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Histamine release from mast cells and monocytes: the effects of azelastine, reproterol and vitamin A-analogues
In addition to basophils, monocytes and lymphocytes are important sources of histamine in blood which may be released on stimulation with either A 23187, C5a or substance P. This release may be inhibited significantly by high concentrations of disodium cromoglycate (DSCG) but not by ketotifen. Free...
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Published in: | Inflammation research 1996-03, Vol.45 Suppl 1 (S1), p.S5-S6 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In addition to basophils, monocytes and lymphocytes are important sources of histamine in blood which may be released on stimulation with either A 23187, C5a or substance P. This release may be inhibited significantly by high concentrations of disodium cromoglycate (DSCG) but not by ketotifen. Free radicals have been shown to originate from monocytes and to activate mast cells. This might be an important process in inflammatory reactions. Therefore we tested the effects of some radical scavengers, e.g. superoxide dismutase (SOD), two dihydrochinolines (MG and MDS), beta -carotene and two vitamin A-analogues (isotretinoin and etretinate) on the histamine release induced by Con A from human adenoidal mast cells. beta -Carotene was also tested in C5a-stimulated human peripheral blood monocytes. The H sub(1)-blocker azelastine and the beta sub(2)-agonist reproterol were included in the study for comparison. |
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ISSN: | 1023-3830 1420-908X |
DOI: | 10.1007/BF03354062 |