Huang Cheng, Long Hua, Shi Yu-Shun, Han Ji-Sheng, Wan You
Neuroscience Research Institute, Peking University, 38 Xueyuan Road, Beijing 100083, China.
Neurosci Lett. 2003 Oct 23;350(2):93-6. doi: 10.1016/s0304-3940(03)00863-2.
Nocistatin (NST) and nociception/orphanin FQ (OFQ) are peptides derived from the same precursor that play opposing roles in pain modulation. OFQ antagonizes morphine analgesia and electroacupuncture (EA)-induced antinociceptive effect. The present study investigates whether NST potentiates EA-induced antinociceptive effect and reverses chronic tolerance to EA in mice. Injection of NST (0.5, 5.0 and 50.0 ng) intracerebroventricularly had no effect on basal thermal latency, but produced a dose-dependent potentiation of EA-induced antinociceptive effect in mice with the maximum response at 5.0 ng. NST (5.0 ng) partly reversed chronic tolerance to EA. These results suggest that NST in the brain might play roles in EA-induced antinociceptive effect and the development of chronic tolerance to EA in mice.
痛稳素(NST)和痛敏肽/孤啡肽(OFQ)是由同一前体衍生而来的肽类,它们在疼痛调节中发挥相反作用。OFQ可拮抗吗啡镇痛作用以及电针(EA)诱导的镇痛效应。本研究探讨NST是否能增强EA诱导的镇痛效应并逆转小鼠对EA的慢性耐受。脑室内注射NST(0.5、5.0和50.0纳克)对基础热潜伏期无影响,但能剂量依赖性地增强EA诱导的小鼠镇痛效应,5.0纳克时反应最大。NST(5.0纳克)部分逆转了对EA的慢性耐受。这些结果表明,脑内的NST可能在EA诱导的镇痛效应以及小鼠对EA慢性耐受的形成中发挥作用。