Se. Blank et al., MECHANISTIC DIFFERENCES IN NK CELL CYTOLYTIC ACTIVITY IN TREADMILL-TRAINED AND CHRONIC ETHANOL-CONSUMING MICE, Journal of applied physiology, 76(5), 1994, pp. 2031-2036
The present study was undertaken to investigate mechanisms contributin
g to differences in natural killer (NK) cell activity in moderately en
durance-trained and ethanol-consuming mice. Independent of ethanol exp
osure, NK cell activity in nylon wool-nonadherent (NWNA) splenocytes i
s lower in trained than in sedentary control mice (Blank et al. J. App
l. Physiol. 72: 8-14, 1992). Reduced activity may result from a genera
lized loss of cytolytically active cells, redistribution of NK cells f
rom the spleen to other body compartments, or disruption of paracrine
regulation of NK cells after removal of nylon wool-adherent cells. To
examine these possibilities, NK cell cytolytic activity was determined
in nonenriched splenocytes from treadmill-trained and ethanol-consumi
ng mice. Lymphocyte subpopulations in nonenriched splenocytes and NWNA
splenocytes were also compared. Peripheral blood lymphocyte subpopula
tions were determined to examine combined effects of training and etha
nol intake on regional distribution of lymphocytes in blood and spleen
. NK cell activity in nonenriched splenocytes from trained water-drink
ing mice was not reduced compared with that in sedentary mice; rather,
cytolytic activity was moderately enhanced (17% increase in lytic uni
ts, P < 0.05). Training did not change percentages of T-cells, B-cells
, and NK [NK1.1(+) and large granular lymphocytes (LGL-1(+))] cells or
the LGL/ NK ratio in the spleen and blood. NK cell cytolytic activity
was significantly reduced in nonenriched splenocytes from ethanol-con
suming mice, independent of training. These findings support the hypot
hesis that moderate-intensity endurance training influences splenic NK
cell function by modulating paracrine regulation of NK cells. In the
case of combined chronic exercise and ethanol intake, training did not
protect against ethanol-related decrease in percentage of NK1.1(+) ce
lls or in its LGL-1 subset, indicating that loss of cytolytically acti
ve cells contributes to decreased NK cytotoxicity in trained ethanol-c
onsuming mice.