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Revenge is sweet: Investigation of the effects of Approach‐Motivated anger on the RewP in the motivated anger delay (MAD) paradigm

Past research has found that neural activity associated with feedback processing is enhanced by positive approach‐motivated states. However, no past work has examined how reward processing changes in the context of revenge. Using a novel aggression paradigm, we sought to explore the influence of app...

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Detalles Bibliográficos
Autores principales: Threadgill, A. Hunter, Gable, Philip A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643382/
https://www.ncbi.nlm.nih.gov/pubmed/32856760
http://dx.doi.org/10.1002/hbm.25177
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author Threadgill, A. Hunter
Gable, Philip A.
author_facet Threadgill, A. Hunter
Gable, Philip A.
author_sort Threadgill, A. Hunter
collection PubMed
description Past research has found that neural activity associated with feedback processing is enhanced by positive approach‐motivated states. However, no past work has examined how reward processing changes in the context of revenge. Using a novel aggression paradigm, we sought to explore the influence of approach‐motivated anger on neural responses to feedback indicating the opportunity to seek revenge against an offending opponent by examining the reward positivity (RewP), an event‐related potential indexing performance feedback. In Experiment 1, after receiving insulting feedback from an opponent, participants played a reaction time game with three trial types: revenge trials, aggravation trials, and no‐consequence trials. Results revealed that RewP amplitudes were larger to revenge trial win feedback than no‐consequence trial win feedback or revenge trial loss feedback. RewP amplitudes were larger to both aggravation trial win and loss feedback than on no‐consequence trials. Experiment 2 examined the influence of approach‐motivated anger during the acquisition of rewards on the RewP without the possibility of retribution from the offending individual. Participants played a reaction time game similar to Experiment 1, except instead of giving or receiving noise blasts, participants could win money from the insulter (revenge trials) or a neutral‐party (e.g., bank). Results indicated that revenge wins elicited larger RewP amplitudes than bank wins. These results suggest that anger enhances revenge‐related RewP amplitudes to obtaining revenge opportunities and further aggravation wins or losses. Anger appears to enhance the pleasurable feelings of revenge.
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spelling pubmed-76433822020-11-13 Revenge is sweet: Investigation of the effects of Approach‐Motivated anger on the RewP in the motivated anger delay (MAD) paradigm Threadgill, A. Hunter Gable, Philip A. Hum Brain Mapp Research Articles Past research has found that neural activity associated with feedback processing is enhanced by positive approach‐motivated states. However, no past work has examined how reward processing changes in the context of revenge. Using a novel aggression paradigm, we sought to explore the influence of approach‐motivated anger on neural responses to feedback indicating the opportunity to seek revenge against an offending opponent by examining the reward positivity (RewP), an event‐related potential indexing performance feedback. In Experiment 1, after receiving insulting feedback from an opponent, participants played a reaction time game with three trial types: revenge trials, aggravation trials, and no‐consequence trials. Results revealed that RewP amplitudes were larger to revenge trial win feedback than no‐consequence trial win feedback or revenge trial loss feedback. RewP amplitudes were larger to both aggravation trial win and loss feedback than on no‐consequence trials. Experiment 2 examined the influence of approach‐motivated anger during the acquisition of rewards on the RewP without the possibility of retribution from the offending individual. Participants played a reaction time game similar to Experiment 1, except instead of giving or receiving noise blasts, participants could win money from the insulter (revenge trials) or a neutral‐party (e.g., bank). Results indicated that revenge wins elicited larger RewP amplitudes than bank wins. These results suggest that anger enhances revenge‐related RewP amplitudes to obtaining revenge opportunities and further aggravation wins or losses. Anger appears to enhance the pleasurable feelings of revenge. John Wiley & Sons, Inc. 2020-08-28 /pmc/articles/PMC7643382/ /pubmed/32856760 http://dx.doi.org/10.1002/hbm.25177 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Threadgill, A. Hunter
Gable, Philip A.
Revenge is sweet: Investigation of the effects of Approach‐Motivated anger on the RewP in the motivated anger delay (MAD) paradigm
title Revenge is sweet: Investigation of the effects of Approach‐Motivated anger on the RewP in the motivated anger delay (MAD) paradigm
title_full Revenge is sweet: Investigation of the effects of Approach‐Motivated anger on the RewP in the motivated anger delay (MAD) paradigm
title_fullStr Revenge is sweet: Investigation of the effects of Approach‐Motivated anger on the RewP in the motivated anger delay (MAD) paradigm
title_full_unstemmed Revenge is sweet: Investigation of the effects of Approach‐Motivated anger on the RewP in the motivated anger delay (MAD) paradigm
title_short Revenge is sweet: Investigation of the effects of Approach‐Motivated anger on the RewP in the motivated anger delay (MAD) paradigm
title_sort revenge is sweet: investigation of the effects of approach‐motivated anger on the rewp in the motivated anger delay (mad) paradigm
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643382/
https://www.ncbi.nlm.nih.gov/pubmed/32856760
http://dx.doi.org/10.1002/hbm.25177
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