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糖尿病神经痛大鼠背根神经节细胞动作电位特征变化

Changes of action potential properties in dorsal root ganglion neurons of rats with diabetic neuropathy pain
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摘要 目的通过观察背根神经节细胞的动作电位特征在糖尿病大鼠周围神经病变中的变化,探讨糖尿病大鼠周围神经病变引起痛觉过敏的发生机制。方法运用全细胞电流钳技术对糖尿病周围神经痛觉过敏大鼠背根神经节细胞进行电生理记录,与正常大鼠比较静息电位水平、动作电位峰值、基强度、动作电位爆发阈值、动作电位时程变化。结果糖尿病神经痛大鼠与正常大鼠静息电位水平和动作电位峰值无显著性差异;糖尿病神经痛大鼠大、中、小直径神经元动作电位爆发阈值下降,动作电位时程变宽,中、小直径神经元基强度降低。结论糖尿病大鼠周围神经病变引起初级感觉神经元背根神经节细胞的兴奋性增强,这可能是引起糖尿病大鼠周围神经痛觉过敏原因之一。 Objective It is to observe the action potential electrophysiological changes of dorsal root ganglion neurons in rats with painful diabetic peripheral neuropathy,and thus to elucidate the mechanism of hyperalgesia during diabetic peripheral neuropathy.Methods Dorsal root ganglion neurons from rats with painful diabetic peripheral neuropathy selected for electrophysiological recording the whole cell current.V rest,V peak,rheobase,Vthreshold,APD level changes were recorded and compared with that of normal rats.Results V rest and V peak showed no significant difference between the rats with painful diabetic peripheral neuropathy and the normal rats.The threshold of action potential outbreak were reduced and the duration of action potential were broadened in large,medium and small dorsal root ganglion neurons in the rats with diabetic peripheral neuropathy;The lower rheobase was observed in both small and medium dorsal root ganglion neurons from diabetic peripheral neuropathy.Conclusion Painful diabetic peripheral neuropathy could induce hyperexcitability of primary sensory neurons,which might be an important mechanism for hyperalgesia during diabetic peripheral neuropathy.
出处 《现代中西医结合杂志》 CAS 2011年第22期2751-2753,共3页 Modern Journal of Integrated Traditional Chinese and Western Medicine
基金 湖北医药学院学生科研基金资助项目(2010XSA13)
关键词 糖尿病神经疼痛 动作电位 背根神经节 diabetic neuropathy pain action potential dorsal root ganglion
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参考文献20

  • 1Bridges D,Thompson SWN,Rice ASC. Mechanisms of neuropathie pain[ J]. British J Anaesthesia,2001,87 : 12 - 26.
  • 2罗放.神经病理性疼痛的背根神经节机制[J].国外医学(麻醉学与复苏分册),2003,24(2):68-70. 被引量:10
  • 3Hirade M, Yasuda H, Omatsu M, et al. Tetrodotoxin-resistant sodi- um channels of dorsal root ganglion neurons are readily activated in diabetic rats[ J ]. Neuroscienee, 1999,90 ( 3 ) :933 - 939.
  • 4Study RE,Kral MG. Spontaneous action potential activity in isolated dorsal root ganglion neurons from rats with a painful neuropathy[ J]. Pain, 1996,65 (2) :235 - 242.
  • 5李洁,李秀钧.糖尿病痛性神经病变的诊断和处理[J].国外医学(内分泌学分册),2004,24(2):90-92. 被引量:56
  • 6Hays L,Reid C,Doran M,et al. Use of methatone for the treatment of diabetic neuropatby[J]. Diabetes Care,2005,28(2) :485 -487.
  • 7邓伦斌,姚磊,王贺春,曹晓杰,万有,韩济生.神经病理性痛大鼠背根神经节细胞电生理学特征的改变[J].中国疼痛医学杂志,2003,9(1):31-34. 被引量:7
  • 8Waxman SG,Kocsis JD,Black JA. Type III sodium channel mRNA is expressed in embryonic but not adult spinal sensory neurons, and is reexpressed following axotomy [ J ]. J Neurophysiol, 1994,72 ( 1 ) :466 -470.
  • 9Shah BS, Rush AM, Liu S, et al. Contactin associates with sodium channel Navl. 3 in native tissues and increases channel density at the cell surface [ J ]. J Neurosci ,2004,24 ( 33 ) :7387 - 7399.
  • 10Hains BC, Klein JP,Saab CY,et al. Upregulation of sodium channel Navl. 3"and functional involvement in neuronal hyperexcitability as- sociated with central neuropathic pain after spinal cord injury[ J]. J Neurosci ,2003,23 ( 26 ) : 8881 - 8892.

二级参考文献19

  • 1[1]Bridges D, Thompson SWN, Rice ASC. Mechanisms of neuropathic pain. British J Anaesthesia, 2001, 87: 12~26.
  • 2[2]Zhang JM, Donnelly DF, Song XJ, et al. Axotomy increases the excitability of dorsal root ganglion cells with unmyelinated axons. J. Neurophysiol, 1997, 78: 2790~2794.
  • 3[3]Kim, SH, and Chung, JM. An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat. Pain, 1992, 50: 355~363.
  • 4[4]Study RE, Kral MG. Spontaneous action potential activity in isolated dorsal root ganglion neurons from rats with a painful neuropathy. Pain, 1996, 65: 235~242.
  • 5[5]Harper AA, Lawson SN. Conduction velocity is related to morphological cell type in rat dorsal root ganglion neurons. J Physiol, 1985, 359: 31~46.
  • 6[6]Rose RD, Koerber HR, Sedivec MJ, et al. Somal action potential duration differs in identified primary afferents. Neurosci Lett, 1986, 63: 259~264.
  • 7[7]Yoshimura N, Groat WC. Increased excitability of afferent neurons innervating rat urinary bladder after chronic bladder inflammation. J. Neuroscience, 1999, 19: 4644~4653 .
  • 8[8]Cohe AS, Weinreich D, Kao JP. Nitric oxide regulates spike frequency accommodation in nodosee neurons of the rabbit. Neurosci Lett, 1994, 173: 17~20.
  • 9[9]Zhang L, Weiner JL, Vallante TA, et al. Whole-cell recording of the Ca2+-dependent slow afterhyperpolarization in hippocampal neurons: effects of internally applied anions. Pflugers Arch, 1994, 426: 247~253
  • 10Ametor AS,Barinov A,Dyck PJ,et al.The sensory symptoms of diabetic polyneuropathy are improved with alpha-lipoic acid:the SYDNEY trial.Diabetes Care,2003,26:770-776.

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