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脊髓背角P物质在电针调控炎性痛大鼠神经-免疫网络中的作用研究
引用本文:王振宇,李淑莲,王希文,孙忠人.脊髓背角P物质在电针调控炎性痛大鼠神经-免疫网络中的作用研究[J].中医药学报,2012,40(3):88-90.
作者姓名:王振宇  李淑莲  王希文  孙忠人
作者单位:黑龙江中医药大学,黑龙江省普通高校重点实验室针灸临床神经生物学实验室,黑龙江 哈尔滨 150001
基金项目:教育部春晖计划课题(Z2009-1-15027); 黑龙江中医药大学博士创新基金(B201004); 黑龙江省教育厅面上项目(12511505)
摘    要:目的:通过阐明在脊髓背角疼痛信号传输中的关键神经肽SP在电针夹脊穴治疗大鼠单发关节炎中的作用,揭示夹脊电针抑制炎性痛的神经-免疫机制。方法:随机数字表法将大鼠分为假造模组、模型组、西乐葆组、电针组、电针+西乐葆组,采用弗氏完全佐剂建立的单侧足底慢性炎症痛大鼠模型,采用实时定量PCR法检测大鼠脊髓中SP mRNA在电针夹脊穴治疗大鼠单发关节炎中过程中的变化。结果:各组单侧足底慢性炎症痛大鼠模型脊髓中的SP mRNA表达与假造模组比较显著性增加(P0.001);电针夹脊穴组大鼠SP mRNA的表达与模型组比较明显降低(P0.01),且电针夹脊穴增强灌饲西乐葆对炎性痛大鼠脊髓中SP mRNA表达的抑制作用(P0.01)。结论:电针通过下调炎性痛大鼠神经-免疫网络环路中的重要神经肽脊髓背角SP的表达,从而发挥镇痛作用。

关 键 词:夹脊电针  神经-免疫网络  单侧炎症痛  镇痛  P物质

Involvement of Substance P in Inflammmatory Pain and Electroacupuncture Regulating Network of Immune - neuroendocrine Interactions
WANG Zhen-yu , LI Shu-lian , WANG Xi-wen , SUN Zhong-ren.Involvement of Substance P in Inflammmatory Pain and Electroacupuncture Regulating Network of Immune - neuroendocrine Interactions[J].Acta Chinese Medicine and Pharmacology,2012,40(3):88-90.
Authors:WANG Zhen-yu  LI Shu-lian  WANG Xi-wen  SUN Zhong-ren
Institution:WANG Zhen - yu, LI Shu - lian, WANG Xi - wen, SUN Zhong - ren ( Institute of Acupuncture, Institute of Neurobiology, Heilongfiang University of Chinese Medicine ,Harbin 150040, China)
Abstract:Objective : To reveal the mechanism of involvement of spinal cord pain control system SP in inflammatory pain and the regulation of network of immune - neuroendocrine interactions by electroacupuncture (EA). Methods : The rats were randomly divided into sham surgery group, model group, Celebre group, EA group, EA plus Celebre group. Monoar- thritis (MA) was induced by an injection of complete Freund' s adjuvant (CFA). The present study was designed to ex- plore the changes mRNA levels of SP in spinal cord of MA rats and EA analgesia by using Real - time PCR. Results :The mRNA levels detected by Real - time PCR of SP in spinal cord in EA group were significantly decreaced as compared to those in MA group ( P 〈 0.01 ) ;Combination of EA with Celebre significantly enhanced the inhibitory effects ( P 〈 0.01 ). Conclusion:Celebre and EA synergistically block activation of spinal microglia and subsequent astrocytes can reduce the release of SP in the spinal cord, thereby leading to a reinforcing inhibitory effect on MA - induced thermal hyperalgesia.
Keywords:EA  Immune - neuroendocrine interactions  Monoarthritis  Analgesia  Substance P
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