TY - JOUR
T1 - Cardiac effects of 3,5-diiodothyropropionic acid, a thyroid hormone analog with inotropic selectivity
AU - Pennock, G. D.
AU - Raya, T. E.
AU - Bahl, J. J.
AU - Goldman, S.
AU - Morkin, E.
PY - 1992
Y1 - 1992
N2 - Thyroid hormone exerts a strong positive inotropic action on the heart and induces α-myosin heavy chain (MHC) gene expression. 3,5-Diiodothyropropionic acid (DITPA), a carboxylic acid analog with low metabolic activity, was observed to induce α-MHC mRNA in heart cell culture with EC50 ≃ 5 x 10- 7 M. To determine if the compound has positive inotropic actions, the effects of DITPA and L-thyroxine on heart rate, left ventricular pressures, left ventricular dP/dt, myosin isoenzymes and hepatic α-glycerolphosphate dehydrogenase activity were compared in hypothyroid rats. Binding affinities of DITPA and triiodothyronine for bacterially expressed alpha-1 and beta-1 thyroid hormone receptors (TRs) also were determined. Over the dosage range of 150 to 1500 μg/100 g, DITPA produced increases in left ventricular dP/dt comparable to those obtained with L-thyroxine at dosages of 1.5 to 15 μg/100 g, but with significantly less tachycardia. The increase in α-MHC mRNA was about the same with both compounds whereas α-MHC protein content and GPDH activity increased less with DITPA. These differences could not be explained by preferential binding of DITPA to TR subtypes. Because heart rate is a major determinant of myocardial oxygen consumption, DITPA is able to achieve increased cardiac performance at lower myocardial oxygen costs.
AB - Thyroid hormone exerts a strong positive inotropic action on the heart and induces α-myosin heavy chain (MHC) gene expression. 3,5-Diiodothyropropionic acid (DITPA), a carboxylic acid analog with low metabolic activity, was observed to induce α-MHC mRNA in heart cell culture with EC50 ≃ 5 x 10- 7 M. To determine if the compound has positive inotropic actions, the effects of DITPA and L-thyroxine on heart rate, left ventricular pressures, left ventricular dP/dt, myosin isoenzymes and hepatic α-glycerolphosphate dehydrogenase activity were compared in hypothyroid rats. Binding affinities of DITPA and triiodothyronine for bacterially expressed alpha-1 and beta-1 thyroid hormone receptors (TRs) also were determined. Over the dosage range of 150 to 1500 μg/100 g, DITPA produced increases in left ventricular dP/dt comparable to those obtained with L-thyroxine at dosages of 1.5 to 15 μg/100 g, but with significantly less tachycardia. The increase in α-MHC mRNA was about the same with both compounds whereas α-MHC protein content and GPDH activity increased less with DITPA. These differences could not be explained by preferential binding of DITPA to TR subtypes. Because heart rate is a major determinant of myocardial oxygen consumption, DITPA is able to achieve increased cardiac performance at lower myocardial oxygen costs.
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M3 - Article
C2 - 1403782
AN - SCOPUS:0026707452
SN - 0022-3565
VL - 263
SP - 163
EP - 169
JO - Journal of Pharmacology and Experimental Therapeutics
JF - Journal of Pharmacology and Experimental Therapeutics
IS - 1
ER -