| Literature DB >> 35084659 |
Lucas Dantas Maia Forte1, Natália de Almeida Rodrigues2, André Vitor Cordeiro2, Thais de Fante3, Laís Angélica de Paula Simino3, Adriana de Souza Torsoni3, Márcio Alberto Torsoni3, Claudio Alexandre Gobatto2, Fúlvia Barros Manchado-Gobatto2.
Abstract
Acute metabolic and molecular response to exercise may vary according to exercise's intensity and duration. However, there is a lack regarding specific tissue alterations after acute exercise with aerobic or anaerobic predominance. The present study investigated the effects of acute exercise performed at different intensities, but with equal total load on molecular and physiological responses in swimming rats. Sixty male rats were divided into a control group and five groups performing an acute bout of swimming exercise at different intensities (80, 90, 100, 110 and 120% of anaerobic threshold [AnT]). The exercise duration of each group was balanced so all groups performed at the same total load. Gene expression (HIF-1α, PGC-1α, MCT1 and MCT4 mRNA), blood biomarkers and tissue glycogen depletion were analyzed after the exercise session. ANOVA One-Way was used to indicate statistical mean differences considering 5% significance level. Blood lactate concentration was the only biomarker sensitive to acute exercise, with a significant increase in rats exercised above AnT intensities (p < 0.000). Glycogen stores of gluteus muscle were significantly reduced in all exercised animals in comparison to control group (p = 0.02). Hepatic tissue presented significant reduction in glycogen in animals exercised above AnT (p = 0.000, as well as reduced HIF-1α mRNA and increased MCT1 mRNA, especially at the highest intensity (p = 0.002). Physiological parameters did not alter amongst groups for most tissues. Our results indicate the hepatic tissue alterations (glycogen stores and gene expressions) in response to different exercise intensities of exercise, even with the total load matched.Entities:
Keywords: Anaerobic threshold; Exercise; Hypoxia-inducible factor 1; Monocarboxylic acid transporters; Peroxisome proliferator-activated receptor gamma coactivator 1-alpha; Physiological stress
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Year: 2022 PMID: 35084659 DOI: 10.1007/s10974-022-09614-4
Source DB: PubMed Journal: J Muscle Res Cell Motil ISSN: 0142-4319 Impact factor: 2.698