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Reinforcement omission effects in rats with bilateral lesions in the substantia nigra pars compacta and ventral tegmental area
Reinforcement omission effects (ROEs) are characterized by higher response rates after reinforcement omission than after reinforcement delivery. This pattern of behavior is interpreted in terms of motivational and attentional processes. Recent studies from our laboratory have shown that the amygdala...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Divulgação Científica
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694775/ https://www.ncbi.nlm.nih.gov/pubmed/31291382 http://dx.doi.org/10.1590/1414-431X20198303 |
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author | Tavares, T.F. Judice-Daher, D.M. Bueno, J.L.O. |
author_facet | Tavares, T.F. Judice-Daher, D.M. Bueno, J.L.O. |
author_sort | Tavares, T.F. |
collection | PubMed |
description | Reinforcement omission effects (ROEs) are characterized by higher response rates after reinforcement omission than after reinforcement delivery. This pattern of behavior is interpreted in terms of motivational and attentional processes. Recent studies from our laboratory have shown that the amygdala, nucleus accumbens, and medial prefrontal cortex are involved in ROE modulation. Also, the literature has demonstrated a role of other areas such as substantia nigra pars compacta (SNc) and the ventral tegmental area (VTA) in processes related to surprising events, such as prediction error and presentation or omission of an event (exteroceptive stimulus and reinforcement). Since these structures send projections to areas related to ROE modulation such as the amygdala, nucleus accumbens, and prefrontal cortex, the objective of the present study was to determine whether the SNc and VTA also integrate the circuit involved in ROE modulation. Rats were trained on a fixed-interval 12 s with limited-hold 6 s signaled schedule of reinforcement (Pre-lesion training). After acquisition of stable performance, the rats received bilateral neurotoxic lesions of the SNc (Experiment 1) and VTA (Experiment 2). Following postoperative recovery, the rats were submitted to two refresher sessions (Post-lesion training). Subsequently, the training was changed from a 100 to a 50% schedule of reinforcement (Post-lesion testing). In both experiments, the results showed that there was no difference in performance between sham rats and rats with bilateral lesions of the SNc or the VTA. |
format | Online Article Text |
id | pubmed-6694775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Associação Brasileira de Divulgação Científica |
record_format | MEDLINE/PubMed |
spelling | pubmed-66947752019-09-04 Reinforcement omission effects in rats with bilateral lesions in the substantia nigra pars compacta and ventral tegmental area Tavares, T.F. Judice-Daher, D.M. Bueno, J.L.O. Braz J Med Biol Res Research Article Reinforcement omission effects (ROEs) are characterized by higher response rates after reinforcement omission than after reinforcement delivery. This pattern of behavior is interpreted in terms of motivational and attentional processes. Recent studies from our laboratory have shown that the amygdala, nucleus accumbens, and medial prefrontal cortex are involved in ROE modulation. Also, the literature has demonstrated a role of other areas such as substantia nigra pars compacta (SNc) and the ventral tegmental area (VTA) in processes related to surprising events, such as prediction error and presentation or omission of an event (exteroceptive stimulus and reinforcement). Since these structures send projections to areas related to ROE modulation such as the amygdala, nucleus accumbens, and prefrontal cortex, the objective of the present study was to determine whether the SNc and VTA also integrate the circuit involved in ROE modulation. Rats were trained on a fixed-interval 12 s with limited-hold 6 s signaled schedule of reinforcement (Pre-lesion training). After acquisition of stable performance, the rats received bilateral neurotoxic lesions of the SNc (Experiment 1) and VTA (Experiment 2). Following postoperative recovery, the rats were submitted to two refresher sessions (Post-lesion training). Subsequently, the training was changed from a 100 to a 50% schedule of reinforcement (Post-lesion testing). In both experiments, the results showed that there was no difference in performance between sham rats and rats with bilateral lesions of the SNc or the VTA. Associação Brasileira de Divulgação Científica 2019-07-10 /pmc/articles/PMC6694775/ /pubmed/31291382 http://dx.doi.org/10.1590/1414-431X20198303 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Tavares, T.F. Judice-Daher, D.M. Bueno, J.L.O. Reinforcement omission effects in rats with bilateral lesions in the substantia nigra pars compacta and ventral tegmental area |
title | Reinforcement omission effects in rats with bilateral lesions in the substantia nigra pars compacta and ventral tegmental area |
title_full | Reinforcement omission effects in rats with bilateral lesions in the substantia nigra pars compacta and ventral tegmental area |
title_fullStr | Reinforcement omission effects in rats with bilateral lesions in the substantia nigra pars compacta and ventral tegmental area |
title_full_unstemmed | Reinforcement omission effects in rats with bilateral lesions in the substantia nigra pars compacta and ventral tegmental area |
title_short | Reinforcement omission effects in rats with bilateral lesions in the substantia nigra pars compacta and ventral tegmental area |
title_sort | reinforcement omission effects in rats with bilateral lesions in the substantia nigra pars compacta and ventral tegmental area |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6694775/ https://www.ncbi.nlm.nih.gov/pubmed/31291382 http://dx.doi.org/10.1590/1414-431X20198303 |
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