Why the study?
Does long-term treatment with amlodipine or MCI-154 improve progressive cardiac dysfunction and microvasculature in dilated cardiomyopathic hamsters?
Does long-term treatment with amlodipine or MCI-154 improve progressive cardiac dysfunction and microvasculature in dilated cardiomyopathic hamsters?
Amlodipine and MCI-154 preserve coronary microvasculature and improve cardiac systolic and diastolic function in a hamster model of dilated cardiomyopathy, potentially through angiogenesis.
No immediate clinical implications; extends microvascular preservation findings in dilated cardiomyopathy models.
The present study examined the effect of long-term treatment with amlodipine and MCI-154 (a Ca2+ sensitizer) on progressive cardiac dysfunction and microvasculature in the dilated cardiomyopathic (DCM) hamster heart. After treatment of DCM hamsters (Bio 53.58) with amlodipine or MCI-154 for 15 wk from the age of 5 wk, amlodipine and MCI-154 were found to cause an increase in left ventricular percent fractional shortening and decreases in left ventricular diastolic dimension and isovolumic relaxation time in echocardiograms (P < 0.01). A hemodynamic study showed that the diastolic time constant decreased in the amlodipine-treatment group (P < 0.05). In a morphometric study employing a double-staining method that discriminated arteriolar and venular capillaries, amlodipine and MCI-154 caused increases in total capillary density (P < 0.05) and the proportion of venular capillaries (P < 0.05). Moreover, Northern blot analysis showed that the expression of mRNA for vascular endothelial growth factor was significantly increased by amlodipine and MCI-154. They preserve coronary microvasculature in the DCM hamster and might induce angiogenesis of small vessels, thereby contributing to preservation of cardiac systolic and diastolic function.
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Kumamoto et al. (1999) studied this question.
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