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dc.contributor.authorSousa Neto, Ivo Vieira de-
dc.contributor.authorDurigan, João Luiz Quagliotti-
dc.contributor.authorFarias Junior, Gonçalo Carreiro de-
dc.contributor.authorBogni, Fabio Henrique-
dc.contributor.authorRuivo, Amanda Lima-
dc.contributor.authorAraújo, Juliana Oliveira de-
dc.contributor.authorNonaka, Keico Okino-
dc.contributor.authorSelistre-de-Araújo, Heloísa-
dc.contributor.authorMarqueti, Rita de Cássia-
dc.date.accessioned2021-02-19T14:06:32Z-
dc.date.available2021-02-19T14:06:32Z-
dc.date.issued2021-01-08-
dc.identifier.citationSOUSA NETO, Ivo Vieira de et al. Resistance training modulates the matrix mtalloproteinase-2 activity in different trabecular bones in aged rats. Clinical Interventions in Aging, v. 16, p. 71-81, 8 jan. 2021. DOI https://doi.org/10.2147/CIA.S276518. Disponível em: https://www.dovepress.com/resistance-training-modulates-the-matrix-metalloproteinase-2-activity--peer-reviewed-article-CIA. Acesso em: 19 fev. 2021pt_BR
dc.identifier.urihttps://repositorio.unb.br/handle/10482/40093-
dc.language.isoInglêspt_BR
dc.publisherDove Presspt_BR
dc.rightsAcesso Abertopt_BR
dc.titleResistance training modulates the matrix mtalloproteinase-2 activity in different trabecular bones in aged ratspt_BR
dc.typeArtigopt_BR
dc.subject.keywordEnvelhecimentopt_BR
dc.subject.keywordSistema musculoesqueléticopt_BR
dc.subject.keywordRemodelaçãopt_BR
dc.subject.keywordMetaloproteinasept_BR
dc.subject.keywordExercícios físicospt_BR
dc.rights.license© 2021 de Sousa Neto et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/ terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).pt_BR
dc.identifier.doihttps://doi.org/10.2147/CIA.S276518pt_BR
dc.description.abstract1Background: Aging decreases osteogenic ability, inducing harmful effects on the bone extracellular matrix (ECM), while exercise training has been indicated as a tool to counteract bone disorders related to advancing age. The modulation of bone ECM is regulated by several types of matrix metalloproteinase (MMP); however, MMP-2 activity in different trabecular bones in response to resistance training (RT) has been neglected. Remodeling differs in different bones under the application of the same mechanical loading. Thus, we investigated the effects of 12 weeks of RT on MMP-2 activity in the lumbar vertebra (L6), tibia, and femur of young (3 months) and older rats (21 months). Methods: Twenty Wistar rats were divided into four groups (five animals per group): young sedentary or trained and older sedentary or trained. The 12-week RT consisted of climbing a 1.1-m vertical ladder three times per week with progressive weights secured to the animals’ tails. The animals were killed 48 h after the end of the experimental period. The MMP-2 activity was assessed by the zymography method. Results: The aging process induced lower MMP-2 activity in the lumbar vertebrae and tibia (p=0.01). RT upregulated pro, intermediate, and active MMP-2 activity in the tibia of young rats (p=0.001). RT also upregulated pro and active MMP-2 activity in the lumbar vertebrae and tibia with advancing age (p=0.01). There was no significant difference (p> 0.05) between groups for MMP-2 of the femur, regardless of age and RT. Conclusion: The aging process impairs MMP-2 activity, but RT is a potential therapeutic approach to minimize the deleterious effects of ECM degeneration in different aged bones. Distinct MMP-2 responses to exercise training may result in specific remodeling processes.pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-1479-5866pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-2372-7814pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0001-9126-3882pt_BR
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