Immunometabolic Responses after Short and Moderate Rest Intervals to Strength Exercise with and without Similar Total Volume

dc.contributor.authorAgostinete, Ricardo R. [UNESP]
dc.contributor.authorRossi, Fabricio E. [UNESP]
dc.contributor.authorMagalhaes, Alan Jose B. [UNESP]
dc.contributor.authorRocha, Ana Paula R. [UNESP]
dc.contributor.authorParmezzani, Sergio S. [UNESP]
dc.contributor.authorGerosa-Neto, Jose [UNESP]
dc.contributor.authorCholewa, Jason M.
dc.contributor.authorLira, Fabio S. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionCoastal Carolina Univ
dc.date.accessioned2018-11-26T17:07:13Z
dc.date.available2018-11-26T17:07:13Z
dc.date.issued2016-10-25
dc.description.abstractThis study investigated the influence of short and moderate intervals of recovery with and without equated volume during an acute bout exhaustive strength exercise on metabolic, hormonal and inflammatory responses in healthy adults. Eight physically active men (23.5 +/- 3.1) performed three randomized sequences: Short (70% of 1 RM with 30s of rest): Moderate (70% of 1 RM with 90s of rest): and Volume-Equated Short (70% of 1 RM with 30s of rest between sets with a repetition volume equal to that performed in Moderate). All sequences of exercises were performed until movement failure in the squat, bench press and T-bar row exercises, respectively. Glucose, lactate, testosterone, IL-6, IL-10, IL-1ra, and MCP-1 levels were assessed at rest, immediate post-exercise, and 1 h post. There was a main effect of time for testosterone (p < 0.001). The post hoc indicated differences between post exercise and rest and post-1 h and post-exercise (p < 0.001). Lactate increased post-exercise when compared to pre and post-1 h (p < 0.001) and maintained higher post-1 h in relation to rest. IL-6 was greater post-exercise than rest (p = 0.045) and post-1 h and rest (p = 0.020). IL-10 was greater post exercise (p = 0.007) and post-1 h (p = 0.002) than rest. IL-1ra increased post-exercise in relation to rest (p = 0.003) and MCP-1 was greater post-exercise than rest (p < 0.001) and post-1 h (p = 0.043). There were no significant differences between conditions or interaction. Thus, both short and moderate intervals of recovery induced greater metabolic, hormonal and inflammatory responses after acute bout of exhaustive strength exercise in healthy adult.en
dc.description.affiliationSao Paulo State Univ, Dept Physiotherapy, Sao Paulo, Brazil
dc.description.affiliationSao Paulo State Univ, Inst Biosci, Dept Phys Educ, Rio Claro, Brazil
dc.description.affiliationSao Paulo State Univ, Dept Phys Educ, Exercise & Immunometab Res Grp, Residente Prudente, Brazil
dc.description.affiliationCoastal Carolina Univ, Dept Kinesiol Recreat & Sport Studies, Conway, SC USA
dc.description.affiliationUnespSao Paulo State Univ, Dept Physiotherapy, Sao Paulo, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Inst Biosci, Dept Phys Educ, Rio Claro, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Dept Phys Educ, Exercise & Immunometab Res Grp, Residente Prudente, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2013/25310-2
dc.format.extent8
dc.identifierhttp://dx.doi.org/10.3389/fphys.2016.00444
dc.identifier.citationFrontiers In Physiology. Lausanne: Frontiers Media Sa, v. 7, 8 p., 2016.
dc.identifier.doi10.3389/fphys.2016.00444
dc.identifier.fileWOS000386093400001.pdf
dc.identifier.issn1664-042X
dc.identifier.urihttp://hdl.handle.net/11449/162084
dc.identifier.wosWOS:000386093400001
dc.language.isoeng
dc.publisherFrontiers Media Sa
dc.relation.ispartofFrontiers In Physiology
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectstrength exercise
dc.subjectintervals of recovery
dc.subjecttestosterone
dc.subjectinflammation
dc.subjectmetabolism
dc.titleImmunometabolic Responses after Short and Moderate Rest Intervals to Strength Exercise with and without Similar Total Volumeen
dc.typeArtigo
dcterms.rightsHolderFrontiers Media Sa

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