Chagasic sera alter the effects of ouabain on isolated rat atria. Participation of adrenergic mechanisms

The effects of chagasic sera, containing an antibody (EVI antibody) which reacts with the plasma membrane of working myocardial cells, on 'toxic' and 'non-toxic' actions of ouabain upon isolated self beating or paced rat atria suspended in different media, were explored. Although...

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Autores principales: Sterin-Borda, L., Canga, L., Borda, E., Cossio, P., Diez, C., Arana, R., Gimeno, A.L.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00142999_v69_n1_p1_SterinBorda
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spelling todo:paper_00142999_v69_n1_p1_SterinBorda2023-10-03T14:12:10Z Chagasic sera alter the effects of ouabain on isolated rat atria. Participation of adrenergic mechanisms Sterin-Borda, L. Canga, L. Borda, E. Cossio, P. Diez, C. Arana, R. Gimeno, A.L. Adrenergic mechanisms Atria Chagasic sera Ouabain endothelium antibody noradrenalin ouabain propranolol unclassified drug animal experiment article Chagas disease drug response drug toxicity heart heart atrium heart muscle contractility intoxication rat serum Animals Antibodies Chagas Cardiomyopathy Heart Heart Rate Male Myocardial Contraction Norepinephrine Ouabain Propranolol Rats Sympathetic Nervous System The effects of chagasic sera, containing an antibody (EVI antibody) which reacts with the plasma membrane of working myocardial cells, on 'toxic' and 'non-toxic' actions of ouabain upon isolated self beating or paced rat atria suspended in different media, were explored. Although ouabain produced a dose-dependent positive inotropic influence on atria suspended in Krebs-Ringer-bicarbonate (KRB) and in KRB plus normal human serum (KRB + NHS) it did not elicit any significant positive inotropic effect on atria beating in KRB plus EVI positive human chagasic serum (EVI(+)S). Additionally, in EVI(+)S dose-response curves of classical signs of digitalis cardiac toxicity shifted to the left. The threshold concentration of ouabain required to elicit the onset of 'toxic' effects was higher in control preparations (kept in KRB or KRB + NHS) than in EVI(+)S exposed preparations. (-)-Propranolol attenuated the overall toxic action of ouabain in EVI(+)S and facilitated its positive inotropic influence. In control media, the β-adrenoceptor blocker failed to modify either the 'non-toxic' or the 'toxic' effect of ouabain. On the other hand, with control atria, subthreshold exogenous norepinephrine inhibited the positive inotropism of ouabain. The data suggest that an adrenergic mechanism is involved in the action of ouabain on cardiac tissue immersed in an EVI(+)S-containing solution. The foregoing results may explain the severe 'toxic' effects observed with cardioactive glycosides when they are used in patients with Chagas' heart disease, even at low doses. © 1981. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00142999_v69_n1_p1_SterinBorda
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Adrenergic mechanisms
Atria
Chagasic sera
Ouabain
endothelium antibody
noradrenalin
ouabain
propranolol
unclassified drug
animal experiment
article
Chagas disease
drug response
drug toxicity
heart
heart atrium
heart muscle contractility
intoxication
rat
serum
Animals
Antibodies
Chagas Cardiomyopathy
Heart
Heart Rate
Male
Myocardial Contraction
Norepinephrine
Ouabain
Propranolol
Rats
Sympathetic Nervous System
spellingShingle Adrenergic mechanisms
Atria
Chagasic sera
Ouabain
endothelium antibody
noradrenalin
ouabain
propranolol
unclassified drug
animal experiment
article
Chagas disease
drug response
drug toxicity
heart
heart atrium
heart muscle contractility
intoxication
rat
serum
Animals
Antibodies
Chagas Cardiomyopathy
Heart
Heart Rate
Male
Myocardial Contraction
Norepinephrine
Ouabain
Propranolol
Rats
Sympathetic Nervous System
Sterin-Borda, L.
Canga, L.
Borda, E.
Cossio, P.
Diez, C.
Arana, R.
Gimeno, A.L.
Chagasic sera alter the effects of ouabain on isolated rat atria. Participation of adrenergic mechanisms
topic_facet Adrenergic mechanisms
Atria
Chagasic sera
Ouabain
endothelium antibody
noradrenalin
ouabain
propranolol
unclassified drug
animal experiment
article
Chagas disease
drug response
drug toxicity
heart
heart atrium
heart muscle contractility
intoxication
rat
serum
Animals
Antibodies
Chagas Cardiomyopathy
Heart
Heart Rate
Male
Myocardial Contraction
Norepinephrine
Ouabain
Propranolol
Rats
Sympathetic Nervous System
description The effects of chagasic sera, containing an antibody (EVI antibody) which reacts with the plasma membrane of working myocardial cells, on 'toxic' and 'non-toxic' actions of ouabain upon isolated self beating or paced rat atria suspended in different media, were explored. Although ouabain produced a dose-dependent positive inotropic influence on atria suspended in Krebs-Ringer-bicarbonate (KRB) and in KRB plus normal human serum (KRB + NHS) it did not elicit any significant positive inotropic effect on atria beating in KRB plus EVI positive human chagasic serum (EVI(+)S). Additionally, in EVI(+)S dose-response curves of classical signs of digitalis cardiac toxicity shifted to the left. The threshold concentration of ouabain required to elicit the onset of 'toxic' effects was higher in control preparations (kept in KRB or KRB + NHS) than in EVI(+)S exposed preparations. (-)-Propranolol attenuated the overall toxic action of ouabain in EVI(+)S and facilitated its positive inotropic influence. In control media, the β-adrenoceptor blocker failed to modify either the 'non-toxic' or the 'toxic' effect of ouabain. On the other hand, with control atria, subthreshold exogenous norepinephrine inhibited the positive inotropism of ouabain. The data suggest that an adrenergic mechanism is involved in the action of ouabain on cardiac tissue immersed in an EVI(+)S-containing solution. The foregoing results may explain the severe 'toxic' effects observed with cardioactive glycosides when they are used in patients with Chagas' heart disease, even at low doses. © 1981.
format JOUR
author Sterin-Borda, L.
Canga, L.
Borda, E.
Cossio, P.
Diez, C.
Arana, R.
Gimeno, A.L.
author_facet Sterin-Borda, L.
Canga, L.
Borda, E.
Cossio, P.
Diez, C.
Arana, R.
Gimeno, A.L.
author_sort Sterin-Borda, L.
title Chagasic sera alter the effects of ouabain on isolated rat atria. Participation of adrenergic mechanisms
title_short Chagasic sera alter the effects of ouabain on isolated rat atria. Participation of adrenergic mechanisms
title_full Chagasic sera alter the effects of ouabain on isolated rat atria. Participation of adrenergic mechanisms
title_fullStr Chagasic sera alter the effects of ouabain on isolated rat atria. Participation of adrenergic mechanisms
title_full_unstemmed Chagasic sera alter the effects of ouabain on isolated rat atria. Participation of adrenergic mechanisms
title_sort chagasic sera alter the effects of ouabain on isolated rat atria. participation of adrenergic mechanisms
url http://hdl.handle.net/20.500.12110/paper_00142999_v69_n1_p1_SterinBorda
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