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Fluoxetine degrades luminance perceptual thresholds while enhancing motivation and reward sensitivity

Selective serotonin reuptake inhibitors (SSRIs) increase serotonin activity in the brain. While they are mostly known for their antidepressant properties, they have been shown to improve visual functions in amblyopia and impact cognitive functions ranging from attention to motivation and sensitivity...

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Autores principales: Gacoin, Maëva, Ben Hamed, Suliann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157648/
https://www.ncbi.nlm.nih.gov/pubmed/37153796
http://dx.doi.org/10.3389/fphar.2023.1103999
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author Gacoin, Maëva
Ben Hamed, Suliann
author_facet Gacoin, Maëva
Ben Hamed, Suliann
author_sort Gacoin, Maëva
collection PubMed
description Selective serotonin reuptake inhibitors (SSRIs) increase serotonin activity in the brain. While they are mostly known for their antidepressant properties, they have been shown to improve visual functions in amblyopia and impact cognitive functions ranging from attention to motivation and sensitivity to reward. Yet, a clear understanding of the specific action of serotonin to each of bottom-up sensory and top-down cognitive control components and their interaction is still missing. To address this question, we characterize, in two adult male macaques, the behavioral effects of fluoxetine, a specific SSRI, on visual perception under varying bottom-up (luminosity, distractors) and top-down (uncertainty, reward biases) constraints while they are performing three different visual tasks. We first manipulate target luminosity in a visual detection task, and we show that fluoxetine degrades luminance perceptual thresholds. We then use a target detection task in the presence of spatial distractors, and we show that under fluoxetine, monkeys display both more liberal responses as well as a degraded perceptual spatial resolution. In a last target selection task, involving free choice in the presence of reward biases, we show that monkeys display an increased sensitivity to reward outcome under fluoxetine. In addition, we report that monkeys produce, under fluoxetine, more trials and less aborts, increased pupil size, shorter blink durations, as well as task-dependent changes in reaction times. Overall, while low level vision appears to be degraded by fluoxetine, performances in the visual tasks are maintained under fluoxetine due to enhanced top-down control based on task outcome and reward maximization.
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spelling pubmed-101576482023-05-05 Fluoxetine degrades luminance perceptual thresholds while enhancing motivation and reward sensitivity Gacoin, Maëva Ben Hamed, Suliann Front Pharmacol Pharmacology Selective serotonin reuptake inhibitors (SSRIs) increase serotonin activity in the brain. While they are mostly known for their antidepressant properties, they have been shown to improve visual functions in amblyopia and impact cognitive functions ranging from attention to motivation and sensitivity to reward. Yet, a clear understanding of the specific action of serotonin to each of bottom-up sensory and top-down cognitive control components and their interaction is still missing. To address this question, we characterize, in two adult male macaques, the behavioral effects of fluoxetine, a specific SSRI, on visual perception under varying bottom-up (luminosity, distractors) and top-down (uncertainty, reward biases) constraints while they are performing three different visual tasks. We first manipulate target luminosity in a visual detection task, and we show that fluoxetine degrades luminance perceptual thresholds. We then use a target detection task in the presence of spatial distractors, and we show that under fluoxetine, monkeys display both more liberal responses as well as a degraded perceptual spatial resolution. In a last target selection task, involving free choice in the presence of reward biases, we show that monkeys display an increased sensitivity to reward outcome under fluoxetine. In addition, we report that monkeys produce, under fluoxetine, more trials and less aborts, increased pupil size, shorter blink durations, as well as task-dependent changes in reaction times. Overall, while low level vision appears to be degraded by fluoxetine, performances in the visual tasks are maintained under fluoxetine due to enhanced top-down control based on task outcome and reward maximization. Frontiers Media S.A. 2023-04-20 /pmc/articles/PMC10157648/ /pubmed/37153796 http://dx.doi.org/10.3389/fphar.2023.1103999 Text en Copyright © 2023 Gacoin and Ben Hamed. https://creativecommons.org/licenses/by/4.0/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) and the copyright owner(s) 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 Pharmacology
Gacoin, Maëva
Ben Hamed, Suliann
Fluoxetine degrades luminance perceptual thresholds while enhancing motivation and reward sensitivity
title Fluoxetine degrades luminance perceptual thresholds while enhancing motivation and reward sensitivity
title_full Fluoxetine degrades luminance perceptual thresholds while enhancing motivation and reward sensitivity
title_fullStr Fluoxetine degrades luminance perceptual thresholds while enhancing motivation and reward sensitivity
title_full_unstemmed Fluoxetine degrades luminance perceptual thresholds while enhancing motivation and reward sensitivity
title_short Fluoxetine degrades luminance perceptual thresholds while enhancing motivation and reward sensitivity
title_sort fluoxetine degrades luminance perceptual thresholds while enhancing motivation and reward sensitivity
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157648/
https://www.ncbi.nlm.nih.gov/pubmed/37153796
http://dx.doi.org/10.3389/fphar.2023.1103999
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