@article {Singh195, author = {Ashvani K. Singh and Bruce D. Schultz and John A. Katzenellenbogen and Elmer M. Price and Robert J. Bridges and Neil A. Bradbury}, title = {Estrogen Inhibition of Cystic Fibrosis Transmembrane Conductance Regulator-Mediated Chloride Secretion}, volume = {295}, number = {1}, pages = {195--204}, year = {2000}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {Cystic fibrosis (CF) is an autosomal genetic disease associated with impaired epithelial ion transport. Mutations in the CF gene alter the primary sequence of the CF transmembrane conductance regulator (CFTR). Several therapeutic modalities have been proposed for CF patients, including the phytoestrogen genistein. Experiments were completed in cellular and subcellular systems to evaluate the impact of naturally occurring and synthetic estrogens on epithelial ion transport, and specifically on the CF protein CFTR. 17β-Estradiol, a naturally occurring estrogen, caused a rapid and reversible inhibition of forskolin-stimulated chloride secretion across T84 epithelial cell monolayers with a Ki of 8 μM. In addition, 17α-estradiol, a stereoisomer that fails to bind and activate nuclear estrogen receptors was equipotent with 17β-estradiol, arguing against a genomic-mediated mechanism of action. Synthetic estrogens, including diethylstilbesterol and the antiestrogen tamoxifen likewise inhibited forskolin-stimulated ion transport. Aldosterone, dexamethasone, and cholesterol were without effect at the highest concentrations tested (>=1 mM). Studies indicated that diethylstilbesterol and other synthetic estrogens that inhibited anion secretion in intact monolayers likewise inhibited CFTR chloride channel activity with similar concentration dependencies in excised membrane patches. Experiments with radioactive photoactivatable estrogen derivatives demonstrated that these compounds bind directly to CFTR expressed in insect cells. Taken together, the data suggest that estrogens can interact directly with CFTR to alter anion transport. The American Society for Pharmacology and Experimental Therapeutics}, issn = {0022-3565}, URL = {https://jpet.aspetjournals.org/content/295/1/195}, eprint = {https://jpet.aspetjournals.org/content/295/1/195.full.pdf}, journal = {Journal of Pharmacology and Experimental Therapeutics} }