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On the Similarity Between the Reinforcing and the Discriminative Properties of Intracranial Self-Stimulation

Rats work very hard for intracranial self-stimulation (ICSS) and tradeoff effort or time allocation for intensity and frequency parameters producing a sigmoidal function of the subjective reward magnitude of ICSS. Previous studies using electrical intracranial stimuli (ICS) as a discriminative cue f...

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Autores principales: Velazquez-Martinez, David N., Pacheco-Gomez, Benita Lizeth, Toscano-Zapien, Ana Laura, Lopez-Guzman, Maria Almudena, Velazquez-Lopez, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899289/
https://www.ncbi.nlm.nih.gov/pubmed/35264936
http://dx.doi.org/10.3389/fnbeh.2022.799015
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author Velazquez-Martinez, David N.
Pacheco-Gomez, Benita Lizeth
Toscano-Zapien, Ana Laura
Lopez-Guzman, Maria Almudena
Velazquez-Lopez, Daniel
author_facet Velazquez-Martinez, David N.
Pacheco-Gomez, Benita Lizeth
Toscano-Zapien, Ana Laura
Lopez-Guzman, Maria Almudena
Velazquez-Lopez, Daniel
author_sort Velazquez-Martinez, David N.
collection PubMed
description Rats work very hard for intracranial self-stimulation (ICSS) and tradeoff effort or time allocation for intensity and frequency parameters producing a sigmoidal function of the subjective reward magnitude of ICSS. Previous studies using electrical intracranial stimuli (ICS) as a discriminative cue focused on estimating detection thresholds or on the discrimination between intensities. To our knowledge, there is no direct comparison of the reinforcer tradeoff functions with the discriminative functions. Rats were trained to press and hold the lever for ICSS using the maximum reinforcing intensity below motor alterations or avoidance behavior. First, rats were trained to hold the lever for 1 s; after stability, they undergo trials where intensity or frequency was decreased on 0.1 log step. Thereafter, they undergo further training with a hold of 2 and later of 4 s to determine tradeoff with intensity or frequency. The same rats were trained on a discrimination task where the previously used ICSS signaled a lever where a 1 s hold response was followed by a reinforcing ICSS; on randomly alternating trials, a −0.6 log ICS signaled an alternate lever where a similar hold response led to a reinforcer. After mastering discrimination, generalization tests were carried out with varying intensity or frequency. Rats completed training with 2 and later 4 s hold response. After the completion of each task, the rats had different doses of a pimozide challenge while their intensity and hold-down requirement were varied. With regards to the rats’ tradeoff response time allocation as a function of intensity or frequency, sigmoid functions were displaced to the right when long responses were required. Rats that learned the discrimination task attained a discrimination index of 90–98%. Discrimination accuracy decreased slightly with the increase of hold requirement, but generalization gradients were not displaced to the right as a function of the response requirement. Pimozide induced a dose-dependent displacement of the time-allocation gradients, but it did not affect the generalization gradients. It is concluded that rats integrate response requirements as part of the reinforcement tradeoff function, but the response cost is not integrated into the discriminative function of ICSS.
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spelling pubmed-88992892022-03-08 On the Similarity Between the Reinforcing and the Discriminative Properties of Intracranial Self-Stimulation Velazquez-Martinez, David N. Pacheco-Gomez, Benita Lizeth Toscano-Zapien, Ana Laura Lopez-Guzman, Maria Almudena Velazquez-Lopez, Daniel Front Behav Neurosci Neuroscience Rats work very hard for intracranial self-stimulation (ICSS) and tradeoff effort or time allocation for intensity and frequency parameters producing a sigmoidal function of the subjective reward magnitude of ICSS. Previous studies using electrical intracranial stimuli (ICS) as a discriminative cue focused on estimating detection thresholds or on the discrimination between intensities. To our knowledge, there is no direct comparison of the reinforcer tradeoff functions with the discriminative functions. Rats were trained to press and hold the lever for ICSS using the maximum reinforcing intensity below motor alterations or avoidance behavior. First, rats were trained to hold the lever for 1 s; after stability, they undergo trials where intensity or frequency was decreased on 0.1 log step. Thereafter, they undergo further training with a hold of 2 and later of 4 s to determine tradeoff with intensity or frequency. The same rats were trained on a discrimination task where the previously used ICSS signaled a lever where a 1 s hold response was followed by a reinforcing ICSS; on randomly alternating trials, a −0.6 log ICS signaled an alternate lever where a similar hold response led to a reinforcer. After mastering discrimination, generalization tests were carried out with varying intensity or frequency. Rats completed training with 2 and later 4 s hold response. After the completion of each task, the rats had different doses of a pimozide challenge while their intensity and hold-down requirement were varied. With regards to the rats’ tradeoff response time allocation as a function of intensity or frequency, sigmoid functions were displaced to the right when long responses were required. Rats that learned the discrimination task attained a discrimination index of 90–98%. Discrimination accuracy decreased slightly with the increase of hold requirement, but generalization gradients were not displaced to the right as a function of the response requirement. Pimozide induced a dose-dependent displacement of the time-allocation gradients, but it did not affect the generalization gradients. It is concluded that rats integrate response requirements as part of the reinforcement tradeoff function, but the response cost is not integrated into the discriminative function of ICSS. Frontiers Media S.A. 2022-02-21 /pmc/articles/PMC8899289/ /pubmed/35264936 http://dx.doi.org/10.3389/fnbeh.2022.799015 Text en Copyright © 2022 Velazquez-Martinez, Pacheco-Gomez, Toscano-Zapien, Lopez-Guzman and Velazquez-Lopez. 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 Neuroscience
Velazquez-Martinez, David N.
Pacheco-Gomez, Benita Lizeth
Toscano-Zapien, Ana Laura
Lopez-Guzman, Maria Almudena
Velazquez-Lopez, Daniel
On the Similarity Between the Reinforcing and the Discriminative Properties of Intracranial Self-Stimulation
title On the Similarity Between the Reinforcing and the Discriminative Properties of Intracranial Self-Stimulation
title_full On the Similarity Between the Reinforcing and the Discriminative Properties of Intracranial Self-Stimulation
title_fullStr On the Similarity Between the Reinforcing and the Discriminative Properties of Intracranial Self-Stimulation
title_full_unstemmed On the Similarity Between the Reinforcing and the Discriminative Properties of Intracranial Self-Stimulation
title_short On the Similarity Between the Reinforcing and the Discriminative Properties of Intracranial Self-Stimulation
title_sort on the similarity between the reinforcing and the discriminative properties of intracranial self-stimulation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899289/
https://www.ncbi.nlm.nih.gov/pubmed/35264936
http://dx.doi.org/10.3389/fnbeh.2022.799015
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