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Closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man

Reward hypersensitization is a common feature of neuropsychiatric disorders, manifesting as impulsivity for anticipated incentives. Temporally specific changes in activity within the nucleus accumbens (NAc), which occur during anticipatory periods preceding consummatory behavior, represent a critica...

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Autores principales: Wu, Hemmings, Miller, Kai J., Blumenfeld, Zack, Williams, Nolan R., Ravikumar, Vinod K., Lee, Karen E., Kakusa, Bina, Sacchet, Matthew D., Wintermark, Max, Christoffel, Daniel J., Rutt, Brian K., Bronte-Stewart, Helen, Knutson, Brian, Malenka, Robert C., Halpern, Casey H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776799/
https://www.ncbi.nlm.nih.gov/pubmed/29255043
http://dx.doi.org/10.1073/pnas.1712214114
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author Wu, Hemmings
Miller, Kai J.
Blumenfeld, Zack
Williams, Nolan R.
Ravikumar, Vinod K.
Lee, Karen E.
Kakusa, Bina
Sacchet, Matthew D.
Wintermark, Max
Christoffel, Daniel J.
Rutt, Brian K.
Bronte-Stewart, Helen
Knutson, Brian
Malenka, Robert C.
Halpern, Casey H.
author_facet Wu, Hemmings
Miller, Kai J.
Blumenfeld, Zack
Williams, Nolan R.
Ravikumar, Vinod K.
Lee, Karen E.
Kakusa, Bina
Sacchet, Matthew D.
Wintermark, Max
Christoffel, Daniel J.
Rutt, Brian K.
Bronte-Stewart, Helen
Knutson, Brian
Malenka, Robert C.
Halpern, Casey H.
author_sort Wu, Hemmings
collection PubMed
description Reward hypersensitization is a common feature of neuropsychiatric disorders, manifesting as impulsivity for anticipated incentives. Temporally specific changes in activity within the nucleus accumbens (NAc), which occur during anticipatory periods preceding consummatory behavior, represent a critical opportunity for intervention. However, no available therapy is capable of automatically sensing and therapeutically responding to this vulnerable moment in time when anticipation-related neural signals may be present. To identify translatable biomarkers for an off-the-shelf responsive neurostimulation system, we record local field potentials from the NAc of mice and a human anticipating conventional rewards. We find increased power in 1- to 4-Hz oscillations predominate during reward anticipation, which can effectively trigger neurostimulation that reduces consummatory behavior in mice sensitized to highly palatable food. Similar oscillations are present in human NAc during reward anticipation, highlighting the translational potential of our findings in the development of a treatment for a major unmet need.
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spelling pubmed-57767992018-01-23 Closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man Wu, Hemmings Miller, Kai J. Blumenfeld, Zack Williams, Nolan R. Ravikumar, Vinod K. Lee, Karen E. Kakusa, Bina Sacchet, Matthew D. Wintermark, Max Christoffel, Daniel J. Rutt, Brian K. Bronte-Stewart, Helen Knutson, Brian Malenka, Robert C. Halpern, Casey H. Proc Natl Acad Sci U S A Biological Sciences Reward hypersensitization is a common feature of neuropsychiatric disorders, manifesting as impulsivity for anticipated incentives. Temporally specific changes in activity within the nucleus accumbens (NAc), which occur during anticipatory periods preceding consummatory behavior, represent a critical opportunity for intervention. However, no available therapy is capable of automatically sensing and therapeutically responding to this vulnerable moment in time when anticipation-related neural signals may be present. To identify translatable biomarkers for an off-the-shelf responsive neurostimulation system, we record local field potentials from the NAc of mice and a human anticipating conventional rewards. We find increased power in 1- to 4-Hz oscillations predominate during reward anticipation, which can effectively trigger neurostimulation that reduces consummatory behavior in mice sensitized to highly palatable food. Similar oscillations are present in human NAc during reward anticipation, highlighting the translational potential of our findings in the development of a treatment for a major unmet need. National Academy of Sciences 2018-01-02 2017-12-18 /pmc/articles/PMC5776799/ /pubmed/29255043 http://dx.doi.org/10.1073/pnas.1712214114 Text en Copyright © 2017 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Wu, Hemmings
Miller, Kai J.
Blumenfeld, Zack
Williams, Nolan R.
Ravikumar, Vinod K.
Lee, Karen E.
Kakusa, Bina
Sacchet, Matthew D.
Wintermark, Max
Christoffel, Daniel J.
Rutt, Brian K.
Bronte-Stewart, Helen
Knutson, Brian
Malenka, Robert C.
Halpern, Casey H.
Closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man
title Closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man
title_full Closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man
title_fullStr Closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man
title_full_unstemmed Closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man
title_short Closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man
title_sort closing the loop on impulsivity via nucleus accumbens delta-band activity in mice and man
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776799/
https://www.ncbi.nlm.nih.gov/pubmed/29255043
http://dx.doi.org/10.1073/pnas.1712214114
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