Cargando…

The Origin of Behavioral Bursts in Decision-Making Circuitry

From ants to humans, the timing of many animal behaviors comes in bursts of activity separated by long periods of inactivity. Recently, mathematical modeling has shown that simple algorithms of priority-driven behavioral choice can result in bursty behavior. To experimentally test this link between...

Descripción completa

Detalles Bibliográficos
Autores principales: Sorribes, Amanda, Armendariz, Beatriz G., Lopez-Pigozzi, Diego, Murga, Cristina, de Polavieja, Gonzalo G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121695/
https://www.ncbi.nlm.nih.gov/pubmed/21731478
http://dx.doi.org/10.1371/journal.pcbi.1002075
_version_ 1782206853169545216
author Sorribes, Amanda
Armendariz, Beatriz G.
Lopez-Pigozzi, Diego
Murga, Cristina
de Polavieja, Gonzalo G.
author_facet Sorribes, Amanda
Armendariz, Beatriz G.
Lopez-Pigozzi, Diego
Murga, Cristina
de Polavieja, Gonzalo G.
author_sort Sorribes, Amanda
collection PubMed
description From ants to humans, the timing of many animal behaviors comes in bursts of activity separated by long periods of inactivity. Recently, mathematical modeling has shown that simple algorithms of priority-driven behavioral choice can result in bursty behavior. To experimentally test this link between decision-making circuitry and bursty dynamics, we have turned to Drosophila melanogaster. We have found that the statistics of intervals between activity periods in endogenous activity-rest switches of wild-type Drosophila are very well described by the Weibull distribution, a common distribution of bursty dynamics in complex systems. The bursty dynamics of wild-type Drosophila walking activity are shown to be determined by this inter-event distribution alone and not by memory effects, thus resembling human dynamics. Further, using mutant flies that disrupt dopaminergic signaling or the mushroom body, circuitry implicated in decision-making, we show that the degree of behavioral burstiness can be modified. These results are thus consistent with the proposed link between decision-making circuitry and bursty dynamics, and highlight the importance of using simple experimental systems to test general theoretical models of behavior. The findings further suggest that analysis of bursts could prove useful for the study and evaluation of decision-making circuitry.
format Online
Article
Text
id pubmed-3121695
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-31216952011-06-30 The Origin of Behavioral Bursts in Decision-Making Circuitry Sorribes, Amanda Armendariz, Beatriz G. Lopez-Pigozzi, Diego Murga, Cristina de Polavieja, Gonzalo G. PLoS Comput Biol Research Article From ants to humans, the timing of many animal behaviors comes in bursts of activity separated by long periods of inactivity. Recently, mathematical modeling has shown that simple algorithms of priority-driven behavioral choice can result in bursty behavior. To experimentally test this link between decision-making circuitry and bursty dynamics, we have turned to Drosophila melanogaster. We have found that the statistics of intervals between activity periods in endogenous activity-rest switches of wild-type Drosophila are very well described by the Weibull distribution, a common distribution of bursty dynamics in complex systems. The bursty dynamics of wild-type Drosophila walking activity are shown to be determined by this inter-event distribution alone and not by memory effects, thus resembling human dynamics. Further, using mutant flies that disrupt dopaminergic signaling or the mushroom body, circuitry implicated in decision-making, we show that the degree of behavioral burstiness can be modified. These results are thus consistent with the proposed link between decision-making circuitry and bursty dynamics, and highlight the importance of using simple experimental systems to test general theoretical models of behavior. The findings further suggest that analysis of bursts could prove useful for the study and evaluation of decision-making circuitry. Public Library of Science 2011-06-23 /pmc/articles/PMC3121695/ /pubmed/21731478 http://dx.doi.org/10.1371/journal.pcbi.1002075 Text en Sorribes 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
Sorribes, Amanda
Armendariz, Beatriz G.
Lopez-Pigozzi, Diego
Murga, Cristina
de Polavieja, Gonzalo G.
The Origin of Behavioral Bursts in Decision-Making Circuitry
title The Origin of Behavioral Bursts in Decision-Making Circuitry
title_full The Origin of Behavioral Bursts in Decision-Making Circuitry
title_fullStr The Origin of Behavioral Bursts in Decision-Making Circuitry
title_full_unstemmed The Origin of Behavioral Bursts in Decision-Making Circuitry
title_short The Origin of Behavioral Bursts in Decision-Making Circuitry
title_sort origin of behavioral bursts in decision-making circuitry
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121695/
https://www.ncbi.nlm.nih.gov/pubmed/21731478
http://dx.doi.org/10.1371/journal.pcbi.1002075
work_keys_str_mv AT sorribesamanda theoriginofbehavioralburstsindecisionmakingcircuitry
AT armendarizbeatrizg theoriginofbehavioralburstsindecisionmakingcircuitry
AT lopezpigozzidiego theoriginofbehavioralburstsindecisionmakingcircuitry
AT murgacristina theoriginofbehavioralburstsindecisionmakingcircuitry
AT depolaviejagonzalog theoriginofbehavioralburstsindecisionmakingcircuitry
AT sorribesamanda originofbehavioralburstsindecisionmakingcircuitry
AT armendarizbeatrizg originofbehavioralburstsindecisionmakingcircuitry
AT lopezpigozzidiego originofbehavioralburstsindecisionmakingcircuitry
AT murgacristina originofbehavioralburstsindecisionmakingcircuitry
AT depolaviejagonzalog originofbehavioralburstsindecisionmakingcircuitry