Focal cerebral ischemia in the cat: pretreatment with a competitive NMDA receptor antagonist, D-CPP-ene (Q41978254)

14 October 2017

title

Focal cerebral ischemia in the cat: pretreatment with a competitive NMDA receptor antagonist, D-CPP-ene (English)

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14 October 2017

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Bullock R

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14 October 2017

Graham DI

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14 October 2017

Chen MH

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14 October 2017

Lowe D

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14 October 2017

McCulloch J

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14 October 2017

publication date

1 September 1990

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Journal of Cerebral Blood Flow & Metabolism

14 October 2017

published in

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14 October 2017

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14 October 2017

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14 October 2017

page(s)

668-674

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Elevation of the Extracellular Concentrations of Glutamate and Aspartate in Rat Hippocampus During Transient Cerebral Ischemia Monitored by Intracerebral Microdialysis

14 October 2017

cites work

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Kynurenic acid antagonises responses to NMDA via an action at the strychnine-insensitive glycine receptor

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The N-methyl-D-aspartate antagonists CGS 19755 and CPP reduce ischemic brain damage in gerbils

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Ifenprodil and SL 82.0715 are antagonists at the polyamine site of the N-methyl-D-aspartate (NMDA) receptor

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Pharmacology of glutamate neurotoxicity in cortical cell culture: attenuation by NMDA antagonists

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Neurobiology. Taking apart NMDA receptors

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7 January 2021

The competitive N-methyl-D-aspartate (NMDA) antagonist CGS 19755 attenuates the rate-decreasing effects of NMDA in rhesus monkeys without producing ketamine-like discriminative stimulus effects

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Direct evidence that excitotoxicity in cultured neurons is mediated via N-methyl-D-aspartate (NMDA) as well as non-NMDA receptors

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Kynurenate inhibition of cell excitation decreases stroke size and deficits

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7-Chlorokynurenic acid is a selective antagonist at the glycine modulatory site of the N-methyl-D-aspartate receptor complex

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Effects of MK-801 upon local cerebral glucose utilisation in conscious rats and in rats anaesthetised with halothane

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7 January 2021

Effects of NMDA antagonists, MK-801 and CPP, upon local cerebral glucose use

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7 January 2021

Possible therapeutic applications of antagonists of excitatory amino acid neurotransmitters

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Differential effects of competitive and non-competitive N-methyl-D-aspartate antagonists on glucose use in the limbic system

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7 January 2021

The effects of N-methyl-D-aspartate receptor blockade with MK-801 upon the relationship between cerebral blood flow and glucose utilisation

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Protective effect of the glutamate antagonist, MK-801 in focal cerebral ischemia in the cat.

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7 January 2021

Focal cerebral ischaemia in the cat: treatment with the glutamate antagonist MK-801 after induction of ischaemia

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7 January 2021

The glutamate antagonist MK-801 reduces focal ischemic brain damage in the rat

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7 January 2021

Effect of the NMDA antagonist MK-801 on local cerebral blood flow in focal cerebral ischaemia in the rat

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7 January 2021

An iontophoretic investigation of the actions of convulsant kynurenines and their interaction with the endogenous excitant quinolinic acid

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Glutamate and the pathophysiology of hypoxic--ischemic brain damage

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7 January 2021

Phencyclidine reduces postischemic neuronal necrosis in rat hippocampus without changing blood flow

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7 January 2021

Blockade of N -Methyl-D-Aspartate Receptors May Protect Against Ischemic Damage in the Brain

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7 January 2021

The novel anticonvulsant MK-801: a potent and specific ligand of the brain phencyclidine/sigma-receptor

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7 January 2021

Dextromethorphan protects against cerebral injury following transient focal ischemia in rabbits

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7 January 2021

Long-term development of selective neuronal loss and the mechanism of protection by 2-amino-7-phosphonoheptanoate in a rat model of incomplete forebrain ischaemia

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7 January 2021

Alterations in local cerebral glucose utilization induced by phencyclidine

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7 January 2021

Hypoglycemia-induced neuronal damage prevented by an N-methyl-D-aspartate antagonist

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https://api.crossref.org/works/10.1038%2FJCBFM.1990.120

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FJCBFM.1990.120

7 January 2021

Identifiers

DOI

10.1038/JCBFM.1990.120

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14 October 2017

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