Yuan Y, Yan S C, Chen X H, Han J S
Department of Orthopedics, First Hospital, Beijing Medical University.
Chin Med J (Engl). 1994 Mar;107(3):192-5.
The effect and mechanism of kappa opiate receptor agonist and high-frequency electrostimulation of acupoints in treating spinal spasticity were studied. The spinal spastic models were made by gradual mechanical compression on the cervical spinal cord of rabbits. 24 prepared rabbits were divided into 3 groups randomly, and each group with 8 rabbits was given intrathecally kappa-receptor agonist 66A-078, kappa-receptor antagonist +66A-078 and normal saline respectively. The degree of spasticity was quantified by both clinical score and electrophysiological examinations. The result showed that the spasticity was markedly inhibited by intrathecal injection of 66A-078 and that the kappa-receptor antagonist (naloxone) reversed this effect. We can infer that the antispastic effect of 66A-078 is mediated by kappa-receptors. This result is helpful in explaining the immediate antispastic mechanism of high-frequency electrostimulation of acupoints discussed in previous study.
研究了κ阿片受体激动剂及穴位高频电刺激治疗脊髓痉挛的效果及机制。通过对兔颈脊髓进行逐渐机械压迫制作脊髓痉挛模型。将24只制备好的兔随机分为3组,每组8只,分别鞘内注射κ受体激动剂66A - 078、κ受体拮抗剂 + 66A - 078和生理盐水。通过临床评分和电生理检查对痉挛程度进行量化。结果显示,鞘内注射66A - 078可显著抑制痉挛,且κ受体拮抗剂(纳洛酮)可逆转此效应。我们可以推断,66A - 078的抗痉挛作用是由κ受体介导的。该结果有助于解释先前研究中讨论的穴位高频电刺激的即时抗痉挛机制。