Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans

Detalhes bibliográficos
Autor(a) principal: Kim, Jun-Sung
Data de Publicação: 2017
Outros Autores: Kim, So-Hyeon, Park, Sang-Kyu
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/138275
Resumo: OBJECTIVE: The free radical theory of aging suggests that cellular oxidative damage caused by free radicals is a leading cause of aging. In the present study, we examined the effects of a well-known anti-oxidant amino acid derivative, selenocysteine, in response to environmental stress and aging using Caenorhabditis elegans as a model system. METHOD: The response to oxidative stress induced by H2O2 or ultraviolet irradiation was compared between the untreated control and selenocysteine-treated groups. The effect of selenocysteine on lifespan and fertility was then determined. To examine the effect of selenocysteine on muscle aging, we monitored the change in motility with aging in both the untreated control and selenocysteine-treated groups. RESULTS: Dietary supplementation with selenocysteine significantly increased resistance to oxidative stress. Survival after ultraviolet irradiation was also increased by supplementation with selenocysteine. Treatment with selenocysteine confers a longevity phenotype without an accompanying reduction in fertility, which is frequently observed in lifespan-extending interventions as a trade-off in C. elegans. In addition, the age-related decline in motility was significantly delayed by supplementation of selenocysteine. CONCLUSION: These findings suggest that dietary supplementation of selenocysteine can modulate response to stressors and lead to lifespan extension, thus supporting the free radical theory of aging.
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spelling Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegansSelenocysteineStress ResponseLifespanAgingC. elegansOBJECTIVE: The free radical theory of aging suggests that cellular oxidative damage caused by free radicals is a leading cause of aging. In the present study, we examined the effects of a well-known anti-oxidant amino acid derivative, selenocysteine, in response to environmental stress and aging using Caenorhabditis elegans as a model system. METHOD: The response to oxidative stress induced by H2O2 or ultraviolet irradiation was compared between the untreated control and selenocysteine-treated groups. The effect of selenocysteine on lifespan and fertility was then determined. To examine the effect of selenocysteine on muscle aging, we monitored the change in motility with aging in both the untreated control and selenocysteine-treated groups. RESULTS: Dietary supplementation with selenocysteine significantly increased resistance to oxidative stress. Survival after ultraviolet irradiation was also increased by supplementation with selenocysteine. Treatment with selenocysteine confers a longevity phenotype without an accompanying reduction in fertility, which is frequently observed in lifespan-extending interventions as a trade-off in C. elegans. In addition, the age-related decline in motility was significantly delayed by supplementation of selenocysteine. CONCLUSION: These findings suggest that dietary supplementation of selenocysteine can modulate response to stressors and lead to lifespan extension, thus supporting the free radical theory of aging.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2017-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/13827510.6061/clinics/2017(08)07Clinics; Vol. 72 No. 8 (2017); 491-498Clinics; v. 72 n. 8 (2017); 491-498Clinics; Vol. 72 Núm. 8 (2017); 491-4981980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/138275/133716Copyright (c) 2017 Clinicsinfo:eu-repo/semantics/openAccessKim, Jun-SungKim, So-HyeonPark, Sang-Kyu2017-09-22T16:20:24Zoai:revistas.usp.br:article/138275Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2017-09-22T16:20:24Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans
title Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans
spellingShingle Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans
Kim, Jun-Sung
Selenocysteine
Stress Response
Lifespan
Aging
C. elegans
title_short Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans
title_full Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans
title_fullStr Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans
title_full_unstemmed Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans
title_sort Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans
author Kim, Jun-Sung
author_facet Kim, Jun-Sung
Kim, So-Hyeon
Park, Sang-Kyu
author_role author
author2 Kim, So-Hyeon
Park, Sang-Kyu
author2_role author
author
dc.contributor.author.fl_str_mv Kim, Jun-Sung
Kim, So-Hyeon
Park, Sang-Kyu
dc.subject.por.fl_str_mv Selenocysteine
Stress Response
Lifespan
Aging
C. elegans
topic Selenocysteine
Stress Response
Lifespan
Aging
C. elegans
description OBJECTIVE: The free radical theory of aging suggests that cellular oxidative damage caused by free radicals is a leading cause of aging. In the present study, we examined the effects of a well-known anti-oxidant amino acid derivative, selenocysteine, in response to environmental stress and aging using Caenorhabditis elegans as a model system. METHOD: The response to oxidative stress induced by H2O2 or ultraviolet irradiation was compared between the untreated control and selenocysteine-treated groups. The effect of selenocysteine on lifespan and fertility was then determined. To examine the effect of selenocysteine on muscle aging, we monitored the change in motility with aging in both the untreated control and selenocysteine-treated groups. RESULTS: Dietary supplementation with selenocysteine significantly increased resistance to oxidative stress. Survival after ultraviolet irradiation was also increased by supplementation with selenocysteine. Treatment with selenocysteine confers a longevity phenotype without an accompanying reduction in fertility, which is frequently observed in lifespan-extending interventions as a trade-off in C. elegans. In addition, the age-related decline in motility was significantly delayed by supplementation of selenocysteine. CONCLUSION: These findings suggest that dietary supplementation of selenocysteine can modulate response to stressors and lead to lifespan extension, thus supporting the free radical theory of aging.
publishDate 2017
dc.date.none.fl_str_mv 2017-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/138275
10.6061/clinics/2017(08)07
url https://www.revistas.usp.br/clinics/article/view/138275
identifier_str_mv 10.6061/clinics/2017(08)07
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/138275/133716
dc.rights.driver.fl_str_mv Copyright (c) 2017 Clinics
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2017 Clinics
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 72 No. 8 (2017); 491-498
Clinics; v. 72 n. 8 (2017); 491-498
Clinics; Vol. 72 Núm. 8 (2017); 491-498
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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