Lin Jaung-Geng, Lee Yu-Chen, Tseng Chien-Hsin, Chen Dai-Yin, Shih Chieh-Yun, MacDonald Iona, Hung Shih-Ya, Chen Yi-Hung
School of Chinese Medicine, China Medical University, Taichung 40402, Taiwan.
Department of Acupuncture, China Medical University Hospital, Taichung 40447, Taiwan; Graduate Institute of Acupuncture Science, China Medical University, Taichung 40402, Taiwan.
Brain Res. 2016 Oct 15;1649(Pt A):23-29. doi: 10.1016/j.brainres.2016.07.007. Epub 2016 Jul 8.
In this study, we examined whether electroacupuncture (EA) represses pruritogen-induced microglial activation. Immunohistochemical studies revealed that a subcutaneous (s.c.) injection of the pruritogen 5'-guanidinonaltrindole (GNTI; 0.3mg/kg) to the back of the neck in mice induced acute expression of the ionized calcium-binding adaptor molecule 1 (Iba1) in both gray and white matter of the spinal cord, with the highest expression in the dorsal horn area. EA application (2Hz) to LI4 and LI11 attenuated GNTI-induced scratching behavior and repressed GNTI-induced Iba1 expression and Iba1 (+) microglia in the dorsal horn. In contrast, EA at the ST36 acupoint had no such effects. Confocal image analysis revealed co-expression of phosphorylated p38 and Iba1 in microglia with EA at the ST36 acupoint, but not at the LI4 or LI11 acupoints. In Western blot analysis, s.c. injection of GNTI to the back of the neck increased Iba1 and phospho-p38 expression in the spinal cord as compared with injection of saline, while EA at LI4 and LI11 reduced GNTI-induced expression of Iba1 and phospho-p38. These findings indicate that EA at LI4 and LI11, but not at ST36, reduces GNTI-induced microglial activation in the mouse spinal cord.
在本研究中,我们检测了电针(EA)是否能抑制致痒原诱导的小胶质细胞激活。免疫组织化学研究显示,向小鼠颈部背部皮下注射致痒原5'-胍基诺他林(GNTI;0.3mg/kg)可诱导脊髓灰质和白质中离子钙结合衔接分子1(Iba1)的急性表达,在背角区域表达最高。对LI4和LI11进行电针刺激(2Hz)可减轻GNTI诱导的搔抓行为,并抑制GNTI诱导的背角中Iba1表达和Iba1(+)小胶质细胞。相比之下,在ST36穴位进行电针则没有这种效果。共聚焦图像分析显示,在ST36穴位进行电针刺激时,小胶质细胞中磷酸化p38和Iba1共表达,但在LI4或LI11穴位则没有。在蛋白质印迹分析中,与注射生理盐水相比,向小鼠颈部背部皮下注射GNTI可增加脊髓中Iba1和磷酸化p38的表达,而在LI4和LI11进行电针可降低GNTI诱导的Iba1和磷酸化p38的表达。这些发现表明,在LI4和LI11而非ST36进行电针可减少GNTI诱导的小鼠脊髓小胶质细胞激活。