Age-Related Changes in Risky Decision Making and Associated Neural Circuitry in a Rat Model
Altered decision making at advanced ages can have a significant impact on an individual's quality of life and the ability to maintain personal independence. Relative to young adults, older adults make less impulsive and less risky choices; although these changes in decision making could be cons...
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Published in | eNeuro Vol. 10; no. 1; p. ENEURO.0385-22.2022 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Society for Neuroscience
01.01.2023
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Abstract | Altered decision making at advanced ages can have a significant impact on an individual's quality of life and the ability to maintain personal independence. Relative to young adults, older adults make less impulsive and less risky choices; although these changes in decision making could be considered beneficial, they can also lead to choices with potentially negative consequences (e.g., avoidance of medical procedures). Rodent models of decision making have been invaluable for dissecting cognitive and neurobiological mechanisms that contribute to age-related changes in decision making, but they have predominantly used costs related to timing or probability of reward delivery and have not considered other equally important costs, such as the risk of adverse consequences. The current study therefore used a rat model of decision making involving risk of explicit punishment to examine age-related changes in this form of choice behavior in male rats, and to identify potential cognitive and neurobiological mechanisms that contribute to these changes. Relative to young rats, aged rats displayed greater risk aversion, which was not attributable to reduced motivation for food, changes in shock sensitivity, or impaired cognitive flexibility. Functional MRI analyses revealed that, overall, functional connectivity was greater in aged rats compared with young rats, particularly among brain regions implicated in risky decision making such as basolateral amygdala, orbitofrontal cortex, and ventral tegmental area. Collectively, these findings are consistent with greater risk aversion found in older humans, and reveal age-related changes in brain connectivity. |
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AbstractList | Altered decision making at advanced ages can have a significant impact on an individual's quality of life and the ability to maintain personal independence. Relative to young adults, older adults make less impulsive and less risky choices; although these changes in decision making could be considered beneficial, they can also lead to choices with potentially negative consequences (e.g., avoidance of medical procedures). Rodent models of decision making have been invaluable for dissecting cognitive and neurobiological mechanisms that contribute to age-related changes in decision making, but they have predominantly used costs related to timing or probability of reward delivery and have not considered other equally important costs, such as the risk of adverse consequences. The current study therefore used a rat model of decision making involving risk of explicit punishment to examine age-related changes in this form of choice behavior in male rats, and to identify potential cognitive and neurobiological mechanisms that contribute to these changes. Relative to young rats, aged rats displayed greater risk aversion, which was not attributable to reduced motivation for food, changes in shock sensitivity, or impaired cognitive flexibility. Functional MRI analyses revealed that, overall, functional connectivity was greater in aged rats compared with young rats, particularly among brain regions implicated in risky decision making such as basolateral amygdala, orbitofrontal cortex, and ventral tegmental area. Collectively, these findings are consistent with greater risk aversion found in older humans, and reveal age-related changes in brain connectivity. Abstract Altered decision making at advanced ages can have a significant impact on an individual’s quality of life and the ability to maintain personal independence. Relative to young adults, older adults make less impulsive and less risky choices; although these changes in decision making could be considered beneficial, they can also lead to choices with potentially negative consequences (e.g., avoidance of medical procedures). Rodent models of decision making have been invaluable for dissecting cognitive and neurobiological mechanisms that contribute to age-related changes in decision making, but they have predominantly used costs related to timing or probability of reward delivery and have not considered other equally important costs, such as the risk of adverse consequences. The current study therefore used a rat model of decision making involving risk of explicit punishment to examine age-related changes in this form of choice behavior in male rats, and to identify potential cognitive and neurobiological mechanisms that contribute to these changes. Relative to young rats, aged rats displayed greater risk aversion, which was not attributable to reduced motivation for food, changes in shock sensitivity, or impaired cognitive flexibility. Functional MRI analyses revealed that, overall, functional connectivity was greater in aged rats compared with young rats, particularly among brain regions implicated in risky decision making such as basolateral amygdala, orbitofrontal cortex, and ventral tegmental area. Collectively, these findings are consistent with greater risk aversion found in older humans, and reveal age-related changes in brain connectivity. |
Author | Pompilus, Marjory Febo, Marcelo Wheeler, Alexa-Rae Setlow, Barry Faraji, Mojdeh Pyon, Wonn S Dragone, Richard J Orsini, Caitlin A Bizon, Jennifer L |
Author_xml | – sequence: 1 givenname: Caitlin A orcidid: 0000-0001-5644-2316 surname: Orsini fullname: Orsini, Caitlin A organization: Department of Psychiatry, University of Florida, Gainesville, Florida 32610 – sequence: 2 givenname: Wonn S surname: Pyon fullname: Pyon, Wonn S organization: Department of Neuroscience, University of Florida, Gainesville, Florida 32610 – sequence: 3 givenname: Richard J surname: Dragone fullname: Dragone, Richard J organization: Department of Psychiatry, University of Florida, Gainesville, Florida 32610 – sequence: 4 givenname: Mojdeh surname: Faraji fullname: Faraji, Mojdeh organization: Department of Psychiatry, University of Florida, Gainesville, Florida 32610 – sequence: 5 givenname: Alexa-Rae surname: Wheeler fullname: Wheeler, Alexa-Rae organization: Department of Neuroscience, University of Florida, Gainesville, Florida 32610 – sequence: 6 givenname: Marjory surname: Pompilus fullname: Pompilus, Marjory organization: Department of Psychiatry, University of Florida, Gainesville, Florida 32610 – sequence: 7 givenname: Marcelo surname: Febo fullname: Febo, Marcelo organization: McKnight Brain Institute, University of Florida, Gainesville, Florida 32610 – sequence: 8 givenname: Jennifer L surname: Bizon fullname: Bizon, Jennifer L organization: McKnight Brain Institute, University of Florida, Gainesville, Florida 32610 – sequence: 9 givenname: Barry orcidid: 0000-0001-9133-9445 surname: Setlow fullname: Setlow, Barry email: setlow@ufl.edu organization: McKnight Brain Institute, University of Florida, Gainesville, Florida 32610 |
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Keywords | risk taking punishment aging rat decision making neuroimaging |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author contributions: C.A.O., M. Faraji, M. Febo, J.L.B., and B.S. designed research; C.A.O., W.S.P., R.J.D., A.-R.W., and M.P. performed research; C.A.O., W.S.P., R.J.D., and M. Faraji analyzed data; C.A.O., W.S.P., M. Faraji, M. Febo, J.L.B., and B.S. wrote the paper. C.A.O. and W.S.P. are co-first authors. The authors declare no competing financial interests. A.-R. Wheeler’s present address: Institute for Neuroscience, The University of Texas at Austin, Austin, TX 78712. This work was supported by Department of Health and Human Services (HHS) | National Institutes of Health (NIH) | National Institute on Aging (NIA) Grant RF1-AG-060778 (J.L.B., B.S.), a McKnight Brain Institute Fellowship, a Thomas H. Maren Fellowship, HHS | NIH | National Institute on Drug Abuse Grant K99-DA-041493 (C.A.O.), HHS | NIH | NIA T32-AG-061892 (W.S.P., R.J.D.), and the McKnight Brain Research Foundation (J.L.B.). C.A. Orsini’s present address: Department of Psychology, Waggoner Center for Alcohol & Addiction Research, The University of Texas at Austin, Austin, TX 78712. |
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Snippet | Altered decision making at advanced ages can have a significant impact on an individual's quality of life and the ability to maintain personal independence.... Abstract Altered decision making at advanced ages can have a significant impact on an individual’s quality of life and the ability to maintain personal... Altered decision making at advanced ages can have a significant impact on an individual’s quality of life and the ability to maintain personal independence.... |
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SubjectTerms | Aged Animals Basolateral Nuclear Complex Brain - diagnostic imaging Decision Making Humans Male New Research Prefrontal Cortex Quality of Life Rats Reward Risk-Taking Young Adult |
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Title | Age-Related Changes in Risky Decision Making and Associated Neural Circuitry in a Rat Model |
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