Skip to main content
Log in

Influence of the thyroid state on myocardial myosin in the adult pig heart

  • Original Contributions
  • Published:
Basic Research in Cardiology Aims and scope Submit manuscript

Summary

The influence of hyper- and hypothyroidism on atrial and ventricular myosin structure and Ca2+-activated ATPase activity has been analyzed in adult mini-pigs. Whereas no difference could be demonstrated between hypo- and euthyroid ventricular myocardium, Ca2+-activated ATPase activity was significantly higher in the hyperthyroid than in the hypo- or euthyroid state. Using pyrophosphate electrophoresis and isoelectric focusing of subfragment 1 this could be ascribed to an additional ventricular myosin in the hyperthyroid myocardium. Atrial myosin ATPase activity and structure were not influenced by the thyroid state of the animals. These results present evidence that thyreotoxicosis induces an additional isomyosin in the pig ventricular myocardium, albeit to a lesser degree than in the rodent heart. The lacking difference between the hypothyroid and the euthyroid states indicates that a myosin with a lower enzymatic activity than the normal ventricular myosin is not synthesized in the heart of higher mammals.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Balint M, Sreter FA, Gergely J (1975) Fragmentation of myosin by papain-studies on myosin from adult fast and slow skeletal and cardiac and embryonic muscle. Arch Biochem Biophys 168: 557–566

    Article  PubMed  Google Scholar 

  2. Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254

    PubMed  Google Scholar 

  3. Clark WA, Chizzonite RA, Everett AW, Rabinowitz M, Zak R (1982) Species correlations between cardiac isomyosins. J Biol Chem 257:5449–5454

    PubMed  Google Scholar 

  4. Conway G, Heazlitt RA, Fowler N, Gabel M, Green S (1976) The effect of hyperthyroidism on the sarcoplasmic reticulum and myosin ATPase of dog. J Mol Cell Cardiol 8:39–51

    Article  PubMed  Google Scholar 

  5. Hoh JFY, McGrath PA, Hale PT (1977) Electrophoretic analysis of multiple forms of rat cardiac myosins: effects of hypothysectomy and thyroxine replacement. J Mol Cell Cardiol 10:1053–1076

    Article  Google Scholar 

  6. Kasper CB (1975) Fragmentation of proteins for sequence studies and separation of peptide mixtures. In: Needleman SB (ed) Molecular biology biochemistry and biophysics 8, Protein sequence determination, Springer-Verlag, Berlin München Heidelberg New York, 114–161

    Google Scholar 

  7. Litten RZ, Martin BJ, Howe ER, Alpert NR (1981) Phosphorylation and adenosine triphosphatase activity of myofibrils from thyrotoxic rabbit hearts. Circulat Res 48:498–501

    PubMed  Google Scholar 

  8. Litten RZ, Martin BJ, Low RB, Alpert NR (1981) Altered myosin isozyme patterns from pressure overloaded and thyrotoxic hypertrophied rabbit hearts. Circulat Res 50:856–864

    Google Scholar 

  9. Lompre AM, Mercadier JJ, Wisnewsky C (1981) Species and age dependent changes in relative amounts of cardiac myosin isozymes in mammals. Dev Biol 84:286–290

    Article  Google Scholar 

  10. Martin AF, Pagani ED, Solaro RJ (1982) Thyroxine induced redistribution of isoenzymes of rabbit ventricular myosin. Circulat Res 50:117–124

    PubMed  Google Scholar 

  11. Mercadier JJ, Bouveret P, Gorza L, Schiaffino S, Clark WA, Zak R, Swynghedauw B, Schwartz K (1983) Myosin isoenzymes in normal and hypertrophied human ventricular myocardium. Circulat Res 53:52–62

    PubMed  Google Scholar 

  12. Mercadier JJ, Lompré AM, Wisnewsky C, Samuel JC, Bercovici J, Swynghedauw B, Schwartz K (1981) Myosin isoenzymic changes in several models of rat cardiac hypertrophy. Circulat Res 49:525–532

    PubMed  Google Scholar 

  13. Morgan M, Perry S, Ottaway J (1976) Myosin light-chain phosphatase. Biochem J 157:687–687

    PubMed  Google Scholar 

  14. Morkin E, Flink IL, Goldman S (1983) Myosin isozymes in cardiac hypertrophy. In: Alpert NR (ed) Perspectives in cardiovascular research 7, Myocardial hypertrophy and failure, Raven Press, New York, 393–404

    Google Scholar 

  15. Pollard TD (1982) Myosin purification and characterization. In: Wilson L (ed) Methods in cell biology 24, Academic Press, 333–371

  16. Rupp H (1982) Polymorphic myosin as the common determinant of myofibrillar ATPase in different hemodynamic and thyroid states. Basic Res Cardiol 77:34–46

    PubMed  Google Scholar 

  17. Rupp H (1981) The adaptive changes in the isoenzyme pattern of myosin from hypertrophied rat myocardium as a result of pressure overload and physical training. Basic Res Cardiol 76:79–88

    PubMed  Google Scholar 

  18. Sachs L (1974) Angewandte Statistik. Springer-Verlag, Berlin Heidelberg New York

    Google Scholar 

  19. Schiaffino S, Gorza L, Sartore S, Valfré C, Pauletto P (1983) Adaptive changes in cardiac isomyosins as visualized by immunofluorescence. In: Jacob r, Gülich RW, Kissling G (eds) Cardiac adaption to hemodynamic overload, training and stress, Steinkopff Verlag, Darmstadt 101:103

    Google Scholar 

  20. Schier JJ, Adelstein RS (1982) Structural and enzymatic comparison of human cardiac muscle myosins isolated from infants, adults and patients with hypertrophic cardiomyopathy. J Clin Invest 69:816–825

    PubMed  Google Scholar 

  21. Schwartz K, Lompre AM, Bouveret P, Wisnewsky C, Whalen RG (1982) Comparisons of rat cardiac myosins at fetal stages, in young animals and in hypothyroid adults. J Biol Chem 257:14412–14418

    PubMed  Google Scholar 

  22. Shiverick KT, Thomas LL, Alpert NR (1975) Purification of cardiac myosin. Application to hypertrophied myocardium. Biochem Biophys Acta 393:124–133

    PubMed  Google Scholar 

  23. Toste AP, Cooke R (1979) Interactions of contractile proteins with free and immobilized cibacron Blue F3GA. Anal Biochem 95:317–328

    Article  PubMed  Google Scholar 

  24. Wiegand V, Stroh E, Henniges A, Lossnitzer K, Kreuzer H (1983) Altered distribution of myosin isoenzymes in the cardiomyopathic Syrian hamster (BIO 8.262). Basic Res Cardiol 78:665–670

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported by the SFB 89

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wiegand, V., Henniges, H., Oberschmidt, R. et al. Influence of the thyroid state on myocardial myosin in the adult pig heart. Basic Res Cardiol 80, 12–17 (1985). https://doi.org/10.1007/BF01906739

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01906739

Key words

Navigation