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Pregabalin: Potential for Addiction and a Possible Glutamatergic Mechanism

Drug addiction remains a prevalent and fatal disease worldwide that carries significant social and economic impacts. Recent reports suggest illicit pregabalin (Lyrica) use may be increasing among youth, however the addictive potential of pregabalin has not been well established. Drug seeking behavio...

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Autores principales: Althobaiti, Yusuf S., Almalki, Atiah, Alsaab, Hashem, Alsanie, Walaa, Gaber, Ahmed, Alhadidi, Qasim, Hardy, Ana Maria Gregio, Nasr, Abdulrahman, Alzahrani, Omar, Stary, Creed M., Shah, Zahoor A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805907/
https://www.ncbi.nlm.nih.gov/pubmed/31641170
http://dx.doi.org/10.1038/s41598-019-51556-4
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author Althobaiti, Yusuf S.
Almalki, Atiah
Alsaab, Hashem
Alsanie, Walaa
Gaber, Ahmed
Alhadidi, Qasim
Hardy, Ana Maria Gregio
Nasr, Abdulrahman
Alzahrani, Omar
Stary, Creed M.
Shah, Zahoor A.
author_facet Althobaiti, Yusuf S.
Almalki, Atiah
Alsaab, Hashem
Alsanie, Walaa
Gaber, Ahmed
Alhadidi, Qasim
Hardy, Ana Maria Gregio
Nasr, Abdulrahman
Alzahrani, Omar
Stary, Creed M.
Shah, Zahoor A.
author_sort Althobaiti, Yusuf S.
collection PubMed
description Drug addiction remains a prevalent and fatal disease worldwide that carries significant social and economic impacts. Recent reports suggest illicit pregabalin (Lyrica) use may be increasing among youth, however the addictive potential of pregabalin has not been well established. Drug seeking behavior and chronic drug use are associated with deficits in glutamate clearance and activation of postsynaptic glutamatergic receptors. In the current study, we investigated the abuse potential of pregabalin using conditioned place preference (CPP) paradigm. Different doses of pregabalin (30, 60, 90, and 120 mg/kg) were used to assess the seeking behavior in mice. Glutamate homeostasis is maintained by glutamate transporter type-1 (GLT-1), which plays a vital role in clearing the released glutamate from synapses and drug seeking behavior. Therefore, we investigated the role of glutamate in pregabalin-seeking behavior with ceftriaxone (CEF), a potent GLT-1 upregulator. Mice treated with pregabalin 60 and 90 mg/kg doses demonstrated drug seeking-like behavior, which was significantly blocked by CEF pretreatment. These results suggest that pregabalin-induced CPP was successfully modulated by CEF which could serve as a lead compound for developing treatment for pregabalin abuse.
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spelling pubmed-68059072019-10-24 Pregabalin: Potential for Addiction and a Possible Glutamatergic Mechanism Althobaiti, Yusuf S. Almalki, Atiah Alsaab, Hashem Alsanie, Walaa Gaber, Ahmed Alhadidi, Qasim Hardy, Ana Maria Gregio Nasr, Abdulrahman Alzahrani, Omar Stary, Creed M. Shah, Zahoor A. Sci Rep Article Drug addiction remains a prevalent and fatal disease worldwide that carries significant social and economic impacts. Recent reports suggest illicit pregabalin (Lyrica) use may be increasing among youth, however the addictive potential of pregabalin has not been well established. Drug seeking behavior and chronic drug use are associated with deficits in glutamate clearance and activation of postsynaptic glutamatergic receptors. In the current study, we investigated the abuse potential of pregabalin using conditioned place preference (CPP) paradigm. Different doses of pregabalin (30, 60, 90, and 120 mg/kg) were used to assess the seeking behavior in mice. Glutamate homeostasis is maintained by glutamate transporter type-1 (GLT-1), which plays a vital role in clearing the released glutamate from synapses and drug seeking behavior. Therefore, we investigated the role of glutamate in pregabalin-seeking behavior with ceftriaxone (CEF), a potent GLT-1 upregulator. Mice treated with pregabalin 60 and 90 mg/kg doses demonstrated drug seeking-like behavior, which was significantly blocked by CEF pretreatment. These results suggest that pregabalin-induced CPP was successfully modulated by CEF which could serve as a lead compound for developing treatment for pregabalin abuse. Nature Publishing Group UK 2019-10-22 /pmc/articles/PMC6805907/ /pubmed/31641170 http://dx.doi.org/10.1038/s41598-019-51556-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Althobaiti, Yusuf S.
Almalki, Atiah
Alsaab, Hashem
Alsanie, Walaa
Gaber, Ahmed
Alhadidi, Qasim
Hardy, Ana Maria Gregio
Nasr, Abdulrahman
Alzahrani, Omar
Stary, Creed M.
Shah, Zahoor A.
Pregabalin: Potential for Addiction and a Possible Glutamatergic Mechanism
title Pregabalin: Potential for Addiction and a Possible Glutamatergic Mechanism
title_full Pregabalin: Potential for Addiction and a Possible Glutamatergic Mechanism
title_fullStr Pregabalin: Potential for Addiction and a Possible Glutamatergic Mechanism
title_full_unstemmed Pregabalin: Potential for Addiction and a Possible Glutamatergic Mechanism
title_short Pregabalin: Potential for Addiction and a Possible Glutamatergic Mechanism
title_sort pregabalin: potential for addiction and a possible glutamatergic mechanism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6805907/
https://www.ncbi.nlm.nih.gov/pubmed/31641170
http://dx.doi.org/10.1038/s41598-019-51556-4
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