Increased beta2-adrenoceptors in doxorubicin-induced cardiomyopathy in rat

PLoS One. 2013 May 31;8(5):e64711. doi: 10.1371/journal.pone.0064711. Print 2013.

Abstract

Background: The toxicity of doxorubicin, leading to an irreversible heart failure, limits its use as chemotherapeutic agent. The beneficial effects of early administration of β-blocker were reported in patients with heart failure due to doxorubicin, suggesting an important role of β-adrenoceptors (β-ARs). This study aimed to identify a putative target (β-AR and/or its effectors) at the early phase of a chronic doxorubicin-induced cardiomyopathy (Dox-CM) in a rat model.

Methodology: Dox-CM was induced by six doxorubicin injections (cumulative dose: 15 mg x kg(-1)) and validated by echocardiography and left ventricle (LV) catheterization. The β-AR protein expressions in LV were evaluated by western-blot at days 35 (d35) and 70 (d70) after the first doxorubicin injection. Ex vivo cardiac contractility (dP/dtmax, dP/dtmin) was evaluated on isolated heart in response to specific β-AR stimulations at d35.

Results: At d35, Dox-CM hearts were characterized by mild LV systolic and diastolic dysfunctions, which were exacerbated at d70. In Dox-CM hearts, β3-AR expression was only decreased at d70 (-37±8%). At d35, β1-AR expression was decreased by 68±6%, but ex vivo β1-AR function was preserved due to, at least in part, an increased adenylyl cyclase response assessed by forskolin. β2-AR expression was increased both at d35 (+58±22%) and d70 (+174±35%), with an increase of ex vivo β2-AR response at d35. Inhibition of Gi protein with pertussis toxin did not affect β2-AR response in Dox-CM hearts, suggesting a decoupling of β2-AR to Gi protein.

Conclusion: This study highlights the β1/β2-AR imbalance in early Dox-CM and reveals the important role that β2-AR/Gi coupling could play in this pathology. Our results suggest that β2-AR could be an interesting target at early stage of Dox-CM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic beta-Antagonists / pharmacology
  • Animals
  • Cardiomyopathies / chemically induced
  • Cardiomyopathies / metabolism*
  • Cardiomyopathies / mortality
  • Cardiomyopathies / physiopathology
  • Cardiotonic Agents / pharmacology
  • Colforsin / pharmacology
  • Doxorubicin
  • GTP-Binding Protein alpha Subunits, Gi-Go / antagonists & inhibitors
  • GTP-Binding Protein alpha Subunits, Gi-Go / genetics*
  • GTP-Binding Protein alpha Subunits, Gi-Go / metabolism
  • Gene Expression Regulation
  • Heart / drug effects
  • Heart / physiopathology*
  • Isoproterenol / pharmacology
  • Male
  • Myocardial Contraction / drug effects
  • Pertussis Toxin / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Adrenergic, beta-1 / genetics*
  • Receptors, Adrenergic, beta-1 / metabolism
  • Receptors, Adrenergic, beta-2 / genetics*
  • Receptors, Adrenergic, beta-2 / metabolism
  • Receptors, Adrenergic, beta-3 / genetics
  • Receptors, Adrenergic, beta-3 / metabolism
  • Survival Analysis

Substances

  • Adrenergic beta-Antagonists
  • Cardiotonic Agents
  • Receptors, Adrenergic, beta-1
  • Receptors, Adrenergic, beta-2
  • Receptors, Adrenergic, beta-3
  • Colforsin
  • Doxorubicin
  • Pertussis Toxin
  • GTP-Binding Protein alpha Subunits, Gi-Go
  • Isoproterenol

Grants and funding

This work was supported by the “Association Française contre les Myopathies”, the “Fédération Française de Cardiologie”, the “Fondation de France” and the “Fondation Genavie”. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.