Cargando…

Human decisions about when to act originate within a basal forebrain–nigral circuit

Decisions about when to act are critical for survival in humans as in animals, but how a desire is translated into the decision that an action is worth taking at any particular point in time is incompletely understood. Here we show that a simple model developed to explain when animals decide it is w...

Descripción completa

Detalles Bibliográficos
Autores principales: Khalighinejad, Nima, Priestley, Luke, Jbabdi, Saad, Rushworth, Matthew F. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260969/
https://www.ncbi.nlm.nih.gov/pubmed/32385157
http://dx.doi.org/10.1073/pnas.1921211117
_version_ 1783540423529070592
author Khalighinejad, Nima
Priestley, Luke
Jbabdi, Saad
Rushworth, Matthew F. S.
author_facet Khalighinejad, Nima
Priestley, Luke
Jbabdi, Saad
Rushworth, Matthew F. S.
author_sort Khalighinejad, Nima
collection PubMed
description Decisions about when to act are critical for survival in humans as in animals, but how a desire is translated into the decision that an action is worth taking at any particular point in time is incompletely understood. Here we show that a simple model developed to explain when animals decide it is worth taking an action also explains a significant portion of the variance in timing observed when humans take voluntary actions. The model focuses on the current environment’s potential for reward, the timing of the individual’s own recent actions, and the outcomes of those actions. We show, by using ultrahigh-field MRI scanning, that in addition to anterior cingulate cortex within medial frontal cortex, a group of subcortical structures including striatum, substantia nigra, basal forebrain (BF), pedunculopontine nucleus (PPN), and habenula (HB) encode trial-by-trial variation in action time. Further analysis of the activity patterns found in each area together with psychophysiological interaction analysis and structural equation modeling suggested a model in which BF integrates contextual information that will influence the decision about when to act and communicates this information, in parallel with PPN and HB influences, to nigrostriatal circuits. It is then in the nigrostriatal circuit that action initiation per se begins.
format Online
Article
Text
id pubmed-7260969
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-72609692020-06-08 Human decisions about when to act originate within a basal forebrain–nigral circuit Khalighinejad, Nima Priestley, Luke Jbabdi, Saad Rushworth, Matthew F. S. Proc Natl Acad Sci U S A Biological Sciences Decisions about when to act are critical for survival in humans as in animals, but how a desire is translated into the decision that an action is worth taking at any particular point in time is incompletely understood. Here we show that a simple model developed to explain when animals decide it is worth taking an action also explains a significant portion of the variance in timing observed when humans take voluntary actions. The model focuses on the current environment’s potential for reward, the timing of the individual’s own recent actions, and the outcomes of those actions. We show, by using ultrahigh-field MRI scanning, that in addition to anterior cingulate cortex within medial frontal cortex, a group of subcortical structures including striatum, substantia nigra, basal forebrain (BF), pedunculopontine nucleus (PPN), and habenula (HB) encode trial-by-trial variation in action time. Further analysis of the activity patterns found in each area together with psychophysiological interaction analysis and structural equation modeling suggested a model in which BF integrates contextual information that will influence the decision about when to act and communicates this information, in parallel with PPN and HB influences, to nigrostriatal circuits. It is then in the nigrostriatal circuit that action initiation per se begins. National Academy of Sciences 2020-05-26 2020-05-08 /pmc/articles/PMC7260969/ /pubmed/32385157 http://dx.doi.org/10.1073/pnas.1921211117 Text en Copyright © 2020 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Khalighinejad, Nima
Priestley, Luke
Jbabdi, Saad
Rushworth, Matthew F. S.
Human decisions about when to act originate within a basal forebrain–nigral circuit
title Human decisions about when to act originate within a basal forebrain–nigral circuit
title_full Human decisions about when to act originate within a basal forebrain–nigral circuit
title_fullStr Human decisions about when to act originate within a basal forebrain–nigral circuit
title_full_unstemmed Human decisions about when to act originate within a basal forebrain–nigral circuit
title_short Human decisions about when to act originate within a basal forebrain–nigral circuit
title_sort human decisions about when to act originate within a basal forebrain–nigral circuit
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260969/
https://www.ncbi.nlm.nih.gov/pubmed/32385157
http://dx.doi.org/10.1073/pnas.1921211117
work_keys_str_mv AT khalighinejadnima humandecisionsaboutwhentoactoriginatewithinabasalforebrainnigralcircuit
AT priestleyluke humandecisionsaboutwhentoactoriginatewithinabasalforebrainnigralcircuit
AT jbabdisaad humandecisionsaboutwhentoactoriginatewithinabasalforebrainnigralcircuit
AT rushworthmatthewfs humandecisionsaboutwhentoactoriginatewithinabasalforebrainnigralcircuit