Isa T, Pettersson L G
Department of Physiology, University of Göteborg, Sweden.
Neurosci Res. 1991 Oct;12(2):388-91. doi: 10.1016/0168-0102(91)90006-k.
The effect of systemic administration of naloxone on transmission in hindlimb reflex pathways was investigated in acute low spinal cats by conditioning monosynaptic reflexes. A marked enhancement of excitatory effects from cutaneous, joint, group II and III muscle afferents was observed in posterior biceps and semitendinosus motoneurones in 4 out of 6 experiments. In contrast, inhibitory synaptic effects in gastrocnemius and soleus motoneurones were not enhanced except weakly in one experiment. The effects of naloxone are different from those observed after spinal cord lesions interrupting axons of a previously described group of upper lumbar propriospinal neurones, which tonically suppress reflex transmission in the acute low spinal state. It is postulated that the suppression exerted by this group of neurones is not dependent on endogenous opioid peptides.
通过条件性单突触反射,在急性低位脊髓猫中研究了全身给予纳洛酮对后肢反射通路传递的影响。在6个实验中的4个实验中,观察到在肱二头肌后束和半腱肌运动神经元中,来自皮肤、关节、II类和III类肌肉传入纤维的兴奋作用显著增强。相比之下,除了在一个实验中有轻微增强外,腓肠肌和比目鱼肌运动神经元中的抑制性突触效应并未增强。纳洛酮的作用与脊髓损伤中断先前描述的一组上腰段脊髓固有神经元的轴突后所观察到的作用不同,该组神经元在急性低位脊髓状态下可紧张性抑制反射传递。据推测,这组神经元所施加的抑制作用不依赖于内源性阿片肽。