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Practice explains abolished behavioural adaptation after human dorsal anterior cingulate cortex lesions

The role of mid-cingulate cortex (MCC), also referred to as dorsal anterior cingulate cortex, in regulating cognitive control is a topic of primary importance in cognitive neuroscience. Although many studies have shown that MCC responds to cognitive demands, lesion studies in humans are inconclusive...

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Autores principales: van Steenbergen, H., Haasnoot, E., Bocanegra, B. R., Berretty, E. W., Hommel, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389810/
https://www.ncbi.nlm.nih.gov/pubmed/25853432
http://dx.doi.org/10.1038/srep09721
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author van Steenbergen, H.
Haasnoot, E.
Bocanegra, B. R.
Berretty, E. W.
Hommel, B.
author_facet van Steenbergen, H.
Haasnoot, E.
Bocanegra, B. R.
Berretty, E. W.
Hommel, B.
author_sort van Steenbergen, H.
collection PubMed
description The role of mid-cingulate cortex (MCC), also referred to as dorsal anterior cingulate cortex, in regulating cognitive control is a topic of primary importance in cognitive neuroscience. Although many studies have shown that MCC responds to cognitive demands, lesion studies in humans are inconclusive concerning the causal role of the MCC in the adaptation to these demands. By elegantly combining single-cell recordings with behavioural methods, Sheth et al. [Sheth, S. et al. Human dorsal anterior cingulate cortex neurons mediate ongoing behavioural adaptation. Nature 488, 218–22 (2012).] recently were able to show that neurons in MCC encode cognitive demand. Importantly, this study also claimed that focal lesions of the MCC abolished behavioural adaptation to cognitive demands. Here we show that the absence of post-cingulotomy behavioural adaptation reported in this study may have been due to practice effects. We run a control condition where we tested subjects before and after a dummy treatment, which substituted cingulotomy with a filler task (presentation of a documentary). The results revealed abolished behavioural adaptation following the dummy treatment. Our findings suggest that future work using proper experimental designs is needed to advance the understanding of the causal role of the MCC in behavioural adaptation.
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spelling pubmed-43898102015-04-08 Practice explains abolished behavioural adaptation after human dorsal anterior cingulate cortex lesions van Steenbergen, H. Haasnoot, E. Bocanegra, B. R. Berretty, E. W. Hommel, B. Sci Rep Article The role of mid-cingulate cortex (MCC), also referred to as dorsal anterior cingulate cortex, in regulating cognitive control is a topic of primary importance in cognitive neuroscience. Although many studies have shown that MCC responds to cognitive demands, lesion studies in humans are inconclusive concerning the causal role of the MCC in the adaptation to these demands. By elegantly combining single-cell recordings with behavioural methods, Sheth et al. [Sheth, S. et al. Human dorsal anterior cingulate cortex neurons mediate ongoing behavioural adaptation. Nature 488, 218–22 (2012).] recently were able to show that neurons in MCC encode cognitive demand. Importantly, this study also claimed that focal lesions of the MCC abolished behavioural adaptation to cognitive demands. Here we show that the absence of post-cingulotomy behavioural adaptation reported in this study may have been due to practice effects. We run a control condition where we tested subjects before and after a dummy treatment, which substituted cingulotomy with a filler task (presentation of a documentary). The results revealed abolished behavioural adaptation following the dummy treatment. Our findings suggest that future work using proper experimental designs is needed to advance the understanding of the causal role of the MCC in behavioural adaptation. Nature Publishing Group 2015-04-08 /pmc/articles/PMC4389810/ /pubmed/25853432 http://dx.doi.org/10.1038/srep09721 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
van Steenbergen, H.
Haasnoot, E.
Bocanegra, B. R.
Berretty, E. W.
Hommel, B.
Practice explains abolished behavioural adaptation after human dorsal anterior cingulate cortex lesions
title Practice explains abolished behavioural adaptation after human dorsal anterior cingulate cortex lesions
title_full Practice explains abolished behavioural adaptation after human dorsal anterior cingulate cortex lesions
title_fullStr Practice explains abolished behavioural adaptation after human dorsal anterior cingulate cortex lesions
title_full_unstemmed Practice explains abolished behavioural adaptation after human dorsal anterior cingulate cortex lesions
title_short Practice explains abolished behavioural adaptation after human dorsal anterior cingulate cortex lesions
title_sort practice explains abolished behavioural adaptation after human dorsal anterior cingulate cortex lesions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389810/
https://www.ncbi.nlm.nih.gov/pubmed/25853432
http://dx.doi.org/10.1038/srep09721
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