RUDN Medical Institute – One more step on the way to fighting cardiologic diseases

The study was carried out on male Chinchilla rabbits (3-3.5 kg) distributed into 4 groups, 4 per group: control (intact animals) and 3 experimental (rabbits with acute LV overload after 1, 3, and 5 days).

The animals were kept and handled in accordance with the Order No. 755 of the Ministry of Health of the USSR (August 12, 1977), and the European Convention for protection of Vertebrates Used in Experiments or with Other Research Purposes (Strasbourg, 1986). Pressure overload of LV was created surgically by narrowing grid. The proportion of equally distant points occupied by positively stained cardiomyocyte cytoplasm to the total count of points occupied by the cytoplasm was calculated.

Morphometric analysis of the myocardium was performed on histological sections stained with he- matoxylin and eosin. The content (vol%) of muscular fiber, cardiomyocyte nuclei, foci of destruction and infiltration, and volume of extracellular space were measured under a microscope at ×400 in 30 visual fields using Avtandilov grid. The nucleus/cytoplasm ratio, i.e. the ratio of cardiomyocyte nuclei to muscular fiber was calculated (in %).

Our previous study of LV cardiomyocyte apoptosis on an identical experimental model showed an increase in activities of effector caspase-3 and initiatory caspase-8 mediating realization of apoptotic cell death by the external pathway [2]. The decrease in Bax protein expression detected in the present study indicated that initiation of apoptotic processes in LV cardiomyocytes in acute LV overload did not depend on the mitochondrial pathway and was caused mainly by the receptor-mediated signal mechanisms.

Hence, acute LV pressure overload is associated with lesser Bax expression protein in LV cardiomyocytes combined with manifest morphological changes in the myocardium most pronounced on day 5 of the process.