Relaxant effect of 7-ethoxy-4-methyl-2H-chromen-2-one by calcium channel blockade: computational and ex vivo studies.
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Date
2014-01
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Abstract
Current work was conducted in order to determine the underlying mode of relaxant action of 7-ethoxy-4-methyl-
2H-chromen-2-one (1), a coumarin obtained by semisynthesis from umbelliferone (2), with significant relaxant
effect in a concentration-dependent manner on tracheal rat rings pre-contracted with carbachol (1 μM). In a
previous study it was demonstrated that compound 1 and 2 showed significant relaxant effect, being 1 the most
active compound (Emax= 100% and EC50= 83 μM) even more active than theophylline an unspecific
phosphodiesterases (PDE’s) inhibitor used as positive control. Moreover, pretreatment with 1 significantly
shifted to the right the carbachol-induced contraction. On the other hand, compound 1 (83 μM) produces
significant (100%) relaxant effect on the contraction induced by KCl (80 mM) and the CaCl2-induced contraction
was significantly reduced by the coumarin 1 as nifedipine does (a L-type calcium channel blocker), used as
positive control. Indomethacin (10 μM, unspecific COX inhibitor) significantly reduced 1-relaxation. Meanwhile,
in the presence of isoproterenol (a -adrenergic agonist), and K+ channel blockers glibenclamide (10 μM) and 2-
AP (100 μM) the relaxant curve was not modified. Compound 1 was docked on an outer cavity located on the
extracellular side of the human L-type calcium channel model (affinity energy -6.8 kcal/mol). However,
compound 1 was also found on the same location as nifedipine with the same affinity energy (-6.3 kcal/mol) as
previously described. Both conformations were stabilized by aliphatic interactions on both binding sites,
primordially by a π-π interaction between FIVS6.7 and aromatic rings from compound 1. In conclusion, 7-ethoxy-4-
methyl-2H-chromen-2-one (1) induces a significant relaxant action on rat trachea rings, through L-type calcium
channel blockade and, as a second mechanism of action, by a possible intracellular cyclic AMP increasing.
Description
Keywords
Coumarin, docking, 7-ethoxy-4-methyl-2Hchromen-2-one, umbelliferone, calcium channel, trachea
Citation
Sánchez-Recillas Amanda, Navarrete-Vázquez Gabriel, Millán-Pacheco César, Aguilar-Guadarrama Berenice, Ortiz-Andrade Rolffy, Estrada-Soto Samuel. Relaxant effect of 7-ethoxy-4-methyl-2H-chromen-2-one by calcium channel blockade: computational and ex vivo studies. Journal of Applied Pharmaceutical Science. 2014 Jan; 4(1): 46-51.