Lu Kung-Wen, Hsu Chao-Kuei, Hsieh Ching-Liang, Yang Jun, Lin Yi-Wen
College of Chinese Medicine, School of Post-Baccalaureate Chinese Medicine, China Medical University, Taichung 40402, Taiwan.
China Medical University Hospital, Department of Chinese Medicine, Taichung 40402, Taiwan.
Sci Rep. 2016 Feb 24;6:22123. doi: 10.1038/srep22123.
Transient receptor potential vanilloid 1 (TRPV1) and associated signaling pathways have been reported to be increased in inflammatory pain signaling. There are accumulating evidences surrounding the therapeutic effect of electroacupuncture (EA). EA can reliably attenuate the increase of TRPV1 in mouse inflammatory pain models with unclear signaling mechanisms. Moreover, the difference in the clinical therapeutic effects between using the contralateral and ipsilateral acupoints has been rarely studied. We found that inflammatory pain, which was induced by injecting the complete Freund's adjuvant (CFA), (2.14 ± 0.1, p < 0.05, n = 8) can be alleviated after EA treatment at either ipsilateral (3.91 ± 0.21, p < 0.05, n = 8) or contralateral acupoints (3.79 ± 0.25, p < 0.05, n = 8). EA may also reduce nociceptive Nav sodium currents in dorsal root ganglion (DRG) neurons. The expression of TRPV1 and associated signaling pathways notably increased after the CFA injection; this expression can be further attenuated significantly in EA treatment. TRPV1 and associated signaling pathways can be prevented in TRPV1 knockout mice, suggesting that TRPV1 knockout mice are resistant to inflammatory pain. Through this study, we have increased the understanding of the mechanism that both ipsilateral and contralateral EA might alter TRPV1 and associated signaling pathways to reduce inflammatory pain.
据报道,瞬时受体电位香草酸亚型1(TRPV1)及其相关信号通路在炎性疼痛信号传导中会增加。围绕电针(EA)的治疗效果有越来越多的证据。在小鼠炎性疼痛模型中,电针能可靠地减弱TRPV1的增加,但其信号机制尚不清楚。此外,使用对侧穴位和同侧穴位的临床治疗效果差异鲜有研究。我们发现,注射完全弗氏佐剂(CFA)诱导的炎性疼痛(2.14±0.1,p<0.05,n = 8),在同侧(3.91±0.21,p<0.05,n = 8)或对侧穴位进行电针治疗后均可缓解(3.79±0.25,p<0.05,n = 8)。电针还可能降低背根神经节(DRG)神经元中的伤害性Nav钠电流。注射CFA后,TRPV1及其相关信号通路的表达显著增加;在电针治疗中,这种表达可进一步显著减弱。在TRPV1基因敲除小鼠中,TRPV1及其相关信号通路可被阻断,这表明TRPV1基因敲除小鼠对炎性疼痛具有抗性。通过这项研究,我们加深了对同侧和对侧电针可能通过改变TRPV1及其相关信号通路来减轻炎性疼痛机制的理解。