Hypertension, Vol 21, 185-194, Copyright © 1993 by American Heart Association
DW Pascual, VH Pascual, KL Bost, JR McGhee and S Oparil
The immune system of the spontaneously hypertensive rat is dysfunctional
compared with that of normotensive control strains. Previous studies from
our laboratory have shown that immunodepression in the spontaneously
hypertensive rat was mediated by macrophages. The current study examines
the mechanism for the depressed proliferative responses to concanavalin A
typically observed by splenic mononuclear cells of spontaneously
hypertensive rats. We tested various inhibitors of known macrophage
products responsible for suppressing lymphoid function. The nitric oxide
synthetase inhibitor NG-monomethyl L- arginine produced dose-dependent
derepression of the proliferative responses of splenic mononuclear cells to
concanavalin A. In contrast, indomethacin and catalase exhibited only weak
derepression of the proliferative responses. Subsequent analysis showed
that splenic mononuclear cells from spontaneously hypertensive rats
generated greater nitric oxide levels than cells from Wistar-Kyoto rats,
and nitric oxide levels were reduced when the inhibitor was added to
splenic mononuclear cell cultures from spontaneously hypertensive rats. We
further demonstrated that L-arginine is required for the development of the
depressed mitogen-induced proliferative responses in these cells. Addition
of L-arginine in excess of 10 microM to cultures diminished cell
proliferation and increased nitric oxide. Polyclonal antibodies to murine
interferon gamma reduced nitric oxide accumulation by approximately 50%,
suggesting that interferon gamma is partially responsible for enhancing
nitric oxide production in mitogen-stimulated splenic mononuclear cell
cultures from spontaneously hypertensive rats. Thus, this study provides
evidence that the immune depression observed in the spontaneously
hypertensive rat is nitric oxide dependent.
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Nitric oxide mediates immune dysfunction in the spontaneously hypertensive rat
Department of Oral Biology, Baptist Medical Centers, Birmingham, Ala.
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