Formation and development of lamellar histoarchitecture of the ventricular myocardium of chick embryos

Authors

DOI:

https://doi.org/10.26641/1997-9665.2024.1.26-31

Keywords:

prenatal ontogeny, heart, ventricular myocardium, histoarchitecture, endomysium, perimysium, muscle plates.

Abstract

Background. The existence of several models of the myolamellar structure of the ventricular myocardium, which currently has a number of contradictory provisions, reflects the need for a reasonable integration of the results of different methods. Under these circumstances, the study of those ontogenetic mechanisms that are responsible for the formation and development of the myolamellar architecture of the myocardium is of great interest. The purpose of the study is to determine the ontogenetic transformations of the embryonic chicken heart that ensure the formation and development of the myolamellar structure of the ventricular myocardium. Methods. The work examined the embryos of Cobb500 cross chickens from the beginning of the 10th day to the 21st day of incubation. The lamellar organization of the ventricular myocardium was studied using light and transmission electron microscopy. Results. Starting from the 36th stage according to NN (the beginning of the 10th day of incubation), the active development of the stromal component was observed in the heart of chicken embryos, which led to the division of the tissue of the compact ventricular myocardium into groups of muscle fibers in the form of narrow elongated flat plates containing thicker than 3 to 5 rows of cardiomyocytes. At the 41st and 43rd stages of development, active development of the intercellular matrix and division of the myocardium mass into muscle plates continued as part of the compact ventricular myocardium. The intercellular spaces within the plates narrowed, and between the myolamellae, the perimysium accumulated elements of the microcirculatory bed, functionally active fibroblasts, a large amount of amorphous substance, and bundles of formed collagen fibers. At the final stages of embryogenesis, the muscle plates of the left ventricle acquired a pronounced spiral orientation with a gradual displacement of the long axis of the muscle fibers in the direction from the apex of the ventricle to its base. In the wall of the right ventricle, the location of the myolamella acquired a transverse oblique-circular orientation. Conclusion. A comparison of the structure and geometry of the myolamella made it possible to reveal that starting from the 38th stage of development in the left ventricle, the conditions for the translational-rotational mechanism of chamber contraction were formed and increased, in which the formation of the difference between the systolic and diastolic volumes of the left ventricle is ensured not only by the longitudinal apico-basal vector compression of the cavity, but also by mutual sliding of spirally oriented plates in the ventricular wall. In right ventricle, the contraction mechanism is based on the longitudinal-circular compression of the chamber in accordance with the oblique-circular orientation of the muscle fibers in the composition of the myolamella without displacement in the state of systole.

References

  1. Zhou J, Shu Y, Lü S. The spatiotemporal development of intercalated disk in three-dimensional engineered heart tissues based on collagen/matrigel matrix. PLoS One. 2013;8(11):814-20.
  2. Kocica MJ, Corno AF, Carreras-Costa F. Helical ventricular myocardial band: global, three-dimensional, functional architecture of the ventricular myocardium. The Eur. J. Cardiothorac Surg. 2006;29:21-40.
  3. Gilbert SH, Benson AP, Li P. Localisation of left ventricular sheet structure: integration with current models of cardiac fibre, sheet and band structure. Regional Eur. J. Cardiothorac Surg. 2007;32:231-49.
  4. Arts T, Costa KD, Covell JW, McCulloch AD. Relating myocardial laminar architecture to shear strain and muscle fiber orientation. Am. J. Physiol. Heart. Circ. Physiol. 2001;280:2222-9.
  5. Ewald AJ, McBride H, Reddington M. Imaging microscopy, an automated method for visualizing whole embryo samples in three dimensions at high resolution. Dev. Dyn. 2002;12:369–75.
  6. Helm PA, Younes L, Beg MF et al. Evidence of structural remodeling in the dyssynchronous failing heart. Circ. Res. 2006;98:125-32.
  7. Tseng WY, Wedeen VJ, Reese TG. Diffusion tensor MRI of myocardial fibers and sheets: correspondence with visible cut-face texture. J. Magn. Reson. Imaging. 2003;17:31-42.
  8. Buckberg GD. Stonehenge and the heart: similar construction. Eur. J. Cardiothorac. Surg. 2006;29:286-90.
  9. Kresh JY, Chopra A. Intercellular and extracellular mechanotransduction in cardiac myocytes. Pflugers Arch. 2011;462(1):75-87.
  10. Chen J, Liu W, Zhang H. Regional ventricular wall thickening reflects changes in cardiac fiber and sheet structure during contraction: quantification with diffusion tensor MRI. Am. J. Physiol. Heart. Circ. Physiol. 2005;289:1898-907.
  11. Harrington KB, Rodriguez F, Cheng A. Direct measurement of transmural laminar architecture in the anterolateral wall of the ovine left ventricle: new implications for wall thickening mechanics. Am. J. Physiol. Heart Circ. Physiol. 2005;288:1324-30.
  12. Martinsen BJ. Reference guide to the stages of chick heart embryology. Dev. Dyn. 2005;233:1217–37.
  13. Rijcken J, Bovendeerd P, Schoofs A. Optimization of cardiac fiber orientation for homogeneous fiber strain during ejection. Ann. Biomed. Eng. 1999;27:289–97.
  14. Dokos S, Smaill BH, Young AA, LeGrice IJ. Shear properties of passive ventricular myocardium. Am. J. Physiol. Heart Circ. Physiol. 2002;283:2650-9.
  15. Chen J, Song SK, Liu W. Remodeling of cardiac fiber structure after infarction in rats quantified with diffusion tensor MRI. Am. J. Physiol. Heart Circ. Physiol. 2003;285:946-54.
  16. LeGrice IJ, Hunter PJ, Smaill BH. Laminar structure of the heart: a mathematical model. Am. J. Physiol. 1997;272:2466-76.
  17. Hamburger V. A series of normal stages in the development of the chick embryo. J. Morphol. 1951;88(1):49-92.
  18. Kuo J. Electron microscopy: methods and protocols. Totowa, New Jersey : Humana Press Inc; 2007. 608 p.
  19. Tverdokhlib IV, Petruk NS, Ivanchenko MV, Silkina JuV, Khripkov IS, Pertseva NO, Shevchenko KM, Goodlett TO, Malkov II, Berehovenko IM, Zinenko DYu, Galaida NO, Varin VV, inventors; State Institution «Dnipropetrovsk medical academy of the Health Ministry of Ukraine». Method of determining the coordinates of ultrastructures in transmission electron microscopy of biological objects. Ukrainian patent UA 83611. 2013 Sep 25. Int. CI. G01N 1/28. Ukrainian.
  20. European convention for the protection of vertebrate animals used for experimental and other scientific purposes. Strasbourg: Council of Europe. 18 Mar 1986. 53 p.

Published

2024-04-01

How to Cite

Bumeister, V., & Dudok, O. (2024). Formation and development of lamellar histoarchitecture of the ventricular myocardium of chick embryos. Морфологія / Morphologia / Morfologìâ, 18(1), 26–31. https://doi.org/10.26641/1997-9665.2024.1.26-31

Issue

Section

Статті