Why the study?
Does receptor blockade with bisoprolol or otenzepad prevent myocardial damage in a rabbit model of experimental autoimmune cardiomyopathy?
Does receptor blockade with bisoprolol or otenzepad prevent myocardial damage in a rabbit model of experimental autoimmune cardiomyopathy?
Beta1-adrenoceptor and M2-muscarinic receptor blockade prevents myocardial damage in an experimental rabbit model of autoimmune cardiomyopathy, supporting their pathogenic role and therapeutic potential in dilated cardiomyopathy.
Receptor blockade attenuates damage in rabbit autoimmune cardiomyopathy model; hypothesis-generating for therapeutic role in human dilated cardiomyopathy.
We investigated the effects of beta1-adrenoceptor blockade and M2-muscarinic receptor antagonist in rabbits which have developed dilated cardiomyopathy-like changes after immunization with the peptides from the second extracellular loop of human beta1-adrenoceptor (beta1-peptide) and M2-muscarinic receptor (M2-peptide). Ten rabbits, which were immunized with beta1-peptide once a month for one year, were treated with bisoprolol and 10 rabbits, which were immunized with M2-peptide, were treated with otenzepad. Although both groups treated with receptor blockade or antagonist showed an increased titer of anti-beta1-adrenoceptor or anti-M2-muscarinic receptor antibodies, myocardial damages were markedly less than those in beta1-peptide- or M2-peptide-immunized rabbits. This study indicates that anti-beta1-adrenoceptor and anti-M2-muscarinic receptor antibodies are of pathogenic importance in the development of human dilated cardiomyopathy, and that beta-adrenoceptor blockade, bisoprolol, and M2-muscarinic receptor antagonist, otenzepad, might be clinically useful for treatment of dilated cardiomyopathy.
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Matsui et al. (2001) studied this question.
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