Abstract
The effects of three K+-channel blockers, quinine, quinidine and sparteine on K+-evoked histamine (HA) release have been investigated. KCl (150 mM) initiated 40–55% release of HA from rat peritoneal mast cells in the absence of extracellular Ca++, and this could be suppressed by pretreating the cells with K+-channel blockers. In the concentration range of 0.05–2 mM, reductions were dose-dependent and the IC50-s (in mM) obtained were 0.15 and 0.25 for quinine and quinidine and 0.20 for sparteine. The light microscopic studies showed close parallelism between the KCl-evoked HA-release and mast cell degranulation in the absence and also in the presence of K+-channel blockers. Present results strenghthened the involvement of K+-channels in the KCl-evoked HA release and showed that these channels are sensitive to quinine/quinidine and also to sparteine. These data appeared, however, insufficient to clarify fully the mechanism of K+-induced HA secretion or to classify the K+-channels involved in this mechanism.
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Németh, A., Huszti, Z. Characterization of potassium channels in mast cell plasma membranes: Their possible existence and involvement in potassium-evoked histamine release. Agents and Actions 36 (Suppl 2), C308–C310 (1992). https://doi.org/10.1007/BF01997359
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DOI: https://doi.org/10.1007/BF01997359