Abstract
Abstract
Experiments were done to test the hypothesis that aggregation of human platelets induced by platelet activating factor (PAF) may be mediated by calmodulin-dependent processes. W-7 [N-(6-aminohexyl)-5-chloro-l-naphthalene sulfonamide], a potent calmodulin antagonist, caused dose-dependent inhibition of PAF induced aggregation of human platelets in vitro. The ED5o for W-7 was 51.5 ± 9.5 μM (mean ± SEM). This concentration is known to be platelet calmodul in-specific. These data are consistent with the hypothesis.
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