Literature DB >> 7042024

The effects of a series of omega-phosphonic alpha-carboxylic amino acids on electrically evoked and excitant amino acid-induced responses in isolated spinal cord preparations.

R H Evans, A A Francis, A W Jones, D A Smith, J C Watkins.   

Abstract

1 The depressant actions on evoked electrical activity and the excitant amino acid antagonist properties of a range of omega-phosphonic alpha-carboxylic amino acids have been investigated in the isolated spinal cord preparations of the frog or immature rat. 2 When tested on dorsal root-evoked ventral root potentials, members of the homologous series from 2- amino-5-phosphonovaleric acid to 2-amino-8-phosphonooctanoic acid showed depressant actions which correlated with the ability of the substances to antagonize selectivity motoneuronal depolarizations induced by N-methyl-D-aspartate. 3 2-Amino-5-phosphonovalerate was the most potent substance of the series giving an apparent KD of 1.4 microM for the antagonism of responses to N-methyl-D-aspartate. 4 A comparison of the (+)- and (-)-forms of 2-amino-5-phosphonovalerate indicated that the N-methyl-D-aspartate antagonist activity and the neuronal depressant action of this substance were both due mainly to the (-)-isomer. 5 The (-)- and (+)-forms of 2-amino-4-phosphonobutyrate had different actions. The (-)-forms of this substance had a relatively weak and non-selective antagonist action on depolarizations induced by N-methyl-D-aspartate, quisqualate and kainate and a similarly weak depressant effect when tested on evoked electrical activity. The (+)-form was more potent than he (-)-form in depressing electrically evoked activity but did not antagonize responses to amino acid excitants. At concentrations higher than those required to depress electrically evoked activity, the (+)-form produced depolarization. This action was blocked by 2-amino-5-phosphonovalerate.

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Year:  1982        PMID: 7042024      PMCID: PMC2071472          DOI: 10.1111/j.1476-5381.1982.tb08758.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  27 in total

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2.  The interpretation of potential changes in the spinal cord.

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3.  Glutamate as transmitter of hippocampal perforant path.

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Authors:  J C Watkins; R H Evans
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6.  Selective antagonism of amino acid-induced and synaptic excitation in the cat spinal cord.

Authors:  J Davies; J C Watkins
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7.  The effects of amino acids and antagonists on the isolated hemisected spinal cord of the immature rat.

Authors:  R H Evans
Journal:  Br J Pharmacol       Date:  1978-02       Impact factor: 8.739

8.  gamma-Aminobutyric acid agonists: an in vitro comparison between depression of spinal synaptic activity and depolarization of spinal root fibres in the rat.

Authors:  R D Allan; R H Evans; G A Johnston
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9.  Structure-activity relations of excitatory amino acids on frog and rat spinal neurones.

Authors:  T J Biscoe; R H Evans; P M Headley; M R Martin; J C Watkins
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10.  Micromolar L-2-amino-4-phosphonobutyric acid selectively inhibits perforant path synapses from lateral entorhinal cortex.

Authors:  J F Koerner; C W Cotman
Journal:  Brain Res       Date:  1981-07-06       Impact factor: 3.252

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7.  Pharmacological characterization of D-aminophosphonovaleric acid antagonism of amino acid and synaptically evoked excitations on frog motoneurones in vitro: an intracellular study.

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8.  Synaptic and extrasynaptic plasticity in glutamatergic circuits involving dentate granule cells following chronic N-methyl-D-aspartate receptor inhibition.

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10.  Effects of excitatory amino acid antagonists on evoked and spontaneous excitatory potentials in guinea-pig hippocampus.

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