Frenk H, Bossut D, Mayer D J
Department of Psychology, Tel-Aviv University, Ramat Aviv, Israel.
Brain Res. 1988 Jul 12;455(2):240-6. doi: 10.1016/0006-8993(88)90082-0.
Intrathecal (i.t.) injections of substance P (SP) and kainic acid in rats produced rostrally directed scratches with the hindlimbs and caudally directed bites or licks. These behaviors, together with myoclonic twitches and vocalization, were also produced by I.T. morphine and strychnine. Intrathecal valproic acid (VA) significantly reduced all behaviors when these occurred spontaneously, and VA and chlordiazepoxide both reduced these behaviors when they were evoked by a light cotton swab tap to the lumbosacral region, in rats treated with the excitatory compounds. Since neither anticonvulsant affected the thermal or mechanical pain threshold at these doses, these results suggest that (a) the behaviors elicited by i.t. injection of the excitatory compounds are not responses to perceived pain, but rather the expression of a spinal convulsive-like state, and (b), since scratching and biting were the only behaviors produced by SP, this peptide is neither necessary nor sufficient for the elicitation of pain at the spinal level. Although our experiments do not rule out other roles for SP in pain processes such as that of a neuromodulator, it is unlikely that this compound is a traditional primary afferent neurotransmitter of pain.
向大鼠鞘内注射P物质(SP)和红藻氨酸会导致后肢向前抓挠以及向后咬或舔。鞘内注射吗啡和士的宁也会引发这些行为,同时还伴有肌阵挛性抽搐和发声。当这些行为自发出现时,鞘内注射丙戊酸(VA)能显著减少所有行为;在用兴奋性化合物处理的大鼠中,当用轻棉棒轻拍腰骶部诱发这些行为时,VA和氯氮卓都能减少这些行为。由于在这些剂量下两种抗惊厥药都未影响热痛或机械痛阈值,这些结果表明:(a)鞘内注射兴奋性化合物引发的行为并非对感知到的疼痛的反应,而是一种脊髓惊厥样状态的表现;(b)由于抓挠和咬是SP产生的唯一行为,该肽对于在脊髓水平引发疼痛既非必要条件也不充分。尽管我们的实验并未排除SP在疼痛过程中的其他作用,如作为神经调节剂的作用,但这种化合物不太可能是传统的疼痛初级传入神经递质。