Zhang Z H, Yang S W, Chen J Y, Xie Y F, Qiao J T, Dafny N
Department of Neurobiology, Shanxi Medical College, Taiyuan, P.R. China.
Brain Res Bull. 1995;38(2):167-71. doi: 10.1016/0361-9230(95)00084-r.
The interactions between different doses of serotonin (5-HT) and norepinephrine (NE) in in vivo experiments on rat spinal cord dorsal horn cells was investigated using the integrated electromyography (EMG) measurement of the nociceptive hindlimb flexor reflex (FR). The results indicate that (1) intrathecal (IT) administration of low doses of 5-HT (60 nmol) or NE (1.5 nmol) suppresses the nociceptive FR by 40% for 20 min, respectively; (2) administration of higher doses of 5-HT (240 nmol, IT) multiplies the suppression of the nociceptive FR by 80% for 40 min, and NE (15 nmol, IT) produces similar suppression of the nociceptive FR for 80 min; (3) concomitant administration of low doses of 5-HT (60 nmol, IT) and NE (1.5 nmol, IT) produces a summation of the nociceptive FR suppression both in amplitude and duration; (4) concomitant administration of the higher doses of 5-HT (240 nmol IT) with NE (15 nmol, IT) produces similar effect obtained as 5-HT given separately, and no summation was obtained as observed following the lower dosages; (5) serotonin (240 nmol, IT) given 40 min before NE (15 nmol, IT) attenuates the duration of the suppression induced by NE; (6) pretreatment with a selective 5-HT2 receptor antagonist ketanserin (60 nmol, IT) failed to abolish the 5-HT effects; (7) pretreatment with ketanserin prior to concomitant administration of the higher doses of 5-HT and NE prolongs the time duration of the nociceptive FR suppression.(ABSTRACT TRUNCATED AT 250 WORDS)
采用伤害性后肢屈肌反射(FR)的肌电图(EMG)综合测量方法,研究了不同剂量的血清素(5-羟色胺,5-HT)和去甲肾上腺素(NE)在大鼠脊髓背角细胞体内实验中的相互作用。结果表明:(1)鞘内(IT)注射低剂量的5-HT(60 nmol)或NE(1.5 nmol)分别在20分钟内将伤害性FR抑制40%;(2)注射较高剂量的5-HT(240 nmol,IT)在40分钟内将伤害性FR的抑制作用增强至80%,而NE(15 nmol,IT)在80分钟内产生类似的伤害性FR抑制作用;(3)同时注射低剂量的5-HT(60 nmol,IT)和NE(1.5 nmol,IT)在幅度和持续时间上均产生伤害性FR抑制的叠加效应;(4)同时注射较高剂量的5-HT(240 nmol IT)和NE(15 nmol,IT)产生的效果与单独给予5-HT时相似,且未观察到低剂量时出现的叠加效应;(5)在给予NE(15 nmol,IT)前40分钟给予5-HT(240 nmol,IT)可缩短NE诱导的抑制持续时间;(6)用选择性5-HT2受体拮抗剂酮色林(60 nmol,IT)预处理未能消除5-HT的作用;(7)在同时给予较高剂量的5-HT和NE之前用酮色林预处理可延长伤害性FR抑制的持续时间。(摘要截断于250字)