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Influences of Dopaminergic System Dysfunction on Late-Life Depression

Deficits in cognition, reward processing, and motor function are clinical features relevant to both aging and depression. Individuals with late-life depression often show impairment across these domains, all of which are moderated by the functioning of dopaminergic circuits. As dopaminergic function...

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Autores principales: Taylor, Warren D., Zald, David H., Felger, Jennifer C., Christman, Seth, Claassen, Daniel O., Horga, Guillermo, Miller, Jeffrey M., Gifford, Katherine, Rogers, Baxter, Szymkowicz, Sarah M., Rutherford, Bret R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850529/
https://www.ncbi.nlm.nih.gov/pubmed/34404915
http://dx.doi.org/10.1038/s41380-021-01265-0
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author Taylor, Warren D.
Zald, David H.
Felger, Jennifer C.
Christman, Seth
Claassen, Daniel O.
Horga, Guillermo
Miller, Jeffrey M.
Gifford, Katherine
Rogers, Baxter
Szymkowicz, Sarah M.
Rutherford, Bret R.
author_facet Taylor, Warren D.
Zald, David H.
Felger, Jennifer C.
Christman, Seth
Claassen, Daniel O.
Horga, Guillermo
Miller, Jeffrey M.
Gifford, Katherine
Rogers, Baxter
Szymkowicz, Sarah M.
Rutherford, Bret R.
author_sort Taylor, Warren D.
collection PubMed
description Deficits in cognition, reward processing, and motor function are clinical features relevant to both aging and depression. Individuals with late-life depression often show impairment across these domains, all of which are moderated by the functioning of dopaminergic circuits. As dopaminergic function declines with normal aging and increased inflammatory burden, the role of dopamine may be particularly salient for late-life depression. We review the literature examining the role of dopamine in the pathogenesis of depression, as well as how dopamine function changes with aging and is influenced by inflammation. Applying a Research Domain Criteria (RDoC) Initiative perspective, we then review work examining how dopaminergic signaling affects these domains, specifically focusing on Cognitive, Positive Valence, and Sensorimotor Systems. We propose a unified model incorporating the effects of aging and low-grade inflammation on dopaminergic functioning, with a resulting negative effect on cognition, reward processing, and motor function. Interplay between these systems may influence development of a depressive phenotype, with an initial deficit in one domain reinforcing decline in others. This model extends RDoC concepts into late-life depression while also providing opportunities for novel and personalized interventions.
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spelling pubmed-88505292022-03-31 Influences of Dopaminergic System Dysfunction on Late-Life Depression Taylor, Warren D. Zald, David H. Felger, Jennifer C. Christman, Seth Claassen, Daniel O. Horga, Guillermo Miller, Jeffrey M. Gifford, Katherine Rogers, Baxter Szymkowicz, Sarah M. Rutherford, Bret R. Mol Psychiatry Article Deficits in cognition, reward processing, and motor function are clinical features relevant to both aging and depression. Individuals with late-life depression often show impairment across these domains, all of which are moderated by the functioning of dopaminergic circuits. As dopaminergic function declines with normal aging and increased inflammatory burden, the role of dopamine may be particularly salient for late-life depression. We review the literature examining the role of dopamine in the pathogenesis of depression, as well as how dopamine function changes with aging and is influenced by inflammation. Applying a Research Domain Criteria (RDoC) Initiative perspective, we then review work examining how dopaminergic signaling affects these domains, specifically focusing on Cognitive, Positive Valence, and Sensorimotor Systems. We propose a unified model incorporating the effects of aging and low-grade inflammation on dopaminergic functioning, with a resulting negative effect on cognition, reward processing, and motor function. Interplay between these systems may influence development of a depressive phenotype, with an initial deficit in one domain reinforcing decline in others. This model extends RDoC concepts into late-life depression while also providing opportunities for novel and personalized interventions. 2022-01 2021-08-17 /pmc/articles/PMC8850529/ /pubmed/34404915 http://dx.doi.org/10.1038/s41380-021-01265-0 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms
spellingShingle Article
Taylor, Warren D.
Zald, David H.
Felger, Jennifer C.
Christman, Seth
Claassen, Daniel O.
Horga, Guillermo
Miller, Jeffrey M.
Gifford, Katherine
Rogers, Baxter
Szymkowicz, Sarah M.
Rutherford, Bret R.
Influences of Dopaminergic System Dysfunction on Late-Life Depression
title Influences of Dopaminergic System Dysfunction on Late-Life Depression
title_full Influences of Dopaminergic System Dysfunction on Late-Life Depression
title_fullStr Influences of Dopaminergic System Dysfunction on Late-Life Depression
title_full_unstemmed Influences of Dopaminergic System Dysfunction on Late-Life Depression
title_short Influences of Dopaminergic System Dysfunction on Late-Life Depression
title_sort influences of dopaminergic system dysfunction on late-life depression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850529/
https://www.ncbi.nlm.nih.gov/pubmed/34404915
http://dx.doi.org/10.1038/s41380-021-01265-0
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