(Q41991056)

English

The mechanism of action and pharmacological specificity of the anticonvulsant NMDA antagonist MK-801: a voltage clamp study on neuronal cells in culture

scientific article published on February 1989

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

The mechanism of action and pharmacological specificity of the anticonvulsant NMDA antagonist MK-801: a voltage clamp study on neuronal cells in culture (English)

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

author name string

Halliwell RF

1

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Peters JA

2

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Lambert JJ

3

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

language of work or name

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publication date

1 February 1989

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

British Journal of Pharmacology

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

96

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

2

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

480-494

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

The mechanism and site of action of ketamine on skeletal muscle.

1 reference

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The dissociative anaesthetics, ketamine and phencyclidine, selectively reduce excitation of central mammalian neurones by N-methyl-aspartate

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Drug-Induced Modification of Ionic Conductance at the Neuromuscular Junction

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Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

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The anticonvulsant MK-801 is a potent N-methyl-D-aspartate antagonist

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Systemic administration of MK-801 protects against ischemia-induced hippocampal neurodegeneration in the gerbil.

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Quantitative autoradiography of [3H]-MK-801 binding sites in mammalian brain

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The novel anticonvulsant MK-801 binds to the activated state of the N-methyl-D-aspartate receptor in rat brain

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Ketamine acts as a non-competitive N-methyl-D-aspartate antagonist on frog spinal cord in vitro.

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Distribution of N-methyl-D-aspartate-sensitive L-[3H]glutamate-binding sites in rat brain.

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Quantitative studies on some antagonists of N-methyl D-aspartate in slices of rat cerebral cortex

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Possible therapeutic applications of antagonists of excitatory amino acid neurotransmitters

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Modulation of the GABAA receptor by depressant barbiturates and pregnane steroids

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Effect of the selective N-methyl-D-aspartate receptor agonist 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid on [3H]flunitrazepam binding

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Coexpression of N-methyl-D-aspartate and phencyclidine receptors in Xenopus oocytes injected with rat brain mRNA

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Differences in results from in vivo and in vitro studies on the use-dependency of N-methylaspartate antagonism by MK-801 and other phencyclidine receptor ligands

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Glycine modulates [3H]MK-801 binding to the NMDA receptor in rat brain

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Block of N-methyl-D-aspartate-activated current by the anticonvulsant MK-801: selective binding to open channels

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Ketamine and phencyclidine cause a voltage-dependent block of responses to L-aspartic acid.

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Effect of the benzodiazepine receptor antagonist Ro 15-1788 on the anticonvulsant and anticonflict actions of MK-801.

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Identifiers

10.1111/J.1476-5381.1989.TB11841.X

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

ResearchGate publication ID

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