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Loss of physical contact in space alters the dopamine system in C. elegans
Progressive neuromuscular decline in microgravity is a prominent health concern preventing interplanetary human habitation. We establish functional dopamine-mediated impairments as a consistent feature across multiple spaceflight exposures and during simulated microgravity in C. elegans. Animals gro...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810405/ https://www.ncbi.nlm.nih.gov/pubmed/35141505 http://dx.doi.org/10.1016/j.isci.2022.103762 |
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author | Sudevan, Surabhi Muto, Kasumi Higashitani, Nahoko Hashizume, Toko Higashibata, Akira Ellwood, Rebecca A. Deane, Colleen S. Rahman, Mizanur Vanapalli, Siva A. Etheridge, Timothy Szewczyk, Nathaniel J. Higashitani, Atsushi |
author_facet | Sudevan, Surabhi Muto, Kasumi Higashitani, Nahoko Hashizume, Toko Higashibata, Akira Ellwood, Rebecca A. Deane, Colleen S. Rahman, Mizanur Vanapalli, Siva A. Etheridge, Timothy Szewczyk, Nathaniel J. Higashitani, Atsushi |
author_sort | Sudevan, Surabhi |
collection | PubMed |
description | Progressive neuromuscular decline in microgravity is a prominent health concern preventing interplanetary human habitation. We establish functional dopamine-mediated impairments as a consistent feature across multiple spaceflight exposures and during simulated microgravity in C. elegans. Animals grown continuously in these conditions display reduced movement and body length. Loss of mechanical contact stimuli in microgravity elicits decreased endogenous dopamine and comt-4 (catechol-O-methyl transferase) expression levels. The application of exogenous dopamine reverses the movement and body length defects caused by simulated microgravity. In addition, increased physical contact made comt-4 and dopamine levels rise. It also increased muscular cytoplasmic Ca(2+) firing. In dop-3 (D2-like receptor) mutants, neither decrease in movement nor in body length were observed during simulated microgravity growth. These results strongly suggest that targeting the dopamine system through manipulation of the external environment (contact stimuli) prevents muscular changes and is a realistic and viable treatment strategy to promote safe human deep-space travel. |
format | Online Article Text |
id | pubmed-8810405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-88104052022-02-08 Loss of physical contact in space alters the dopamine system in C. elegans Sudevan, Surabhi Muto, Kasumi Higashitani, Nahoko Hashizume, Toko Higashibata, Akira Ellwood, Rebecca A. Deane, Colleen S. Rahman, Mizanur Vanapalli, Siva A. Etheridge, Timothy Szewczyk, Nathaniel J. Higashitani, Atsushi iScience Article Progressive neuromuscular decline in microgravity is a prominent health concern preventing interplanetary human habitation. We establish functional dopamine-mediated impairments as a consistent feature across multiple spaceflight exposures and during simulated microgravity in C. elegans. Animals grown continuously in these conditions display reduced movement and body length. Loss of mechanical contact stimuli in microgravity elicits decreased endogenous dopamine and comt-4 (catechol-O-methyl transferase) expression levels. The application of exogenous dopamine reverses the movement and body length defects caused by simulated microgravity. In addition, increased physical contact made comt-4 and dopamine levels rise. It also increased muscular cytoplasmic Ca(2+) firing. In dop-3 (D2-like receptor) mutants, neither decrease in movement nor in body length were observed during simulated microgravity growth. These results strongly suggest that targeting the dopamine system through manipulation of the external environment (contact stimuli) prevents muscular changes and is a realistic and viable treatment strategy to promote safe human deep-space travel. Elsevier 2022-01-11 /pmc/articles/PMC8810405/ /pubmed/35141505 http://dx.doi.org/10.1016/j.isci.2022.103762 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sudevan, Surabhi Muto, Kasumi Higashitani, Nahoko Hashizume, Toko Higashibata, Akira Ellwood, Rebecca A. Deane, Colleen S. Rahman, Mizanur Vanapalli, Siva A. Etheridge, Timothy Szewczyk, Nathaniel J. Higashitani, Atsushi Loss of physical contact in space alters the dopamine system in C. elegans |
title | Loss of physical contact in space alters the dopamine system in C. elegans |
title_full | Loss of physical contact in space alters the dopamine system in C. elegans |
title_fullStr | Loss of physical contact in space alters the dopamine system in C. elegans |
title_full_unstemmed | Loss of physical contact in space alters the dopamine system in C. elegans |
title_short | Loss of physical contact in space alters the dopamine system in C. elegans |
title_sort | loss of physical contact in space alters the dopamine system in c. elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810405/ https://www.ncbi.nlm.nih.gov/pubmed/35141505 http://dx.doi.org/10.1016/j.isci.2022.103762 |
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