Mjellem N, Lund A, Eide P K, Størkson R, Tjølsen A
Department of Physiology, University of Bergen, Norway.
Neuroreport. 1992 Dec;3(12):1061-4. doi: 10.1097/00001756-199212000-00007.
The effects on nociception of intrathecal (i.th.) administration of selective 5-HT1A and 5-HT1B agonists were studied in rats. Nociception was evaluated using the tail-flick test with adjustments for tail-skin temperature, the increasing temperature hot-plate test and the scoring of biting and scratching behaviour after i.th. N-methyl-D-aspartate (NMDA). Activation of the spinal 5-HT1A receptor induced an antinociceptive effect in the increasing temperature hot-plate test and produced a dose dependent decrease in NMDA-receptor mediated behaviour. No significant change in nociception measured by either of the nociceptive tests was found after administration of the 5-HT1B agonist. These results support the hypothesis that spinal 5-HT1A receptor activation has an antinociceptive effect, and indicate a possible interaction between the serotonergic and glutaminergic transmitter systems.
研究了鞘内注射选择性5-羟色胺1A(5-HT1A)和5-羟色胺1B(5-HT1B)激动剂对大鼠伤害感受的影响。采用甩尾试验评估伤害感受,并对尾皮温度进行调整,采用升温热板试验以及鞘内注射N-甲基-D-天冬氨酸(NMDA)后对撕咬和抓挠行为进行评分。脊髓5-HT1A受体的激活在升温热板试验中诱导了抗伤害感受作用,并使NMDA受体介导的行为呈剂量依赖性降低。注射5-HT1B激动剂后,通过任何一种伤害感受测试所测得的伤害感受均未发现显著变化。这些结果支持了脊髓5-HT1A受体激活具有抗伤害感受作用这一假说,并表明5-羟色胺能和谷氨酰胺能递质系统之间可能存在相互作用。