Effect of increased pressure loading on heart growth in neonatal rats

Journal of Molecular and Cellular Cardiology

Volumn 35, Issue 3, 2003, Pages 301-309

  Sedmera, David ^a,b   Thompson, Robert P ^b   Kolar, Frantisek ^c  

^a UNIVERSITY OF LAUSANNE   (Switzerland)

^b MEDICAL UNIVERSITY OF SOUTH CAROLINA   (United States)

^c Ctr for Exp Cardiovasc Research   (Czech Republic)

Author keywords

Apoptosis; Cell proliferation; Experimental aortic stenosis; Hyperplasia; Hypertrophy; Left ventricle; Myocardium

Indexed keywords

BROXURIDINE; DNA; THYMIDINE DERIVATIVE;

ABDOMINAL AORTA; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; AORTA CONSTRICTION; APOPTOSIS; ARTICLE; CELL DIVISION; CELL PROLIFERATION; CELL SIZE; CHEMICAL LABELING; CONTROLLED STUDY; DNA SYNTHESIS; HEART DEVELOPMENT; HEART LEFT VENTRICLE OVERLOAD; HEART MUSCLE CELL; HEART VENTRICLE WALL; MALE; NEWBORN; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; RAT;

EID: 0037348215     PISSN: 00222828     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-2828(03)00011-7     Document Type: Article

References (45)

1. Hutchins G.M., Bulkley B.H., Moore G.W., Piasio M.A., Lohr F.T. Shape of the human cardiac ventricles. Am J Cardiol. 41:1978;646-654.
2. Jacob R., Gulch R.W. The functional significance of ventricular geometry for the transition from hypertrophy to cardiac failure. Does a critical degree of structural dilatation exist? Basic Res Cardiol. 93:1998;423-429. [editorial].
3. Zak R. Development and proliferative capacity of cardiac muscle cells. II-17-. Circ Res. 34:(26):1974.
4. Kajstura J., Leri A., Finato N., Di Loreto C., Beltrami C.A., Anversa P. Myocyte proliferation in end-stage cardiac failure in humans. Proc Natl Acad Sci USA. 95:1998;8801-8805.
5. Li J.M., Poolman R.A., Brooks G. Role of G1 phase cyclins and cyclin-dependent kinases during cardiomyocyte hypertrophic growth in rats. Am J Physiol. 275:1998;H814-822.
6. Soonpaa M.H., Field L.J. Survey of studies examining mammalian cardiomyocyte DNA synthesis. Circ Res. 83:1998;15-26.
7. Rumyantsev P.P. Cardiomyocytes in the processes of reproduction, differentiation, and regeneration. 1982;Nauka, Leningrad.
8. Saiki Y., Konig A., Waddell J., Rebeyka I.M. Hemodynamic alteration by fetal surgery accelerates myocyte proliferation in fetal guinea pig hearts. Surgery. 122:1997;412-419.
9. Toussaint M., Bical O., Galliz P., Neveux J.Y. Effect of intrauterine creation of pulmonary stenosis and atresia on ventricular hypertrophy in the foetal lamb; haemodynamic, morphometric and ultrastructural study. Eur Heart J. 19:1998;654.
10. Clark E.B., Hu N., Rosenquist G.C. Effect of conotruncal constriction on aortic-mitral valve continuity in the stage 18, 21 and 24 chick embryo. Am J Cardiol. 53:1984;324-327.
11. Clark E.B., Hu N., Frommelt P., Vandekieft G.K., Dummett J.L., Tomanek R.J. Effect of increased pressure on ventricular growth in stage 21 chick embryos. Am J Physiol. 257:1989;H55-61.
12. Sedmera D., Pexieder T., Rychterova V., Hu N., Clark E.B. Remodeling of chick embryonic ventricular myoarchitecture under experimentally changed loading conditions. Anat Rec. 254:1999;238-252.
13. Clubb Jr F.J., Bishop S.P. Formation of binucleated myocardial cells in the neonatal rat. An index for growth hypertrophy. Lab Invest. 50:1984;571-577.
14. Beinlich C.J., Rissinger C.J., Morgan H.E. Mechanisms of rapid growth in the neonatal pig heart. J Mol Cell Cardiol. 27:1995;273-281.
15. Campbell S.E., Rakusan K., Gerdes A.M. Change in cardiac myocyte size distribution in aortic-constricted neonatal rats. Basic Res Cardiol. 84:1989;247-258.
16. Kajstura J., Mansukhani M., Cheng W., Reiss K., Krajewski S., Reed J.C., et al. Programmed cell death and expression of the protooncogene bcl-2 in myocytes during postnatal maturation of the heart. Exp Cell Res. 219:1995;110-121.
17. Korecky B., Sweet S., Rakusan K. Number of nuclei in mammalian cardiac myocytes. Can J Physiol Pharmacol. 57:1979;1122-1129.
18. Claycomb W.C. Biochemical aspects of cardiac muscle differentiation. Deoxyribonucleic acid synthesis and nuclear and cytoplasmic deoxyribonucleic acid polymerase activity. J Biol Chem. 250:1975;3229-3235.
19. Li F., Wang X., Capasso J.M., Gerdes A.M. Rapid transition of cardiac myocytes from hyperplasia to hypertrophy during postnatal development. J Mol Cell Cardiol. 28:1996;1737-1746.
20. Kolar F., Papousek F., Pelouch V., Ostadal B., Rakusan K. Pressure overload induced in newborn rats: effects on left ventricular growth, morphology, and function. Pediatr Res. 43:1998;521-526.
21. Oliviero P., Chassagne C., Kolar F., Adamy C., Marotte F., Samuel J.L., et al. Effect of pressure overload on angiotensin receptor expression in the rat heart during early postnatal life. J Mol Cell Cardiol. 32:2000;1631-1645.
22. Rakusan K., Raman S., Layberry R., Korecky B. The influence of aging and growth on the postnatal development of cardiac muscle in rats. Circ Res. 42:1978;212-218.
23. Pelouch V., Kolar F., Milerova M., Ostadal B. Effect of the preweaning nutritional state on the cardiac protein profile and functional performance of the rat heart. Mol Cell Biochem. 177:1997;221-228.
24. Sedmera D., Hu N., Weiss K.M., Keller B.B., Denslow S., Thompson R.P. Cellular changes in experimental left heart hypoplasia. Anat Rec. 267:2002;137-145.
25. Sedmera D., Pexieder T., Hu N., Clark E.B. Developmental changes in the myocardial architecture of the chick. Anat Rec. 248:1997;421-432.
26. Sedmera D., Pexieder T., Vuillemin M., Thompson R.P., Anderson R.H. Developmental patterning of the myocardium. Anat Rec. 258:2000;319-337.
27. Bical O., Gallix P., Toussaint M., Landais P., Gaillard D., Karam J., et al. Intrauterine versus postnatal repair of created pulmonary artery stenosis in the lamb. Morphologic comparison. J Thorac Cardiovasc Surg. 99:1990;685-690.
28. Zheng L., Wibo M., Kolar F., Godfraind T. Calcium channels and cation transport ATPases in cardiac hypertrophy induced by aortic constriction in newborn rats. Mol Cell Biochem. 163-164:1996;23-29.
29. Knaapen M.W., Vrolijk B.C., Wenink A.C. Nuclear and cellular size of myocytes in different segments of the developing rat heart. Anat Rec. 244:1996;118-125.
30. Clubb Jr F.J., Bell P.D., Kriseman J.D., Bishop S.P. Myocardial cell growth and blood pressure development in neonatal spontaneously hypertensive rats. Lab Invest. 56:1987;189-197.
31. Gerdes A.M., Moore J.A., Hines J.M., Kirkland P.A., Bishop S.P. Regional differences in myocyte size in normal rat heart. Anat Rec. 215:1986;420-426.
32. Grohmann D. Mitotische Wachstumsintensitat des embryonalen und fetalen Hunchenherzens und ihre Bedeutung fur die entstehung von Herzmissbildungen. Z f Zellforschung. 55:1961;104-122.
33. Jeter J.R. Jr, Cameron I.L. Cell proliferation patterns during cytodifferentiation in embryonic chick tissues: liver, heart and erythrocytes. J Embryol Exp Morphol. 25:1971;405-422.
34. Li F., McNelis M.R., Lustig K., Gerdes A.M. Hyperplasia and hypertrophy of chicken cardiac myocytes during posthatching development. Am J Physiol. 273:1997;R518-526.
35. Rumyantsev P.P. Interrelations of the proliferation and differentiation processes during cardiact myogenesis and regeneration. Int Rev Cytol. 51:1977;186-273.
36. Anversa P., Kajstura J. Ventricular myocytes are not terminally differentiated in the adult mammalian heart. Circ Res. 83:1998;1-14.
37. Kellerman S., Moore J.A., Zierhut W., Zimmer H.G., Campbell J., Gerdes A.M. Nuclear DNA content and nucleation patterns in rat cardiac myocytes from different models of cardiac hypertrophy. J Mol Cell Cardiol. 24:1992;497-505.
38. Hefti M.A., Harder B.A., Eppenberger H.M., Schaub M.C. Signaling pathways in cardiac myocyte hypertrophy. J Mol Cell Cardiol. 29:1997;2873-2892.
39. Pasumarthi K.B., Field L.J. Cardiomyocyte cell cycle regulation. Circ Res. 90:2002;1044-1054.
40. Manasek F.J. Myocardial cell death in the embryonic chick ventricle. J Embryol Exp Morphol. 21:1969;271-284.
41. Cheng G., Wessels A., Gourdie R.G., Thompson R.P. Spatiotemporal distribution of apoptosis in embryonic chicken heart. Dev Dyn. 223:2002;119-133.
42. Anversa P., Leri A., Beltrami C.A., Guerra S., Kajstura J. Myocyte death and growth in the failing heart. Lab Invest. 78:1998;767-786.
43. Cheng W., Reiss K., Kajstura J., Kowal K., Quaini F., Anversa P. Down-regulation of the IGF-1 system parallels the attenuation in the proliferative capacity of rat ventricular myocytes during postnatal development. Lab Invest. 72:1995;646-655.
44. Bitar F.F., Bitar H., El Sabban M., Nasser M., Yunis K.A., Tawil A., et al. Modulation of ceramide content and lack of apoptosis in the chronically hypoxic neonatal rat heart. Pediatr Res. 51:2002;144-149.
45. Widdowson E.M., Crabb D.E., Milner R.D. Cellular development of some human organs before birth. Arch Dis Child. 47:1972;652-655.