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Turk J Med Sci ; 54(1): 148-156, 2024.
Artigo em Inglês | MEDLINE | ID: mdl-38812641

RESUMO

Background/aim: Although high muscle strength worsens the sense of force, it is unknown whether there is a relationship between this deterioration and the underlying molecular mechanisms. This study examined the relationship between decreased force sense (FS) acuity and strength-related gene expressions. Materials and methods: Maximal voluntary isometric contraction (MVIC) and FS (50% MVIC) tests were performed on the knee joints of twenty-two subjects. The expression analyses were evaluated by qRT-PCR in blood samples taken before, after MVIC, after 50% MVIC, and 15 min after the test. Results: MVIC and FS error values were significantly correlated with each other (r = .659, p = .001). The qRT-PCR analyses demonstrated that the expressed mRNAs of the interleukin 6 (IL-6), alpha-actinin 3 (ACTN3), angiotensin-converting enzyme (ACE), brain-derived neurotrophic factor (BDNF), and ciliary neurotrophic factor receptor (CNTFR) genes dramatically increased until 50% MVIC and subsequently decreased 15 min after the exercise (p < .05). The muscle-specific creatine kinase (CKMM), myosin light chain kinase (MLCK), and G-protein ß3 subunit (GNB3) genes reached their peak expression levels 30 min after MVIC (p < .05). ACE and ACTN3 gene expression increased significantly in parallel with the increased FS error (p < .05). These gene expression fluctuations observed at 50% MVIC and after the rest could be related to changes in cellular metabolism leading to fatigue. Conclusion: The time points of gene expression levels during exercise need to be considered. The force acuity of those whose maximal force develops too much may deteriorate.


Assuntos
Contração Isométrica , Força Muscular , Humanos , Masculino , Força Muscular/genética , Força Muscular/fisiologia , Contração Isométrica/fisiologia , Adulto , Adulto Jovem , Expressão Gênica , Músculo Esquelético/metabolismo , Músculo Esquelético/fisiologia , Interleucina-6/genética , Feminino , Fator Neurotrófico Derivado do Encéfalo/genética , Peptidil Dipeptidase A/genética , Actinina/genética , Articulação do Joelho
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