Abstract
Mutations occurring in the CFTR gene, encoding for the cystic fibrosis transmembrane conductance regulator chloride channel, cause cystic fibrosis (CF). Mutations belonging to class II, such as ΔPhe508, give rise to a protein with both a defective maturation and altered channel gating. Mutations belonging to class III, such as G551D and G1349D, cause only a gating defect. We have previously identified antihypertensive 1,4-dihydropyridines (DHPs), a class of drugs that block voltage-dependent Ca2+ channels, as effective potentiators of CFTR gating, able to correct the defective activity of CFTR mutants (Mol Pharmacol68:1736-1746, 2005). However, optimization of potency for CFTR versus Ca2+ channels is required to design selective compounds for CFTR pharmacotherapy. In the present study, we have established DHP structure-activity relationship for both CFTR potentiation and Ca2+ channel inhibition using cell-based assays for both types of channels. A panel of 333 felodipine analogs was studied to understand the effect of various substitutions and modifications in the DHP scaffold. Our results show that alkyl substitutions at the para position of the 4-phenyl ring lead to compounds with very low activity on Ca2+ channels and strong effect as potentiators on the ΔPhe508, G551D, and G1349D CFTR mutants.
Footnotes
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This work was supported by grants from the Cystic Fibrosis Foundation Therapeutics, Telethon-Italy (GGP05103), CIPE-Regione Liguria (Biofarma 2), and Fondazione Italiana per la Ricerca sulla Fibrosi Cistica.
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ABBREVIATIONS: CF, cystic fibrosis; CFTR, cystic fibrosis transmembrane conductance regulator; NBD, nucleotide-binding domain; DHP, 1,4-dihydropyridine; VDCC, voltage-dependent Ca2+ channel; FRT, Fischer rat thyroid; YFP, yellow fluorescent protein; BayK-8644, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-[trifluoromethyl]phenyl)-3-pyridine carboxylic acid methyl ester.
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The online version of this article (available at http://molpharm.aspetjournals.org) contains supplemental material.
- Received February 1, 2007.
- Accepted April 23, 2007.
- The American Society for Pharmacology and Experimental Therapeutics
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