期刊文献+

Effect of Electroacupuncture on the Pathomorphology of the Sciatic Nerve and the Sensitization of P2X_3 Receptors in the Dorsal Root Ganglion in Rats with Chronic Constrictive Injury 被引量:7

Effect of Electroacupuncture on the Pathomorphology of the Sciatic Nerve and the Sensitization of P2X_3 Receptors in the Dorsal Root Ganglion in Rats with Chronic Constrictive Injury
原文传递
导出
摘要 Objective: To explore the effect of electroacupuncture (EA) on the pathomorphology of the sciatic nerve and the role of P2X3 receptors in EA analgesia. Methods: The chronic constriction injury (CCI) model was adopted in this study. A total of 32 rats were randomly divided into four groups: sham CCI, CCI, CCI plus contralateral EA (CCI + conEA) and CCI plus ipsilateral EA (CCI + ipsEA). Mechanical withdrawal threshold (MWT) and thermal withdrawal latency OWL) were measured. EA began at day 7 after the CCI operation and was applied to the Zusanli (ST 36) and Yanglingquan acupoints (GB 34). At day 14, the pathomorphologic changes of the operated sciatic nerve were demonstrated by hematoxylin and eosin staining. In addition, dorsal root ganglion (DRG) neurons isolated from rats were examined by electrophysiological recording to determine if the P2X3 receptor agonists, adenosine 5'-tdphosphate disodium (ATP) and α, 13 -methylen-ATP (or, 13 -meATP) evoked inward currents. Results: Pain thresholds in the CCI group were obviously decreased post CCI surgery (P〈0.01). In the EA groups, thermal and mechanical threshold values were increased after the last EA treatment (P〈0.05, P〈0.01). There was no significant difference in light microscopic examination among the four groups (P〉0.05). Current amplitude after application of ATP and or, 13 -meATP in DRG neurons were much larger in the CCI group compared to those obtained in sham CCI (P〈0.05). ATP and α, 13 -meATP invoked amplitudes in the CCI + EA groups were reduced. There was no significant difference between the CCI + conEA group and the CCI + ipsEA group (P〉0.05). Conclusion: EA analgesia may be mediated by decreasing the response of P2X8 receptors to the agonists ATP and or, 13 -meATP in the DRG of rats with CCI. No pathological changes of the sciatic nerve of rats were observed after EA treatment. Objective: To explore the effect of electroacupuncture (EA) on the pathomorphology of the sciatic nerve and the role of P2X3 receptors in EA analgesia. Methods: The chronic constriction injury (CCI) model was adopted in this study. A total of 32 rats were randomly divided into four groups: sham CCI, CCI, CCI plus contralateral EA (CCI + conEA) and CCI plus ipsilateral EA (CCI + ipsEA). Mechanical withdrawal threshold (MWT) and thermal withdrawal latency OWL) were measured. EA began at day 7 after the CCI operation and was applied to the Zusanli (ST 36) and Yanglingquan acupoints (GB 34). At day 14, the pathomorphologic changes of the operated sciatic nerve were demonstrated by hematoxylin and eosin staining. In addition, dorsal root ganglion (DRG) neurons isolated from rats were examined by electrophysiological recording to determine if the P2X3 receptor agonists, adenosine 5'-tdphosphate disodium (ATP) and α, 13 -methylen-ATP (or, 13 -meATP) evoked inward currents. Results: Pain thresholds in the CCI group were obviously decreased post CCI surgery (P〈0.01). In the EA groups, thermal and mechanical threshold values were increased after the last EA treatment (P〈0.05, P〈0.01). There was no significant difference in light microscopic examination among the four groups (P〉0.05). Current amplitude after application of ATP and or, 13 -meATP in DRG neurons were much larger in the CCI group compared to those obtained in sham CCI (P〈0.05). ATP and α, 13 -meATP invoked amplitudes in the CCI + EA groups were reduced. There was no significant difference between the CCI + conEA group and the CCI + ipsEA group (P〉0.05). Conclusion: EA analgesia may be mediated by decreasing the response of P2X8 receptors to the agonists ATP and or, 13 -meATP in the DRG of rats with CCI. No pathological changes of the sciatic nerve of rats were observed after EA treatment.
出处 《Chinese Journal of Integrative Medicine》 SCIE CAS 2013年第5期374-379,共6页 中国结合医学杂志(英文版)
基金 Supported by the National Natural Science Foundation of China (No.30901924)
关键词 ELECTROACUPUNCTURE PATHOMORPHOLOGY patch clamp P2X3 receptor ATP dorsal root ganglia neuropathic pain electroacupuncture pathomorphology patch clamp, P2X3 receptor ATP dorsal root ganglia neuropathic pain
  • 相关文献

参考文献22

  • 1Jiang SH, Yang GH, eds. Clinical research and application of acupuncture and tuina. Beijing: People's Medical Publishing House; 2008:121-126.
  • 2Burnstock G. Historical review: ATP as a neurotransmitter. Trends Pharmacol Sci 2006;27:166-176.
  • 3Abbracchio MP, Burnstock G, Verkhratsky A, Zimmermann H. Purinergic signalling in the nervous system: an overview. Trends Neurosci 2009;32:19-29.
  • 4Burnstock G. Physiology and pathophysiology of purinergic neurotransmission. Physiol Rev 2007;87:659-797.
  • 5Bumstock G. Acupuncture: a novel hypothesis for the involvement of purinergic signalling. Med Hypotheses 2009;73:470-472.
  • 6Lau WK, Lau YM, Zhang HQ, Wong SC, Bian ZX. Electroacupuncture versus celecoxib for neuropathic pain in rat SNL model. Neuroscience 2010; 170:655-661.
  • 7Sun S, Cao H, Han M, Li TT, Zhao ZQ, Zhang YQ. Evidence for suppression of electroacupuncture on spinal glial activation and behavioral hypersensitivity in a rat model of monoarthritis. Brain Res Bull 2008;75:83-93.
  • 8Patel S, Naeem S, Kesingland A, Froestl W, Capogna M, Urban L, et al. The effects of GABA(B) agonists and gabapentin on mechanical hyperalgesia in modelsof neuropathic and inflammatory pain in the rat, Pain 2001 ;90:217-226.
  • 9Fox A, Kesingland A, Gentry C, McNair K, Patel S, Urban L, et al. The role of central and peripheral Cannabinoidl receptors in the antihyperalgesic activity of cannabinoids in a model of neuropathic pain. Pain 2001 ;92:91-100.
  • 10Zhang A, Xu C, Liang S, Gao Y, Li G, Wei J, et al. Role of sodium ferulate in the nociceptive sensory facilitation of neuropathic pain injury mediated by P2X(3) receptor. Neurochem Int 2008:53:278-282.

同被引文献77

引证文献7

二级引证文献112

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