Cridland R A, Henry J L
Department of Psychiatry, McGill University, Montreal, Que., Canada.
Neurosci Lett. 1988 Jan 22;84(2):203-8. doi: 10.1016/0304-3940(88)90408-9.
Substance P (10 micrograms) was administered intrathecally (i.t.) via a chronic catheter to the L5 vertebral level in rats with spinal cords transected at the T10-12 level (n = 11) and in intact rats pretreated 25 min earlier with morphine (5 micrograms i.t., n = 5). In both experimental paradigms, substance P decreased the reaction time in the tail flick test at 1 min after injection; the magnitude of this effect resembled that which occurs in intact rats given substance P alone. In both paradigms, substance P failed to produce the behavioural responses typically observed in untreated rats given substance P. These results indicate that substance P-induced facilitation of the tail flick reflex may occur via spinal mechanisms alone. The results also suggest that in the spinal cord morphine preferentially blocks the relay of substance P-induced information to supraspinal structures. Finally, as the behavioural response is blocked by the analgesic and by spinal transection, this is interpreted as further support for the proposal that this behavioural response indicates that the animal has perceived a noxious stimulus.
将P物质(10微克)通过慢性导管经鞘内注射至脊髓在T10 - 12水平横断的大鼠(n = 11)的L5椎体水平,以及25分钟前预先经鞘内注射吗啡(5微克,n = 5)的完整大鼠。在这两种实验范式中,P物质在注射后1分钟时缩短了甩尾试验中的反应时间;这种效应的程度类似于单独给予P物质的完整大鼠所出现的效应。在这两种范式中,P物质均未产生未处理的给予P物质的大鼠中通常观察到的行为反应。这些结果表明,P物质诱导的甩尾反射促进可能仅通过脊髓机制发生。结果还表明,在脊髓中吗啡优先阻断P物质诱导的信息向脊髓上结构的传递。最后,由于行为反应被镇痛药和脊髓横断所阻断,这被解释为进一步支持如下提议,即这种行为反应表明动物已感知到有害刺激。