Abstract

Vessels of the microcirculatory bed ensure the full trophism of the body at the level of capillary-tissue relations and are the first to respond to various functional and pathological conditions of organs. At the same time, morphological changes in prostate microvasculature with age under conditions of prolonged ethanol poisoning have been understudied. The purpose of this study was to determine the age-related remodelling of the prostate vessels of the microcirculatory bed in case of prolonged alcohol intoxication. Injection, histological, morphometric, and statistical methods were used. The microvasculature of the prostate gland of 80 sexually mature white male rats of different ages was studied, 40 animals served as controls, and 40 rats were injected daily for 28 days with a 30% ethanol solution at a dose of 20 ml/kg intragastrically. Morphometric analysis indicated that chronic ethanol poisoning in white rats significantly reduces the lumens of arterial microvessels and hemocapillaries, while expanding the venous vessels in the microcirculatory bed of the prostate gland. When venous congestion occurs, the density of microvessels decreases, and microcirculation bed is disturbed. This disruption is accompanied by atrophic, dystrophic, and necrobiotic changes in endotheliocytes, epithelial cells, muscle cells, stromal structures, infiltration, and sclerosing. Intragastric 28-day administration of a 30% ethanol solution at a dose of 20 ml/kg to laboratory mature white male rats leads to pronounced structural changes in the microvasculature of the prostate microcirculatory bed: constriction of arterioles, precapillary arterioles and hemocapillaries, dilation of the capillary venules and venules, which is complicated by significant venous haemorrhage, development of atrophy, dystrophy, necrosis of vascular endothelial cells, glandular epithelial cells, muscle cells, connective tissue structures, cellular infiltration, and sclerosis. Vessels of the microcirculatory bed play a leading role in ethanol-induced damage of prostate structures, which dominate in 24-month-old experimental animals

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