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Disrupted GABAergic facilitation of working memory performance in people with schizophrenia

OBJECTIVES: Gamma-Amiobutyric acid (GABA) is a primary inhibitory neurotransmitter that facilitates neural oscillations that coordinate neural activity between brain networks to facilitate cognition. The present magnetic resonance spectroscopy (MRS) study tests the hypothesis that GABAergic facilita...

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Autores principales: Ragland, J.D., Maddock, R.J., Hurtado, M.Y., Tanase, C., Lesh, T.A., Niendam, T.A., Carter, C.S., Ranganath, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928454/
https://www.ncbi.nlm.nih.gov/pubmed/31864216
http://dx.doi.org/10.1016/j.nicl.2019.102127
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author Ragland, J.D.
Maddock, R.J.
Hurtado, M.Y.
Tanase, C.
Lesh, T.A.
Niendam, T.A.
Carter, C.S.
Ranganath, C.
author_facet Ragland, J.D.
Maddock, R.J.
Hurtado, M.Y.
Tanase, C.
Lesh, T.A.
Niendam, T.A.
Carter, C.S.
Ranganath, C.
author_sort Ragland, J.D.
collection PubMed
description OBJECTIVES: Gamma-Amiobutyric acid (GABA) is a primary inhibitory neurotransmitter that facilitates neural oscillations that coordinate neural activity between brain networks to facilitate cognition. The present magnetic resonance spectroscopy (MRS) study tests the hypothesis that GABAergic facilitation of working memory is disrupted in people with schizophrenia (PSZ). METHODS: 51 healthy participants and 40 PSZ from the UC Davis Early Psychosis Program performed an item and temporal order working memory (WM) task and underwent resting MRS to measure GABA and glutamate concentrations in dorsolateral prefrontal (DLPFC) and anterior cingulate (ACC) regions of interest. MRS was acquired on a 3 Tesla Siemens scanner and GABA and glutamate concentrations were referenced to creatine. Percent correct on the WM task indexed performance and correlation coefficients examined GABAergic or Glutamatergic facilitation of WM, with Fisher's Z transformation testing for group differences. RESULTS: There were no group differences in GABA or glutamate concentrations, but WM correlations were reversed between groups. In patients, higher DLPFC GABA was associated with worse rather than better WM performance. This pattern was not observed for glutamate or in the ACC. Although under-powered, there was no indication of medication effects. CONCLUSIONS AND RELEVANCE: Results cannot be explained by group differences in DLPFC GABA or glutamate concentrations but, instead, indicate that schizophrenia disrupts the GABAergic facilitation of WM seen in healthy individuals. Results appear to parallel post mortem findings in suggesting that schizophrenia alters the distribution of different classes of GABAergic interneurons rather than producing a general deficit across the total population of neurons.
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spelling pubmed-69284542019-12-30 Disrupted GABAergic facilitation of working memory performance in people with schizophrenia Ragland, J.D. Maddock, R.J. Hurtado, M.Y. Tanase, C. Lesh, T.A. Niendam, T.A. Carter, C.S. Ranganath, C. Neuroimage Clin Regular Article OBJECTIVES: Gamma-Amiobutyric acid (GABA) is a primary inhibitory neurotransmitter that facilitates neural oscillations that coordinate neural activity between brain networks to facilitate cognition. The present magnetic resonance spectroscopy (MRS) study tests the hypothesis that GABAergic facilitation of working memory is disrupted in people with schizophrenia (PSZ). METHODS: 51 healthy participants and 40 PSZ from the UC Davis Early Psychosis Program performed an item and temporal order working memory (WM) task and underwent resting MRS to measure GABA and glutamate concentrations in dorsolateral prefrontal (DLPFC) and anterior cingulate (ACC) regions of interest. MRS was acquired on a 3 Tesla Siemens scanner and GABA and glutamate concentrations were referenced to creatine. Percent correct on the WM task indexed performance and correlation coefficients examined GABAergic or Glutamatergic facilitation of WM, with Fisher's Z transformation testing for group differences. RESULTS: There were no group differences in GABA or glutamate concentrations, but WM correlations were reversed between groups. In patients, higher DLPFC GABA was associated with worse rather than better WM performance. This pattern was not observed for glutamate or in the ACC. Although under-powered, there was no indication of medication effects. CONCLUSIONS AND RELEVANCE: Results cannot be explained by group differences in DLPFC GABA or glutamate concentrations but, instead, indicate that schizophrenia disrupts the GABAergic facilitation of WM seen in healthy individuals. Results appear to parallel post mortem findings in suggesting that schizophrenia alters the distribution of different classes of GABAergic interneurons rather than producing a general deficit across the total population of neurons. Elsevier 2019-12-13 /pmc/articles/PMC6928454/ /pubmed/31864216 http://dx.doi.org/10.1016/j.nicl.2019.102127 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Ragland, J.D.
Maddock, R.J.
Hurtado, M.Y.
Tanase, C.
Lesh, T.A.
Niendam, T.A.
Carter, C.S.
Ranganath, C.
Disrupted GABAergic facilitation of working memory performance in people with schizophrenia
title Disrupted GABAergic facilitation of working memory performance in people with schizophrenia
title_full Disrupted GABAergic facilitation of working memory performance in people with schizophrenia
title_fullStr Disrupted GABAergic facilitation of working memory performance in people with schizophrenia
title_full_unstemmed Disrupted GABAergic facilitation of working memory performance in people with schizophrenia
title_short Disrupted GABAergic facilitation of working memory performance in people with schizophrenia
title_sort disrupted gabaergic facilitation of working memory performance in people with schizophrenia
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928454/
https://www.ncbi.nlm.nih.gov/pubmed/31864216
http://dx.doi.org/10.1016/j.nicl.2019.102127
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