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Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non‐cell‐autonomous stress response
Oxidative stress has long been associated with aging and has recently been linked to psychiatric disorders, including psychosis and depression. We identified multiple antipsychotics and antidepressants that extend Caenorhabditis elegans lifespan and protect the animal from oxidative stress. Here, we...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693466/ https://www.ncbi.nlm.nih.gov/pubmed/26255886 http://dx.doi.org/10.1111/acel.12379 |
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author | Rangaraju, Sunitha Solis, Gregory M. Andersson, Sofia I. Gomez‐Amaro, Rafael L. Kardakaris, Rozina Broaddus, Caroline D. Niculescu, Alexander B. Petrascheck, Michael |
author_facet | Rangaraju, Sunitha Solis, Gregory M. Andersson, Sofia I. Gomez‐Amaro, Rafael L. Kardakaris, Rozina Broaddus, Caroline D. Niculescu, Alexander B. Petrascheck, Michael |
author_sort | Rangaraju, Sunitha |
collection | PubMed |
description | Oxidative stress has long been associated with aging and has recently been linked to psychiatric disorders, including psychosis and depression. We identified multiple antipsychotics and antidepressants that extend Caenorhabditis elegans lifespan and protect the animal from oxidative stress. Here, we report that atypical antidepressants activate a neuronal mechanism that regulates the response to oxidative stress throughout the animal. While the activation of the oxidative stress response by atypical antidepressants depends on synaptic transmission, the activation by reactive oxygen species does not. Lifespan extension by atypical antidepressants depends on the neuronal oxidative stress response activation mechanism. Neuronal regulation of the oxidative stress response is likely to have evolved as a survival mechanism to protect the organism from oxidative stress, upon detection of adverse or dangerous conditions by the nervous system. |
format | Online Article Text |
id | pubmed-4693466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46934662016-01-04 Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non‐cell‐autonomous stress response Rangaraju, Sunitha Solis, Gregory M. Andersson, Sofia I. Gomez‐Amaro, Rafael L. Kardakaris, Rozina Broaddus, Caroline D. Niculescu, Alexander B. Petrascheck, Michael Aging Cell Original Articles Oxidative stress has long been associated with aging and has recently been linked to psychiatric disorders, including psychosis and depression. We identified multiple antipsychotics and antidepressants that extend Caenorhabditis elegans lifespan and protect the animal from oxidative stress. Here, we report that atypical antidepressants activate a neuronal mechanism that regulates the response to oxidative stress throughout the animal. While the activation of the oxidative stress response by atypical antidepressants depends on synaptic transmission, the activation by reactive oxygen species does not. Lifespan extension by atypical antidepressants depends on the neuronal oxidative stress response activation mechanism. Neuronal regulation of the oxidative stress response is likely to have evolved as a survival mechanism to protect the organism from oxidative stress, upon detection of adverse or dangerous conditions by the nervous system. John Wiley and Sons Inc. 2015-08-08 2015-12 /pmc/articles/PMC4693466/ /pubmed/26255886 http://dx.doi.org/10.1111/acel.12379 Text en © 2015 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Rangaraju, Sunitha Solis, Gregory M. Andersson, Sofia I. Gomez‐Amaro, Rafael L. Kardakaris, Rozina Broaddus, Caroline D. Niculescu, Alexander B. Petrascheck, Michael Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non‐cell‐autonomous stress response |
title | Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non‐cell‐autonomous stress response |
title_full | Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non‐cell‐autonomous stress response |
title_fullStr | Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non‐cell‐autonomous stress response |
title_full_unstemmed | Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non‐cell‐autonomous stress response |
title_short | Atypical antidepressants extend lifespan of Caenorhabditis elegans by activation of a non‐cell‐autonomous stress response |
title_sort | atypical antidepressants extend lifespan of caenorhabditis elegans by activation of a non‐cell‐autonomous stress response |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693466/ https://www.ncbi.nlm.nih.gov/pubmed/26255886 http://dx.doi.org/10.1111/acel.12379 |
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