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Biomedical subjects

U Order

Publications and source records attributed to U Order.

9 recordsLinked to original sources

Effect of a short maximal physical exercise on coagulation, fibrinolysis, and complement system.

In 11 healthy young subjects, the plasma concentrations of the thrombin-antithrombin III complex, fibrinopeptide A, tissue-plasminogen activator, complement fragments C3a and C4a, and histamine were measured before and after a graded maximal bicycle exercise test. The analyses were carried out 30 min before and immediately before exercise, immediately after exercise, and 30 and 60 min later. All post-exercise values were corrected for plasma volume changes, which were calculated from hematocrit and hemoglobin values. Immediately post-exercise, thrombin-antithrombin III, tissue-plasminogen activator, complement fragments C3a and C4a, and histamine were all significantly elevated (p less than 0.01), compared with the pre-exercise values; 30 and 60 min later the values normalized and significant differences from the pre-exercise values could no longer be measured. Fibrinopeptide A did not change significantly after exercise. The present results provide evidence for a simultaneous activation of coagulation, fibrinolysis, and complement system as well as for a release of histamine after a short maximal exercise.

Adult↗

Can endurance sports stimulate immune mechanisms against cancer and metastasis?

Proceeding from a brief historical contemplation of the problematic nature of "exercise and malignancy" a training investigation (running on a treadmill) with animals is presented. By means of the experimental tumor model fibrosarcoma L-1 of BALB/c mice differences in growth, size, and metastatic spreading have been proven depending upon the mode and more significantly on the intensity of training and upon the mode of application and inoculation of tumor cells. Accordingly the best cancer protective effect could be observed when the animals performed a pre- and a post-running training before and after inoculation. More over mechanisms of the acute phase response of human athletes are discussed in relation to possible prophylactic effects on the prevention of infections and on the development of cancer.

Animals↗

Lymphocyte subsets during the first hours and days after a 2.5 h running test.

After a 2.5 h running test on eight healthy young males the lymphocyte subsets in peripheral blood were analyzed by flow cytometry. The analysis was carried out immediately post-exercise, after a 1 h and 3 h interval as well as a one day, a two day and five day interval. Lymphocyte subpopulations were also measured in five control subjects who did not exercise. Compared with the pre-exercise level the total lymphocyte and T-cell count was decreased 1 h and 3 h after the run and one and two days after exercise (p less than 0.01). The absolute number of monocytes and B-lymphocytes fell significantly (p less than 0.01) on the first and second day after exercise. No consistent change of helper-/suppressor-inducer T-lymphocytes (CD4+) and cytotoxic-suppressor T-cells (CD8+) cells was observed immediately after exercise. One and 3 h later, however, the absolute number of both cell types dropped below pre-exercise values (p less than 0.01). The decrease of the CD8+ cells was more pronounced, causing an increase of the CD4+ to CD8+ ratio (p less than 0.01). Among the CD4+ cells only the Leu 8+ subpopulation showed a relative increase 1 h after the exercise (p less than 0.01) while the Leu 8- population remained unaffected. 1 h and 3 h after the end of the run there was a significant fall of the absolute number and percentage of natural killer cells (Leu 7+) and cytotoxic T-cells (CD8+ Leu 7+) (p less than 0.01). These cells remained low during the first and second day after the exercise (p less than 0.01). In the control subjects the changes of cell counts for all cells examined were much smaller than in the runners. The results indicate that strenuous and prolonged exercise causes a delayed redistribution of lymphocyte subpopulations with a reduction of lymphocytes and particularly of natural killer and cytotoxic cells beginning 1 h after the exercise followed by a reduction of monocytes 24 h later. The percentage increase of CD4+ cells 1 h after the exercise could be explained by an increase of the CD4+ Leu 8+ subpopulation.

Adult↗

Complement activation after prolonged exercise.

The effects of a 2.5-h running test on the concentrations of the complement cleavage products C3a, C4a and C5a in plasma were examined in eight healthy young males. In all participants the C3a and C4a values were raised during (1 h after the start) and immediately after exercise. C4a was also raised 1 and 3 h after the race. These results provide evidence for complement activation after prolonged exercise.

Adult↗

Plasma elastase-alpha 1-antitrypsin, neopterin, tumor necrosis factor, and soluble interleukin-2 receptor after prolonged exercise.

The effects of a 2.5-h running test on the plasma concentrations of elastase-alpha 1-antitrypsin, neopterin, tumor necrosis factor, and soluble interleukin-2 receptor were evaluated in eight healthy young male subjects. Neopterin was measured by radioimmunoassay, elastase-alpha 1-antitrypsin, tumor necrosis factor, and soluble interleukin-2 receptor by enzyme immunoassay. The post-exercise values were corrected for plasma volume changes which were calculated from hematocrit and hemoglobin values. Compared with the concentrations before exercise, elastase-alpha 1-antitrypsin values were significantly increased during the run (1 h after the start) (P less than 0.01) as well as during the first few hours after the end of the running test (P less than 0.01). A significant increase of tumor necrosis factor and neopterin was observed 1 h after the end and 1,3, and 24 h after the end of the running test, respectively, (P less than 0.01), and soluble interleukin-2 receptor concentrations were significantly elevated 1 and 2 days after exercise (P less than 0.01). The increase of elastase-alpha 1-antitrypsin, neopterin, tumor necrosis factor, and soluble interleukin-2 receptor supports the concept of a functional involvement of polymorphonuclear neutrophils and an activation of macrophages and T-lymphocytes after prolonged exercise.

Adult↗

Delayed effects of prolonged exercise on serum lipoproteins.

The delayed lipoprotein changes after a 3-hour running test were examined in 14 moderately trained young male subjects. Fasting blood samples were obtained one day before, immediately before, and one, two, and four days after the race. Nonfasting samples were collected immediately after, one, and three hours after exercise. Three hours after the race, the ratio of unesterified cholesterol to cholesteryl esters was significantly increased, and one and two days after the race it was significantly decreased compared to the preexercise value. The HDL2/HDL3 ratio, measured by density-gradient ultracentrifugation was one and three hours after the running significantly elevated. However, no redistribution of the HDL2/HDL3 cholesterol ratio determined by a precipitation method with polyanions was found at this time. One day postexercise HDL cholesterol rose significantly above the preexercise value, and this was associated with an elevation of the HDL3 subfraction. On the following day a significant increase of HDL2 cholesterol and the HDL2/HDL3 cholesterol ratio was found. The apolipoproteins A-I, A-II, and B, measured by radial immunodiffusion, did not change during the first hours and the first two days after the race. On the second postexercise day the Lp(a) lipoprotein rose significantly above the preexercise value. Compared with the preexercise level the LCAT activity was significantly elevated three hours after the race and significantly decreased two days later. The present study suggests that during the first few days after prolonged exercise a number of plasma lipoprotein changes take place that are similar to those observed after a period of physical training.

Adult↗

Can physical exercise induce an effective fibrinolysis?

The study examined serum fibrin(ogen) degradation products (FDP/fdp) after short and prolonged exercise, before and after training, in young and elderly subjects. Six of 15 well-trained soccer players demonstrated an increase of FDP/fdp after a short graded maximal treadmill test. In 12 elderly subjects short maximal exercise produced no increase of FDP/fdp. However, in most of these subjects an exhaustive work load was not reached. Three of 16 moderately trained young subjects exhibited a small FDP/fdp increase after 45 minutes of submaximal exercise and in 3 of 10 participants an elevation of FDP/fdp was found after a 3 h-running test. Immediately after the race there was a significant (p less than 0.001) increase of fragment D, measured by an enzyme immunoassay. During a second 3 h-race after an 8 week physical training program, the post-exercise FDP/fdp and fragment D increase was slightly enhanced. Plasma fibrinogen was significantly (p less than 0.05) elevated on the fourth day after the 3 h-race before but not after the training program. In conclusion intense and/or prolonged physical exercise caused only a modest increase of FDP/fdp. Physical training seems only minimally to affect this response. It is speculated that in the trained subject, daily exercise-induced fibrinolytic activation might be more relevant to the risk of thrombotic or atherosclerotic disease than a higher absolute resting or post-exercise fibrinolytic level compared with the untrained.

Acute-Phase Proteins↗

C-reactive protein serum concentrations in well-trained athletes.

Previously it had been shown that there is a sharp increase in C-reactive protein (CRP) serum concentration during the first few days after severe exercise. To evaluate the effect of physical training on the CRP levels, a sensitive enzyme immunoassay was developed and used to assess the basal CRP concentrations in 356 male and 103 female athletes, who trained at least 4 times per week in various disciplines, in 45 male and 40 female untrained controls, and in 35 elderly coronary patients. In male athletes the lowest CRP values were found in swimmers (median: 102 ng/ml, n = 59), which were significantly lower (P less than 0.001) than those of male controls (median: 502 ng/ml, n = 45). The CRP concentrations in rowers (median: 260 ng/ml, n = 108) were also significantly lower (P less than 0.01) than in the control group. CRP levels in middle- and long-distance runners (median: 315 ng/ml, n = 53), racing cyclists (median: 620 ng/ml, n = 111), and soccer players (median: 660 ng/ml, n = 25) did not differ significantly from those of the controls. In female athletes the lowest CRP concentrations were also found in swimmers (median: 110 ng/ml, n = 49), which were significantly lower (P less than 0.001) than those of the female controls (median: 396 ng/ml, n = 40). Female middle- and long-distance runners (n = 36) and female rowers (n = 18) had median CRP values of 250 and 285 ng/ml, respectively. This results suggest that training induces a suppressive effect upon CRP, responsible for the low serum levels in athletes (particularly swimmers) when compared to controls.(ABSTRACT TRUNCATED AT 250 WORDS)

Adolescent↗