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From the Molecular Physiology Laboratory, Division of Cardiology, Departments of Medicine & Physiology/Biophysics, Albert Einstein College of Medicine, Bronx, NY.
Correspondence to Jagdish Gulati, PhD, Molecular Physiology Laboratory, Division of Cardiology, F-G48 Departments of Medicine & Physiology/Biophysics, Albert Einstein College of Medicine, Bronx, NY 10461. E-mail jgulati@aecom.yu.edu.
Abstract We have measured the apparent Ca2+ sensitivities of force development in skinned cardiac trabeculae at different sarcomere lengths together with shifts in troponin (Tn) T subunits on specimens from the same hearts and drawn insights into the pathogenesis of myocardial dysfunction in the diabetic rat. The Ca2+-force relations were measured at a long (2.4-µm) and a short (1.9-µm) sarcomere length. In disease, compared with the control condition, the apparent Ca2+ sensitivity was greatly diminished at a sarcomere length of 1.9 µm but not affected at all at the long length (2.4 µm). We also examined the alterations in contractile regulatory proteins TnT and TnI by both sodium dodecyl sulfatepolyacrylamide gel electrophoresis and Western blots. The TnI band was largely unperturbed, but major changes were discerned in TnT. The normal rat heart indicated two major bands (TnT1 and TnT2) and a faint third band (TnT3); in the diabetic rat heart, there was a significant shift in intensity from TnT1 to TnT3. Since myosin isozyme shifts also accompany diabetes in the rat, we used a prototypical hypothyroid rat as well to evaluate the myosin influence in the length-induced effects on Ca2+ sensitivity. Myosin shifts during hypothyroidism were unaccompanied by significant changes in TnT, and there were also no length-dependent modifications in Ca2+ sensitivity. The findings raise the possibility that diabetic Ca2+-sensitivity changes in the myocardium are coupled with TnT alterations. A plausible explanation is offered whereby these TnT alterations modify the length dependence of Ca2+ sensitivity.
Key Words: troponin T diabetes heart failure hypothyroidism Ca2+
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