Lee P H, Obie J, Hong J S
Laboratory of Behavioral and Neurological Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709.
Brain Res. 1988 Feb 16;441(1-2):381-5. doi: 10.1016/0006-8993(88)91419-9.
The effects of a selective mu-agonist, [NMe-Phe3-D-Pro4]morphiceptin (PL017), and a selective mu-antagonist, beta-funaltrexamine (beta-FNA), on convulsions and wet dog shakes (WDS) were studied. Electroencephalogram demonstrated that a single injection of PL017 into the ventral hippocampus evoked epileptiform spiking which appeared initially in the ventral hippocampus and spread to the cortical area when the animal developed generalized convulsion. Behavioral studies showed that PL017-induced convulsions and WDS were dose-dependent, and these behavioral changes were blocked by beta-FNA pretreatment. The results indicate that mu-receptors in the hippocampus may play an important role in seizure activities evoked by opioids.
研究了选择性μ-激动剂[N-甲基苯丙氨酸3-D-脯氨酸4]吗啡肽(PL017)和选择性μ-拮抗剂β-芬太尼丁(β-FNA)对惊厥和湿狗样抖动(WDS)的影响。脑电图显示,向腹侧海马单次注射PL017可诱发癫痫样棘波,最初出现在腹侧海马,当动物出现全身性惊厥时扩散至皮质区域。行为学研究表明,PL017诱导的惊厥和WDS呈剂量依赖性,且这些行为变化可被β-FNA预处理阻断。结果表明,海马中的μ受体可能在阿片类药物诱发的癫痫活动中起重要作用。