Kádár T, Telegdy G, Schally A V
Department of Pathophysiology, A. Szent-Györgyi University Medical School, Szeged, Hungary.
Neuropeptides. 1990 Oct;17(2):81-6. doi: 10.1016/0143-4179(90)90053-2.
The neuropharmacological actions of the agonist analog D-Trp-6-LH-RH were investigated in several tests after subcutaneous administrations to male mice. The doses applied were in the range 1-1000 micrograms/kg. D-Trp-6-LH-RH doses of 10 micrograms/kg and higher induced significant analgesic effects in the hot-plate and tail-flick tests, and decreased the open-field parameters (ambulation, rearing, grooming). The 100 and 1000 micrograms/kg doses increased the latencies of picrotoxin-induced seizures, significantly inhibited apomorphine-induced cage climbing and also exerted a cataleptogenic effect. The results indicate that this agonist analog of LH-RH has an inhibitory effect on the central nervous system, and the mechanism of its action may involve dopaminergic transmission and/or endogenous opiates.
在对雄性小鼠皮下给药后,通过多项试验研究了激动剂类似物D-色氨酸-6-促黄体生成素释放激素(D-Trp-6-LH-RH)的神经药理学作用。给药剂量范围为1-1000微克/千克。10微克/千克及以上剂量的D-Trp-6-LH-RH在热板试验和甩尾试验中诱导出显著的镇痛作用,并降低旷场试验参数(行走、竖毛、理毛)。100和1000微克/千克剂量增加了印防己毒素诱导惊厥的潜伏期,显著抑制阿扑吗啡诱导的笼内攀爬,并且还产生了僵住效应。结果表明,这种促黄体生成素释放激素的激动剂类似物对中枢神经系统有抑制作用,其作用机制可能涉及多巴胺能传递和/或内源性阿片类物质。