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Enhanced functional connectivity and volume between cognitive and reward centers of naïve rodent brain produced by pro-dopaminergic agent KB220Z

Dopaminergic reward dysfunction in addictive behaviors is well supported in the literature. There is evidence that alterations in synchronous neural activity between brain regions subserving reward and various cognitive functions may significantly contribute to substance-related disorders. This stud...

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Autores principales: Febo, Marcelo, Blum, Kenneth, Badgaiyan, Rajendra D., Perez, Pablo D., Colon-Perez, Luis M., Thanos, Panayotis K., Ferris, Craig F., Kulkarni, Praveen, Giordano, John, Baron, David, Gold, Mark S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405923/
https://www.ncbi.nlm.nih.gov/pubmed/28445527
http://dx.doi.org/10.1371/journal.pone.0174774
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author Febo, Marcelo
Blum, Kenneth
Badgaiyan, Rajendra D.
Perez, Pablo D.
Colon-Perez, Luis M.
Thanos, Panayotis K.
Ferris, Craig F.
Kulkarni, Praveen
Giordano, John
Baron, David
Gold, Mark S.
author_facet Febo, Marcelo
Blum, Kenneth
Badgaiyan, Rajendra D.
Perez, Pablo D.
Colon-Perez, Luis M.
Thanos, Panayotis K.
Ferris, Craig F.
Kulkarni, Praveen
Giordano, John
Baron, David
Gold, Mark S.
author_sort Febo, Marcelo
collection PubMed
description Dopaminergic reward dysfunction in addictive behaviors is well supported in the literature. There is evidence that alterations in synchronous neural activity between brain regions subserving reward and various cognitive functions may significantly contribute to substance-related disorders. This study presents the first evidence showing that a pro-dopaminergic nutraceutical (KB220Z) significantly enhances, above placebo, functional connectivity between reward and cognitive brain areas in the rat. These include the nucleus accumbens, anterior cingulate gyrus, anterior thalamic nuclei, hippocampus, prelimbic and infralimbic loci. Significant functional connectivity, increased brain connectivity volume recruitment (potentially neuroplasticity), and dopaminergic functionality were found across the brain reward circuitry. Increases in functional connectivity were specific to these regions and were not broadly distributed across the brain. While these initial findings have been observed in drug naïve rodents, this robust, yet selective response implies clinical relevance for addicted individuals at risk for relapse, who show reductions in functional connectivity after protracted withdrawal. Future studies will evaluate KB220Z in animal models of addiction.
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spelling pubmed-54059232017-05-14 Enhanced functional connectivity and volume between cognitive and reward centers of naïve rodent brain produced by pro-dopaminergic agent KB220Z Febo, Marcelo Blum, Kenneth Badgaiyan, Rajendra D. Perez, Pablo D. Colon-Perez, Luis M. Thanos, Panayotis K. Ferris, Craig F. Kulkarni, Praveen Giordano, John Baron, David Gold, Mark S. PLoS One Research Article Dopaminergic reward dysfunction in addictive behaviors is well supported in the literature. There is evidence that alterations in synchronous neural activity between brain regions subserving reward and various cognitive functions may significantly contribute to substance-related disorders. This study presents the first evidence showing that a pro-dopaminergic nutraceutical (KB220Z) significantly enhances, above placebo, functional connectivity between reward and cognitive brain areas in the rat. These include the nucleus accumbens, anterior cingulate gyrus, anterior thalamic nuclei, hippocampus, prelimbic and infralimbic loci. Significant functional connectivity, increased brain connectivity volume recruitment (potentially neuroplasticity), and dopaminergic functionality were found across the brain reward circuitry. Increases in functional connectivity were specific to these regions and were not broadly distributed across the brain. While these initial findings have been observed in drug naïve rodents, this robust, yet selective response implies clinical relevance for addicted individuals at risk for relapse, who show reductions in functional connectivity after protracted withdrawal. Future studies will evaluate KB220Z in animal models of addiction. Public Library of Science 2017-04-26 /pmc/articles/PMC5405923/ /pubmed/28445527 http://dx.doi.org/10.1371/journal.pone.0174774 Text en © 2017 Febo et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Febo, Marcelo
Blum, Kenneth
Badgaiyan, Rajendra D.
Perez, Pablo D.
Colon-Perez, Luis M.
Thanos, Panayotis K.
Ferris, Craig F.
Kulkarni, Praveen
Giordano, John
Baron, David
Gold, Mark S.
Enhanced functional connectivity and volume between cognitive and reward centers of naïve rodent brain produced by pro-dopaminergic agent KB220Z
title Enhanced functional connectivity and volume between cognitive and reward centers of naïve rodent brain produced by pro-dopaminergic agent KB220Z
title_full Enhanced functional connectivity and volume between cognitive and reward centers of naïve rodent brain produced by pro-dopaminergic agent KB220Z
title_fullStr Enhanced functional connectivity and volume between cognitive and reward centers of naïve rodent brain produced by pro-dopaminergic agent KB220Z
title_full_unstemmed Enhanced functional connectivity and volume between cognitive and reward centers of naïve rodent brain produced by pro-dopaminergic agent KB220Z
title_short Enhanced functional connectivity and volume between cognitive and reward centers of naïve rodent brain produced by pro-dopaminergic agent KB220Z
title_sort enhanced functional connectivity and volume between cognitive and reward centers of naïve rodent brain produced by pro-dopaminergic agent kb220z
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405923/
https://www.ncbi.nlm.nih.gov/pubmed/28445527
http://dx.doi.org/10.1371/journal.pone.0174774
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