Author:
Bartošová L.,Frydrych M.,Vaculová G.,Beránková K.,Bébarová M.,Opatřilová R.,Strnadová V.,Mokrý P.,Brunclík V.,Kolevská J.,Krčmář J.,Bartošíková L.,Florian T.,Nečas J.
Abstract
Changes in the heart rate induced by four different doses of two newly synthesized potential ultrashort-action antagonists of beta adrenergic receptors were tested in 90 male laboratory Wistar rats. The isoprenaline-induced tachycardia model was used. Their effects were compared with those of esmolol. In the second part of the study, approximate electro-physiological measurements were made in vitro to assess the influence of the compounds tested on ion membrane currents in isolated ventricular cardiomyocytes. Both compounds demonstrated significant bradycardic effects in all concentrations tested compared with the control group, but they differed in the time of the onset of their action. Both newly synthesized compounds induced blockade of the fast sodium current (INa) and potassium currents (Ito, IK1, IK,end).
Publisher
University of Veterinary and Pharmaceutical Sciences
Cited by
3 articles.
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