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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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.
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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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