Abstract
Conclusion
Several types of electrophysiological tests have been applied to the analysis of the pharmacological actions of amino acids. Only the ω-amino acids have been found to have pronounced synaptic effects among the available C2 to C8 compounds. The α-amino acids, with the exception of glycine which has its amino group in the terminal position, are not synaptically active. Synaptic action is reduced or abolished by conversion to the α, ω-diamino compound. The ω-amino acids all act to blockade synapses, but quantitative and qualitative differences characterize the compounds of different carbon length. The C2 to C5 compounds block predominantly the depolarizing, excitatory synapses, while the C6 and C8 ω-amino acids block selectively the hyperpolarizing, inhibitory synapses. Within each group there are quantitative differences in effectiveness of selective action. The findings provide a new series of pharmacological tools for the analysis of the molecular structure and organization of central nervous synapses.
Get full access to this article
View all access options for this article.
