Key result
Pranidipine ameliorated the progression of left ventricular dysfunction and cardiac remodeling in rats with heart failure at a lower dose compared to amlodipine.
Why the study?
Does pranidipine improve left ventricular dysfunction and cardiac remodeling compared to amlodipine in a rat model of heart failure?
RCT
randomized
Does pranidipine improve left ventricular dysfunction and cardiac remodeling compared to amlodipine in a rat model of heart failure?
Pranidipine ameliorates the progression of left ventricular dysfunction and cardiac remodeling in rats with heart failure at a lower dose compared to amlodipine.
Hypothesis-generating in rat heart failure; leaves open translation to human LV dysfunction versus amlodipine.
The aim of the present study was to compare the cardioprotective properties of long-acting calcium channel antagonist pranidipine with amlodipine in rat model of heart failure induced by autoimmune myocarditis. Twenty-eight days after immunization the surviving rats were randomized for the oral administration of low-dose amlodipine (1 mg/kg/day), high-dose amlodipine (5 mg/kg/day), pranidipine (0.3 mg/kg/day) or vehicle (0.5% methylcellulose). After oral administration for 1 month, the animals underwent echocardiography and hemodynamic analysis. Histopathology, immunohistochemistry, and Western immunoblotting were carried out in the heart samples. Both pranidipine and high-dose amlodipine increased survival rate. Although the heart rate did not differ among the four groups, left ventricular end-diastolic pressure was significantly decreased and +/-dP/dt was increased in the pranidipine- and high-dose amlodipine-treated rats, but not in low-dose amlodipine-treated rats. In comparison to amlodipine treatment, pranidipine treatment significantly reduced myocyte size and central venous pressure. Furthermore, both pranidipine and high-dose amlodipine treatment significantly reduced myocardial protein levels of atrial natriuretic peptide and inducible nitric oxide synthase, whereas pranidipine only significantly decreased tumor necrosis factor-alpha, and improved sarcoplasmic reticulum Ca2+ ATPase2 protein levels. We conclude that pranidipine ameliorates the progression of left ventricular dysfunction and cardiac remodeling in rats with heart failure after autoimmune myocarditis in a lower dose when compared to amlodipine and which may be a clinically potential therapeutic agent for the treatment of heart failure.
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Veeraveedu et al. (2006) conducted an RCT in Heart failure induced by autoimmune myocarditis (rat model). Pranidipine vs. Amlodipine (1 mg/kg/day or 5 mg/kg/day) or vehicle was evaluated on Survival rate, hemodynamics, and cardiac remodeling. Pranidipine ameliorated the progression of left ventricular dysfunction and cardiac remodeling in rats with heart failure at a lower dose compared to amlodipine.
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