Lee Bong Hyo, Ku Ji Young, Zhao Rong Jie, Kim Hee Young, Yang Chae Ha, Gwak Young S, Chang Su Chan, Kim Nam Jun, Kim Jae Su, Lee Yun Kyu, Lee Hyun Jong, Lim Sung Chul
Department of Acupuncture, Moxibustion, and Acupoint, College of Oriental Medicine, Daegu Haany University, Daegu 706-828, South Korea.
Department of Acupuncture, Moxibustion, and Acupoint, College of Oriental Medicine, Daegu Haany University, Daegu 706-828, South Korea.
Neurosci Lett. 2014 Jul 25;576:34-9. doi: 10.1016/j.neulet.2014.05.050. Epub 2014 Jun 4.
In the previous study, acupuncture at HT7 has shown to attenuate the self-administration of morphine at a low dose (0.1mg/kg). In this study, it was further investigated whether acupuncture at HT7 could attenuate the morphine self-administration at a high dose (0.5mg/kg). Male Sprague-Dawley rats weighing 270-300g were used. After surgery of catheterization, animals were trained to self-administer morphine solution (0.5mg/kg) using daily 1h session under fixed ratio 1 schedule for 3 weeks. Animals that had shown stable morphine-taking (establish baseline: variation less than 20% of the mean of three consecutive days) were subjected to the acupuncture treatment. Bicuculline and SCH 50911 were used to investigate the possible relation between the effect of acupuncture and the GABA receptor system. Acupuncture at HT7, but not at control acupoint, LI5, suppressed spontaneous morphine-taking behavior significantly. In addition, the effect of acupuncture was blocked by both GABA receptor antagonists. The results of this study suggest that acupuncture at HT7 suppresses morphine-taking behavior through the mediation of GABA receptor system.
在先前的研究中,已表明针刺心经的神门穴(HT7)能在低剂量(0.1mg/kg)时减弱吗啡的自我给药行为。在本研究中,进一步探究了针刺心经的神门穴(HT7)在高剂量(0.5mg/kg)时是否能减弱吗啡的自我给药行为。使用体重为270 - 300g的雄性斯普拉格-道利大鼠。在进行插管手术后,让动物在固定比率1的模式下,每天进行1小时的训练,以自我给药吗啡溶液(0.5mg/kg),持续3周。对那些已表现出稳定吗啡摄取量(建立基线:变化小于连续三天平均值的20%)的动物进行针刺治疗。使用荷包牡丹碱和SCH 50911来研究针刺效果与GABA受体系统之间的可能关系。针刺心经的神门穴(HT7)而非对照穴位合谷穴(LI5)能显著抑制自发的吗啡摄取行为。此外,针刺的效果被两种GABA受体拮抗剂所阻断。本研究结果表明,针刺心经的神门穴(HT7)通过GABA受体系统的介导来抑制吗啡摄取行为。