Effect of Electroacupuncture on the Expression of Spinal Glial Fibrillary Acidic Protein,Tumor Necrosis Factor-α and Interleukin-1β in Chronic Neuropathic Pain Rats
SUN Tao, CUI Cheng-bin1, LUO Jian-gang, et al. Effect of Electroacupuncture on the Expression of Spinal Glial Fibrillary Acidic Protein,Tumor Necrosis Factor-α and Interleukin-1β in Chronic Neuropathic Pain Rats[J]. Acupuncture research, 2010, 35(1): 12-16.
SUN Tao, CUI Cheng-bin1, LUO Jian-gang, et al. Effect of Electroacupuncture on the Expression of Spinal Glial Fibrillary Acidic Protein,Tumor Necrosis Factor-α and Interleukin-1β in Chronic Neuropathic Pain Rats[J]. Acupuncture research, 2010, 35(1): 12-16. DOI: 10.13702/j.1000-0607.2010.01.013.
Objective To observe the effect of electroacupuncture(EA) on the expression of spinal glial fibrillary acidic protein(GFAP)
tumor necrosis factor-α(TNF-α) and interleukin-1β(IL-1β) in chronic constriction injury(CCI) rats.Methods Seventy-two SD rats were randomized into sham operation(sham)
CCI(model) and EA groups(n=24/group).The mechanical and thermal pain thresholds were measured by using Von Frey filaments and radiant-heat irridiation separately.The immunoactivity of GFAP of spinal dorsal horn(L4-L5) was assessed by immunohistochemistry
and the expression of spinal TNF-α mRNA and IL-1β mRNA was detected by real time-PCR.Results Compared with pre-CCI and sham group
both mechanical and thermal pain thresholds decreased considerably in rats with CCI(P<0.05)
and in comparison with model group
those of EA group increased markedly(P<0.05).Compared with sham group
GFAP immunoactivity(mainly in the lamina Ⅰ-Ⅱ of the spinal dorsal horn)
TNF-α mRNA and IL-1β mRNA expression in the ipsilateral spinal cord on the CCI side in model group increased consi-derably(P<0.05)
while compared with model group
the expression of GFAP
TNF-α mRNA and IL-1β mRNA in EA group was down-regulated remarkably(P<0.05).Conclusion EA can effectively suppress CCI-induced up-regulation of expression of spinal GFAP
TNF-α mRNA and IL-1β mRNA
which may contribute to its effect in reducing mechanical allodynia and thermal hyperalgesia in neuropathic pain rats.