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1.
Sci Rep ; 10(1): 21735, 2020 12 10.
Article in English | MEDLINE | ID: mdl-33303928

ABSTRACT

In this study, we evaluated the effects of autologous serum collected after two types of exercise on the in vitro inflammatory profile and T cell phenotype of resting peripheral blood mononuclear cells (PBMCs) in obese men. Serum samples and PBMCs were obtained from eight obese men who performed two exercise bouts-high intensity interval exercise (HIIE) and exhaustive exercise session to voluntary fatigue-in a randomized cross-over trial. Pre-exercise PBMCs were incubated with 50% autologous serum (collected before and after each exercise bout) for 4 h. In vitro experiments revealed that post-HIIE serum reduced the histone H4 acetylation status and NF-κB content of PBMCs and suppressed the production of both TNF-α and IL-6 by PBMCs, while increasing IL-10 production. Post-exhaustive exercise serum induced histone H4 hyperacetylation and mitochondrial depolarization in lymphocytes and increased TNF-α production. In vitro post-HIIE serum incubation resulted in an increase in the frequencies of CD4 + CTLA-4 + and CD4 + CD25+ T cells expressing CD39 and CD73. Post-exhaustive exercise serum decreased the frequency of CD4 + CD25 + CD73+ T cells but increased CD4 + CD25-CD39 + T cell frequency. Both post-exercise serums increased the proportions of CD4 + PD-1 + and CD8 + PD-1+ T cells. Blood serum factors released during exercise altered the immune response and T cell phenotype. The type of exercise impacted the immunomodulatory activity of the post-exercise serum on PBMCs.


Subject(s)
Antigens, CD , Exercise/physiology , Immunomodulation/immunology , Leukocytes, Mononuclear/immunology , Obesity/immunology , T-Lymphocytes/immunology , Acetylation , Adult , Cross-Over Studies , Histones/metabolism , Humans , Interleukin-10/metabolism , Leukocytes, Mononuclear/metabolism , Male , NF-kappa B/metabolism , Tumor Necrosis Factor-alpha/metabolism , Young Adult
2.
Appl Physiol Nutr Metab ; 45(6): 659-666, 2020 Jun.
Article in English | MEDLINE | ID: mdl-31782931

ABSTRACT

The aim of this study was to evaluate the impact of high-intensity strength training (ST) or low-intensity strength training with blood flow restriction (ST-BFR) on monocyte subsets, the expression of C-C chemokine receptor 5 (CCR5), and CD16 on monocytes, and tumor necrosis factor alpha (TNF-α) production of overweight men. Thirty overweight men were randomly assigned to conventional ST or ST-BFR. Both groups performed exercises of knee extension and biceps curl with equal volume (3 sessions/week) over 8 weeks, and the peripheral frequency of monocytes (CD14+CD16-, classical monocytes; CD14+CD16+, intermediate monocytes; CD14-CD16+, nonclassical monocytes), the mean fluorescence intensity (MFI) of CCR5 and CD16 on CD14+ monocytes; and the production of TNF-α by lipopolysaccharide (LPS)-stimulated cells were quantified. Eight weeks of ST increased the frequency of CD14+CD16- monocytes (p = 0.04) and reduced the percentage of CD14-CD16+ (p = 0.02) and the production of TNF-α by LPS-stimulated cells (p = 0.03). The MFI of CD16 on CD14+ monocytes decreased after the ST intervention (p = 0.02). No difference in monocyte subsets, CCR5 or CD16 expression, and TNF-α production were identified after ST-BFR intervention (p > 0.05). The adoption of ST promotes anti-inflammatory effects on monocyte subsets of overweight men, but this effect was lost when BFR was adopted. Novelty High-intensity strength training reduces the production of TNF-α and the peripheral frequency of CD16+ monocytes in overweight men. Blood flow restriction method blunts the strength training adaptations on monocyte subsets and pro-inflammatory TNF-α production in overweight men.


Subject(s)
Inflammation , Overweight , Physical Conditioning, Human/physiology , Resistance Training , Adaptation, Physiological/immunology , Adaptation, Physiological/physiology , Adult , Cells, Cultured , Humans , Inflammation/immunology , Inflammation/physiopathology , Male , Monocytes/immunology , Monocytes/metabolism , Overweight/immunology , Overweight/physiopathology , Overweight/therapy , Tumor Necrosis Factor-alpha/blood , Vascular Diseases/immunology , Vascular Diseases/physiopathology , Young Adult
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