Abstract |
We have tested the hypothesis that thyroid state may influence both the flow of cellular Ca2+ and the myofilament response to Ca2+ by effects on intracellular pH (pHi) and Na+ (Nai+). Single cardiac myocytes isolated from hypothyroid, euthyroid and hyperthyroid animals were loaded with fura-2/AM (Cai2+ probe), BCECF/AM (pHi probe) or SBFI/AM (Nai+ probe). Compared with hypothyroid animals, myocytes isolated from hyperthyroid rat hearts demonstrated a significant: (1) increase in extent of shortening; (2) decrease in the time to peak contraction; (3) increase in the peak amplitude of the fura-2 fluorescence ratio; (4) decrease in pHi (DeltapHi=0. 19+/-0.05); and (5) increase in Nai+ (DeltaNai+=2.88+/-0.55 mM). We have also compared pHi in Langendorff perfused hypo- and hyperthyroid rat hearts using NMR. We have found that hyperthyroid hearts are 0.15+/-0.03 pH units more acidic than hypothyroid hearts. Analysis of mRNA levels demonstrated that hyperthyroidism increased expression of both the Na+/Ca2+ exchanger and Na+/H+ antiporter, and decreased expression of Na+ channel mRNAs. These changes appear partially responsible for the observed changes in Nai+ and pHi. Our results provide the first evidence that changes in cardiac contractility associated with altered thyroid state not only involve effects on Ca2+, but may also involve changes in the response of the myofilaments to Cai2+mediated by altered pHi and Nai+.
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Authors | B M Wolska, V Averyhart-Fullard, A Omachi, M O Stojanović, R G Kallen, R J Solaro |
Journal | Journal of molecular and cellular cardiology
(J Mol Cell Cardiol)
Vol. 29
Issue 10
Pg. 2653-63
(Oct 1997)
ISSN: 0022-2828 [Print] England |
PMID | 9344760
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Copyright | Copyright 1997 Academic Press Limited. |
Chemical References |
- RNA, Messenger
- Sodium Channels
- Sodium-Calcium Exchanger
- Sodium-Hydrogen Exchangers
- Thyroid Hormones
- Sodium
- Calcium
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Topics |
- Animals
- Calcium
(metabolism)
- Heart Ventricles
(cytology, metabolism)
- Homeostasis
- Hydrogen-Ion Concentration
- Hyperthyroidism
(metabolism)
- Hypothyroidism
(metabolism)
- Male
- Myocardial Contraction
- Myocardium
(metabolism)
- RNA, Messenger
- Rats
- Rats, Sprague-Dawley
- Sodium
(metabolism)
- Sodium Channels
(genetics, metabolism)
- Sodium-Calcium Exchanger
(metabolism)
- Sodium-Hydrogen Exchangers
(metabolism)
- Thyroid Gland
(metabolism)
- Thyroid Hormones
(metabolism)
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