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Antibodies against the β1-adrenergic receptor induce progressive development of cardiomyopathy
被引:25
作者:
Buvall, Lisa
Tang, Margareta Scharin
Isic, Azra
Andersson, Bert
Fu, Michael
机构:
[1] Gothenburg Univ, Sahlgrenska Acad, Inst Med, Dept Mol & Clin Med Cardiol, S-41124 Gothenburg, Sweden
[2] Sahlgrens Univ Hosp, Dept Med, S-41345 Gothenburg, Sweden
关键词:
beta(1)-adrenergic receptor;
antibody;
dilated cardiomyopathy;
immunization;
cardiac function;
D O I:
10.1016/j.yjmcc.2007.02.007
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Different immune disturbances have been found among patients with dilated cardiomyopathy (DCM), including antibodies directed against different cardiac antigens, such as the second extracellular loop of the beta(1)-adrenergic receptor. The aim of our study was to investigate antibodies directed against the second extracellular loop of the beta(1)-adrenergic receptor effect on cardiac functions at an early and late stage during DCM development. This was made in a mouse model, in which DCM was induced by immunization with the second extracellular loop of the beta(1)-adrenergic receptor. Mice were immunized for 14 or 25 weeks respectively with the second extracellular loop of the I-adrenergic receptor. At 14 weeks, there was no decreased heart function reviled by echocardiography at rest, but when dobutamine stress echocardiography was used, a lower cardiac reserve was shown in the mice with antibodies against the second extracellular loop of the beta(1)-adrenergic receptor. By 25 weeks, decreased heart function, dilatation of the left ventricle and thinner left ventricular posterior wall were observed. Further biochemical analyses at 25 weeks showed increased mRNA expressions for beta(1)-adrenergic receptor kinase, monocyte chemoattractant protein-1 and the brain natriuretic peptide as well as increased concentrations of complement factor 3 in sera in the immunized animals. Our data suggest a cardiotoxic effect of antibodies directed against the second extracellular loop of the beta(1)-adrenergic receptor and a capacity to induce DCM with progressive remodeling, decreased cardiac function, altered beta(1)AR signaling and upregulation of proinflammatory components. (C) 2007 Elsevier Inc. All rights reserved.
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页码:1001 / 1007
页数:7
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