Dynamics of morphometric parameters and the glycogen content in rat hearts after аntenatal antigen influence
DOI:
https://doi.org/10.14739/2310-1237.2013.1.15314Keywords:
heart morphogenesis, glycogen, rats, body weight, antenatal influence of antigensAbstract
Cardiovascular pathology may be formed on the background of the heart morphogenesis disturbances during fetal development. 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 into the fetus in the last decade. Pathology of the antenatal period has negative health consequences over lifetime. 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 have not been studied.
Objective To determine the dynamics of body weight, heart weight and their ratio and glycogen content in cardiomyocytes 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 been 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) has been 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 VAXIGRIP, IV - intrauterine injection of Sodium Chloride solution 0.9% (control group). Relative heart weight was calculated as heart weight x100, mg / body weight, mg. The histochemical PAS diastase staining of heart sections has been investigated for the differentiation of glycogen and other glycoproteins in the rats of three age groups (1, 7 and 60 days of postnatal period). The histochemical index of the glycogen content in cardiomyocytes was determined by the method of Kaplow L.S.
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 has been noted. From 14 to 60 days increased body weight of animals of groups II and III was significant as compared with indexes of groups I and IV. Significant differences in body weight in any terms of postnatal period of ontogenesis in intact and control animals groups were not detected. The absolute heart weight had no significant differences in the animals of different groups from 1 to 60 days of postnatal period, except group 7 days. The relative heart weight of animals of 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. The downward trend at neonatal period and the significant increasing at the age of 60 days of postnatal development of glycogen content in cardiomyocytes of II and III groups animals compared with intact (I) and control (IV) groups indexes have been established.
Conclusions Disproportion in development of rat hearts in experiment with a significant reduction of its relative weight at the period from 7 days of life on the background trend in early terms and significant from 30 to 60 days overweight of experimental animals, significant increasing of glycogen content in cardiomyocytes at the age of 60 days of postnatal development have been established. Revealed changes do not depend on the nature of the antigen and demonstrate the heart morphofunctional disorders in rats with antenatal antigens exposure.
References
Бережний В.В. Стан надання кардіоревматологічної допомоги дітям України (за матеріалами діяльності кардіоревматологічної служби у 2009 році) / В.В. Бережний, Т.В. Марушко, І.В. Романкевич // Современная педиатрия. – 2010. – №5 (33). – С. 15–17.
Моніторинг здоров'я дітей як визначальна складова в забезпеченні здоров'я людини / О.М. Лук'янова, Ю.Г. Антипкін, В.Г. Майданник, Л.І. Омельченко // Педіатрія, акушерство та гінекологія. – 2008. – №4. – С. 6.
Марковский В.Д. Патологическая анатомия сердца при задержке внутриутробного развития / В.Д. Марковский, В.В. Гаргин, М.С. Мирошниченко – Харьков: «Финарт», 2010. – 158 с.
Внутрішньоутробні інфекції. Епідеміологія, клініка, діагностика та сучасні принципи терапії у вагітних жінок та дітей / Ю.П. Ткаченко, Г.О. Леженко, Ю.Г. Резніченко, Г.І. Резніченко. – 2-е вид., доп. та переробл. – Донецьк: Видавець Заславський О.Ю., 2012. –144 с.
Barker D.J.P. Fetal programming of coronary heart disease / Barker D.J.P. // Trends Endocrinology Metabol. – 2002. – №9. – P. 364–368.
Godfrey K.M. Developmental origins of metabolic disease: life course and intergenerational perspectives / K.M. Godfrey, P.D. Gluckman, M.A. Hanson // Trends in Endocrinology & Metabolism. – 2010. – Vol. 21. – P. 199–205.
Екосистема великого промислового міста України та діти першого року життя / [О.М. Лук’янова, Ю.Г. Резніченко, Ю.Г. Антипкін, Г.І. Резніченко, З.А. Шкіряк-Нижник] – Запоріжжя, 2005. – 254 с.
Шабалов Н.П. Общебиологическая проблема: закономерности и последствия перинатального инфицирования человека / Н.П. Шабалов // Педиатрия. – 2012. – №91 (3). – С. 26–31.
Волошин Н.А. Лимфоцит – фактор морфогенеза / Н.А. Волошин // Запорожский медицинский журнал. – 2005. – №3 (30). – С. 122.
Волошин Н.А. Внутриутробная антигенная стимуляция как модель для изучения морфогенеза органов. / Волошин Н.А., Григорьева Е.А., Кущ О.Г. и др. // Морфологические ведомости. – 2006. – № 1–2, приложение №1. – С.57–59.
Kaplow L.S. Histochemical procedure for localizing and evaluationg leukocyte alcaline phosphatase activity marrow / L. S. Kaplow // Blood. – 1955. – Vol. 10.–P. 1023 – 1029.
Западнюк И.П. Лабораторные животные. Разведение, содержание, использование в эксперименте / И.П. Западнюк, В.И. Западнюк, Е.А. Захария, Б.В. Западнюк – К.: Вища школа, 1983. – 384 с.
Rat’s age versus human’s age: what is the relationship? / Andreollo N.A., Santos E.F., Araújo M.R., Lopes L.R. // Arq. Bras. Cir. Dig. – 2012. – №25 (1). – Р. 49–51.
Перфилова В.Н. Влияние соединения РГПУ-147 на морфофункциональное состояние миокарда животных после длительного стрессорного воздействия / В.Н. Перфилова, И.Н. Тюренков, А.В. Смирнов // Бюллетень Волгоградского научного центра РАМН. – 2010. – №4. – С. 45–49.
Cardiac glycogen accumulation after dexamethasone is regulated by AMPK / Puthanveetil, F. Wang, G. Kewalramani et al. // Am J Physiol Heart Circ Physiol. – 2008. – Vol. 295, №4. – P. 1753–1762.
Omar M.A. Ischemia-induced activation of AMPK does not increase glucose uptake in glycogen-replete isolated working rat hearts / M.A.Omar, H. Fraser, A.S. Clanachan // Am J Physiol Heart Circ Physiol. – 2008. – №294.– Р. 1266–1273.
Абатуров А.Е. Особенности метаболического синдрома у детей / А.Е. Абатуров // Дитячий лікар. – 2011. – №4. – С. 54–61.
Downloads
How to Cite
Issue
Section
License
Authors who publish with this journal agree to the following terms:- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (SeeThe Effect of Open Access).