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DYNAMICS OF BODY AND HEART WEIGHTS IN THE RATS AFTER АNTENATAL ANTIGEN INFLUENCE Lebedinets A. N., Voloshin N. A., ReznichenkoYu.G. Zaporozhye State Medical University, Ukraine Abstract Rationale There is a high prevalence of pathological pregnancy, intrauterine infections of different etiology, accompanied by dysfunction of the placenta and the penetration of foreign antigens to the fetus in the last decade. Pathology of the antenatal period has negative health consequences over lifetime. Cardiovascular pathology may be formed on the background of the heart morphogenesis disturbances during fetal development. Intrauterine administration of antigens in experiment causes acceleration of immunologically immature lymphocytes migration from the thymus to the internal organs. These lymphocytes affect the formation of morphological and functional units of the internal organs. Features of the morphogenesis of heart after antenatal antigens exposure not studied. Objective Determine the dynamics of the body and heart weights and their ratio in experimental animals (rats) after antenatal antigens exposure. Research design and Methods Experimental study of the heart morphogenesis in rats of Wistar line after intrauterine injection of antigens at 18 days of pregnancy by the method of Voloshin N.A. has performed. The dynamics of the body and heart weights in the rats of six age groups (1, 7, 14, 30, 45 and 60 days of postnatal period of ontogenesis) have investigated. Animals were divided in 4 groups: I - intact group, II - intrauterine injection of Human Immunoglobulin for intramuscular administration, III - intrauterine injection of Influenza Vaccine (split virion, inactivated) VAXIGRIP, IV - intrauterine injection of Sodium Chloride solution 0.9% (control group). Ratio of weight to length of the body was calculated. Relative heart weight was determined by the formula: heart weight x 100, mg / body weight, mg. Results Increased body weight in animals of II and III groups compared with body weight of intact (I) and control (IV) groups in all terms of postnatal period of ontogenesis from the first day of life have noted. From 14 to 60 days increased body weight in animals of groups II and III was significant as compared with indexes of groups I and IV. There were no significant changes in the length of the body in different groups of animals throughout the period of postnatal development. Ratio of the weight and length of the body in the neonatal period and at 14, 30, 45 and 60 days were significantly higher in animals of groups II and III in comparison with indexes of intact and control groups. In intact and control animals groups were not detected significant differences in body weight and length in any terms of postnatal period of ontogenesis that excluded the impact of surgical intervention on the dynamics of the body weight and length. The absolute heart weight had no significant differences in the animals of different groups from 1 to 60 days of postnatal period, except for 7 days. The relative heart weight of animals groups II and III was significantly lower than both the intact and control groups indexes from 7 days of life for all age groups up to 60 days. Conclusions Disproportion in development of rats hearts in experiment with significant reduction of its relative weight at the period from 7 to 60 days of life on the background trend in early terms and significant from 14 to 60 days of postnatal development overweight of experimental animals have established. Detected changes do not depend on the nature of the antigen and demonstrate the heart morphofunctional disorders after antenatal antigens exposure. These features indicate changes of the heart morphogenesis after an antenatal antigen influence that may have essential contribution in the formation of cardiovascular diseases of children. Further efforts should be directed to the study of the features of cardiovascular system disorders in infants with antenatal antigen influence of foreign antigens. Keywords: heart morphogenesis, rats, body weight, heart weight, antenatal antigens exposure.