Analysis of left ventricular function of the mouse heart during experimentally induced hyperthyroidism and recovery

Many of the clinical manifestations of hyperthyroidism are due to the ability of thyroid hormones to alter myocardial contractility and cardiovascular hemodynamics, leading to cardiovascular impairment. In contrast, recent studies highlight also the potential beneficial effects of thyroid hormone ad...

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Veröffentlicht in:NMR in biomedicine 2015-01, Vol.28 (1), p.116-123
Hauptverfasser: Hübner, Neele Saskia, Merkle, Annette, Jung, Bernd, von Elverfeldt, Dominik, Harsan, Laura-Adela
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Sprache:eng
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Zusammenfassung:Many of the clinical manifestations of hyperthyroidism are due to the ability of thyroid hormones to alter myocardial contractility and cardiovascular hemodynamics, leading to cardiovascular impairment. In contrast, recent studies highlight also the potential beneficial effects of thyroid hormone administration for clinical or preclinical treatment of different diseases such as atherosclerosis, obesity and diabetes or as a new therapeutic approach in demyelinating disorders. In these contexts and in the view of developing thyroid hormone‐based therapeutic strategies, it is, however, important to analyze undesirable secondary effects on the heart. Animal models of experimentally induced hyperthyroidism therefore represent important tools for investigating and monitoring changes of cardiac function. In our present study we use high‐field cardiac MRI to monitor and follow‐up longitudinally the effects of prolonged thyroid hormone (triiodothyronine) administration focusing on murine left ventricular function. Using a 9.4 T small horizontal bore animal scanner, cinematographic MRI was used to analyze changes in ejection fraction, wall thickening, systolic index and fractional shortening. Cardiac MRI investigations were performed after sustained cycles of triiodothyronine administration and treatment arrest in adolescent (8 week old) and adult (24 week old) female C57Bl/6 N mice. Triiodothyronine supplementation of 3 weeks led to an impairment of cardiac performance with a decline in ejection fraction, wall thickening, systolic index and fractional shortening in both age groups but with a higher extent in the group of adolescent mice. However, after a hormonal treatment cessation of 3 weeks, only young mice are able to partly restore cardiac performance in contrast to adult mice lacking this recovery potential and therefore indicating a presence of chronically developed heart pathology. Copyright © 2014 John Wiley & Sons, Ltd. High‐field mouse cardiac MRI was performed to monitor and follow‐up longitudinally the effects of long‐term thyroid hormone (T3) administration, inducing hyperthyroidism in adolescent and adult female mice. Sustained cycles of T3 administration and arrest lead to an impairment of cardiac performance with a decline in ejection fraction and wall thickening. Treatment cessation for 3 weeks resulted in partly restored cardiac performance in adolescent mice but not in adult animals, indicating a presence of chronically developed heart pathology
ISSN:0952-3480
1099-1492
DOI:10.1002/nbm.3233