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Glycine antagonist activity
- Publisher
- Wiley
- Copyright
- Copyright © 1990 Wiley Subscription Services, Inc., A Wiley Company
- ISSN
- 0022-3042
- eISSN
- 1471-4159
- DOI
- 10.1111/j.1471-4159.1990.tb02355.x
- Publisher site
- See Article on Publisher Site
Abstract
Abstract: In synaptic plasma membranes from rat forebrain, the potencies of glycine recognition site agonists and antagonists for modulating (3H)1‐(1‐(2‐thienyl)cyclohexyl)piperidine ((3H)TCP) binding and for displacing strychnine‐insensitive (3H)glycine binding are altered in the presence of N‐methyl‐D‐aspartate (NMDA) recognition site ligands. The NMDA competitive antagonist, cis‐4‐phosphonomethyl‐2‐piperidine carboxylate (CGS 19755), reduces (3H)glycine binding, and the reduction can be fully reversed by the NMDA recognition site agonist, L‐glutamate. Scatchard analysis of (3H)glycine binding shows that in the presence of CGS 19755 there is no change in Bmax (8.81 vs. 8.79 pmol/mg of protein), but rather a decrease in the affinity of glycine (KD of 0.202 γM vs. 0.129 γM). Similar decreases in affinity are observed for the glycine site agonists, D‐serine and 1‐aminocyclopropane‐1‐carboxylate, in the presence of CGS 19755. In contrast, the affinity of glycine antagonists, 1‐hydroxy‐3‐amino‐2‐pyrrolidone and 1‐aminocyclobutane‐1‐carboxylate, at this (3H)glycine recognition site increases in the presence of CGS 19755. The functional consequence of this change in affinity was addressed using the modulation of (3H)TCP binding. In the presence of L‐glutamate, the potency of glycine agonists for the stimulation of (3H)TCP binding increases, whereas the potency of glycine antagonists decreases. These data are consistent with NMDA recognition site ligands, through their interactions at the NMDA recognition site, modulating activity at the associated glycine recognition site.
Journal
Journal of Neurochemistry – Wiley
Published: Mar 1, 1990