Changes in myosin and creatine kinase mRNA levels with cardiac hypertrophy and hypothyroidism
- 1 September 1990
- journal article
- research article
- Published by Springer Nature in Basic Research in Cardiology
- Vol. 85 (5) , 481-494
- https://doi.org/10.1007/bf01931494
Abstract
Rats were treated with three methods which produce alterations in the expression of myosin isozymes: coarctation of the abdominal aorta, treatment with low doses of isoproterenol, and administration of propylthiouracil. The steady-state levels of the left ventricle mRNAs for α myosin heavy chain (α-MHC), β myosin heavy chain (β-MHC), M creatine kinase (MCK), and B creatine kinase (BCK) were then determined using Northern and slot blot hybridizations. Cardiac hypertrophy was induced by an acute systolic pressure overload, or β adrenergic stimulation. At 7 days following systolic pressure overload, the induced cardiac hypertrophy was accompanied by alterations in the levels of MHC mRNAs, as has been previously reported. In RNA from left ventricles of treated animals α-MHC mRNA levels decreased by 15% by day 3 and 20% by day 7. In contrast, β-MHC mRNA levels increased to 250% of control levels by day 3 and then declined to a value 150% of controls by day 7. Levels of MCK and BCK mRNAs showed little or no changes by day 3; at day 7 both MCK and BCK mRNAs showed decreases of 20% relative to controls. Cardiac hypertrophy induced by low doses of isoproterenol produced decreases of α-MHC mRNA levels to 70% of control values at day 3 and 50% at day 7. Over the same time periods there was an increase in the levels of the fetal mRNA isoform (β-MHC) to 190%, then 130% of control values, respectively. At 3 days, both BCK and MCK mRNA levels had declined by approximately 20–25%. By 7 days, MCK mRNA levels had decreased by approximately 50% and BCK mRNA levels by 30%. Hypothyroidism induced by PTU treatment led to a 50% decrease in α-MHC mRNA levels by day 3, which then further decreased to 10% of control levels at day 7. β-MHC mRNA levels increased to 350% of control levels at day 3 and then decreased to 275% of control levels at day 7. For creatine kinase mRNAs the level of the M isoform was increased by 30% at day 3, whereas there appeared to be no significant change in levels of B isoform mRNA at this time. At day 7 neither BCK nor MCK mRNA levels were significantly different from controls. These results show three treatments which produce an alteration in myosin mRNA isoforms produce little or no change in creatine kinase isoform mRNAs. Thus, the MHC and CK genes respond differently to either cardiac hypertrophy or a reduction in thyroid hormone levels.Keywords
This publication has 60 references indexed in Scilit:
- Effect of triiodothyronine on cultured neonatal rat heart cells: Beating rate, myosin subunits and CK-isozymesJournal of Molecular and Cellular Cardiology, 1988
- MOLECULAR GENETICS OF MYOSINAnnual Review of Biochemistry, 1987
- Myosin heavy chain messenger RNA and protein isoform transitions during cardiac hypertrophy. Interaction between hemodynamic and thyroid hormone-induced signals.Journal of Clinical Investigation, 1987
- Cardiac myofibrillar creatine kinase is not influenced by hypothyroidismCanadian Journal of Physiology and Pharmacology, 1985
- Hemodynamic versus adrenergic control of cat right ventricular hypertrophy.Journal of Clinical Investigation, 1985
- Expression of a rat brain creatine kinase-β-galactosidase fusion protein in Escherichia coli and derivation of the complete amino acid sequence of rat brain creatine kinaseGene, 1985
- Redistribution of creatine kinase isoenzymes in chronically overloaded myocardiumCardiovascular Research, 1985
- Development of isoproterenol-indueed cardiac hypertrophyCanadian Journal of Physiology and Pharmacology, 1984
- Isoenzyme pattern and activity of myocardial creatine phosphokinase under heart adaptation to prolonged overloadBasic Research in Cardiology, 1982
- Protein synthesis, amino acid uptake, and pools during isoproterenol-induced hypertrophy of the rat heart and tibialis muscleCanadian Journal of Physiology and Pharmacology, 1981