Planta Med 1985; 51(1): 16-20
DOI: 10.1055/s-2007-969381
Research Articles

© Georg Thieme Verlag Stuttgart · New York

Inhibition of Mast Cell Histamine Release by Flavonoids and Biflavonoids

M. Amellal1 , C. Bronner1 , F. Briancon2 , M. Haag2 , R. Anton2 , Y. Landry1
  • 1Laboratoire d'Allergopharmacologie, Faculté de Pharmacie, B. P. 10, F-67048 Strasbourg Cedex, France
  • 2Laboratoire de Pharmacognosie, Faculté de Pharmacie, B. P. 10, F-67048 Strasbourg Cedex, France
Further Information

Publication History

1984

1984

Publication Date:
26 February 2007 (online)

Abstract

The effect of 11 flavonoids and 4 biflavonoids on the release of histamine from peritoneal rat mast cells induced by compound 48/80 and calcium ionophore A23187 was studied. Dihydroflavonoids (flavanones) and (+)-catechin did not modify histamine release induced by both secretagogues. Flavone, apigenin and cromoglycate inhibited the secretion elicited by compound 48/80 but did not modify the A23187-induced secretion. The effect of kaempferol on the compound 48/80-induced histamine release was biphasic. Low doses (10-6 to 10-5M) of the compound potentiated secretion whereas higher doses inhibited histamine secretion. Some of the drugs tested revealed a higher potency as referred to quercetin. Luteolin, a tetrahydroxyflavone and amentoflavone, a biapigenin, exhibited the highest inhibitory effects of mast cell histamine secretion.

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