Different responses of apoptotic, inflammatory and heat shock protein gene expression to a single bout of high intensity interval exercise between physically active and inactive men

Author(s):  
Selma Arzu Vardar ◽  
Zeynep Banu Doğanlar ◽  
Oktay Kaya ◽  
Pınar Tayfur ◽  
Necdet Sut ◽  
...  

High mechanical load of muscles may induce muscular apoptosis on the one hand and adaptation to exercise on the other. This study aimed to explore whether changes of circulatory levels of inflammation, apoptosis and heat shock proteins (HSPs) mRNA following single bout of high intensity interval exercise (HIIE) differs between physically active (PA) and inactive (PI) men. Nine PA and nine PI (peak VO2 2.6±0.4 vs. 2.0 ± 0.2 L.min-1) healthy men (age: 28.7+/-6.3 vs. 30.2+/-4.5 years and BMI: 2.6±2.1 vs. 23.3±2.8 kg.m-2) performed HIIE comprising 4 repeats of a Wingate test (load:0.050 kg.kg-1 body weight). Blood samples were collected before exercise, 5 min and 24 h after HIIE for measuring mRNA of inflammation markers IL6 and TNFα, apoptosis markers including Bcl-2, Bax, and HSP27, HSP60, HSP70, HSP90 using quantitative real-time PCR analysis. Post-HIIE IL6, TNFα and HSP60 were higher in the PI than the PA group 5 min after exercise (p=0.003, ES=1.59; p=0.007, ES=1.59 and p=0.027, ES=1.10 respectively). HSP70 acutely increased only in the PA group (p=0.024, ES=1.20). The increase in Bcl-2 (p=0.047, ES=1.08) and Bax (p=0.024, ES=1.20) levels were higher in the PI group 5 min after HIIE. The present study indicated that the response of inflammatory, apoptosis and HSP gene expressions to HIIE in blood of healthy male volunteers strongly depends on their level of regular physical activity. Novelty • Blood IL-6 and HSP60 mRNA levels following high intensity exercise may indicate metabolic stress. • Increased blood HSP70 mRNA in physically active men may show an alternative apoptosis suppression pathway.

2013 ◽  
Vol 38 (8) ◽  
pp. 823-829 ◽  
Author(s):  
Elena Bellou ◽  
Faidon Magkos ◽  
Tonia Kouka ◽  
Eirini Bouchalaki ◽  
Dimitra Sklaveniti ◽  
...  

A single bout of high-intensity interval aerobic exercise has been shown to produce the same or greater metabolic benefits as continuous endurance exercise with considerably less energy expenditure, but whether this applies to very low density lipoprotein (VLDL) metabolism is not known. We sought to examine the effect of a single bout of high-intensity interval aerobic exercise on basal VLDL-triglyceride (TG) kinetics 14 and 48 h after exercise cessation to determine the acute and time-dependent effects of this type of exercise on VLDL-TG metabolism. Eight healthy sedentary men (age, 23.6 ± 6.1 years; body mass index, 23.1 ± 2.2 kg·m−2, peak oxygen consumption (V̇O2peak), 36.3 ± 5.5 mL·kg−1·min−1) participated in three stable isotopically labeled tracer infusion studies: (i) 14 h and (ii) 48 h after a single bout of high-intensity aerobic interval exercise (60% and 90% of V̇O2peak in 4 min intervals for a total of 32 min; gross energy expenditure ∼500 kcal) and (iii) after an equivalent period of rest, in random order. Fasting plasma VLDL-TG concentration was 20% lower at 14 h (P = 0.046) but not at 48 h (P = 1.000) after exercise compared with the resting trial. VLDL-TG plasma clearance rate increased by 21% at 14 h (P < 0.001) but not at 48 h (P = 0.299) after exercise compared with rest, whereas hepatic VLDL-TG secretion rate was not different from rest at any time point after exercise. We conclude that high-intensity interval exercise reduces fasting plasma VLDL-TG concentrations in non-obese men the next day by augmenting VLDL-TG clearance, just like a single bout of continuous endurance exercise. This effect is short-lived and abolished by 48 h after exercise.


2021 ◽  
pp. 1-23
Author(s):  
Kosar Valaei ◽  
Javad Mehrabani ◽  
Alexei Wong

Abstract L-citrulline (L-Cit) is a nonessential amino acid that stimulates nitric oxide (NO) production and improves exercise performance by reducing muscle damage indices; however, the direct benefits of L-Cit on antioxidant markers are unclear. The aim of this study was to examine antioxidant responses to high-intensity interval exercise following acute L-Cit supplementation. Nine young men (21 ± 1 years) participated in a double-blind crossover study in which they received 12 g of L-Cit and placebo (PL) an hour prior to high-intensity interval exercise on two occasions, separated by a seven-day washout period. Blood samples were obtained before (PRE), immediately after (IP), 10 (10P), and 30 min after exercise (30P) from the cubital vein using standard procedures. Serum concentrations of superoxide dismutase (SOD), glutathione peroxidase (GPx), catalase (CAT), and NO metabolites (NOx) were measured. The exercise protocol significantly elevated SOD (p = 0.01) and GPx (p = 0.048) from PRE to 10P in the L-Cit group with greater changes than the PL group. CAT concentrations increased IP (p = 0.014) and remained elevated at 10P (p = 0.03) and 30P (p = 0.015) in both the L-Cit and PL conditions. NOx concentrations increased IP (p = 0.05) in the L-Cit group with greater changes than PL group in PRE to IP, PRE to 10P, and PRE to 30P (p < 0.05). Our data indicate that L-Cit supplementation (single 12 g dose pre-exercise) induces improvements in antioxidant markers following a session of high-intensity interval exercise in young men.


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