Yang S W, Zhang Z H, Wang R, Xie Y F, Qiao J T, Dafny N
Department of Neurobiology, Shanxi Medical College, Taiyuan, P.R. China.
Brain Res Bull. 1994;35(2):113-7. doi: 10.1016/0361-9230(94)90090-6.
The effects of intrathecally (IT) administered naloxone (Nal) on the antinociception produced by IT norepinephrine (NE), serotonin (5-HT), or morphine (Mor) were observed and compared in rats using the tail-flick (TF) assay. The results show that: a) NE, 5-HT, and Mor in doses of 1 nmol, 240 nmol, and 0.5 nmol, respectively, produce similar increases in amplitude and time in TF latency (TFL); b) Nal treatment of 240 and 360 nmol has no effects on TFL; c) the antinociception produced by NE (1 nmol) can be blocked by Nal (240 nmol); d) antinociception produced by Mor (0.5 nmol) can also be blocked by Nal (240 nmol); e) 240 nmol of Nal does not affect the 5-HT (120 nmol)-produced antinociception, while 360 nmol of Nal show a delayed blockade to the 5-HT (120 nmol)-produced antinociception. The results suggest that endogenous opiate-like substances may be involved in both NE- or 5-HT-produced antinociception at the spinal level, and these effects may be mediated through different types of opiate receptors.
在大鼠中使用甩尾试验观察并比较了鞘内注射纳洛酮(Nal)对鞘内注射去甲肾上腺素(NE)、5-羟色胺(5-HT)或吗啡(Mor)所产生的抗伤害感受作用的影响。结果显示:a)分别给予1 nmol的NE、240 nmol的5-HT和0.5 nmol的Mor,可使甩尾潜伏期(TFL)的幅度和时间产生相似的增加;b)240 nmol和360 nmol的Nal处理对TFL无影响;c)240 nmol的Nal可阻断1 nmol的NE所产生的抗伤害感受作用;d)240 nmol的Nal也可阻断0.5 nmol的Mor所产生的抗伤害感受作用;e)240 nmol的Nal不影响120 nmol的5-HT所产生的抗伤害感受作用,而360 nmol的Nal对120 nmol的5-HT所产生的抗伤害感受作用表现出延迟阻断作用。结果表明,内源性阿片样物质可能参与脊髓水平上由NE或5-HT所产生的抗伤害感受作用,并且这些作用可能通过不同类型的阿片受体介导。