scholarly journals Exhaustive Exercise Increases Spontaneous but Not fMLP-Induced Production of Reactive Oxygen Species by Circulating Phagocytes in Amateur Sportsmen

Biology ◽  
2022 ◽  
Vol 11 (1) ◽  
pp. 103
Author(s):  
Adam Chmielecki ◽  
Krzysztof Bortnik ◽  
Szymon Galczynski ◽  
Gianluca Padula ◽  
Hanna Jerczynska ◽  
...  

Strenuous exercise alters the oxidative response of blood phagocytes to various agonists. However, little is known about spontaneous post exercise oxidant production by these cells. In this cross-over trial, we tested whether an exhaustive treadmill run at a speed corresponding to 70% of VO2max affects spontaneous and fMLP-provoked oxidant production by phagocytes in 18 amateur sportsmen. Blood was collected before, just after, and 1, 3, 5 and 24 h post exercise for determination of absolute and normalized per phagocyte count spontaneous (a-rLBCL, rLBCL) and fMLP-induced luminol-enhanced whole blood chemiluminescence (a-fMLP-LBCL, fMLP-LBCL). a-rLBCL and rLBCL increased by 2.5- and 1.5-times just after exercise (p < 0.05) and then returned to baseline or decreased by about 2-times at the remaining time-points, respectively. a-fMLP-LBCL increased 1.7- and 1.6-times just after and at 3 h post-exercise (p < 0.05), respectively, while fMLP-LBCL was suppressed by 1.5- to 2.3-times at 1, 3, 5 and 24 h post-exercise. No correlations were found between elevated post-exercise a-rLBCL, a-fMLP-LBCL and run distance to exhaustion. No changes of oxidants production were observed in the control arm (1 h resting instead of exercise). Exhaustive exercise decreased the blood phagocyte-specific oxidative response to fMLP while increasing transiently spontaneous oxidant generation, which could be a factor inducing secondary rise in antioxidant enzymes activity.

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Robert Stawski ◽  
Konrad Walczak ◽  
Ewelina Perdas ◽  
Anna Wlodarczyk ◽  
Agata Sarniak ◽  
...  

Abstract Strenuous exercise increases circulating cell free DNA (cfDNA) and stimulates blood phagocytes to generate reactive oxygen species (ROS) which may induce DNA strand breaks. We tested whether: (A) elevated cfDNA in response to three repeated bouts of exhaustive exercise has decreased integrity; (B) each bout of exercise increases luminol enhanced whole blood chemiluminescence (LBCL) as a measure of ROS production by polymorphonuclear leukocytes. Eleven men performed three treadmill exercise tests to exhaustion separated by 72 hours of resting. Pre- and post-exercise concentrations and integrity of cf nuclear and mitochondrial DNA (cf n-DNA, cf mt-DNA) and resting (r) and fMLP (n-formyl-methionyl-leucyl-phenylalanine)-stimulated LBCL were determined. Each bout increased concentrations of cf n-DNA by more than 10-times which was accompanied by about 2-times elevated post-exercise rLBCL and fMLP-LBCL. Post-exercise cf n-DNA integrity (integrity index, I229/97) decreased after the first (0.59 ± 0.19 vs. 0.48 ± 0.18) and second (0.53 ± 0.14 vs. 0.44 ± 0.17) bout of exercise. There were negative correlations between I229/97 and rLBCL (ƍ = –0.37), and I229/97 and fMLP-LBCL (ƍ = –0.40) – analysis of pooled pre- and post-exercise data (n = 66). cf mt- DNA integrity (I218/78) did not alter in response to exercise. This suggests an involvement of phagocyte ROS in cf n-DNA strand breaks in response to exhaustive exercise.


2018 ◽  
Author(s):  
Robert Stawski ◽  
Konrad Walczak ◽  
Ewelina Perdas ◽  
Anna Wlodarczyk ◽  
Agata Sarniak ◽  
...  

AbstractStrenuous exercise increases circulating cell free DNA (cf DNA) and stimulates blood phagocytes to generate reactive oxygen species (ROS) which may induce DNA strand breaks. We tested whether: (A) elevated cf DNA in response to three repeated bouts of exhaustive exercise has decreased integrity; (B) each bout of exercise increases luminol enhanced whole blood chemiluminescence (LBCL) as a measure of ROS production by polymorphonuclear leukocytes. Eleven men performed three treadmill exercise tests to exhaustion separated by 72 hours of resting. Pre- and post-exercise concentrations and integrity of cf nuclear and mitochondrial DNA (cf n-DNA, cf mt-DNA) and resting and fMLP-stimulated LBCL were determined. Each bout increased concentrations of cf n-DNA by more than 10-times which was accompanied by about 2-times elevated post-exercise rLBCL and fMLP-LBCL. Post-exercise cf n-DNA integrity (integrity index, I206/78) decreased after the first (0.59±0.19 vs. 0.48±0.18) and second (0.53±0.14 vs. 0.44±0.17) bout of exercise. There were negative correlations between I206/78and rLBCL (ƍ=−0.37) and I206/78and fMLP-LBCL (ƍ=− 0.40) – analysis of pooled pre- and post-exercise data (n=66). cf-mt DNA integrity (I218/97) did not alter in response to exercise. This suggests an involvement of phagocyte ROS in cf n-DNA strand breaks in response to exhaustive exercise.


Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 3224-3224
Author(s):  
Micah J. Mooberry ◽  
Robert Bradford ◽  
Robin Kellerman ◽  
Eric Sobolewski ◽  
Harry C. Stafford ◽  
...  

Abstract Abstract 3224 The acute physiological response to strenuous exercise is characterized by a transient hypercoagulable state as well as an acute inflammatory response. Despite these well-recognized findings, the mechanisms involved in these exercise-induced effects are not well understood. To further evaluate the effect of exercise on multiple hematologic parameters, subjects underwent an exercise protocol with blood samples obtained at several time points. Fifteen healthy male African-American subjects [10 normal hemoglobin (HbAA), 5 sickle cell trait (HbAS)], ages 18–35, exercised at 65% of VO2max × 30 min followed by an increase in treadmill grade of 2.5% every 3 min until volitional exhaustion. Blood was collected at baseline, immediately post-exercise, and at 1 and 2 hours post-exercise. Analyses included CBC, D-dimer, sVCAM, LDH, haptoglobin, plasma free hemoglobin (PF Hb), RBC phosphatidylserine (PS) exposure (by flow cytometry), microparticle (MP) procoagulant activity (Zymuphen MP-activity assay measuring ‘PS equivalents’), and MP-tissue factor (MP-TF) activity (in-house chromogenic assay). Flow cytometric enumeration of MPs in platelet poor plasma was performed using a standardized ISTH protocol, and included platelet MP (PMP: AnnV+/CD41+), endothelial MP (EMP: CD31+/CD41−), red cell MP (RBC MP: AnnV+/CD235a+), leukocyte MP (LMP: AnnV+/CD45+), and monocyte MP (MMP: AnnV+/CD14+) analyses. As previously reported, increases in total WBC count, monocyte count, and sVCAM occurred immediately after exercise, with return towards baseline thereafter. A similar transient increase was seen with both MP procoagulant activity and MP-TF activity (Fig. 1), with a 2.5- (p<0.01) and 3-fold (p<0.01) increase, respectively. Acute increases were also observed for PMPs, EMPs, LMPs and MMPs, which peaked immediately post-exercise. No significant changes were noted for D-dimer, Hb, LDH, or haptoglobin; however, a modest increase in PF Hb was noted following exercise. Interestingly, some unique differences were seen in HbAS compared to HbAA subjects; specifically, EMPs peaked later (at 2 hrs) and were more elevated in HbAS subjects, although the difference was not statistically significant (HbAS 138.2 +/−162.3 EMPs/uL vs. HbAA 65.4 +/− 29.3 EMPs/uL; p=0.26). Additionally, there was a trend towards increased RBC MPs in HbAS subjects (HbAS: 291 +/− 284 RBC MPs/uL at baseline vs. 975 +/− 1033 RBC MPs/uL at 2 hrs; p=0.13). A trend towards increased RBC PS exposure immediately post-exercise in HbAS subjects compared to HbAA was also apparent (Fig. 2), with almost 3× more RBC PS exposure in the HbAS group (post exercise % PS+ RBCs: HbAS 1.28 +/− 1.05% vs. HbAA 0.22 +/− 0.10%; p=0.09, n=4). We also observed a trend towards lower haptoglobin and increased D-dimer in HbAS subjects compared to HbAA subjects at all time points. These data confirm previous observations reporting systemic activation of coagulation occurring after strenuous exercise, and demonstrate a transient increase in MP-TF activity. Interestingly, the time course and magnitude of this activity differs from that seen in the human endotoxemia model (data not shown), in which there is a 5–7 fold increase in MP-TF activity that peaks much later (4 hours) post LPS exposure. The much earlier peak and lower magnitude (∼ 3-fold increase) with exercise suggest a mechanism that does not involve cellular synthesis of TF but is instead likely due to a release of pre-formed TF stores. Other findings in this study may also be relevant to the pathophysiology of the well-documented risk of exertional sudden death with sickle cell trait. In particular, we speculate that the increased RBC PS exposure, elevated RBC MPs and a relative increase in EMPs may contribute to increased activation of coagulation and occlusion of the microvasculature during exercise that may result in DIC, rhabdomyolysis and sudden death. Disclosures: No relevant conflicts of interest to declare.


2007 ◽  
Vol 2 ◽  
pp. 117739010700200 ◽  
Author(s):  
Tamara Zoltan ◽  
Franklin Vargas ◽  
Carla Izzo

We have determined and quantified spectrophotometrically the capacity of producing reactive oxygen species (ROS) as 1O2 during the photolysis with UV-A light of 5 new synthesized naphthyl ester derivates of well-known quinolone antibacterials (nalidixic acid (1), cinoxacin (2), norfloxacin (3), ciprofloxacin (4) and enoxacin (5)). The ability of the naphthyl ester derivatives (6-10) to generate singlet oxygen were detecting and for the first time quantified by the histidine assay, a sensitive, fast and inexpensive method. The following tendency of generation of singlet oxygen was observed: compounds 7 >10 > 6 > 8 > 9 >> parent drugs 1-5.


1987 ◽  
Vol 243 (2) ◽  
pp. 555-559 ◽  
Author(s):  
M C Liu ◽  
M Suiko ◽  
F Lipmann

Rat embryo fibroblasts, line 3Y1, were prelabelled for 24 h with [35S]sulphate and incubated in fresh medium without [35S]sulphate. A rapid efflux of the overall 35S-labelled compounds from the cells into the medium was observed. After 9 h of incubation, about 50% of the total 35S radioactivity appeared in the medium and up to 84.3% did so at the end of a 48 h incubation. Determination of [35S]sulphated macromolecules present in both the cell-associated and the incubation-medium fractions at different time points during incubation indicated that the majority of the 35S-labelled compounds released from the cells were low-Mr products derived from digestion of the [35S]sulphated macromolecules. Further analysis for tyrosine-O-[35S]sulphated proteins, which constituted only a small fraction of the overall [35S]sulphated macromolecules, showed that, after 9 h of incubation, there was a 65% decrease in the cell-associated fraction, and only 16.4% remained after 48 h. During that time, an amount equivalent to 20.7% of the cell-associated tyrosine-O-[35S]sulphated proteins originally present was released into the medium. Free tyrosine O-[35S]sulphate was generated in the cells and excreted into the incubation medium. Its rate of increase with time, however, was slow, and could account for only 12.4% of the tyrosine-O-[35S]sulphated proteins catabolized at the end of the 48 h incubation.


2002 ◽  
Vol 93 (3) ◽  
pp. 813-822 ◽  
Author(s):  
Natalie Hiscock ◽  
Bente Klarlund Pedersen

The amino acid glutamine is known to be important for the function of some immune cells in vitro. It has been proposed that the decrease in plasma glutamine concentration in relation to catabolic conditions, including prolonged, exhaustive exercise, results in a lack of glutamine for these cells and may be responsible for the transient immunodepression commonly observed after acute, exhaustive exercise. It has been unclear, however, whether the magnitude of the observed decrease in plasma glutamine concentration would be great enough to compromise the function of immune cells. In fact, intracellular glutamine concentration may not be compromised when plasma levels are decreased postexercise. In addition, a number of recent intervention studies with glutamine feeding demonstrate that, although the plasma concentration of glutamine is kept constant during and after acute, strenuous exercise, glutamine supplementation does not abolish the postexercise decrease in in vitro cellular immunity, including low lymphocyte number, impaired lymphocyte proliferation, impaired natural killer and lymphokine-activated killer cell activity, as well as low production rate and concentration of salivary IgA. It is concluded that, although the glutamine hypothesis may explain immunodepression related to other stressful conditions such as trauma and burn, plasma glutamine concentration is not likely to play a mechanistic role in exercise-induced immunodepression.


Nutrients ◽  
2018 ◽  
Vol 10 (7) ◽  
pp. 893
Author(s):  
Chihiro Kojima ◽  
Nobukazu Kasai ◽  
Chika Kondo ◽  
Kumiko Ebi ◽  
Kazushige Goto

PURPOSE: The purpose of the present study was to investigate the effect of whole-body cryotherapy (WBC) treatment after exercise on appetite regulation and energy intake. METHODS: Twelve male athletes participated in two trials on different days. In both trials, participants performed high-intensity intermittent exercise. After 10 min following the completion of the exercise, they were exposed to a 3-min WBC treatment (−140 °C, WBC trial) or underwent a rest period (CON trial). Blood samples were collected to assess plasma acylated ghrelin, serum leptin, and other metabolic hormone concentrations. Respiratory gas parameters, skin temperature, and ratings of subjective variables were also measured after exercise. At 30 min post-exercise, energy and macronutrient intake were evaluated during an ad libitum buffet meal test. RESULTS: Although appetite-regulating hormones (acylated ghrelin and leptin) significantly changed with exercise (p = 0.047 for acylated ghrelin and p < 0.001 for leptin), no significant differences were observed between the trials. Energy intake during the buffet meal test was significantly higher in the WBC trial (1371 ± 481 kcal) than the CON trial (1106 ± 452 kcal, p = 0.007). CONCLUSION: Cold exposure using WBC following strenuous exercise increased energy intake in male athletes.


1991 ◽  
Vol 156 (1) ◽  
pp. 153-171 ◽  
Author(s):  
YONG TANG ◽  
ROBERT G. BOUTILIER

The intracellular acid-base status of white muscle of freshwater (FW) and seawater (SW) -adapted rainbow trout was examined before and after exhaustive exercise. Exhaustive exercise resulted in a pronounced intracellular acidosis with a greater pH drop in SW (0.82 pH units) than in FW (0.66 pH units) trout; this was accompanied by a marked rise in intracellular lactate levels, with more pronounced increases occurring in SW (54.4 mmoll−1) than in FW (45.7 mmoll−1) trout. Despite the more severe acidosis, recovery was faster in the SW animals, as indicated by a more rapid clearance of metabolic H+ and lactate loads. Compartmental analysis of the distribution of metabolic H+ and lactate loads showed that the more rapid recovery of pH in SW trout could be due to (1) their greater facility for excreting H+ equivalents to the environmental water [e.g. 15.5 % (SW) vs 5.0 % (FW) of the initial H+ load was stored in external water at 250 min post-exercise] and, to a greater extent, (2) the more rapid removal of H+, facilitated via lactate metabolism in situ (white muscle) and/or the Cori cycle (e.g. heart, liver). The slower pH recovery in FW trout may also be due in part to greater production of an ‘unmeasured acid’ [maximum approx. 8.5 mmol kg−1 fish (FW) vs approx. 6 mmol kg−1 fish (SW) at 70–130 min post-exercise] during the recovery period. Furthermore, the analysis revealed that H+-consuming metabolism is quantitatively the most important mechanism for the correction of an endogenously originating acidosis, and that extracellular pH normalization gains priority over intracellular pH regulation during recovery of acid-base status following exhaustive exercise.


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