首页> 外文期刊>Experimental Neurology >Effects of synchronous or asynchronous electroacupuncture stimulation with low versus high frequency on spinal opioid release and tail flick nociception.
【24h】

Effects of synchronous or asynchronous electroacupuncture stimulation with low versus high frequency on spinal opioid release and tail flick nociception.

机译:低频或高频同步或异步电针刺激对脊髓阿片样物质释放和甩尾痛感受的影响。

获取原文
获取原文并翻译 | 示例
           

摘要

Electroacupuncture stimulation (EAS) is known to change brain neurotransmitter release. In the present study, we investigated the effects of synchronous or asynchronous electroacupuncture stimulation with low versus high frequency on spinal opioid release and tail flick nociception. Rats were given "2/100 Hz" EAS, which stands for an asynchronous mode of stimulation, in which 2 Hz was alternated with 100 Hz, each lasting for 3 s, or "(2 + 100) Hz" EAS, a mode of stimulation in which 2 Hz stimulation was applied to the left hind leg simultaneously with 100 Hz stimulation on the right hind leg. The rats were subjected to the same total number of electrical stimulations in these two modes. Results were as follows: (1) 2/100 Hz EAS was 40% more potent than (2 + 100) Hz EAS (P < 0.01) in producing an anti-nociceptive effect. (2) Intrathecal (i.t.) injection of the mu-opioid receptor antagonist d-Phe-Cys-Tyr-d-Trp-Orn-Thr-Pen-Thr amide (CTOP) blocked in a dose-dependent manner the anti-nociceptive effect produced by 2/100 Hz EAS but not by (2 + 100) Hz EAS, whereas i.t. injection of the kappa-opioid receptor antagonist norbinaltorphimide (Nor-BNI) blocked the anti-nociceptive effect induced by both modes of EAS. (3) I.t. injection of endomorphin-2 antiserum blocked in a dose-dependent manner the anti-nociceptive effect of 2/100 Hz EAS but not that of (2 + 100) Hz EAS, whereas i.t. injection of dynorphin antiserum blocked the anti-nociceptive effect induced by both modes of stimulation. (4) 2/100 Hz EAS increased the release of both endomorphin-2 and dynorphin, whereas (2 + 100) Hz EAS increased the release of dynorphin but not of endmorphin-2. We conclude that the more potent anti-nociceptive effect induced by 2/100 Hz EAS, as compared with that of (2 + 100) Hz EAS, was due, at least partly, to the synergistic interaction of endomorphin-2 and dynorphin in rat spinal cord.
机译:众所周知,电针刺激(EAS)会改变大脑神经递质的释放。在本研究中,我们研究了低频或高频同步或异步电针刺激对脊髓阿片样物质释放和甩尾痛感受的影响。给予大鼠“ 2/100 Hz” EAS,它表示异步刺激模式,其中2 Hz与100 Hz交替,每组持续3 s,或“(2 + 100)Hz” EAS,一种刺激模式。在左侧后腿施加2 Hz刺激的同时在右侧后腿施加100 Hz刺激的刺激。在这两种模式下,大鼠受到相同数量的电刺激。结果如下:(1)2/100 Hz EAS的抗伤害感受作用比(2 + 100)Hz EAS的效力高40%(P <0.01)。 (2)鞘内注射μ阿片受体拮抗剂d-Phe-Cys-Tyr-d-Trp-Orn-Thr-Pen-Thr酰胺(CTOP)以剂量依赖性方式阻断抗伤害感受作用由2/100 Hz EAS产生,但不是由(2 + 100)Hz EAS产生注射阿片受体拮抗剂降冰片Norbinaltorphimide(Nor-BNI)可以阻止这两种EAS诱导的抗伤害感受作用。 (3)内啡肽2抗血清的注射以剂量依赖性方式阻断了2/100 Hz EAS的抗伤害感受作用,而不是(2 + 100)Hz EAS的抗伤害感受作用。强啡肽抗血清的注射阻断了两种刺激方式引起的抗伤害感受作用。 (4)2/100 Hz EAS会增加内啡肽2和强啡肽的释放,而(2 + 100)Hz EAS会增加强啡肽的释放,但不会增加endmorphin-2的释放。我们得出结论,与(2 + 100)Hz EAS相比,由2/100 Hz EAS诱导的更强的抗伤害感受作用至少部分是由于内啡肽2与强啡肽在大鼠中的协同相互作用所致脊髓。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号