βadrenergic cardiac antibody in autoimmune myocarditis
Balb/c mice were immunized with homologous heart in complete Freund's adjuvant to induce autoimmune myocarditis. The myocarditis was characterized by lymphomononuclear infiltration, electrocardiographic abnormalities and antimuscle antibodies by indirect immunofluorescence. In this paper, we de...
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1989
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08916934_v2_n3_p223_Leiros http://hdl.handle.net/20.500.12110/paper_08916934_v2_n3_p223_Leiros |
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paper:paper_08916934_v2_n3_p223_Leiros2023-06-08T15:47:14Z βadrenergic cardiac antibody in autoimmune myocarditis Anti βadrenergic Antibodies Autoimmunity Cardiac contractility Myocarditis Receptor antibody βadrenergic receptors autoantibody beta adrenergic receptor dihydroalprenolol propranolol receptor antibody animal cell animal experiment autoimmunity heart muscle contractility mouse myocarditis nonhuman Animal Autoantibodies Autoimmune Diseases Binding, Competitive Cyclic AMP Dihydroalprenolol Immunoglobulin G In Vitro Male Mice Mice, Inbred BALB C Myocardial Contraction Myocarditis Myocardium Organ Specificity Receptors, Adrenergic, beta Support, Non-U.S. Gov't Balb/c mice were immunized with homologous heart in complete Freund's adjuvant to induce autoimmune myocarditis. The myocarditis was characterized by lymphomononuclear infiltration, electrocardiographic abnormalities and antimuscle antibodies by indirect immunofluorescence. In this paper, we demonstrate that the IgG present in autoimmune myocarditis mice is able to bind to βadrenoreceptors of the heart and also induce a biological effect inhibiting the contractile action of exogenous norepinephrine. Auto-immune IgG inhibited the binding of (3H)-dyhidroalprenolol to a βadrenergic receptor of purified myocardial membranes behaving as non-competitive inhibitor. This IgG also exerted a non-competitive inhibition upon the mechanical effect of exogenous norepinephrine. The recognition appears to be organ specific, because the autoimmune myocarditis IgG did not bind to βlymphocyte, lung and fat adrenoreceptors. The autoimmune IgG inhibited the stimulatory action of isoproterenol on cAMP levels, behaving as a βadrenergic antagonist. © 1989 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted. 1989 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08916934_v2_n3_p223_Leiros http://hdl.handle.net/20.500.12110/paper_08916934_v2_n3_p223_Leiros |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Anti βadrenergic Antibodies Autoimmunity Cardiac contractility Myocarditis Receptor antibody βadrenergic receptors autoantibody beta adrenergic receptor dihydroalprenolol propranolol receptor antibody animal cell animal experiment autoimmunity heart muscle contractility mouse myocarditis nonhuman Animal Autoantibodies Autoimmune Diseases Binding, Competitive Cyclic AMP Dihydroalprenolol Immunoglobulin G In Vitro Male Mice Mice, Inbred BALB C Myocardial Contraction Myocarditis Myocardium Organ Specificity Receptors, Adrenergic, beta Support, Non-U.S. Gov't |
spellingShingle |
Anti βadrenergic Antibodies Autoimmunity Cardiac contractility Myocarditis Receptor antibody βadrenergic receptors autoantibody beta adrenergic receptor dihydroalprenolol propranolol receptor antibody animal cell animal experiment autoimmunity heart muscle contractility mouse myocarditis nonhuman Animal Autoantibodies Autoimmune Diseases Binding, Competitive Cyclic AMP Dihydroalprenolol Immunoglobulin G In Vitro Male Mice Mice, Inbred BALB C Myocardial Contraction Myocarditis Myocardium Organ Specificity Receptors, Adrenergic, beta Support, Non-U.S. Gov't βadrenergic cardiac antibody in autoimmune myocarditis |
topic_facet |
Anti βadrenergic Antibodies Autoimmunity Cardiac contractility Myocarditis Receptor antibody βadrenergic receptors autoantibody beta adrenergic receptor dihydroalprenolol propranolol receptor antibody animal cell animal experiment autoimmunity heart muscle contractility mouse myocarditis nonhuman Animal Autoantibodies Autoimmune Diseases Binding, Competitive Cyclic AMP Dihydroalprenolol Immunoglobulin G In Vitro Male Mice Mice, Inbred BALB C Myocardial Contraction Myocarditis Myocardium Organ Specificity Receptors, Adrenergic, beta Support, Non-U.S. Gov't |
description |
Balb/c mice were immunized with homologous heart in complete Freund's adjuvant to induce autoimmune myocarditis. The myocarditis was characterized by lymphomononuclear infiltration, electrocardiographic abnormalities and antimuscle antibodies by indirect immunofluorescence. In this paper, we demonstrate that the IgG present in autoimmune myocarditis mice is able to bind to βadrenoreceptors of the heart and also induce a biological effect inhibiting the contractile action of exogenous norepinephrine. Auto-immune IgG inhibited the binding of (3H)-dyhidroalprenolol to a βadrenergic receptor of purified myocardial membranes behaving as non-competitive inhibitor. This IgG also exerted a non-competitive inhibition upon the mechanical effect of exogenous norepinephrine. The recognition appears to be organ specific, because the autoimmune myocarditis IgG did not bind to βlymphocyte, lung and fat adrenoreceptors. The autoimmune IgG inhibited the stimulatory action of isoproterenol on cAMP levels, behaving as a βadrenergic antagonist. © 1989 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted. |
title |
βadrenergic cardiac antibody in autoimmune myocarditis |
title_short |
βadrenergic cardiac antibody in autoimmune myocarditis |
title_full |
βadrenergic cardiac antibody in autoimmune myocarditis |
title_fullStr |
βadrenergic cardiac antibody in autoimmune myocarditis |
title_full_unstemmed |
βadrenergic cardiac antibody in autoimmune myocarditis |
title_sort |
βadrenergic cardiac antibody in autoimmune myocarditis |
publishDate |
1989 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_08916934_v2_n3_p223_Leiros http://hdl.handle.net/20.500.12110/paper_08916934_v2_n3_p223_Leiros |
_version_ |
1768542463331401728 |