Functional Effects of Hyperthyroidism on Cardiac Papillary Muscle in Rats

Hyperthyroidism is currently recognized to affect the cardiovascular system, leading to a series of molecular and functional changes. However, little is known about the functional influence of hyperthyroidism in the regulation of cytoplasmic calcium and on the sodium/calcium exchanger (NCX) in the c...

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Published in:Arquivos brasileiros de cardiologia Vol. 107; no. 6; pp. 542 - 549
Main Authors: Vieira, Fabricio Furtado, Olivoto, Robson Ruiz, Silva, Priscyla Oliveira da, Francisco, Julio Cesar, Fogaça, Rosalvo Tadeu Hochmuller
Format: Journal Article
Language:English
Portuguese
Published: Brazil Sociedade Brasileira de Cardiologia - SBC 01-12-2016
Sociedade Brasileira de Cardiologia (SBC)
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Summary:Hyperthyroidism is currently recognized to affect the cardiovascular system, leading to a series of molecular and functional changes. However, little is known about the functional influence of hyperthyroidism in the regulation of cytoplasmic calcium and on the sodium/calcium exchanger (NCX) in the cardiac muscle. To evaluate the functional changes in papillary muscles isolated from animals with induced hyperthyroidism. We divided 36 Wistar rats into a group of controls and another of animals with hyperthyroidism induced by intraperitoneal T3 injection. We measured in the animals' papillary muscles the maximum contraction force, speed of contraction (+df/dt) and relaxation (-df/dt), contraction and relaxation time, contraction force at different concentrations of extracellular sodium, post-rest potentiation (PRP), and contraction force induced by caffeine. In hyperthyroid animals, we observed decreased PRP at all rest times (p < 0.05), increased +df/dt and -df/dt (p < 0.001), low positive inotropic response to decreased concentration of extracellular sodium (p < 0.001), reduction of the maximum force in caffeine-induced contraction (p < 0.003), and decreased total contraction time (p < 0.001). The maximal contraction force did not differ significantly between groups (p = 0.973). We hypothesize that the changes observed are likely due to a decrease in calcium content in the sarcoplasmic reticulum, caused by calcium leakage, decreased expression of NCX, and increased expression of a-MHC and SERCA2.
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ISSN:0066-782X
1678-4170
1678-4170
DOI:10.5935/abc.20160179