Evans R H, Watkins J C
Eur J Pharmacol. 1978 Jul 15;50(2):123-9. doi: 10.1016/0014-2999(78)90007-9.
The specificity of the neurodepressant actions of D-alpha-aminoadipate, alpha,epsilon-diaminopimelic acid, HA-966 (HAP) and Mg2+ has been investigated. On the isolated spinal cord of the neonatal rat, ventral root depolarizations produced by kainate, substance P, carbachol and noradrenaline were relatively unaffected by the same concentrations (0.25--1 mM) of the agents as those which reduced synaptic activity and ventral root depolarizations produced by N-methyl-D-aspartate (especially), L-aspartate and L-glutamate. The same or higher concentrations of the agents did not affect excitatory transmission in the isolated rat superior cervical ganglion. It is proposed that the agents specifically block synaptic transmission mediated by an excitatory amino acid.
已对D-α-氨基己二酸、α,ε-二氨基庚二酸、HA-966(HAP)和Mg2+的神经抑制作用的特异性进行了研究。在新生大鼠的离体脊髓上,由海藻酸、P物质、卡巴胆碱和去甲肾上腺素引起的腹根去极化相对不受相同浓度(0.25 - 1 mM)这些药物的影响,而这些浓度的药物会降低由N-甲基-D-天冬氨酸(尤其是)、L-天冬氨酸和L-谷氨酸引起的突触活动和腹根去极化。相同或更高浓度的这些药物对离体大鼠颈上神经节中的兴奋性传递没有影响。有人提出,这些药物特异性地阻断由兴奋性氨基酸介导的突触传递。