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Pridopidine Reverses Phencyclidine-Induced Memory Impairment

Pridopidine is in clinical trials for Huntington's disease treatment. Originally developed as a dopamine D(2) receptor (D(2)R) ligand, pridopidine displays about 100-fold higher affinity for the sigma-1 receptor (sigma-1R). Interestingly, pridopidine slows disease progression and improves motor...

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Autores principales: Sahlholm, Kristoffer, Valle-León, Marta, Fernández-Dueñas, Víctor, Ciruela, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902730/
https://www.ncbi.nlm.nih.gov/pubmed/29692729
http://dx.doi.org/10.3389/fphar.2018.00338
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author Sahlholm, Kristoffer
Valle-León, Marta
Fernández-Dueñas, Víctor
Ciruela, Francisco
author_facet Sahlholm, Kristoffer
Valle-León, Marta
Fernández-Dueñas, Víctor
Ciruela, Francisco
author_sort Sahlholm, Kristoffer
collection PubMed
description Pridopidine is in clinical trials for Huntington's disease treatment. Originally developed as a dopamine D(2) receptor (D(2)R) ligand, pridopidine displays about 100-fold higher affinity for the sigma-1 receptor (sigma-1R). Interestingly, pridopidine slows disease progression and improves motor function in Huntington's disease model mice and, in preliminarily reports, Huntington's disease patients. The present study examined the anti-amnesic potential of pridopidine. Thus, memory impairment was produced in mice by administration of phencyclidine (PCP, 10 mg/kg/day) for 10 days, followed by 14 days' treatment with pridopidine (6 mg/kg/day), or saline. Finally, novel object recognition performance was assessed in the animals. Mice receiving PCP and saline exhibited deficits in novel object recognition, as expected, while pridopidine treatment counteracted PCP-induced memory impairment. The effect of pridopidine was attenuated by co-administration of the sigma receptor antagonist, NE-100 (10 mg/kg). Our results suggest that pridopidine exerts anti-amnesic and potentially neuroprotective actions. These data provide new insights into the therapeutic potential of pridopidine as a pro-cognitive drug.
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spelling pubmed-59027302018-04-24 Pridopidine Reverses Phencyclidine-Induced Memory Impairment Sahlholm, Kristoffer Valle-León, Marta Fernández-Dueñas, Víctor Ciruela, Francisco Front Pharmacol Pharmacology Pridopidine is in clinical trials for Huntington's disease treatment. Originally developed as a dopamine D(2) receptor (D(2)R) ligand, pridopidine displays about 100-fold higher affinity for the sigma-1 receptor (sigma-1R). Interestingly, pridopidine slows disease progression and improves motor function in Huntington's disease model mice and, in preliminarily reports, Huntington's disease patients. The present study examined the anti-amnesic potential of pridopidine. Thus, memory impairment was produced in mice by administration of phencyclidine (PCP, 10 mg/kg/day) for 10 days, followed by 14 days' treatment with pridopidine (6 mg/kg/day), or saline. Finally, novel object recognition performance was assessed in the animals. Mice receiving PCP and saline exhibited deficits in novel object recognition, as expected, while pridopidine treatment counteracted PCP-induced memory impairment. The effect of pridopidine was attenuated by co-administration of the sigma receptor antagonist, NE-100 (10 mg/kg). Our results suggest that pridopidine exerts anti-amnesic and potentially neuroprotective actions. These data provide new insights into the therapeutic potential of pridopidine as a pro-cognitive drug. Frontiers Media S.A. 2018-04-10 /pmc/articles/PMC5902730/ /pubmed/29692729 http://dx.doi.org/10.3389/fphar.2018.00338 Text en Copyright © 2018 Sahlholm, Valle-León, Fernández-Dueñas and Ciruela. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Sahlholm, Kristoffer
Valle-León, Marta
Fernández-Dueñas, Víctor
Ciruela, Francisco
Pridopidine Reverses Phencyclidine-Induced Memory Impairment
title Pridopidine Reverses Phencyclidine-Induced Memory Impairment
title_full Pridopidine Reverses Phencyclidine-Induced Memory Impairment
title_fullStr Pridopidine Reverses Phencyclidine-Induced Memory Impairment
title_full_unstemmed Pridopidine Reverses Phencyclidine-Induced Memory Impairment
title_short Pridopidine Reverses Phencyclidine-Induced Memory Impairment
title_sort pridopidine reverses phencyclidine-induced memory impairment
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902730/
https://www.ncbi.nlm.nih.gov/pubmed/29692729
http://dx.doi.org/10.3389/fphar.2018.00338
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