Effect of increased pressure on ventricular growth in stage 21 chick embryos.

We studied the effect of increased ventricular pressure on heart growth in the stage 21 (3.5-day) chick embryo. Ventricular pressure was increased by constricting the conotruncus with a loop of 10-0 nylon tied in an overhand knot. The embryos were reincubated, and physiology and cellular morphology were evaluated at successive stages of development, stages 21, 24, 27, and 29. Ventricular pressure was measured with a servo-null pressure system, and cardiac output was measured with a 20-MHz pulsed Doppler velocity meter. Ventricular and embryo dry weights were measured on an electronic microbalance, myocyte organelle composition was measured by a point counting technique, and cell growth response was measured by DNA and protein assay. The conotruncal loop increased ventricular pressure in experimental compared with control embryos, i.e., at stage 24, 2.88 +/- 0.13 vs. 1.96 +/- 0.05 (SE) mmHg (P less than 0.05), respectively, without affecting cardiac output. Ventricular dry weight increased in experimental vs. control embryos, i.e., at stage 24, 114 +/- 7 vs. 85 +/- 4 micrograms (P less than 0.05), respectively, whereas embryo weights were similar between the two groups. The difference in ventricular weights was due to myocyte hyperplasia, since organelle proportion of myofibrils and mitochondria, DNA-to-protein ratio, and myocyte area were similar in experimental voice control embryos. Thus the adjustment of myocardial mass to ventricular work occurs even during the earliest stages of embryonic development. Cardiac growth and morphogenesis are parallel but separable processes.

[1]  G Olivetti,et al.  Quantitative structural analysis of the myocardium during physiologic growth and induced cardiac hypertrophy: a review. , 1986, Journal of the American College of Cardiology.

[2]  K. Rakušan,et al.  Differences in capillary supply of hypertrophic and hyperplastic hearts. , 1966, Cardiologia.

[3]  E. Clark,et al.  Developmental Hemodynamic Changes in the Chick Embryo from Stage 18 to 27 , 1982, Circulation research.

[4]  D. Higgins,et al.  Development of transmitter secretory mechanisms by adrenergic neurons in the embryonic chick heart ventricle. , 1981, Developmental biology.

[5]  T. W. James,et al.  Assay for nanogram quantities of DNA in cellular homogenates. , 1979, Analytical biochemistry.

[6]  K. Paigen,et al.  A simple, rapid, and sensitive DNA assay procedure. , 1980, Analytical biochemistry.

[7]  A. Pappano The Development of Postsynaptic Cardiac Autonomic Receptors and Their Regulation of Cardiac Function During Embryonic, Fetal, and Neonatal Life , 1984 .

[8]  E. Hasser,et al.  Pressure-induced cardiac enlargement in neonatal and adult rats. Left ventricular weight and hemodynamic responses during the early adaptive period. , 1979, Texas reports on biology and medicine.

[9]  M. Heymann,et al.  Models of Congenital Heart Disease in Fetal Lambs , 1978, Circulation.

[10]  J. Marx The yin and yang of cell growth control. , 1986, Science.

[11]  A. Pappano,et al.  Ontogenetic development of autonomic neuroeffector transmission and transmitter reactivity in embryonic and fetal hearts. , 1977, Pharmacological reviews.

[12]  E. Clark,et al.  Effect of conotruncal constriction on aortic-mitral valve continuity in the stage 18, 21 and 24 chick embryo. , 1984, The American journal of cardiology.

[13]  S. R. Hilfer,et al.  Development of the eye of the chick embryo. , 1983, Scanning electron microscopy.

[14]  M. M. Bradford A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. , 1976, Analytical biochemistry.

[15]  C. Bolognesi,et al.  Improved microfluorometric DNA determination in biological material using 33258 Hoechst. , 1979, Analytical biochemistry.

[16]  Viktor Hamburger,et al.  A series of normal stages in the development of the chick embryo , 1992, Journal of morphology.