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腰5脊神经结扎大鼠腰4背根神经节神经元超极化激活电流的变化

CHANGE OF Ih IN LUMBAR 4 INTACT DRG NEURONS AFTER L5 SPINAL NERVE LIGATION IN RATS
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摘要 目的:研究腰5脊神经结扎(L5spinal nerve ligation,SNL)神经病理痛大鼠腰4背根神经节(dorsal root ganglion,DRG)神经元超极化激活电流(Ih)及其通道超极化激活环核苷酸门控阳离子通道(HCN)发生的可塑性变化。方法:以单侧L5SNL制备神经病理痛大鼠模型,运用全细胞膜片钳技术记录和分析背根神经节神经元Ih的表达和激活特性。结果:L5SNL之后,腰4 DRG神经元Ih的电流密度降低,单位电导下降,而翻转电位及电压依赖特性未发生显著性改变。结论:腰4DRG神经元Ih的这些变化可能贡献于L5SNL大鼠的神经病理痛。 Objective: To investigate the changes of Ih and its channel, hyperpolarization-activated cyclic nucleotide gated cation channel ( HCN), in the intact lumbar 4 DRG neurons following lumbar 5 ( L5 ) spinal nerve ligation (SNL). Methods: Rat neuropathic pain model was produced by tight ligation of L5 spinal nerve and Ih was recorded with whole-cell patch clamp technique. Results: The current density and the maximal conductance of Ih in the SNL group were decreased significantly compared with those in the sham-operation control, while the reversal potential and the channel biophysics properties of HCN channel did not show any significant change. Conclusion: These electrophysiological changes of Ih and HCN channel properties in the L4 intact DRG neurons might contribute to peripheral sensitization in L5 SNL neuropathic pain.
出处 《中国疼痛医学杂志》 CAS CSCD 北大核心 2008年第4期218-221,共4页 Chinese Journal of Pain Medicine
基金 北京市自然科学基金项目(7052039) 国家自然科学基金项目(30470559) "973"项目(2007CB512501)
关键词 神经病理痛 脊神经结扎 IH 背根神经节 全细胞膜片钳 neuropathic pain spinal nerve ligation hyperpolarization-activated cyclic nucleotide gated cation channel (HCN) Ih dorsal root ganglion whole-cell patch clamp
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参考文献9

  • 1Robinson RB, Siegelbaum SA. Hyperpolarization-activated cation currents: from molecules to physiological function. Annu Rev Physiol, 2003, 65 : 453 - 480.
  • 2Tu HY, Deng LB, Sun Q, et al. Hyperpolarization-activated, cyclic nucleotide-gated cation channels: Roles in the differential electrophysiological properties of rat primary afferent neurons. J Neurosci Res, 2004, 76 : 13 -722.
  • 3Ho Kim S, Mo Chung J. An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat. Pain, 1992, 50 : 355 - 363.
  • 4Chaplan SR, Bach FW, Pogrel JW, et al. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods, 1994, 53 : 55 -63.
  • 5Bridges D, Thompson SWN, Rice ASC. Mechanism in neuropathic pain. British Journal of Anaesthesia, 2001, 87 : 12-26.
  • 6Yagi J, Sumino R. Inhibition of a hyperpolarization-activated current by clonidine in rat dorsal root ganglion neurons. J Neurophysiol, 1998, 80 : 1094 - 1104.
  • 7van Welie I, van Hooft JA, Wadman WJ. Homeostatic scaling of neuronal excitability by synaptic modulation of somatic hyperpolarization-activated Ih channels. Proceedings of the National Academy of Sciences of the United States of America, 2004, 101 : 5123-5128.
  • 8Chaplan SR, Guo HQ, Lee DH, et al. Neuronal hyperpolarization-activated pacemaker channels drive neuropathic pain. J Neurosci, 2003, 23 : 1169 - 1178.
  • 9Yao H, Donnelly DF, Ma C, et al. Upregulation of the hyperpolarization-activated cation current after chronic compression of the dorsal root ganglion. J Neurosci, 2003, 23 : 2069 -2074.

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