Wilcox G L
Neuropharmacology. 1982 Aug;21(8):745-50. doi: 10.1016/0028-3908(82)90059-4.
The antinociceptive effectiveness of spinally administered opiates raises the question of their neural target in the spinal cord. A large body of evidence points to a site of action on primary afferent fibers before the first central synapse. The dorsal root potential (DRP) is a consequence of phasic presynaptic inhibitory action on the primary afferent fibers. In these studies in the rat, dorsal root potentials, evoked by non-noxious subcutaneous electrical stimulation, were altered by systemic and spinal administration of opiates and by two types of noxious stimulation. Noxious stimulation was accompanied by increased dorsal root potential amplitude, whereas antinociception was associated with decreased dorsal root potential amplitude. Treatment with morphine decreased the dorsal potential and blocked the increase in amplitude induced by noxious by noxious stimuli. These results indicate that nociception and antinociception differentially modulate the phasic component of presynaptic inhibition on primary afferent fibers in the spinal cord.
脊髓给予阿片类药物的抗伤害感受作用引发了其在脊髓中的神经靶点问题。大量证据表明其作用位点在初级传入纤维的第一个中枢突触之前。背根电位(DRP)是对初级传入纤维的阶段性突触前抑制作用的结果。在这些大鼠研究中,无害的皮下电刺激诱发的背根电位会因阿片类药物的全身和脊髓给药以及两种类型的伤害性刺激而改变。伤害性刺激伴随着背根电位幅度增加,而抗伤害感受则与背根电位幅度降低相关。吗啡治疗可降低背根电位,并阻断伤害性刺激诱导的幅度增加。这些结果表明,伤害感受和抗伤害感受对脊髓中初级传入纤维突触前抑制的阶段性成分有不同的调节作用。