Vol 71, No 7 (2013)
Original articles
Published online: 2013-07-17
The effect of the renin–angiotensin–aldosterone system inhibition on myocardial function in early and late phases of dilated cardiomyopathy in Tgaq*44 mice
DOI: 10.5603/KP.2013.0161
Kardiol Pol 2013;71(7):730-737.
Abstract
Background: The renin–angiotensin–aldosterone system (RAAS) determines progression of heart failure (HF) in humans, and
RAAS inhibition is a major therapeutic strategy in HF.
Aim: To assess the effect of angiotensin-converting enzyme inhibitor (ACE-I) and aldosterone receptor antagonist (ARA) therapy
on the development of HF at its early and late stage in a murine model of dilated cardiomyopathy (Tgaq*44 mice).
Methods: Tgaq*44 mice at the early or advanced stage of HF received combined therapy including ACE-I (perindopril
2 mg/kg) and ARA (canrenone 20 mg/kg). Cardiac function was assessed by magnetic resonance imaging before and after
2 months of treatment.
Results: Combined therapy with perindopril and canrenone resulted in preserved systolic function at the early stage and
reduced chamber dilatation at the advanced stage of HF in Tgaq*44 mice.
Conclusions: Activation of the RAAS is involved in progression of HF in Tgaq*44 mice with dilated cardiomyopathy. Therapeutic
efficacy of ACE-I and ARA to inhibit systolic dysfunction and cardiac chamber dilation depends on the stage of HF development.
RAAS inhibition is a major therapeutic strategy in HF.
Aim: To assess the effect of angiotensin-converting enzyme inhibitor (ACE-I) and aldosterone receptor antagonist (ARA) therapy
on the development of HF at its early and late stage in a murine model of dilated cardiomyopathy (Tgaq*44 mice).
Methods: Tgaq*44 mice at the early or advanced stage of HF received combined therapy including ACE-I (perindopril
2 mg/kg) and ARA (canrenone 20 mg/kg). Cardiac function was assessed by magnetic resonance imaging before and after
2 months of treatment.
Results: Combined therapy with perindopril and canrenone resulted in preserved systolic function at the early stage and
reduced chamber dilatation at the advanced stage of HF in Tgaq*44 mice.
Conclusions: Activation of the RAAS is involved in progression of HF in Tgaq*44 mice with dilated cardiomyopathy. Therapeutic
efficacy of ACE-I and ARA to inhibit systolic dysfunction and cardiac chamber dilation depends on the stage of HF development.
Keywords: Tgaq*44 miceheart failuremagnetic resonance imagingdobutaminerenin–angiotensin–aldosterone systemperindoprilcanrenone