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Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes
Author(s) -
Mall Marcus,
Wissner Andreas,
Seydewitz Hans H,
Hübner Martin,
Kuehr Joachim,
Brandis Matthias,
Greger Rainer,
Kunzelmann Karl
Publication year - 2000
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1038/sj.bjp.0703520
Subject(s) - genistein , ibmx , forskolin , cystic fibrosis transmembrane conductance regulator , ussing chamber , amiloride , endocrinology , dids , medicine , apical membrane , xenopus , chemistry , epithelium , stimulation , biology , microbiology and biotechnology , secretion , biochemistry , cystic fibrosis , genetics , organic chemistry , membrane , gene , sodium
The flavonoid genistein has been shown to activate a Cl − conductance in various cell types expressing CFTR. We examined if similar effects can be observed when genistein is applied to native ex vivo tissues from human respiratory tract and rectum. We further compared the effects when genistein was applied to oocytes of Xenopus laevis expressing CFTR. In oocytes, both wtCFTR and ΔF508‐CFTR were activated by genistein while both cyclic AMP (K v LQT1) and Ca 2+ (SK4) activated K + channels were inhibited at high concentrations of genistein. Biopsies from nasal polyps and rectal mucosa were obtained from normal individuals (non‐CF) and CF patients and in the presence of amiloride (10 μmol l −1 ; mucosal side) the effects of genistein were assessed using a perfused Ussing chamber. In non‐CF airway epithelia, genistein (50 μmol l −1 ; mucosal side) increased lumen negative I sc but had no additional effects on tissues pre‐stimulated with IBMX and forskolin (100 μmol l −1 and 1 μmol l −1 ; both sides). In non‐CF rectal biopsies, in the presence of amiloride (10 μmol l −1 ; mucosal side) and indomethacin (10 μmol l −1 ; basolateral side), genistein increased lumen negative I sc and enabled cholinergic (carbachol; CCH, 100 μmol l −1 ; basolateral side) stimulation of Cl − secretion indicating activation of luminal CFTR Cl − channels. However, after stimulation with IBMX/forskolin, genistein induced opposite effects and significantly inhibited CCH activated I sc . In CF airway and intestinal tissues genistein failed to induce Cl − secretion. Thus, genistein is able to activate luminal CFTR Cl − conductance in non‐CF tissues and mutant CFTR in oocytes. However, additional inhibitory effects on basolateral K + conductance and missing effects in native CF tissues do not support the use for pharmacological intervention in CF.British Journal of Pharmacology (2000) 130 , 1884–1892; doi: 10.1038/sj.bjp.0703520