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pubmed-article:2443458pubmed:abstractTextIn this study we investigated the modulation of natural killer (NK) cell activity by various histamine receptor antagonists in vitro. The histamine H2-receptor antagonists cimetidine, ranitidine and tiotidine suppressed NK cell cytotoxicity (NKCC) at a high concentration (10(-3) M). Cimetidine enhanced NKCC of Ficoll-Hypaque-separated lymphocytes and of lymphocytes enriched for NKCC by Percoll density gradient centrifugation. The enhancing effect of cimetidine was dose-dependent at final concentrations of 10(-4)-10(-7) M and did not require the presence of adherent cells/monocytes. Ranitidine did not affect NKCC over a wide range of concentrations. Tiotidine strongly enhanced NKCC of low-density, large granular lymphocyte-enriched mononuclear cells (MNC) in the presence of adherent cells/monocytes, but was ineffective in nonadherent effector cells. All H2-receptor antagonists clearly antagonized histamine-induced NKCC enhancement in monocyte-containing effector cells. Clemastin, a specific H1-receptor antagonist, effectively suppressed NKCC. This effect was mimicked by a clemastin isomer with very low affinity for H1-receptors. We conclude that (1) cimetidine enhances NKCC in vitro by a mechanism of action that is not specifically related to antagonism of H2-receptors, (2) tiotidine displays mixed agonist/antagonist properties for MNC H2-receptors and (3) NK-suppressive properties of clemastin are unrelated to H1-receptor antagonism.lld:pubmed
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pubmed-article:2443458pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:2443458pubmed:articleTitleDifferential effects of histamine receptor antagonists on human natural killer cell activity.lld:pubmed
pubmed-article:2443458pubmed:affiliationDepartment of Virology, University of Göteborg, Sweden.lld:pubmed
pubmed-article:2443458pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:2443458pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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