Pharmacological detection of AMPA receptor heterogeneity by use of two allosteric potentiators in rat hippocampal cultures (Q24672620)

2

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T Harada

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T Morimoto

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Y Kudo

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S Yamashita

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S Kohsaka

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K Wada

British Journal of Pharmacology

8

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language of work or name

English

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publication date

April 1998

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published in

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volume

123

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issue

7

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page(s)

1294-303

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cites work

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AMPA receptor heterogeneity in rat hippocampal neurons revealed by differential sensitivity to cyclothiazide

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Relative abundance of subunit mRNAs determines gating and Ca2+ permeability of AMPA receptors in principal neurons and interneurons in rat CNS

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Argiotoxin detects molecular differences in AMPA receptor channels.

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Ca2+ permeability of KA-AMPA--gated glutamate receptor channels depends on subunit composition

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Identification of a site in glutamate receptor subunits that controls calcium permeability

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Aniracetam reduces glutamate receptor desensitization and slows the decay of fast excitatory synaptic currents in the hippocampus

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A family of AMPA-selective glutamate receptors

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Identification of a subunit-specific antagonist of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate/kainate receptor channels

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Control of kinetic properties of AMPA receptor channels by nuclear RNA editing

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Glutamate-operated channels: developmentally early and mature forms arise by alternative splicing.

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A molecular determinant for submillisecond desensitization in glutamate receptors

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AMPA receptor flip/flop mutants affecting deactivation, desensitization, and modulation by cyclothiazide, aniracetam, and thiocyanate.

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Hippocampal neurons exhibit cyclothiazide-sensitive rapidly desensitizing responses to kainate.

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A novel allosteric potentiator of AMPA receptors: 4--2-(phenylsulfonylamino)ethylthio--2,6-difluoro-phenoxyaceta mide.

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Flip and Flop: A Cell-Specific Functional Switch in Glutamate-Operated Channels of the CNS

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RNA editing in brain controls a determinant of ion flow in glutamate-gated channels

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Evidence for multiple AMPA receptor complexes in hippocampal CA1/CA2 neurons.

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Benzothiadiazides inhibit rapid glutamate receptor desensitization and enhance glutamatergic synaptic currents.

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release_vc5gmkf7bffirl6vm5t6bmt6ei

Identifiers

DOI

10.1038/SJ.BJP.0701707

0 references

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/vc5gmkf7bffirl6vm5t6bmt6ei

24 November 2022