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    І.V. Dzevulska, О.І. Kovalchuk, E.V. Cherkasov, О.Ye. Majewskyi, Yu.G. Shevchuk, V.A. Pastukhova, T.M. Kyselova

    INFLUENCE OF LACTOPROTEINUM SOLUTION WITH SORBITOL ON DNA CONTENT OF CELLS OF ENDOCRINE GLANDS ON THE BACKGROUND OF SKIN BURN IN RATS


    About the author: І.V. Dzevulska, О.І. Kovalchuk, E.V. Cherkasov, О.Ye. Majewskyi, Yu.G. Shevchuk, V.A. Pastukhova, T.M. Kyselova
    Heading CLINICAL MEDICINE
    Type of article Scentific article
    Annotation Damage to the endocrine glands is one of the key pathogenetic factors in skin burns, but intracellular mechanisms of the effect of burn disease and its therapy on these organs continue to be poorly understood. The article presents the results of the study of DNA content in adenohypophysis, adrenal and thymus cells of rats by flowing DNA-cytometry against the background of thermal skin burn and correction of it with solutions of 0.9% NaCl or Lactoproteinum with sorbitol. The study was performed 1, 3, 7, 14, 21 and 30 days after the thermal burn of 2-3 degrees of 21-23% of the body surface and its correction. The statistical processing of the obtained results was carried out in the license package "STATISTICA 6.1" using nonparametric estimation methods. Against the backdrop of applying 0.9% NaCl solution in adenohypophysis cells, occurs a significant decrease in the parameters of the synthetic S-phase (the percentage ratio of the DNA synthesis phase to all cells of the cell cycle) already from 1 day of the experiment, which were restored to the control level only 21 days after the skin burn. The index of the interval SUB-G0G1 (DNA fragmentation index) against the background of applying 0.9% NaCl solution increased significantly from 3 days, and the decrease in the indicator in adenohypophysis cells was observed from the 14th day of the study. In adrenal cells, a significant increase in the S-phase index was observed with a 0.9% NaCl solution correction followed by a decrease from the 3 days of the experiment, and the SUB-G0G1 interval also increased from 1 day, followed by a decrease in this index. Against the background of correction with 0.9% NaCl solution, a significant decrease in the S-phase index of thymus cells was observed 1 day after the skin burn, and on the 3 day there was an increase in this index with its normalization after 14 days from the beginning of the experiment. The parameters of the SUB-G0G1 interval of thymus cells were elevated from 1 day, but after 7 days did not differ from those of the control group. With the use of a solution of Lactoproteinum with sorbitol, the amplitude of the S-phase and the SUB-G0G1 interval of adenohypophysis, adrenal and thymus cells decreased, indicating a cytoprotective effect of this drug. It was concluded that correcting by the 0.9% NaCl solution not sufficiently compensated the DNA damage of the endocrine glands after thermal skin burn, and the use of Lactoproteinum with sorbitol significantly improves the studied DNA content in these organs.
    Tags DNA-cytometry, thermal damage to the skin of rats, adenohypophysis, adrenal glands, thymus, Lactoproteinum with sorbitol; 0.9% NaCl solution
    Bibliography
    • Kozynets H.P., Osadcha O.I., Boiarska H.M., Kalashnykov V.V. Klinichna efektyvnistʹ preparatu laktoproteyinu sorbitolom u patsiyentiv z hlybokymy ta tryvalymy opikamy [Clinical efficacy of preparation lactoprotein with sorbitol in patients with deep and extended burns]. Klin. Khir., 2008; 9: 31–33. [in Ukrainian]
    • Stefanov O.V. Doklinichni doslidzhennya likarskykh zasobiv. Metodychni rekomendatsiyi [Preclinical studies of medicinal products. Guidelines]. 2001, Avicenna, Kiev. [in Ukrainian]
    • Archana M., Bastian, Yogesh T.L., Kumaraswamy K.L. Various methods available for detection of apoptotic cells – a review. Indian Journal of Cancer, 2013; 50(3): 274–283.
    • Auron M. & Raissouni N. Adrenal insufficiency. Pediatr Rev., 2015; 36(3): 92–102.
    • Bjornson Z.B., Nolan G.P., Fantl W.J. Single Cell Mass Cytometry for Analysis of Immune System Functional States. Current Opinion in Immunology, 2013; 25(4): 10.1016/j.coi.2013.07.004.
    • Blaisdell L.L, Chace R., Hallagan L.D., Clark D.E.J. A half-century of burn epidemiology and burn care in a rural state. Burn Care Res., 2012; 33(3): 347–353.
    • Fan J., Wu J., Wu L.D., Li G.P., Xiong M., Chen X., Meng Q.Y. Effect of parenteral glutamine supplementation combined with enteral nutrition on Hsp90 expression and lymphoid organ apoptosis in severely burned rats. Burns, 2016; 42(7): 1494–1506.
    • Fuzaylov G., Anderson R., Knittel J., Driscoll D.N. Global health: burn outreach program. J. Burn Care Res., 2015; 36(2): 306–309.
    • Fuzaylov G., Murthy S., Dunaev A., Savchyn V., Knittel J., Zabolotina O., Dylewski M.L., Driscoll D.N. Improving burn care and preventing burns by establishing a burn database in Ukraine. Burns, 2014; 40(5): 1007–1012.
    • Gamelli L., Mykychack I., Kushnir A., Driscoll D.N., Fuzaylov G. Targeting burn prevention in Ukraine: evaluation of base knowledge in burn prevention and first aid treatment. G. J. Burn Care Res., 2015; 36(1): 225–231.
    • Graves K.K., Faraklas I., Cochran A. Identification of risk factors associated with critical illness related corticosteroid insufficiency in burn patients. J. Burn Care Res., 2012; 33(3): 330–335.
    • Gunas I., Dovgan I., Masur O. Method of thermal burn trauma correction by means of cryoinfluence. Verhandlungen der Anatomischen Gesellschaft, zusammen mit der Polish Anatomical Society with the participation of the Association des Anatomistes, Olsztyn 24-27. Mai, 1997. Bestell-Nr.: 258655
    • Johnson B.L., Rice T.C., Xia B.T., Boone K.I., Green E.A., Gulbins E., Caldwell C.C. Amitriptyline usage exacerbates the immune suppression following burn injury. Shock (Augusta, Ga.), 2016; 46(5): 541–548.
    • Kawase T., Hayama K., Tsuchimochi M., Nagata M., Okuda K., Yoshie H., Burns D.M., Nakata K. Evaluating the safety of somatic periosteal cells by flow-cytometric analysis monitoring the history of DNA damage. Biopreserv Biobank, 2016; 14: 129–137.
    • Lee K.H., Lim D., Green T., Greenhalgh D., Cho K. Injury-elicited stressors alter endogenous retrovirus expression in lymphocytes depending on cell type and source lymphoid organ. BMC Immunology, 2013; 14: 2.
    • Lee M.O. Determination of the surface area of the white rat with its application to the expression of metabolic results. Am. J. Physiol., 1989; 24: 1223.
    • Mosier M.J., Lasinski A.M., Gamelli R.L. Suspected adrenal insufficiency in critically ill burned patients: etomidate-induced or critical illness-related corticosteroid insufficiency? – A review of the literature. J. Burn Care Res., 2015; 36(2): 272–278.
    • Osterbur K., Mann F.A., Kuroki K., DeClue A. Multiple Organ Dysfunction Syndrome in Humans and Animals. Journal of Veterinary Internal Medicine, 2014; 28(4): 1141–1151. http://doi.org/10.1111/jvim.12364
    • Rani M. & Schwacha M.G. The composition of T-cell subsets are altered in the burn wound early after injury. PLoS ONE, 2017; 12(6): e0179015.
    • Regas F.C. & Ehrlich H.P. Elucidating the vascular response to burns with a new rat model. J. Trauma, 1992; 32(5): 557–563.
    • Rice T.C., Armocida S.M., Kuethe J.W., Midura E.F., Jain A., Hildeman D.A., Healy D.P., Gulbins E., Caldwell C.C. Burn injury influences the T cell homeostasis in a butyrate-acid sphingomyelinase dependent manner. Cell Immunol., 2017; 313: 25–31.
    • Rojas Y., Finnerty C.C., Radhakrishnan R.S., Herndon D.N. Burns: an update on current pharmacotherapy. Expert Opinion on Pharmacotherapy, 2012; 13(17): 2485–2494.
    • Toussaint J. & Singer A.J. The evaluation and management of thermal injuries: 2014 update. Clinical and Experimental Emergency Medicine, 2014; 1(1): 8–18.
    • Venet F., Plassais J., Textoris J., Cazalis M.A., Pachot A., Bertin-Maghit M., Tissot S. Low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial. Critical Care, 2015; 19(1): 21.
    • Vivó C., Galeiras R., del Caz M.D. Initial evaluation and management of the critical burn patient. Med. Intensiva, 2016; 40(1): 49–59.
    • Yamamoto Y., Enkhbaatar P., Sakurai H., Rehberg S., Asmussen S., Ito H., Traber D.L. Development of a long-term ovine model of cutaneous burn and smoke inhalation injury and the effects of early excision and skin autografting. Burns : Journal of the International Society for Burn Injuries, 2012; 38(6): 10.1016/j.burns.2012.01.003.
    • Zhu X.M., Dong N., Wang Y.B., Zhang Q.H., Yu Y., Yao Y.M., Liang H.P. The involvement of endoplasmic reticulum stress response in immune dysfunction of dendritic cells after severe thermal injury in mice. Oncotarget, 2017; 8(6): 9035–9052.
    Publication of the article «World of Medicine and Biology» №2(64), 2018 year, 033-039 pages, index UDK 611.43/47-018.1:577.213-06:616.5-001.17]:615.384-092.9
    DOI 10.26724/2079-8334-2018-2-64-33-39