| Literature DB >> 1976410 |
H Pan-Hou1, Y Suda, Y Ohe, M Sumi, M Yoshioka.
Abstract
Aspartame (L-aspartyl-L-phenylalanine methyl ester), an artificial low-calorie sweetener, was shown to dose-dependently inhibit L-[3H]glutamate binding to its N-methyl-D-aspartate-specific receptors. L-Aspartic acid, a major endogenous metabolite of aspartame, inhibited the binding more stronger than aspartame, while the other metabolites, L-phenylalanine and methanol, had no effect at the same concentration. Aspartame caused a significant change in the affinities of L-[3H]glutamate binding without altering the Vmax values of the binding, suggesting the inhibition is competitive. These in vitro findings suggested that aspartame may act directly on the N-methyl-D-aspartate-sensitive glutamate recognition sites in the brain synaptic membranes.Entities:
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Year: 1990 PMID: 1976410 DOI: 10.1016/0006-8993(90)91729-z
Source DB: PubMed Journal: Brain Res ISSN: 0006-8993 Impact factor: 3.252