Itraconazole-mediated inhibition of calcium entry into platelet-activating factor-stimulated human neutrophils is due to interference with production of leukotriene B4
Authors: Steel, H. C.; Tintinger, G. R.1; Theron, A. J.; Anderson, R.
Source: Clinical & Experimental Immunology, Volume 150, Number 1, October 2007 , pp. 144-150(7)
Publisher: Blackwell Publishing
Abstract:
Summary The primary objective of this study was to probe the involvement of leukotriene B4 (LTB4) in itraconazole (0·1-5 µM)-mediated inhibition of Ca2+ uptake by chemoattractant-activated human neutrophils. Following exposure of the cells to platelet-activating factor (PAF, 200 nM), LTB4 was measured by immunoassay, while neutrophil cytosolic Ca2+ concentrations were determined by a fura-2/AM-based spectrofluorimetric procedure. Activation of neutrophils was accompanied by an abrupt and sustained (for about 1 min) elevation in cytosolic Ca2+ which was associated with increased generation of LTB4, both of which were attenuated significantly by itraconazole at 0·5 µM and higher. The inhibitory effect of the anti-mycotic on Ca2+ uptake by PAF-activated cells was mimicked by an LTB4 antibody, as well as by LY255283 (1 µM) and MK886 (0·5 µM), an antagonist of LTB4 receptors and an inhibitor of 5′-lipoxygenase-activating protein, respectively, while addition of itraconazole to purified 5′-lipoxygenase resulted in inhibition of enzyme activity. A mechanistic relationship between itraconazole-mediated inhibition of LTB4 production and Ca2+ influx was also supported by the observation that pulsed addition of purified LTB4 to PAF-activated neutrophils caused substantial restoration of Ca2+ uptake by cells treated with the anti-mycotic. Taken together, these observations suggest that the potentially beneficial anti-inflammatory interactions of itraconazole with activated neutrophils result from interference with production of LTB4, with consequent attenuation of a secondary LTB4-mediated wave of Ca2+ uptake by the cells.Keywords: 5′-lipoxygenase; calcium; itraconazole; leukotriene B4; neutrophils; platelet-activating factor
Document Type: Research article
DOI: 10.1111/j.1365-2249.2007.03470.x
Affiliations: 1: MRC Unit for Inflammation and Immunity, Department of Immunology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa, and

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