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3.1 ENHANCED PARVALBUMIN NETWORK ACTIVITY PROLONGS CRITICAL PERIOD PLASTICITY
BACKGROUND: Oscillations in neuronal activity tie the pathophysiology of schizophrenia to alterations in local processing and large-scale coordination, and these alterations in turn can lead to the cognitive and perceptual disturbances observed in schizophrenia. Here, we focus on the dual role of fa...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887339/ http://dx.doi.org/10.1093/schbul/sby014.003 |
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author | Takao, Hensch |
author_facet | Takao, Hensch |
author_sort | Takao, Hensch |
collection | PubMed |
description | BACKGROUND: Oscillations in neuronal activity tie the pathophysiology of schizophrenia to alterations in local processing and large-scale coordination, and these alterations in turn can lead to the cognitive and perceptual disturbances observed in schizophrenia. Here, we focus on the dual role of fast-spiking, parvalbumin (PV+) networks in the generation of gamma oscillations and critical periods of brain plasticity. METHODS: We generated a mouse model of reduced recurrent inhibition only within local PV+ cell networks by selective removal of GABAA receptor alpha1 subunits (PV-α1 KO mice). Electroencephalography (EEG), PV+ immunohistochemistry, perineuronal net (PNN) labeling and redox balance were compared to cortical measures of brain plasticity (loss of visual acuity, formation of preference behaviors) that are typically limited to a critical period early in life. RESULTS: PV-α1 KO mice exhibit chronically enhanced gamma-oscillations and extended juvenile forms of cortical plasticity into adulthood. Acute pharmacological suppression of excitatory input restored E-I balance onto these disinhibited PV+ cells and returned baseline EEG power to normal levels, preventing the extended plasticity. Enhanced gamma oscillations were further found to compromise the integrity of perineuronal nets (PNNs) surrounding PV+ cells, elevating oxidative stress and the turnover of metallopeptidases and structural components of the PNN. All of these aspects were also reversed by pharmacological dampening of excitation onto PV+ cells. DISCUSSION: Cortical gamma oscillations are associated with plasticity and cognition. Our results provide a cellular explanation of how elevated gamma oscillations may promote ectopic brain plasticity by regulating the extracellular matrix which normally stabilizes cortical circuitry. These results carry broad implications for subjects at-risk for schizophrenia who exhibit heightened gamma oscillations prior to psychosis onset (see talk by P Uhlhaas). |
format | Online Article Text |
id | pubmed-5887339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58873392018-04-11 3.1 ENHANCED PARVALBUMIN NETWORK ACTIVITY PROLONGS CRITICAL PERIOD PLASTICITY Takao, Hensch Schizophr Bull Abstracts BACKGROUND: Oscillations in neuronal activity tie the pathophysiology of schizophrenia to alterations in local processing and large-scale coordination, and these alterations in turn can lead to the cognitive and perceptual disturbances observed in schizophrenia. Here, we focus on the dual role of fast-spiking, parvalbumin (PV+) networks in the generation of gamma oscillations and critical periods of brain plasticity. METHODS: We generated a mouse model of reduced recurrent inhibition only within local PV+ cell networks by selective removal of GABAA receptor alpha1 subunits (PV-α1 KO mice). Electroencephalography (EEG), PV+ immunohistochemistry, perineuronal net (PNN) labeling and redox balance were compared to cortical measures of brain plasticity (loss of visual acuity, formation of preference behaviors) that are typically limited to a critical period early in life. RESULTS: PV-α1 KO mice exhibit chronically enhanced gamma-oscillations and extended juvenile forms of cortical plasticity into adulthood. Acute pharmacological suppression of excitatory input restored E-I balance onto these disinhibited PV+ cells and returned baseline EEG power to normal levels, preventing the extended plasticity. Enhanced gamma oscillations were further found to compromise the integrity of perineuronal nets (PNNs) surrounding PV+ cells, elevating oxidative stress and the turnover of metallopeptidases and structural components of the PNN. All of these aspects were also reversed by pharmacological dampening of excitation onto PV+ cells. DISCUSSION: Cortical gamma oscillations are associated with plasticity and cognition. Our results provide a cellular explanation of how elevated gamma oscillations may promote ectopic brain plasticity by regulating the extracellular matrix which normally stabilizes cortical circuitry. These results carry broad implications for subjects at-risk for schizophrenia who exhibit heightened gamma oscillations prior to psychosis onset (see talk by P Uhlhaas). Oxford University Press 2018-04 2018-04-01 /pmc/articles/PMC5887339/ http://dx.doi.org/10.1093/schbul/sby014.003 Text en © Maryland Psychiatric Research Center 2018. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstracts Takao, Hensch 3.1 ENHANCED PARVALBUMIN NETWORK ACTIVITY PROLONGS CRITICAL PERIOD PLASTICITY |
title | 3.1 ENHANCED PARVALBUMIN NETWORK ACTIVITY PROLONGS CRITICAL PERIOD PLASTICITY |
title_full | 3.1 ENHANCED PARVALBUMIN NETWORK ACTIVITY PROLONGS CRITICAL PERIOD PLASTICITY |
title_fullStr | 3.1 ENHANCED PARVALBUMIN NETWORK ACTIVITY PROLONGS CRITICAL PERIOD PLASTICITY |
title_full_unstemmed | 3.1 ENHANCED PARVALBUMIN NETWORK ACTIVITY PROLONGS CRITICAL PERIOD PLASTICITY |
title_short | 3.1 ENHANCED PARVALBUMIN NETWORK ACTIVITY PROLONGS CRITICAL PERIOD PLASTICITY |
title_sort | 3.1 enhanced parvalbumin network activity prolongs critical period plasticity |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887339/ http://dx.doi.org/10.1093/schbul/sby014.003 |
work_keys_str_mv | AT takaohensch 31enhancedparvalbuminnetworkactivityprolongscriticalperiodplasticity |