Do stereoisomers of homocysteic acid exhibit different convulsant action in immature rats?

Mechanism of ictogenesis of D- and L-stereroisomers of homocysteic acid was studied in 12-day-old rats by means of antagonists of N-methyl-D-aspartate (NMDA) and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors. There was no qualitative difference between the two stereoisome...

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Veröffentlicht in:Physiological research 2019-01, Vol.68 (Suppl 3), p.S361-S366
Hauptverfasser: Mareš, P, Folbergrová, J, Haugvicová, R, Kubová, H
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Sprache:eng
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Zusammenfassung:Mechanism of ictogenesis of D- and L-stereroisomers of homocysteic acid was studied in 12-day-old rats by means of antagonists of N-methyl-D-aspartate (NMDA) and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors. There was no qualitative difference between the two stereoisomers in generation of emprosthotonic (flexion) as well as generalized tonic-clonic seizures. Moderate differences were observed in the first, nonconvulsive effects of the two isomers. As generation of the two types of seizures is concerned, NMDA and AMPA participate in generalized tonic-clonic seizures whereas NMDA receptors play a dominant role in generation of flexion seizures.
ISSN:0862-8408
1802-9973
DOI:10.33549/physiolres.934347