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Glutathione in the nucleus accumbens regulates motivation to exert reward-incentivized effort

Emerging evidence is implicating mitochondrial function and metabolism in the nucleus accumbens in motivated performance. However, the brain is vulnerable to excessive oxidative insults resulting from neurometabolic processes, and whether antioxidant levels in the nucleus accumbens contribute to mot...

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Autores principales: Zalachoras, Ioannis, Ramos-Fernández, Eva, Hollis, Fiona, Trovo, Laura, Rodrigues, João, Strasser, Alina, Zanoletti, Olivia, Steiner, Pascal, Preitner, Nicolas, Xin, Lijing, Astori, Simone, Sandi, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642999/
https://www.ncbi.nlm.nih.gov/pubmed/36345724
http://dx.doi.org/10.7554/eLife.77791
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author Zalachoras, Ioannis
Ramos-Fernández, Eva
Hollis, Fiona
Trovo, Laura
Rodrigues, João
Strasser, Alina
Zanoletti, Olivia
Steiner, Pascal
Preitner, Nicolas
Xin, Lijing
Astori, Simone
Sandi, Carmen
author_facet Zalachoras, Ioannis
Ramos-Fernández, Eva
Hollis, Fiona
Trovo, Laura
Rodrigues, João
Strasser, Alina
Zanoletti, Olivia
Steiner, Pascal
Preitner, Nicolas
Xin, Lijing
Astori, Simone
Sandi, Carmen
author_sort Zalachoras, Ioannis
collection PubMed
description Emerging evidence is implicating mitochondrial function and metabolism in the nucleus accumbens in motivated performance. However, the brain is vulnerable to excessive oxidative insults resulting from neurometabolic processes, and whether antioxidant levels in the nucleus accumbens contribute to motivated performance is not known. Here, we identify a critical role for glutathione (GSH), the most important endogenous antioxidant in the brain, in motivation. Using proton magnetic resonance spectroscopy at ultra-high field in both male humans and rodent populations, we establish that higher accumbal GSH levels are highly predictive of better, and particularly, steady performance over time in effort-related tasks. Causality was established in in vivo experiments in rats that, first, showed that downregulating GSH levels through micro-injections of the GSH synthesis inhibitor buthionine sulfoximine in the nucleus accumbens impaired effort-based reward-incentivized performance. In addition, systemic treatment with the GSH precursor N-acetyl-cysteine increased accumbal GSH levels in rats and led to improved performance, potentially mediated by a cell-type-specific shift in glutamatergic inputs to accumbal medium spiny neurons. Our data indicate a close association between accumbal GSH levels and an individual’s capacity to exert reward-incentivized effort over time. They also suggest that improvement of accumbal antioxidant function may be a feasible approach to boost motivation.
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spelling pubmed-96429992022-11-15 Glutathione in the nucleus accumbens regulates motivation to exert reward-incentivized effort Zalachoras, Ioannis Ramos-Fernández, Eva Hollis, Fiona Trovo, Laura Rodrigues, João Strasser, Alina Zanoletti, Olivia Steiner, Pascal Preitner, Nicolas Xin, Lijing Astori, Simone Sandi, Carmen eLife Neuroscience Emerging evidence is implicating mitochondrial function and metabolism in the nucleus accumbens in motivated performance. However, the brain is vulnerable to excessive oxidative insults resulting from neurometabolic processes, and whether antioxidant levels in the nucleus accumbens contribute to motivated performance is not known. Here, we identify a critical role for glutathione (GSH), the most important endogenous antioxidant in the brain, in motivation. Using proton magnetic resonance spectroscopy at ultra-high field in both male humans and rodent populations, we establish that higher accumbal GSH levels are highly predictive of better, and particularly, steady performance over time in effort-related tasks. Causality was established in in vivo experiments in rats that, first, showed that downregulating GSH levels through micro-injections of the GSH synthesis inhibitor buthionine sulfoximine in the nucleus accumbens impaired effort-based reward-incentivized performance. In addition, systemic treatment with the GSH precursor N-acetyl-cysteine increased accumbal GSH levels in rats and led to improved performance, potentially mediated by a cell-type-specific shift in glutamatergic inputs to accumbal medium spiny neurons. Our data indicate a close association between accumbal GSH levels and an individual’s capacity to exert reward-incentivized effort over time. They also suggest that improvement of accumbal antioxidant function may be a feasible approach to boost motivation. eLife Sciences Publications, Ltd 2022-11-08 /pmc/articles/PMC9642999/ /pubmed/36345724 http://dx.doi.org/10.7554/eLife.77791 Text en © 2022, Zalachoras, Ramos-Fernández et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Zalachoras, Ioannis
Ramos-Fernández, Eva
Hollis, Fiona
Trovo, Laura
Rodrigues, João
Strasser, Alina
Zanoletti, Olivia
Steiner, Pascal
Preitner, Nicolas
Xin, Lijing
Astori, Simone
Sandi, Carmen
Glutathione in the nucleus accumbens regulates motivation to exert reward-incentivized effort
title Glutathione in the nucleus accumbens regulates motivation to exert reward-incentivized effort
title_full Glutathione in the nucleus accumbens regulates motivation to exert reward-incentivized effort
title_fullStr Glutathione in the nucleus accumbens regulates motivation to exert reward-incentivized effort
title_full_unstemmed Glutathione in the nucleus accumbens regulates motivation to exert reward-incentivized effort
title_short Glutathione in the nucleus accumbens regulates motivation to exert reward-incentivized effort
title_sort glutathione in the nucleus accumbens regulates motivation to exert reward-incentivized effort
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9642999/
https://www.ncbi.nlm.nih.gov/pubmed/36345724
http://dx.doi.org/10.7554/eLife.77791
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