Wang Jun-Ying, Chen Renbo, Chen Shu-Ping, Gao Yong-Hui, Zhang Jian-Liang, Feng Xiu-Mei, Yan Yaxia, Liu Jun-Ling, Gaischek Ingrid, Litscher Daniela, Wang Lu, Lippe Irmgard Th, Litscher Gerhard
Department of Physiology, Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing 100700, China; Research Unit for Complementary and Integrative Laser Medicine, Research Unit of Biomedical Engineering in Anesthesia and Intensive Care Medicine, and TCM Research Center Graz, Medical University of Graz, 8036 Graz, Austria.
Department of Chronic Diseases, Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing 100700, China.
Neural Plast. 2016;2016:6521026. doi: 10.1155/2016/6521026. Epub 2016 Oct 19.
To study the effects of acupuncture analgesia on the hippocampus, we observed the effects of electroacupuncture (EA) and mitogen-activated protein kinase (MEK) inhibitor on pain-excited neurons (PENs) and pain-inhibited neurons (PINs) in the hippocampal area CA1 of sham or chronic constrictive injury (CCI) rats. The animals were randomly divided into a control, a CCI, and a U0126 (MEK1/2 inhibitor) group. In all experiments, we briefly (10-second duration) stimulated the sciatic nerve electrically and recorded the firing rates of PENs and PINs. The results showed that in both sham and CCI rats brief sciatic nerve stimulation significantly increased the electrical activity of PENs and markedly decreased the electrical activity of PINs. These effects were significantly greater in CCI rats compared to sham rats. EA treatment reduced the effects of the noxious stimulus on PENs and PINs in both sham and CCI rats. The effects of EA treatment could be inhibited by U0126 in sham-operated rats. The results suggest that EA reduces effects of acute sciatic nerve stimulation on PENs and PINs in the CA1 region of the hippocampus of both sham and CCI rats and that the ERK (extracellular regulated kinase) signaling pathway is involved in the modulation of EA analgesia.
为研究针刺镇痛对海马的影响,我们观察了电针(EA)和丝裂原活化蛋白激酶(MEK)抑制剂对假手术或慢性压迫性损伤(CCI)大鼠海马CA1区痛兴奋神经元(PENs)和痛抑制神经元(PINs)的作用。将动物随机分为对照组、CCI组和U0126(MEK1/2抑制剂)组。在所有实验中,我们短暂(持续10秒)电刺激坐骨神经,并记录PENs和PINs的放电频率。结果显示,在假手术和CCI大鼠中,短暂的坐骨神经刺激均显著增加了PENs的电活动,并显著降低了PINs的电活动。与假手术大鼠相比,CCI大鼠的这些效应更为显著。EA处理减轻了假手术和CCI大鼠中有害刺激对PENs和PINs的影响。在假手术大鼠中,U0126可抑制EA处理的效应。结果表明,EA减轻了急性坐骨神经刺激对假手术和CCI大鼠海马CA1区PENs和PINs的影响,且细胞外调节激酶(ERK)信号通路参与了EA镇痛的调节。