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Optogenetically evoked gamma oscillations are disturbed by cocaine administration
Drugs of abuse have enormous societal impact by degrading the cognitive abilities, emotional state and social behavior of addicted individuals. Among other events involved in the addiction cycle, the study of a single exposure to cocaine, and the contribution of the effects of that event to the cont...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841795/ https://www.ncbi.nlm.nih.gov/pubmed/24376397 http://dx.doi.org/10.3389/fncel.2013.00213 |
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author | Dilgen, Jonathan E. Tompa, Tamas Saggu, Shalini Naselaris, Thomas Lavin, Antonieta |
author_facet | Dilgen, Jonathan E. Tompa, Tamas Saggu, Shalini Naselaris, Thomas Lavin, Antonieta |
author_sort | Dilgen, Jonathan E. |
collection | PubMed |
description | Drugs of abuse have enormous societal impact by degrading the cognitive abilities, emotional state and social behavior of addicted individuals. Among other events involved in the addiction cycle, the study of a single exposure to cocaine, and the contribution of the effects of that event to the continuous and further use of drugs of abuse are fundamental. Gamma oscillations are thought to be important neural correlates of cognitive processing in the prefrontal cortex (PFC) which include decision making, set shifting and working memory. It follows that cocaine exposure might modulate gamma oscillations, which could result in reduced cognitive ability. Parvalbumin-positive fast-spiking interneurons play an orchestrating role in gamma oscillation induction and it has been shown recently that gamma oscillations can be induced in an anesthetized animal using optogenetic techniques. We use a knock-in mouse model together with optogenetics and in vivo electrophysiology to study the effects of acute cocaine on PFC gamma oscillation as a step toward understanding the cortical changes that may underlie continuous use of stimulants. Our results show that acute cocaine administration increases entrainment of the gamma oscillation to the optogentically induced driving frequency. Our results also suggest that this modulation of gamma oscillations is driven trough activation of D1 receptors. The acute cocaine-mediated changes in mPFC may underlie the enhancement of attention and awareness commonly reported by cocaine users and may contribute to the further use and abuse of psychostimulants. |
format | Online Article Text |
id | pubmed-3841795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-38417952013-12-27 Optogenetically evoked gamma oscillations are disturbed by cocaine administration Dilgen, Jonathan E. Tompa, Tamas Saggu, Shalini Naselaris, Thomas Lavin, Antonieta Front Cell Neurosci Neuroscience Drugs of abuse have enormous societal impact by degrading the cognitive abilities, emotional state and social behavior of addicted individuals. Among other events involved in the addiction cycle, the study of a single exposure to cocaine, and the contribution of the effects of that event to the continuous and further use of drugs of abuse are fundamental. Gamma oscillations are thought to be important neural correlates of cognitive processing in the prefrontal cortex (PFC) which include decision making, set shifting and working memory. It follows that cocaine exposure might modulate gamma oscillations, which could result in reduced cognitive ability. Parvalbumin-positive fast-spiking interneurons play an orchestrating role in gamma oscillation induction and it has been shown recently that gamma oscillations can be induced in an anesthetized animal using optogenetic techniques. We use a knock-in mouse model together with optogenetics and in vivo electrophysiology to study the effects of acute cocaine on PFC gamma oscillation as a step toward understanding the cortical changes that may underlie continuous use of stimulants. Our results show that acute cocaine administration increases entrainment of the gamma oscillation to the optogentically induced driving frequency. Our results also suggest that this modulation of gamma oscillations is driven trough activation of D1 receptors. The acute cocaine-mediated changes in mPFC may underlie the enhancement of attention and awareness commonly reported by cocaine users and may contribute to the further use and abuse of psychostimulants. Frontiers Media S.A. 2013-11-27 /pmc/articles/PMC3841795/ /pubmed/24376397 http://dx.doi.org/10.3389/fncel.2013.00213 Text en Copyright © 2013 Dilgen, Tompa, Saggu, Naselaris and Lavin. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 | Neuroscience Dilgen, Jonathan E. Tompa, Tamas Saggu, Shalini Naselaris, Thomas Lavin, Antonieta Optogenetically evoked gamma oscillations are disturbed by cocaine administration |
title | Optogenetically evoked gamma oscillations are disturbed by cocaine administration |
title_full | Optogenetically evoked gamma oscillations are disturbed by cocaine administration |
title_fullStr | Optogenetically evoked gamma oscillations are disturbed by cocaine administration |
title_full_unstemmed | Optogenetically evoked gamma oscillations are disturbed by cocaine administration |
title_short | Optogenetically evoked gamma oscillations are disturbed by cocaine administration |
title_sort | optogenetically evoked gamma oscillations are disturbed by cocaine administration |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841795/ https://www.ncbi.nlm.nih.gov/pubmed/24376397 http://dx.doi.org/10.3389/fncel.2013.00213 |
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