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Humor as a Reward Mechanism: Event-Related Potentials in the Healthy and Diseased Brain
Humor processing involves distinct processing stages including incongruity detection, emotional response, and engagement of mesolimbic reward regions. Dysfunctional reward processing and clinical symptoms in response to humor have been previously described in both hypocretin deficient narcolepsy-cat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906016/ https://www.ncbi.nlm.nih.gov/pubmed/24489683 http://dx.doi.org/10.1371/journal.pone.0085978 |
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author | Mensen, Armand Poryazova, Rositsa Schwartz, Sophie Khatami, Ramin |
author_facet | Mensen, Armand Poryazova, Rositsa Schwartz, Sophie Khatami, Ramin |
author_sort | Mensen, Armand |
collection | PubMed |
description | Humor processing involves distinct processing stages including incongruity detection, emotional response, and engagement of mesolimbic reward regions. Dysfunctional reward processing and clinical symptoms in response to humor have been previously described in both hypocretin deficient narcolepsy-cataplexy (NC) and in idiopathic Parkinson disease (PD). For NC patients, humor is the strongest trigger for cataplexy, a transient loss of muscle tone, whereas dopamine-deficient PD-patients show blunted emotional responses to humor. To better understand the role of reward system and the various contributions of hypocretinergic and dopaminergic mechanisms to different stages of humor processing we examined the electrophysiological response to humorous and neutral pictures when given as reward feedback in PD, NC and healthy controls. Humor compared to neutral feedback demonstrated modulation of early ERP amplitudes likely corresponding to visual processing stages, with no group differences. At 270 ms post-feedback, conditions showed topographical and amplitudinal differences for frontal and left posterior electrodes, in that humor feedback was absent in PD patients but increased in NC patients. We suggest that this effect relates to a relatively early affective response, reminiscent of increased amygdala response reported in NC patients. Later ERP differences, corresponding to the late positive potential, revealed a lack of sustained activation in PD, likely due to altered dopamine regulation in reward structures in these patients. This research provides new insights into the temporal dynamics and underlying mechanisms of humor detection and appreciation in health and disease. |
format | Online Article Text |
id | pubmed-3906016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39060162014-01-31 Humor as a Reward Mechanism: Event-Related Potentials in the Healthy and Diseased Brain Mensen, Armand Poryazova, Rositsa Schwartz, Sophie Khatami, Ramin PLoS One Research Article Humor processing involves distinct processing stages including incongruity detection, emotional response, and engagement of mesolimbic reward regions. Dysfunctional reward processing and clinical symptoms in response to humor have been previously described in both hypocretin deficient narcolepsy-cataplexy (NC) and in idiopathic Parkinson disease (PD). For NC patients, humor is the strongest trigger for cataplexy, a transient loss of muscle tone, whereas dopamine-deficient PD-patients show blunted emotional responses to humor. To better understand the role of reward system and the various contributions of hypocretinergic and dopaminergic mechanisms to different stages of humor processing we examined the electrophysiological response to humorous and neutral pictures when given as reward feedback in PD, NC and healthy controls. Humor compared to neutral feedback demonstrated modulation of early ERP amplitudes likely corresponding to visual processing stages, with no group differences. At 270 ms post-feedback, conditions showed topographical and amplitudinal differences for frontal and left posterior electrodes, in that humor feedback was absent in PD patients but increased in NC patients. We suggest that this effect relates to a relatively early affective response, reminiscent of increased amygdala response reported in NC patients. Later ERP differences, corresponding to the late positive potential, revealed a lack of sustained activation in PD, likely due to altered dopamine regulation in reward structures in these patients. This research provides new insights into the temporal dynamics and underlying mechanisms of humor detection and appreciation in health and disease. Public Library of Science 2014-01-29 /pmc/articles/PMC3906016/ /pubmed/24489683 http://dx.doi.org/10.1371/journal.pone.0085978 Text en © 2014 Mensen et al http://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 author and source are properly credited. |
spellingShingle | Research Article Mensen, Armand Poryazova, Rositsa Schwartz, Sophie Khatami, Ramin Humor as a Reward Mechanism: Event-Related Potentials in the Healthy and Diseased Brain |
title | Humor as a Reward Mechanism: Event-Related Potentials in the Healthy and Diseased Brain |
title_full | Humor as a Reward Mechanism: Event-Related Potentials in the Healthy and Diseased Brain |
title_fullStr | Humor as a Reward Mechanism: Event-Related Potentials in the Healthy and Diseased Brain |
title_full_unstemmed | Humor as a Reward Mechanism: Event-Related Potentials in the Healthy and Diseased Brain |
title_short | Humor as a Reward Mechanism: Event-Related Potentials in the Healthy and Diseased Brain |
title_sort | humor as a reward mechanism: event-related potentials in the healthy and diseased brain |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906016/ https://www.ncbi.nlm.nih.gov/pubmed/24489683 http://dx.doi.org/10.1371/journal.pone.0085978 |
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