Proton inhibition of N-methyl-D-aspartate receptors in cerebellar neurons.

Article date: 1990/5/24

PubMed ID: 1692970

Journal name: Nature (ISSN: 0028-0836)


Mammalian neurons contain at least three types of excitatory amino-acid receptors, selectively activated by N-methyl-D-aspartate (NMDA) or aspartate, (S)-alpha-amino-3-hydroxy-5-methyl-4-isoxazole proprionate ((S)-AMPA) and kainate. An important aspect of NMDA receptors is their regulation by a variety of factors such as glycine, Mg2+ and Zn2+ that are present in vivo. We show here that NMDA receptor responses are selectively inhibited by protons, with a 50% inhibitory concentration (IC50) that is close to physiological pH, implying that NMDA receptors are not fully active under normal conditions. (S)-AMPA and kainate responses remain unchanged at similar pH levels. Proton inhibition is voltage-insensitive and does not result either from fast channel block, a change in channel conductance, or an increase in the 50% excitatory concentration (EC50) of aspartate/NMDA or glycine. Instead, protons seem to decrease markedly the opening frequency of 30-50 pS NMDA channels, and reduce the relative proportion of longer bursts. This feature of NMDA receptors could be relevant to neurotoxic activation of NMDA receptors during ischaemia, as well as to seizure generation, as extracellular proton changes occur during both of these pathological situations. Furthermore, these results may have implications for normal NMDA receptor function as transient changes in extracellular protons occur during synaptic transmission.

This document is available from: http://directlinks.cc/files/muscimol/1692970.pdf

Author List: Traynelis S F, Cull-Candy S G

Publication Types: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

Substances mentioned in the article: Ion Channels; Protons; Receptors, N-Methyl-D-Aspartate; Receptors, Neurotransmitter; Ibotenic Acid; Aspartic Acid; N-Methylaspartate; alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid; Kainic Acid; Glycine;

Mesh terms: Animals; Aspartic Acid/analogs & derivatives; Binding Sites; Cerebellum/cytology; Electric Conductivity; Glycine/pharmacology; Hydrogen-Ion Concentration; Ibotenic Acid/analogs & derivatives; Ion Channels/physiology; Kainic Acid/pharmacology; N-Methylaspartate; Neurons/metabolism; Protons; Receptors, N-Methyl-D-Aspartate; Receptors, Neurotransmitter/antagonists & inhibitors; alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid;

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