Thompson S W, Urban L, Dray A
Department of Neuropharmacology, Sandoz Institute for Medical Research, London, UK.
Brain Res. 1993 Oct 15;625(1):100-8. doi: 10.1016/0006-8993(93)90142-a.
The contribution of neurokinin and NMDA receptor activation to the generation of the prolonged high threshold evoked ventral root potential (VRP) and its temporal summation has been assessed in the neonatal rat hemisected spinal cord maintained in vitro. High intensity single shock stimulation of the dorsal roots evoked a prolonged VRP (9.81 +/- 0.9 s, n = 11). A low frequency (1-10 Hz) repetitive stimulation (20 s duration) of high threshold afferent fibres evoked a summated VRP. This summated VRP reflected the temporal summation of EPSP's in spinal cord neurones which underlies the phenomenon of 'Windup'. The integrated area and duration of the high threshold evoked VRP were significantly reduced following superfusion of the spinal cord with the NK2 receptor antagonist MEN,10376 (100 nM). In the presence of D-AP5 (20 microM) the area of the C-fibre evoked VRP was also significantly reduced. The VRP duration was unaffected. Superfusion with either CP-96,345 (500 nM) or RP,67580 (100 nM), both non-peptide NK1 antagonist, did not have any significant effect upon the area or duration of the prolonged VRP following high threshold stimulation. The simultaneous application of D-AP5 (20 microM) with either MEN,10376 (100 nM) or CP-96,345 (500 nM) together produced a reduction in the area of the evoked VRP which was comparable to the value obtained by addition of their individual effects. The amplitude of the summated VRP was significantly reduced following application of D-AP5 (20 microM). No significant effect upon the amplitude was observed following separate application of either MEN,10376 (100 nM), CP-96,345 (500 nM) or RP,67580 (100 nM).(ABSTRACT TRUNCATED AT 250 WORDS)
在体外维持的新生大鼠半横断脊髓中,已评估了神经激肽和NMDA受体激活对延长的高阈值诱发腹根电位(VRP)的产生及其时间总和的作用。高强度单次电休克刺激背根可诱发延长的VRP(9.81±0.9秒,n = 11)。高阈值传入纤维的低频(1 - 10赫兹)重复刺激(持续20秒)可诱发总和VRP。这种总和VRP反映了脊髓神经元中EPSP的时间总和,它是“windup”现象的基础。用NK2受体拮抗剂MEN,10376(100 nM)灌注脊髓后,高阈值诱发VRP的积分面积和持续时间显著减少。在存在D - AP5(20 microM)的情况下,C纤维诱发VRP的面积也显著减少。VRP持续时间未受影响。用两种非肽NK1拮抗剂CP - 96,345(500 nM)或RP,67580(100 nM)灌注,对高阈值刺激后延长的VRP的面积或持续时间均无显著影响。D - AP5(20 microM)与MEN,