Key result
Diiodothyropropionic acid (DITPA) and L-thyroxine (T4) reduced chamber diameter during diastole and increased myocardial blood flow in cardiomyopathic hamsters.
Why the study?
Does diiodothyropropionic acid (DITPA) or L-thyroxine (T4) improve chamber remodeling and cardiac function in normal and cardiomyopathic hamsters?
Does diiodothyropropionic acid (DITPA) or L-thyroxine (T4) improve chamber remodeling and cardiac function in normal and cardiomyopathic hamsters?
DITPA and T4 exert beneficial effects on chamber remodeling and vascular supply in cardiomyopathic hamsters, supporting further investigation of thyroid hormone analogs in heart failure.
Supports further investigation of thyroid hormone analogs in heart failure; leaves open translation from hamster models to patients.
Diiodothyropropionic acid (DITPA) is a thyroid hormone analog that is currently in phase II clinical trials. However, there have not been any studies to comprehensively analyze its effect on myocyte morphology. In addition, long-term studies with DITPA have not been done. This study compares the effects of DITPA with L-thyroxine (T4) on chamber remodeling, cardiac function, cellular morphology, cardiac blood flow, and protein expression. Normal and cardiomyopathic hamsters were treated with T4 or DITPA for 2 months. At the end of the treatment, echos, hemodynamics, coronary blood flow, cell morphology, and protein expression data were collected. Both T4 and DITPA treatment reduced chamber diameter during diastole, suggesting attenuated chamber dilatation in cardiomyopathic hamsters. Wall thickness also tended to increase, which was supported by cell morphology data in which DITPA significantly increased cross-sectional growth of myocytes specifically in the minor dimension, which is oriented transmurally. T4 and DITPA also increased myocardial blood flow both at baseline and after maximal dilation. This suggests there was increased angiogenesis or reduced loss of arterioles. Both T4 and DITPA had beneficial effects on chamber remodeling, which was most likely due to beneficial changes in cell shape and improved vascular supply.
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Kuzman et al. (2007) studied Cardiomyopathy. Diiodothyropropionic acid (DITPA) vs. L-thyroxine (T4) was evaluated on Chamber remodeling, cardiac function, cellular morphology, cardiac blood flow, and protein expression. Diiodothyropropionic acid (DITPA) and L-thyroxine (T4) reduced chamber diameter during diastole and increased myocardial blood flow in cardiomyopathic hamsters.
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