Fleetwood-Walker S M, Mitchell R, Hope P J, El-Yassir N, Molony V, Bladon C M
Department of Preclinical Veterinary Sciences, Royal (Dick) School of Veterinary Studies, Summerhall, Edinburgh, U.K.
Brain Res. 1990 Jun 11;519(1-2):169-82. doi: 10.1016/0006-8993(90)90075-m.
As well as substance P (SP), neurokinin A (NKA) and neurokinin B (NKB) have recently been found in the superficial dorsal horn of the spinal cord; NKA originating mainly in fine primary afferents. We have investigated the effects of these tachykinins and a range of analogues on somatosensory responses of single identified dorsal horn neurons, when applied ionophoretically to the region of the substantia gelatinosa. Behavioural reflex tests of thermal nociception were carried out in parallel. The role of NK-1, NK-2 and NK-3 receptors was addressed. NK-1-selective agonists attenuated the non-nociceptive responses of identified multireceptive spinocervical tract (SCT) neurons. Of the endogenous tachykinins, both SP and NKB (a weak NK-1 agonist) showed this effect. No role for NK-3 receptors was identified in our experiments. NK-2-selective agonists (including NKA) caused a unique and selective facilitation of thermal nociceptive responses. NKA also reduced reflex response latency in tail-flick and hot plate tests. NKA as a primary afferent transmitter may thus be involved in mediating or facilitating the expression of thermal nociceptive inputs in the substantia gelatinosa. NKA and SP could be considered as acting in concert in the superficial dorsal horn in an effectively pro-nociceptive modulatory role. Evidence from receptor-selective antagonists supports that obtained with agonists for the roles of particular NK receptors in somatosensory processing. NK-2, but not NK-1 or NK-3 antagonists attenuated endogenous thermal nociceptive responses, supporting the hypothesis that an NK-2 agonist (such as NKA) may normally participate in expression of thermal nociception in the superficial dorsal horn. Behavioural experiments showing increased response latencies with a putative NK-2 selective antagonist further supported the involvement of NK-2 receptors in thermal nociception.
除了P物质(SP)之外,最近还在脊髓背角浅层发现了神经激肽A(NKA)和神经激肽B(NKB);NKA主要起源于细的初级传入纤维。我们研究了这些速激肽及其一系列类似物在通过离子导入法施加到脊髓胶状质区域时,对单个已鉴定的背角神经元体感反应的影响。同时进行了热痛觉行为反射测试。探讨了NK-1、NK-2和NK-3受体的作用。NK-1选择性激动剂减弱了已鉴定的多感受性脊髓颈段束(SCT)神经元的非痛觉反应。在内源性速激肽中,SP和NKB(一种弱NK-1激动剂)都表现出这种作用。在我们的实验中未发现NK-3受体的作用。NK-2选择性激动剂(包括NKA)对热痛觉反应产生独特且选择性的易化作用。NKA还缩短了甩尾和热板试验中的反射反应潜伏期。因此,NKA作为一种初级传入递质可能参与介导或促进脊髓胶状质中热痛觉输入的表达。NKA和SP可被认为在背角浅层协同发挥有效的促痛觉调制作用。来自受体选择性拮抗剂的证据支持了激动剂所获得的关于特定NK受体在体感处理中作用的证据。NK-2拮抗剂而非NK-1或NK-3拮抗剂减弱了内源性热痛觉反应,支持了NK-2激动剂(如NKA)可能正常参与背角浅层热痛觉表达的假说。行为实验显示,使用一种假定的NK-2选择性拮抗剂时反应潜伏期延长,进一步支持了NK-2受体参与热痛觉感受的观点。