Altered in vivo left ventricular torsion and principal strains in hypothyroid rats. Am J Physiol Heart Circ Physiol 299: H1577-H1587, 2010. First published August 20, 2010 doi:10.1152/ajpheart.00406.2010.-The twisting and untwisting motions of the left ventricle (LV) lead to efficient ejection of blood during systole and filling of the ventricle during diastole. Global LV mechanical performance is dependent on the contractile properties of cardiac myocytes; however, it is not known how changes in contractile protein expression affect the pattern and timing of LV rotation. At the myofilament level, contractile performance is largely dependent on the isoforms of myosin heavy chain (MHC) that are expressed. Therefore, in this study, we used MRI to examine the in vivo mechanical consequences of altered MHC isoform expression by comparing the contractile properties of hypothyroid rats, which expressed only the slow -MHC isoform, and euthyroid rats, which predominantly expressed the fast ␣-MHC isoform. Unloaded shortening velocity (Vo) and apparent rate constants of force development (ktr) were measured in the skinned ventricular myocardium isolated from euthyroid and hypothyroid hearts. Increased expression of -MHC reduced LV torsion and fiber strain and delayed the development of peak torsion and strain during systole. Depressed in vivo mechanical performance in hypothyroid rats was related to slowed cross-bridge performance, as indicated by significantly slower Vo and ktr, compared with euthyroid rats. Dobutamine infusion in hypothyroid hearts produced smaller increases in torsion and strain and aberrant transmural torsion patterns, suggesting that the myocardial response to -adrenergic stress is compromised. Thus, increased expression of -MHC alters the pattern and decreases the magnitude of LV rotation, contributing to reduced mechanical performance during systole, especially in conditions of increased workload. magnetic resonance imaging; myosin heavy chain; myocardial contractility; dobutamine; cardiac muscle contraction DURING THE EARLY PHASE of isovolumic contraction, the ventricular apex and base initially rotate in a counterclockwise direction when viewed from the apex to base (55), and later in systole, the base rotates in a clockwise direction, whereas the apex continues to rotate in a counterclockwise direction (36). Toward the end of systole and early diastole, the direction of torsion is reversed as the ventricle untwists (51, 56). The systolic twisting and diastolic untwisting of the left ventricle (LV) optimize the ejection of blood and the filling of the chamber during systole and diastole, respectively. The pattern of ventricular rotation during systole and diastole is facilitated by the architectural design of the LV, in which the subendocardial fibers are oriented in a right-handed helix and the epicardial fibers in an opposing left-handed helix (64), creating the torsion associated with the wringing and unwringing motions of the heart. The sequence of electromechanical activation occurs in ...