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Phenylalanine derivatives with modulating effects on human α1-glycine receptors and anticonvulsant activity in strychnine-induced seizure model in male adult rats.

Abstract
The critical role of α1-glycine receptor (α1-GLYRs) in pathological conditions such as epilepsy is well known. In the present study, structure-activity relations for a series of phenylalanine derivatives carrying selected hydrogen bond acceptors were investigated on the functional properties of human α1-GLYR expressed in Xenopus oocytes. The results indicate that one particular substitution position appeared to be of special importance for control of ligand activity. Among tested ligands (1-8), the biphenyl derivative (2) provided the most promising antagonistic effect on α1-GLYRs, while its phenylbenzyl analogue (5) exhibited the highest potentiation effect. Moreover, ligand 5 with most promising potentiating effect showed in-vivo moderate protection when tested in strychnine (STR)-induced seizure model in male adult rats, whereas ligand 2 with highest antagonistic effect failed to provide appreciable anti(pro)convulsant effect. Furthermore, ligands 2 and 5 with the most promising effects on human α1-GLYRs were examined for their toxicity and potential neuroprotective effect against neurotoxin 6-hydroxydopamine (6-OHDA). The results show that ligands 2 and 5 possessed neither significant antiproliferative effects, nor necrotic and mitochondrial toxicity (up to concentration of 50μM). Moreover, ligand 2 showed weak neuroprotective effect at the 50μM against 100μM toxic dose of 6-OHDA. Our results indicate that modulatory effects of ligands 2 and 5 on human α1-GLYRs as well as on STR-induced convulsion can provide further insights for the design of therapeutic agents in treatment of epilepsy and other pathological conditions requiring enhanced activity of inhibitory glycine receptors.
AuthorsBassem Sadek, Murat Oz, Syed M Nurulain, Petrilla Jayaprakash, Gniewomir Latacz, Katarzyna Kieć-Kononowicz, Ewa Szymańska
JournalEpilepsy research (Epilepsy Res) Vol. 138 Pg. 124-131 (12 2017) ISSN: 1872-6844 [Electronic] Netherlands
PMID28554717 (Publication Type: Journal Article)
CopyrightCopyright © 2017 Elsevier B.V. All rights reserved.
Chemical References
  • Anticonvulsants
  • Convulsants
  • Ligands
  • Receptors, Glycine
  • Phenylalanine
  • Oxidopamine
  • Strychnine
  • Glycine
Topics
  • Animals
  • Anticonvulsants (chemistry, therapeutic use)
  • Convulsants (toxicity)
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Glycine (pharmacology)
  • HEK293 Cells
  • Humans
  • Ligands
  • Male
  • Membrane Potentials (physiology)
  • Microinjections
  • Neuroblastoma (pathology)
  • Oocytes
  • Oxidopamine (pharmacology)
  • Patch-Clamp Techniques
  • Phenylalanine (chemistry, therapeutic use)
  • Rats
  • Rats, Wistar
  • Receptors, Glycine (genetics, metabolism)
  • Seizures (chemically induced, drug therapy, metabolism)
  • Strychnine (toxicity)
  • Transduction, Genetic
  • Xenopus laevis

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