H. Gabriel et al., CIRCULATING LEUKOCYTE SUBPOPULATIONS IN SEDENTARY SUBJECTS FOLLOWING GRADED MAXIMAL EXERCISE WITH HYPOXIA, European journal of applied physiology and occupational physiology, 67(4), 1993, pp. 348-353
Ten healthy sedentary subjects [age, 27.5 (SD 3.5) years; height, 180
(SD 5) cm; mass, 69.3 (SD 6.3) kg] performed two periods of maximal in
cremental graded cycle ergometer exercise in a supine position. Random
ly ordered and using an open spirometric system, one exercise was carr
ied out during normoxia [maximal oxygen consumPtiOn (VO2max) = 38.6 (S
D 3.5) ml . min-1 . kg-1; maximal blood lactate concentration, 9.86 (S
D 1.85) mmol . l-1; test duration, 22.6 (SD 2.7) min], the other durin
g hypoxia [VO2max = 33.2 (SD 3.2) ml . min-1 . kg-1; maximal blood lac
tate concentration, 10.38 (SD 2.02) mmol . l-1; test duration, 19.7 (S
D 2.8) min]. At rest, immediately (0 p) and 60 min (60 p) after exerci
se, counts of leucocyte subpopulations (flow cytometry), cortisol and
catecholamine concentrations were determined. At 0 p in contrast to no
rmoxia, during hypoxia there was no significant increase of granulocyt
es. There were no significant differences between normoxia and hypoxia
in the increases from rest to 0 p in counts of monocytes, total lymph
ocytes and lymphocyte subpopulations [clusters of differentiation (CD)
, CD3+, CD4+CD45RO-, CD4+CD45RO+, CD8+CD45RO-, CD8+CD45RO+, CD3+HLADR, CD3-CD16/CD56+, CD3-CD16/CD56+, CD19+] as well as adrenaline, noradr
enaline and cortisol concentrations. The counts of CD3-CD16/CD56+- and
CD8+CD45RO+-cells increased most. At 60 p, CD3-CD16/CD56+ and CD3+CD1
6/CD56+-cell counts were below pre-exercise levels and under hypoxia s
lightly but significantly lower than under normoxia. We concluded that
the exercise-induced mobilization and redistribution of most leucocyt
e and lymphocyte subpopulations were unimpaired under acute hypoxia at
sea level. Reduced increases of granulocyte counts during the study a
nd reduced cell numbers of natural killer cells and cytotoxic, not maj
or histocompatibility complex-restricted T-cells, only indicated margi
nal effects on the immune system.