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The ventromedial prefrontal cortex and emotion regulation: lost in translation?

Neuroimaging studies implicate the ventromedial prefrontal cortex (vmPFC) in a wide range of emotional and cognitive functions, and changes in activity within vmPFC have been linked to the aetiology and successful treatment of depression. However, this is a large, structurally heterogeneous region a...

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Autores principales: Alexander, Laith, Wood, Christian M., Roberts, Angela C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084434/
https://www.ncbi.nlm.nih.gov/pubmed/35635793
http://dx.doi.org/10.1113/JP282627
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author Alexander, Laith
Wood, Christian M.
Roberts, Angela C.
author_facet Alexander, Laith
Wood, Christian M.
Roberts, Angela C.
author_sort Alexander, Laith
collection PubMed
description Neuroimaging studies implicate the ventromedial prefrontal cortex (vmPFC) in a wide range of emotional and cognitive functions, and changes in activity within vmPFC have been linked to the aetiology and successful treatment of depression. However, this is a large, structurally heterogeneous region and the extent to which this structural heterogeneity reflects functional heterogeneity remains unclear. Causal studies in animals should help address this question but attempts to map findings from vmPFC studies in rodents onto human imaging studies highlight cross‐species discrepancies between structural homology and functional analogy. Bridging this gap, recent studies in marmosets – a species of new world monkey in which the overall organization of vmPFC is more like humans than that of rodents – have revealed that over‐activation of the caudal subcallosal region of vmPFC, area 25, but not neighbouring area 32, heightens reactivity to negatively valenced stimuli whilst blunting responsivity to positively valenced stimuli. These co‐occurring states resemble those seen in depressed patients, which are associated with increased activity in caudal subcallosal regions. In contrast, only reward blunting but not heightening of threat reactivity is seen following over‐activation of the structurally homologous region in rodents. To further advance understanding of the role of vmPFC in the aetiology and treatment of depression, future work should focus on the behaviourally specific networks by which vmPFC regions have their effects, together with characterization of cross‐species similarities and differences in function. [Image: see text]
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spelling pubmed-100844342023-04-11 The ventromedial prefrontal cortex and emotion regulation: lost in translation? Alexander, Laith Wood, Christian M. Roberts, Angela C. J Physiol Symposium Section Reviews: Decoding Prefrontal Cortical Physiology: Circuits of Cognition Neuroimaging studies implicate the ventromedial prefrontal cortex (vmPFC) in a wide range of emotional and cognitive functions, and changes in activity within vmPFC have been linked to the aetiology and successful treatment of depression. However, this is a large, structurally heterogeneous region and the extent to which this structural heterogeneity reflects functional heterogeneity remains unclear. Causal studies in animals should help address this question but attempts to map findings from vmPFC studies in rodents onto human imaging studies highlight cross‐species discrepancies between structural homology and functional analogy. Bridging this gap, recent studies in marmosets – a species of new world monkey in which the overall organization of vmPFC is more like humans than that of rodents – have revealed that over‐activation of the caudal subcallosal region of vmPFC, area 25, but not neighbouring area 32, heightens reactivity to negatively valenced stimuli whilst blunting responsivity to positively valenced stimuli. These co‐occurring states resemble those seen in depressed patients, which are associated with increased activity in caudal subcallosal regions. In contrast, only reward blunting but not heightening of threat reactivity is seen following over‐activation of the structurally homologous region in rodents. To further advance understanding of the role of vmPFC in the aetiology and treatment of depression, future work should focus on the behaviourally specific networks by which vmPFC regions have their effects, together with characterization of cross‐species similarities and differences in function. [Image: see text] John Wiley and Sons Inc. 2022-06-11 2023-01-01 /pmc/articles/PMC10084434/ /pubmed/35635793 http://dx.doi.org/10.1113/JP282627 Text en © 2022 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Symposium Section Reviews: Decoding Prefrontal Cortical Physiology: Circuits of Cognition
Alexander, Laith
Wood, Christian M.
Roberts, Angela C.
The ventromedial prefrontal cortex and emotion regulation: lost in translation?
title The ventromedial prefrontal cortex and emotion regulation: lost in translation?
title_full The ventromedial prefrontal cortex and emotion regulation: lost in translation?
title_fullStr The ventromedial prefrontal cortex and emotion regulation: lost in translation?
title_full_unstemmed The ventromedial prefrontal cortex and emotion regulation: lost in translation?
title_short The ventromedial prefrontal cortex and emotion regulation: lost in translation?
title_sort ventromedial prefrontal cortex and emotion regulation: lost in translation?
topic Symposium Section Reviews: Decoding Prefrontal Cortical Physiology: Circuits of Cognition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10084434/
https://www.ncbi.nlm.nih.gov/pubmed/35635793
http://dx.doi.org/10.1113/JP282627
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