S. Herzig et al., PHARMACOLOGICAL CHARACTERIZATION OF POSITIVE INOTROPIC DERIVATIVES OF4-AMINO-7-METHYL-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID, Arzneimittel-Forschung, 44-2(8), 1994, pp. 937-942
The positive inotropic effect of a series of 4-amino-7- methyl-1,8-nap
hthyridine-3-carboxylic acid derivatives was compared with the effects
of known inotropic agents (ouabain, dihydroouabain, isoproterenol, ad
renaline, histamine and isobutylmethylxanthine) in guinea-pig atrial a
nd ventricular myocardial preparations. With respect to their function
al effects the 1,8-naphthyridine compounds are clearly different from
drugs acting on the cAMP system, whereas several similarities with car
diac glycoside effects were found. Their ability to inhibit [H-3]ouaba
in binding in guinea-pig cardiac membranes correlates well with their
effects on myocardial contractile force. However the latter effect was
exerted by ten-fold lower concentrations. The dissimilarities found b
etween the 1,8-naphthyridines and digitalis may be due to a different
type of interaction with the binding site on the (Na++K+)-ATPase.