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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">sechenov</journal-id><journal-title-group><journal-title xml:lang="en">Sechenov Medical Journal</journal-title><trans-title-group xml:lang="ru"><trans-title>Сеченовский вестник</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2218-7332</issn><issn pub-type="epub">2658-3348</issn><publisher><publisher-name>Сеченовский Университет</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.47093/2218-7332.2020.11.3.47-56</article-id><article-id custom-type="elpub" pub-id-type="custom">sechenov-222</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>PATHOLOGICAL PHYSIOLOGY</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ПАТОЛОГИЧЕСКАЯ ФИЗИОЛОГИЯ</subject></subj-group></article-categories><title-group><article-title>VEGF-C — a biomarker of renal injury in the experimental model of intra-abdominal hypertension</article-title><trans-title-group xml:lang="ru"><trans-title>VEGF-C — биомаркер повреждения почек при экспериментальной интраабдоминальной гипертензии</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1833-3028</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Яковлев</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Iakovlev</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Яковлев Владислав Вячеславович, аспирант кафедры патофизиологии</p><p>ул. Трубецкая, д. 8, стр. 2, г. Москва, 119991</p><p>+7 (926) 761-20-68</p></bio><bio xml:lang="en"><p>Vladislav V. Iakovlev, Postgraduate, Pathophysiology Department </p><p>8/2, Trubetskaya str., Moscow, 119991</p><p>8 (926) 761-20-68 </p></bio><email xlink:type="simple">vladislav.iak@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9870-4414</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бадаева</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Badaeva</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бадаева Анастасия Викторовна, студентка</p><p>ул. Трубецкая, д. 8, стр. 2, г. Москва, 119991</p></bio><bio xml:lang="en"><p>Anastasiia V. Badaeva, student </p><p>8/2, Trubetskaya str., Moscow, 119991</p></bio><email xlink:type="simple">nastyabadaeva1507@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-5601-0465</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Иванова</surname><given-names>Е. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Ivanova</surname><given-names>E. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Иванова Елена Ильинична, врач-патологоанатом</p><p>пер. Абрикосовский, д. 2, ГСП-1, г. Москва, 119991</p></bio><bio xml:lang="en"><p>Elena I. Ivanova, pathologist </p><p>2, Abrikosovsky lane, GSP-1, Moscow, 119991</p></bio><email xlink:type="simple">ellen151@rambler.ru</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2422-3463</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Севергина</surname><given-names>Л. О.</given-names></name><name name-style="western" xml:lang="en"><surname>Severgina</surname><given-names>L. O.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Севергина Любовь Олеговна, д-р мед. наук, врачпатологоанатом, профессор кафедры патологической анатомии им. А.И. Струкова</p><p>ул. Трубецкая, д. 8, стр. 2, г. Москва, 119991</p></bio><bio xml:lang="en"><p>Lyubov O. Severgina, Dr. of Sci. (Medicine), pathologist, Professor, Department of Pathological Anatomy named after A.I. Strukov </p><p>8/2, Trubetskaya str., Moscow, 119991</p></bio><email xlink:type="simple">losevergina@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4380-4522</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Мальцева</surname><given-names>Л. Д.</given-names></name><name name-style="western" xml:lang="en"><surname>Maltseva</surname><given-names>L. D.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Мальцева Лариса Дмитриевна, канд. мед. наук, доцент кафедры патофизиологии</p><p>ул. Трубецкая, д. 8, стр. 2, г. Москва, 119991</p></bio><bio xml:lang="en"><p>Larisa D. Maltseva, Cand. of Sci. (Medicine), Associate Professor, Pathophysiology Department </p><p>8/2, Trubetskaya str., Moscow, 119991</p></bio><email xlink:type="simple">lamapost@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2453-1319</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Морозова</surname><given-names>О. Л.</given-names></name><name name-style="western" xml:lang="en"><surname>Morozova</surname><given-names>O. L.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Морозова Ольга Леонидовна, д-р мед. наук, профессор кафедры патофизиологии</p><p>ул. Трубецкая, д. 8, стр. 2, г. Москва, 119991</p></bio><bio xml:lang="en"><p>Olga L. Morozova, Dr. of Sci. (Medicine), Professor, Pathophysiology Department </p><p>8/2, Trubetskaya str., Moscow, 119991</p></bio><email xlink:type="simple">morozova_ol@list.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГАОУ ВО «Первый Московский государственный медицинский университет им. И.М. Сеченова» Минздрава России (Сеченовский Университет)</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Sechenov First Moscow State Medical University (Sechenov University)</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ФГБНУ «Российский научный центр хирургии им. академика Б.В. Петровского»</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Petrovsky National Research Centre of Surgery</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2020</year></pub-date><pub-date pub-type="epub"><day>25</day><month>11</month><year>2020</year></pub-date><volume>11</volume><issue>3</issue><fpage>47</fpage><lpage>56</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Iakovlev V.V., Badaeva A.V., Ivanova E.I., Severgina L.O., Maltseva L.D., Morozova O.L., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Яковлев В.В., Бадаева А.В., Иванова Е.И., Севергина Л.О., Мальцева Л.Д., Морозова О.Л.</copyright-holder><copyright-holder xml:lang="en">Iakovlev V.V., Badaeva A.V., Ivanova E.I., Severgina L.O., Maltseva L.D., Morozova O.L.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.sechenovmedj.com/jour/article/view/222">https://www.sechenovmedj.com/jour/article/view/222</self-uri><abstract><p>Lymphangiogenesis plays an important role in development of renal parenchyma inflammation during kidney injury. Vascular endothelial growth factor type C (VEGF-C), cytokine that regulates lymphangiogenesis, is a potential early biomarker for acute kidney injury. Aim. To study the concentration of VEGF-C in renal homogenate and blood serum of newborn rats with experimental intraabdominal hypertension (IAH) of varying severity and duration, to establish a relationship with morphological changes in the renal tissue. Materials and methods. The experiment was conducted on 50 newborn Wistar rats. Rats were divided into 5 groups of 10 rats each: groups 1 and 2 with mild IAH lasting 5 and 10 days, respectively, and groups 3 and 4 with severe IAH lasting 5 and 10 days, respectively, and the control group. IAH was modelled by injecting sterile vaseline into the abdominal cavity to a predetermined level of IAH under the control of intra-vesical manometry. VEGF-C content was measured by ELISA. Morphological examination of the biopsy material and its photography were carried out using a Leica DM2000 microscope. The Mann—Whitney, Kruskal—Wallis, Wilcoxon tests, as well as one-way ANOVA, were used for statistical analysis. Results. The level of VEGF-C in the renal homogenate was increased in all groups (pc &lt; 0.001); the degree of VEGF-C increase depended on the severity of IAH (p &lt; 0.05) but not on the duration of IAH exposure. The VEGF-C blood serum level was increased only in group 3 (pc = 0.011). Morphological analysis showed hydropic dystrophy: changes in the height of the tubular epithelium, an increase in interstitial edema, expansion of the urinary spaces of glomeruli. The degree of morphological changes depended on the severity and duration of IAH. Conclusion. Changes in VEGF-C level assessed in the renal homogenate correlated with morphological changes in renal tissue of rats with different severity and duration of IAH.</p></abstract><trans-abstract xml:lang="ru"><p>Лимфангиогенез играет важную роль в развитии воспаления паренхимы почек при их повреждении. Васкулоэндотелиальный фактор роста тип С (vascular endothelial growth factor, VEGF-C) — цитокин, регулирующий лимфангиогенез, — является потенциальным ранним биомаркером острого повреждения почек.Цель. Изучить содержание VEGF-C в почечном гомогенате и сыворотке крови новорожденных крыс с экспериментальной интраабдоминальной гипертензией (ИАГ) различной тяжести и длительности, установить взаимосвязь с морфологическими изменениями в паренхиме почек.Материалы и методы. Эксперимент проведен на 50 новорожденных крысах линии Wistar, которые были разделены на 5 групп по 10 особей: группы 1 и 2 с легкой ИАГ длительностью 5 и 10 дней соответственно, группы 3 и 4 с тяжелой ИАГ длительностью 5 и 10 дней соответственно и 5-я контрольная группа. ИАГ достигалась введением стерильного вазелина в брюшную полость до заданного уровня интраабдоминального давления под контролем интравезикальной манометрии. Содержание VEGF-C измерялось методом ELISA. Морфологическое исследование биопсийного материала и его фотосъемка осуществлялись на микроскопе Leica DM2000. Сравнение групп проводилось с помощью критериев Манна — Уитни, Краскела — Уоллиса, Вилкоксона; проводился однофакторный дисперсионный анализ.Результаты. Отмечено увеличение концентрации VEGF-C в почечном гомогенате во всех экспериментальных группах (pк &lt; 0,001). Степень повышения VEGF-C зависела от тяжести ИАГ (p &lt; 0,05), но не от длительности экспозиции ИАГ. Содержание VEGF-C в сыворотке крови было повышено только в 3-й группе (pк = 0,011). При морфологическом исследовании установлены изменения, которые характерны для гидропической дистрофии: изменение высоты канальцевого эпителия, нарастание отека интерстиция, расширение мочевых пространств гломерул. Степень морфологических изменений паренхимы почек зависела от тяжести и длительности ИАГ.Заключение. Наблюдалась взаимосвязь между морфологическими изменениями паренхимы почек при ИАГ различной тяжести и длительности и изменением уровня VEGF-C в почечном гомогенате.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>интраабдоминальная гипертензия</kwd><kwd>повреждение почек</kwd><kwd>лимфангиогенез</kwd><kwd>биомаркер</kwd><kwd>VEGF-C</kwd><kwd>дети</kwd></kwd-group><kwd-group xml:lang="en"><kwd>intra-abdominal hypertension</kwd><kwd>kidney injury</kwd><kwd>lymphangiogenesis</kwd><kwd>biomarker</kwd><kwd>VEGF-C</kwd><kwd>children</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Исследование выполнено при финансовой поддержке Российского фонда фундаментальных исследований (РФФИ) в рамках научного проекта № 20-315-90075.</funding-statement><funding-statement xml:lang="en">The reported study was funded by Russian Foundation for Basic Research (RFBR), project number № 20-315-90075.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Rauniyar K., Jha S.K., Jeltsch M. Biology of Vascular Endothelial Growth Factor C in the Morphogenesis of Lymphatic Vessels. Front Bioeng Biotechnol. 2018; 6: 7. https://doi.org/10.3389/fbioe.2018.00007 PMID: 29484295</mixed-citation><mixed-citation xml:lang="en">Rauniyar K, Jha SK, Jeltsch M. Biology of Vascular Endothelial Growth Factor C in the Morphogenesis of Lymphatic Vessels. Front Bioeng Biotechnol 2018;6. DOI:10.3389/fbioe.2018.00007.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Veikkola T., Jussila L., Makinen T., et al. Signalling via vascular endothelial growth factor receptor-3 is sufficient for lymphangiogenesis in transgenic mice. EMBO J. 2001; 20(6): 1223–31. https://doi.org/10.1093/emboj/20.6.1223 PMID: 11250889</mixed-citation><mixed-citation xml:lang="en">Veikkola T, Jussila L, Makinen T, Karpanen T, Jeltsch M, Petrova TV, et al. Signalling via vascular endothelial growth factor receptor-3 is sufficient for lymphangiogenesis in transgenic mice. EMBO J 2001;20:1223–31. DOI:10.1093/emboj/20.6.1223.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Mäkinen T., Veikkola T., Mustjoki S., et al. Isolated lymphatic endothelial cells transduce growth, survival and migratory signals via the VEGF-C/D receptor VEGFR-3. EMBO J. 2001; 20(17): 4762–73. https://doi.org/10.1093/emboj/20.17.4762 PMID: 11532940</mixed-citation><mixed-citation xml:lang="en">Mäkinen T, Veikkola T, Mustjoki S, Karpanen T, Catimel B, Nice EC, et al. Isolated lymphatic endothelial cells transduce growth, survival and migratory signals via the VEGF-C/D receptor VEGFR-3. EMBO J 2001;20:4762–73. DOI:10.1093/emboj/20.17.4762.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Huggenberger R., Ullmann S., Proulx S.T., et al. Stimulation of lymphangiogenesis via VEGFR-3 inhibits chronic skin inflammation. J Exp Med. 2010; 207(10): 2255–69. https://doi.org/10.1084/jem.20100559 PMID: 20837699</mixed-citation><mixed-citation xml:lang="en">Huggenberger R, Ullmann S, Proulx ST, Pytowski B, Alitalo K, Detmar M. Stimulation of lymphangiogenesis via VEGFR-3 inhibits chronic skin inflammation. J Exp Med 2010;207:2255–69. DOI:10.1084/jem.20100559.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Hamada K., Oike Y., Takakura N., et al. VEGF-C signaling pathways through VEGFR-2 and VEGFR-3 in vasculoangiogenesis and hematopoiesis. Blood. 2000; 96(12): 3793–800. https://doi.org/10.1182/blood.V96.12.3793 PMID: 11090062</mixed-citation><mixed-citation xml:lang="en">Hamada K, Oike Y, Takakura N, Ito Y, Jussila L, Dumont DJ, et al. VEGF-C signaling pathways through VEGFR-2 and VEGFR-3 in vasculoangiogenesis and hematopoiesis. Blood 2000;96:3793–800. DOI:10.1182/blood.V96.12.3793.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Kim H., Kataru R.P., Koh G.Y. Inflammation-associated lymphangiogenesis: a double-edged sword? J Clin Invest. 2014; 124(3): 936–42. https://doi.org/10.1172/JCI71607 PMID: 24590279</mixed-citation><mixed-citation xml:lang="en">Kim H, Kataru RP, Koh GY. Inflammation-associated lymphangiogenesis: a double-edged sword? J Clin Invest 2014;124:936–42. DOI:10.1172/JCI71607.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Onimaru M., Yonemitsu Y., Fujii T., et al. VEGF-C regulates lymphangiogenesis and capillary stability by regulation of PDGF-B. Am J Physiol Heart Circ Physiol. 2009; 297(5): H1685–96. https://doi.org/10.1152/ajpheart.00015.2009 PMID: 19734356</mixed-citation><mixed-citation xml:lang="en">Onimaru M, Yonemitsu Y, Fujii T, Tanii M, Nakano T, Nakagawa K, et al. VEGF-C regulates lymphangiogenesis and capillary stability by regulation of PDGF-B. Am J Physiol Heart Circ Physiol 2009;297:H1685-1696. DOI:10.1152/ajpheart.00015.2009.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Lee A.S., Lee J.E., Jung Y.J., et al. Vascular endothelial growth factor-C and -D are involved in lymphangiogenesis in mouse unilateral ureteral obstruction. Kidney Int. 2013; 83(1): 50–62. https://doi.org/10.1016/j.kint.2017.07.006 PMID: 28938942</mixed-citation><mixed-citation xml:lang="en">Lee AS, Lee JE, Jung YJ, et al. Vascular endothelial growth factor-C and -D are involved in lymphangiogenesis in mouse unilateral ureteral obstruction. Kidney Int. 2013;83:50-62. Kidney Int 2017;92:1018. DOI:10.1016/j.kint.2017.07.006.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Hasegawa S., Nakano T., Torisu K., et al. Vascular endothelial growth factor-C ameliorates renal interstitial fibrosis through lymphangiogenesis in mouse unilateral ureteral obstruction. Lab Invest. 2017; 97(12): 1439–52. https://doi.org/10.1016/j.kint.2017.07.00610.1038/labinvest.2017.77 PMID: 29083411</mixed-citation><mixed-citation xml:lang="en">Hasegawa S, Nakano T, Torisu K, Tsuchimoto A, Eriguchi M, Haruyama N, et al. Vascular endothelial growth factor-C ameliorates renal interstitial fibrosis through lymphangiogenesis in mouse unilateral ureteral obstruction. Lab Invest 2017;97:1439–52. DOI:10.1038/labinvest.2017.77.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Chang X., Yang Q., Zhang C., et al. Roles for VEGF-C/NRP-2 axis in regulating renal tubular epithelial cell survival and autophagy during serum deprivation. Cell Biochem Funct. 2019; 37(4): 290– 300. https://doi.org/10.1002/cbf.3402 PMID: 31211440</mixed-citation><mixed-citation xml:lang="en">Chang X, Yang Q, Zhang C, Zhang Y, Liang X, Liu Y, et al. Roles for VEGF-C/NRP-2 axis in regulating renal tubular epithelial cell survival and autophagy during serum deprivation. Cell Biochem Funct 2019;37:290–300. DOI:10.1002/cbf.3402.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Zarjou A., Black L.M., Bolisetty S., et al. Dynamic signature of lymphangiogenesis during AKI and CKD. Lab Invest. 2019; 99(9): 1376–88. https://doi.org/10.1038/s41374-019-0259-0 PMID: 31019289</mixed-citation><mixed-citation xml:lang="en">Zarjou A, Black LM, Bolisetty S, Traylor AM, Bowhay SA, Zhang M-Z, et al. Dynamic signature of lymphangiogenesis during AKI and CKD. Lab Invest 2019;99:1376–88. DOI:10.1038/s41374-019-0259-0.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Kirkpatrick A.W., Roberts D.J., De Waele J., et al. Intraabdominal hypertension and the abdominal compartment syndrome: updated consensus definitions and clinical practice guidelines from the World Society of the Abdominal Compartment Syndrome. Intensive Care Med. 2013; 39(7): 1190–206. https://doi.org/10.1007/s00134-013-2906-z PMID: 23673399</mixed-citation><mixed-citation xml:lang="en">Kirkpatrick AW, Roberts DJ, De Waele J, Jaeschke R, Malbrain MLNG, De Keulenaer B, et al. Intra-abdominal hypertension and the abdominal compartment syndrome: updated consensus definitions and clinical practice guidelines from the World Society of the Abdominal Compartment Syndrome. Intensive Care Med 2013;39:1190–206. DOI:10.1007/s00134-013-2906-z.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Thabet F.C., Bougmiza I.M., Chehab M.S., et al. Incidence, Risk Factors, and Prognosis of Intra-Abdominal Hypertension in Critically Ill Children: A Prospective Epidemiological Study. J Intensive Care Med. 2016; 31(6): 403–8. https://doi.org/10.1177/0885066615583645 PMID: 25922384</mixed-citation><mixed-citation xml:lang="en">Thabet FC, Bougmiza IM, Chehab MS, Bafaqih HA, AlMohaimeed SA, Malbrain MLNG. Incidence, Risk Factors, and Prognosis of Intra-Abdominal Hypertension in Critically Ill Children: A Prospective Epidemiological Study. J Intensive Care Med 2016;31:403–8. DOI:10.1177/0885066615583645.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Steinau G., Kaussen T., Bolten B., et al. Abdominal compartment syndrome in childhood: diagnostics, therapy and survival rate. Pediatr Surg Int. 2011; 27(4): 399–405. https://doi.org/10.1007/s00383-010-2808-x PMID: 21132501</mixed-citation><mixed-citation xml:lang="en">Steinau G, Kaussen T, Bolten B, Schachtrupp A, Neumann UP, Conze J, et al. Abdominal compartment syndrome in childhood: diagnostics, therapy and survival rate. Pediatric Surgery International 2011;27:399–405. DOI:10.1007/s00383-010-2808-x.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Kaussen T., Steinau G., Srinivasan P., et al. Recognition and management of abdominal compartment syndrome among German pediatric intensivists: results of a national survey. Ann Intensive Care. 2012; 2 Suppl 1(Suppl 1): S8. https://doi.org/10.1186/2110-5820-2-S1-S8 PMID: 22873424</mixed-citation><mixed-citation xml:lang="en">Kaussen T, Steinau G, Srinivasan P, Otto J, Sasse M, Staudt F, et al. Recognition and management of abdominal compartment syndrome among German pediatric intensivists: results of a national survey. Annals of Intensive Care 2012;2:S8. DOI:10.1186/2110-5820-2-S1-S8.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Vidal M.G., Ruiz Weisser J., Gonzalez F., et al. Incidence and clinical effects of intra-abdominal hypertension in critically ill patients. Crit Care Med. 2008; 36(6): 1823–31. https://doi.org10.1097/CCM.0b013e31817c7a4d PMID: 18520642</mixed-citation><mixed-citation xml:lang="en">Vidal MG, Ruiz Weisser J, Gonzalez F, Toro MA, Loudet C, Balasini C, et al. Incidence and clinical effects of intra-abdominal hypertension in critically ill patients. Crit Care Med 2008;36:1823–31. DOI:10.1097/CCM.0b013e31817c7a4d.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">De Waele J., Desender L., De Laet I., et al. Abdominal decompression for abdominal compartment syndrome in critically ill patients: a retrospective study. Acta Clin Belg. 2010; 65(6): 399– 403. https://doi.org/10.1179/acb.2010.65.6.005 PMID: 21268953</mixed-citation><mixed-citation xml:lang="en">De Waele J, Desender L, De Laet I, Ceelen W, Pattyn P, Hoste E. Abdominal decompression for abdominal compartment syndrome in critically ill patients: a retrospective study. Acta Clin Belg 2010;65:399–403. DOI:10.1179/acb.2010.65.6.005.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Carr J.A. Abdominal compartment syndrome: a decade of progress. J Am Coll Surg. 2013; 216(1): 135–46. https://doi.org/10.1016/j.jamcollsurg.2012.09.004 PMID: 23062520</mixed-citation><mixed-citation xml:lang="en">Carr JA. Abdominal compartment syndrome: a decade of progress. J Am Coll Surg 2013;216:135–46. DOI:10.1016/j.jamcollsurg.2012.09.004.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Ejike J.C., Humbert S., Bahjri K., Mathur M. Outcomes of children with abdominal compartment syndrome. Acta Clin Belg. 2007; 62 Suppl 1: 141–8. https://doi.org/10.1179/acb.2007.62. s1.018 PMID: 17469712</mixed-citation><mixed-citation xml:lang="en">Ejike JC, Humbert S, Bahjri K, Mathur M. Outcomes of children with abdominal compartment syndrome. Acta Clin Belg 2007;62 Suppl 1:141–8. DOI:10.1179/acb.2007.62.s1.018.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Pearson E.G., Rollins M.D., Vogler S.A., et al. Decompressive laparotomy for abdominal compartment syndrome in children: before it is too late. J Pediatr Surg. 2010; 45(6): 1324–9. https://doi.org/10.1016/j.jpedsurg.2010.02.107 PMID: 20620339</mixed-citation><mixed-citation xml:lang="en">Pearson EG, Rollins MD, Vogler SA, Mills MK, Lehman EL, Jacques E, et al. Decompressive laparotomy for abdominal compartment syndrome in children: before it is too late. J Pediatr Surg 2010;45:1324–9. DOI:10.1016/j.jpedsurg.2010.02.107.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory Animals. Guide for the Care and Use of Laboratory Animals. 8th ed. Washington (DC): National Academies Press (US); 2011. https://doi.org/10.17226/12910 PMID: 21595115</mixed-citation><mixed-citation xml:lang="en">National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory Animals. Guide for the Care and Use of Laboratory Animals. 8th ed. Washington (DC): National Academies Press (US); 2011. ISBN: 978-0-309-15401-7.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Kinashi H., Falke L.L., Nguyen T.Q., et al. Connective tissue growth factor regulates fibrosis-associated renal lymphangiogenesis. Kidney Int. 2017; 92(4): 850–63. https://doi.org/10.1016/j.kint.2017.03.029 PMID: 28545716</mixed-citation><mixed-citation xml:lang="en">Kinashi H, Falke LL, Nguyen TQ, Bovenschen N, Aten J, Leask A, et al. Connective tissue growth factor regulates fibrosis-associated renal lymphangiogenesis. Kidney Int 2017;92:850–63. DOI:10.1016/j.kint.2017.03.029.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Beaini S., Saliba Y., Hajal J., et al. VEGF-C attenuates renal damage in salt-sensitive hypertension. J Cell Physiol. 2019; 234(6): 9616–30. https://doi.org/10.1002/jcp.27648 PMID: 30378108</mixed-citation><mixed-citation xml:lang="en">Beaini S, Saliba Y, Hajal J, Smayra V, Bakhos J-J, Joubran N, et al. VEGF-C attenuates renal damage in salt-sensitive hypertension. J Cell Physiol 2019;234:9616–30. DOI:10.1002/jcp.27648.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Joory K.D, Levick J.R., Mortimer P.S., Bates D.O. Vascular endothelial growth factor-C (VEGF-C) expression in normal human tissues. Lymphat Res Biol. 2006; 4(2): 73–82. https://doi.org/10.1089/lrb.2006.4.73 PMID: 16808669</mixed-citation><mixed-citation xml:lang="en">Joory KD, Levick JR, Mortimer PS, Bates DO. Vascular endothelial growth factor-C (VEGF-C) expression in normal human tissues. Lymphat Res Biol 2006;4:73–82. DOI:10.1089/lrb.2006.4.73.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Divarci E., Karapinar B., Yalaz M., et al. Incidence and prognosis of intraabdominal hypertension and abdominal compartment syndrome in children. J Pediatr Surg. 2016; 51(3): 503–7. https://doi.org/10.1016/j.jpedsurg.2014.03.014 PMID:25783342</mixed-citation><mixed-citation xml:lang="en">Divarci E, Karapinar B, Yalaz M, Ergun O, Celik A. Incidence and prognosis of intraabdominal hypertension and abdominal compartment syndrome in children. J Pediatr Surg 2016;51:503–7. DOI:10.1016/j.jpedsurg.2014.03.014.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Villa G., Samoni S., De Rosa S., Ronco C. The Pathophysiological Hypothesis of Kidney Damage during Intra-Abdominal Hypertension. Front Physiol. 2016 Feb 23; 7: 55. https://doi.org/10.3389/fphys.2016.00055 PMID: 26941652</mixed-citation><mixed-citation xml:lang="en">Villa G, Samoni S, De Rosa S, Ronco C. The Pathophysiological Hypothesis of Kidney Damage during Intra-Abdominal Hypertension. Front Physiol 2016;7. DOI:10.3389/fphys.2016.00055.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Köşüm A., Borazan E., Maralcan G., Aytekin A. Biochemical and histopathological changes of intra-abdominal hypertension on the kidneys: Experimental study in rats. Ulus Cerrahi Derg. 2013; 29(2): 49–53. https://doi.org/5152/UCD.2013.39 PMID: 25931845</mixed-citation><mixed-citation xml:lang="en">Köşüm A, Borazan E, Maralcan G, Aytekin A. Biochemical and histopathological changes of intra-abdominal hypertension on the kidneys: Experimental study in rats. Ulus Cerrahi Derg 2013;29:49–53. DOI:10.5152/UCD.2013.39.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Chang Y., Qi X., Li Z., et al. Hepatorenal syndrome: insights into the mechanisms of intra-abdominal hypertension. Int J Clin Exp Pathol. 2013; 6(11): 2523–8. PMID: 24228115</mixed-citation><mixed-citation xml:lang="en">Chang Y, Qi X, Li Z, Wang F, Wang S, Zhang Z, et al. Hepatorenal syndrome: insights into the mechanisms of intra-abdominal hypertension. Int J Clin Exp Pathol 2013;6:2523–8.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Morozov D., Morozova O., Pervouchine D., et al. Hypoxic renal injury in newborns with abdominal compartment syndrome (clinical and experimental study). Pediatr Res. 2018; 83(2): 520–6. https://doi.org/10.1038/pr.2017.263 PMID: 29053704</mixed-citation><mixed-citation xml:lang="en">Morozov D, Morozova O, Pervouchine D, Severgina L, Tsyplakov A, Zakharova N, et al. Hypoxic renal injury in newborns with abdominal compartment syndrome (clinical and experimental study). Pediatr Res 2018;83:520–6. DOI:10.1038/pr.2017.263.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
