PHARMACOLOGICAL CHARACTERIZATION OF POSITIVE INOTROPIC DERIVATIVES OF4-AMINO-7-METHYL-1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID

Citation
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
Citations number
26
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
Journal title
ISSN journal
00044172
Volume
44-2
Issue
8
Year of publication
1994
Pages
937 - 942
Database
ISI
SICI code
0004-4172(1994)44-2:8<937:PCOPID>2.0.ZU;2-#
Abstract
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.