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Myofibrillar adaptations during cardiac hypertrophy

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Abstract

The main purpose of this study was to determine the transmural adaptive changes that occur in cell size, myofibrils, and myosin isoforms from the endocardium (ENDO) to the epicardium (EPI) of the left ventricle (LV) of the rat heart during compensatory hypertrophy. Hypertrophy was induced by supra-renal aortic constriction for periods of 2, 7, 15 and 30 days. Percent left ventricular hypertrophy averaged 63±9.7% at 30 days following constriction. A significant (p <0.05) transmural gradient in the V3 myosin isoform (9±0.7% ENDO vs. 5±1.8% EPI) was initially observed at 7 days and was still evident by 30 days (25±3.6% ENDO vs 15±2.0% EPI). Cell cross-sectional area was also greater (p <0.05) in the ENDO than in the EPI at 7,15 and 30 days. MF diameter was determined only at 30 days and was found to be similar to control values in both the hypertrophied ENDO (sham 1.24±0.05 vs hyp 1.18±0.09 μm) and EPI (sham 1.17±0.08 vs hyp 1.06±0.08 μm). The combined effects of cardiac myocyte hypertrophy with no change in MF diameter resulted in a calculated increase of approximately 70% in the number of myofibrils per myocyte both in the ENDO and EPI. It was concluded that the adaptive strategy of the left ventricular free wall to pressure overload was to initially increase myocyte cross-sectional area and then switch myosin expression from V1 to V3, both of which proceeds transmurally from the sub-endocardium towards the sub-epicardium. Along with these transmural adaptations, myofibrils increased in number while maintaining myofibrillar diameter with the apparent intent of conserving diffusion distance for calcium from the sarcoplasmic reticulum to the innermost contractile filaments of the myofibrils.

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References

  1. Campbell SE, Rakusan K, Gerdes AM: Change in cardiac myocyte size distribution in aortic-constricted neonatal rats. Basic Res Cardiol 54: 247–258, 1989

    Google Scholar 

  2. Campbell SE, Korecky B, Rakusan K: Remodeling of myocyte dimensions in hypertrophic and atrophic rat hearts. Circ Res 68: 984–996, 1991

    Google Scholar 

  3. Eisenberg BR: Quantitative ultrastructure of mammalian skeletal. In: LD Peachey, RH Adrian, SR Geiger, (eds) Handbook of Physiology: Skeletal Muscle. American Physiological Society, Baltimore, MD, 1983, pp 73–112

    Google Scholar 

  4. Richter GW, Kellner A: Hypertrophy of the human heart at the level of fine structure. J Cell Biol 18: 195–206, 1963

    Google Scholar 

  5. Anversa P, Loud AV, Giacomelli, F, Wiener J: Absolute morphometric study of myocardial hypertrophy in experimental hypertension: II Ultrastructure of myocytes and interstitium. Lab Invest 38: 597–607, 1978

    Google Scholar 

  6. Anversa P, Olivetti G, Melissari M, Loud AV: Stereological measurement of cellular and subcellular hypertrophy and hyperplasia in the papillary muscle of adult rat. J Mol Cell Cardiol 12: 781–795, 1980

    Google Scholar 

  7. Alpert NR, Mulieri LA: Myocardial myosin isoenzymes and thermomechanical economy. In: RC Tarazi, JB Dunbar (eds) Perspectives in Cardiovascular Research. Raven Press, New York, 1983, pp 157–166

    Google Scholar 

  8. Gorza L, Pauletto P, Pessina AC, Sartore S, Schiaffino S: Isomyosin distribution in normal and pressure-overloaded rat ventricular myocardium: An immunohistochemical study. Circ Res 49: 1003–1009, 1981

    Google Scholar 

  9. Lompre A, Schwartz K, d'Albis A, Lacombe G, Van Thien N, Swynghedauw B: Myosin isoenzyme redistribution in chronic heart overload. Nature (London) 282:105–107, 1979

    Google Scholar 

  10. Mercadier J, Lompre A, Wisenewsky C, Sameul J, Bercovici J, Swynghedauw B, Schwartz K: Myosin isoenzymic changes in several models of rat cardiac hypertrophy. Circ Res 49: 525–532, 1981

    Google Scholar 

  11. Bugaisky LB, Anderson PG, Hall RS, Bishop SP: Differences in myosin isoform expression in subepicardial and subendocardial myocardium during cardiac hypertrophy in the rat. Circ Res 66: 1127–1132, 1990

    Google Scholar 

  12. Hoh JFY, McGrath PA, Hale PT: Electrophoretic analysis of multiple forms of rat cardiac myosin: effects of hypophysectomy and thyroxine replacement. J Mol Cell Cardiol 10: 1053–1076, 1978

    Google Scholar 

  13. Lowry OH, Rosenbrough NJ, Farr AL, Randall RJ: Protein measurement with the folin phenol reagent. J Biol Chem 193: 265–275, 1951

    Google Scholar 

  14. Moens P, Earnshaw WC: Anti-topoisomerase II recognizes meiotic chromosome cores. Chromosoma 98: 317–322, 1989

    Google Scholar 

  15. Johnson GD, Arujo de C Nogueira GM: A simple method of reducing the fading of immunofluorescence during microscopy. J Immunol Meth 43: 349–350, 1981

    Google Scholar 

  16. Brooke MH, Kaiser KK: Three ‘myosin adenosine triphosphatase’ systems: the nature of their pH lability and sulphydryl dependence. J Histochem Cytochem 18: 670–672, 1970

    Google Scholar 

  17. Lee RM, McKenzie R, Kobayashi K, Garfield RE, Forrest JB, Daniel EE: Effects of glutaraldehyde fixative osmolarities on smooth muscle cell volume, and osmotic reactivity of the cells after fixation. J Microsc 125: 77–87, 1982

    Google Scholar 

  18. Spurr AR: A low-viscosity epoxy resin embedding medium for electron microscopy. J Ultra Res 26: 31–43, 1969

    Google Scholar 

  19. Fiske S: A adaptation of Reynold's lead citrate stain for high resolution autoradiography. J Microsc 5: 355–360, 1966

    Google Scholar 

  20. Zar JH: Biostatistical Analysis (2nd ed). Prentice Hall, Englewood Cliffs, NJ, 1984, pp 239–241

    Google Scholar 

  21. Zak R: Development and proliferative capacity of cardiac muscle cells. Circ Res (Suppl II) 34: 17–26, 1974

    Google Scholar 

  22. Campbell SE, Gerdes AM, Smith TD: Comparison of regional differences in cardiac myocyte dimensions in rats, hamsters, and guinea pigs. Anat Rec 219: 53–59, 1987

    Google Scholar 

  23. Gerdes AM, Moore JA, Hines JM, Kirkland PA, Bishop SP: Regional differences in myocyte size in normal rat heart. Anat Rec 215:420–426, 1986

    Google Scholar 

  24. Anversa P, Olivetti G, Melissari M, Loud AL: Stereological measurement of cellular and subcellular hypertrophy and hyperplasia in the papillary muscle of the adult rat. J Mol Cell Cardiol 12: 781–795, 1980

    Google Scholar 

  25. Morkin E: Postnatal muscle fiber assembly: Localization of newly synthesized myofibrillar proteins. Science Wash 167: 1499–1501, 1970

    Google Scholar 

  26. Anversa P, Hagopian M, Loud AV: Quantitative radioautographic localization of protein synthesis in experimental cardiac hypertrophy. Lab Invest 29: 282–292, 1973

    Google Scholar 

  27. Bishop SP, Cole CR: Ultrastructural changes in the canine myocardium with right ventricular hypertrophy and congestive heart failure. Lab Invest 20: 219–229, 1969

    Google Scholar 

  28. Ito Y, Suko J, Chidsey CA: Intracellular calcium and myocardial contractility V. Calcium uptake of sarcoplasmic reticulum fractions in hypertrophied and failing rabbit hearts. J Mol Cell Cardiol 6: 237–247, 1974

    Google Scholar 

  29. Sordahl LA, McCollum WB, Wood WG, Schwartz A: Mitochondria and sarcoplasmic reticulum function in cardiac hypertrophy and failure. Am J Physiol 224: 497–502, 1973

    Google Scholar 

  30. Jacob R, Kissling G, Rupp H, Vogt M: Functional significance of contractile proteins in cardiac hypertrophy and failure. J Cardiovas Pharmacol (Suppl) 6: S2-S12, 1987

    Google Scholar 

  31. Kirk ES, Honig CR: An experimental and theoretical analysis of myocardial tissue pressure. Am J Physiol 207: 361–367, 1964

    Google Scholar 

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Toffolo, R.L., Ianuzzo, C.D. Myofibrillar adaptations during cardiac hypertrophy. Mol Cell Biochem 131, 141–149 (1994). https://doi.org/10.1007/BF00925950

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