;regulation by cytokines, lipopolysaccharide, and vitroneetin[J]. Neurochem Int, 2013 (13) : 00130-7.

引证文献4

二级引证文献5

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