Clarke R W, Ford T W, Taylor J S
Department of Physiology and Environmental Science, University of Nottingham, School of Agriculture, Loughborough, Leicestershire, U.K.
Brain Res. 1989 Dec 25;505(1):1-6. doi: 10.1016/0006-8993(89)90108-x.
The short-latency sural to gastrocnemius reflex in the decerebrated rabbit was depressed for 20-30 min following high intensity conditioning stimulation of the common peroneal nerve. This effect was observed in animals with or without spinal section, but was greater in non-spinalized preparations. Graded conditioning stimuli showed that it was necessary to activate fine myelinated common peroneal axons to inhibit the reflex. In spinalized rabbits, maximal inhibition was achieved with conditioning stimulation of fine myelinated axons and was completely reversed by the opioid antagonist naloxone. In non-spinalized rabbits, maximal inhibition was only obtained with conditioning stimuli which activated non-myelinated axons. In these preparations the effects of common peroneal nerve stimuli were only blocked by co-administration of naloxone with the alpha 2-adrenoceptor antagonist idazoxan. Thus high intensity peripheral nerve stimuli activated a segmental opioidergic and a supraspinal adrenergic suppression of the sural-gastrocnemius withdrawal reflex. Such long-lasting suppression of reflex excitability may contribute to recovery from intensely noxious stimuli.
在对去大脑家兔的腓总神经进行高强度条件刺激后,腓肠肌短潜伏期腓肠神经反射被抑制20 - 30分钟。在有或没有脊髓横断的动物中均观察到这种效应,但在未进行脊髓横断的标本中更为明显。分级条件刺激表明,激活细有髓鞘的腓总神经轴突对于抑制该反射是必要的。在脊髓横断的家兔中,通过对细有髓鞘轴突进行条件刺激可实现最大抑制,且这种抑制可被阿片类拮抗剂纳洛酮完全逆转。在未进行脊髓横断的家兔中,只有通过激活无髓鞘轴突的条件刺激才能获得最大抑制。在这些标本中,腓总神经刺激的效应仅在纳洛酮与α₂肾上腺素能受体拮抗剂咪唑克生联合给药时被阻断。因此,高强度外周神经刺激激活了节段性阿片能和脊髓上肾上腺素能对腓肠肌 - 腓肠神经退缩反射的抑制。这种对反射兴奋性的长期抑制可能有助于从强烈的有害刺激中恢复。