Selenocysteine modulates resistance to environmental stress and confers anti-aging effects in C. elegans
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , |
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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Clinics |
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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 |
_version_ |
1800222763229642752 |