Wang Te-wei, Wang Ting-hua, Zhou Xue, Zhang Lian-shuang, Xu Xin-yun
Institute of Neuroscience, Kunming Medical College, Kunming 650031, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2007 Sep;38(5):792-4, 835.
To explore the effect of acupuncture, endogenous c-Fos and c-Jun on the regeneration of neuronal dendrite of spared dorsal root ganglion (DRG) in vitro following partial ganglionectomy.
Five adult male cats were used in this experiment. Their bilateral L1-L5, L7-S2 DRG were removed, and L6 DRG were spared. Then unilaterally, two sets of acupoints (Zusanli(St. 36) and Xuanzhong(G. B. 39); Futu (St. 32) and Sanyinjiao (Sp. 6) located in the distribution area of spinal nerve L6) were electro-stimulated alternately 30 min everyday by electro-needling. Seven days after operation, bilateral L6 DRGs were taken out and were cultured respectively in vitro. Some cultured mediums of the acupuncture lateral wells were totally replaced by each corresponding antibody-cultured medium including respectively 100 ng/mL anti-c-Fos and anti-c-Jun antibody at the 24th hour and terminated after 7 days. The length of the neurite was measured by upside-down light microscopy. Then, cultured cells were stained by the immunohistochemistry ABC method. Data were analyzed by One-way ANOVA and q test.
Immunocytochemical staining revealed that over 95% cells were NSE positive cells which were the typical neuron of DRG in vitro. On the 7th day, the average neurite length of the spared DRG group, the anti-c-Fos antibody and the anti-c-Jun antibody group were shorter than that of the acupuncture group (P < 0.05); the average neurite length of the two antibody groups were longer than that of the spared DRG group (P < 0.05).
These results indicate that acupuncture, endogenous c-Fos and c-Jun probably promote regeneration of neuronal dendrite of spared DRG in vitro.
探讨针刺、内源性c-Fos和c-Jun对部分神经节切除术后备用背根神经节(DRG)神经元树突在体外再生的影响。
本实验选用5只成年雄性猫。切除其双侧L1-L5、L7-S2 DRG,保留L6 DRG。然后,在L6脊神经分布区域,每天交替电针刺激两组穴位(足三里(胃经36)和悬钟(胆经39);扶突(大肠经32)和三阴交(脾经6))30分钟。术后7天,取出双侧L6 DRG并分别在体外培养。在第24小时,将针刺侧培养孔的一些培养基分别完全替换为含100 ng/mL抗c-Fos和抗c-Jun抗体的相应抗体培养基,并培养7天后终止。通过倒置光学显微镜测量神经突长度。然后,用免疫组织化学ABC法对培养细胞进行染色。数据采用单因素方差分析和q检验进行分析。
免疫细胞化学染色显示,超过95%的细胞为NSE阳性细胞,是体外DRG的典型神经元。第7天,备用DRG组、抗c-Fos抗体组和抗c-Jun抗体组的平均神经突长度短于针刺组(P<0.05);两个抗体组的平均神经突长度长于备用DRG组(P<0.05)。
这些结果表明,针刺、内源性c-Fos和c-Jun可能促进备用DRG神经元树突在体外的再生。