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<article 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" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Pharmacy &amp; Pharmacology</journal-id><journal-title-group><journal-title xml:lang="en">Pharmacy &amp; Pharmacology</journal-title><trans-title-group xml:lang="ru"><trans-title>Фармация и фармакология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2307-9266</issn><issn publication-format="electronic">2413-2241</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">352579</article-id><article-id pub-id-type="doi">10.19163/2307-9266-2022-10-6-549-561</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>ORIGINAL ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОРИГИНАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">DF-5 compound delays development of diabetic nephropathy in rats</article-title><trans-title-group xml:lang="ru"><trans-title>Соединение ДФ-5 замедляет развитие диабетической нефропатии у крыс</trans-title></trans-title-group><trans-title-group xml:lang="zh"><trans-title/></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7185-4826</contrib-id><name-alternatives><name xml:lang="en"><surname>Spasov</surname><given-names>Alexander A.</given-names></name><name xml:lang="ru"><surname>Спасов</surname><given-names>Александр Алексеевич</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Doctor of Sciences (Medicine), Academician of RAS, Head of the Pharmacology and Bioinformatics Department, Volgograd State Medical University; Head of the Laboratory of Experimental Pharmacology, Volgograd Medical Research Center</p></bio><bio xml:lang="ru"><p>доктор медицинских наук, академик РАН, заведующий кафедрой фармакологии и биоинформатики, ФГБОУ ВО ВолгГМУ Минздрава России; заведующий лабораторией экспериментальной фармакологии ГБУ ВМНЦ</p></bio><email>aspasov@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2485-2139</contrib-id><name-alternatives><name xml:lang="en"><surname>Zhukovskaya</surname><given-names>Olga N.</given-names></name><name xml:lang="ru"><surname>Жуковская</surname><given-names>Ольга Николаевна</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Candidate of Sciences (Chemistry), Senior researcher of the Organic Synthesis Laboratory</p></bio><bio xml:lang="ru"><p>кандидат химических наук, старший научный сотрудник лаборатории органического синтеза</p></bio><email>zhukowskaia.ol@yandex.ru</email><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Rashchenko</surname><given-names>Andrey I.</given-names></name><name xml:lang="ru"><surname>Ращенко</surname><given-names>Андрей Игоревич</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Candidate of Sciences (Pharmacy), Senior researcher of the Metabotropic Drugs Laboratory</p></bio><bio xml:lang="ru"><p>кандидат фармацевтических наук, старший научный сотрудник лаборатории метаботропных лекарственных средств НЦИЛС</p></bio><email>a.rashencko@yandex.ru</email><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0957-7087</contrib-id><name-alternatives><name xml:lang="en"><surname>Brigadirova</surname><given-names>Anasthasia A.</given-names></name><name xml:lang="ru"><surname>Бригадирова</surname><given-names>Анастасия Андреевна</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Candidate of Sciences (Medicine), Associate Professor, Pharmacology and Bioinformatics Department, Volgograd State Medical University; Volgograd Medical Research Center</p></bio><bio xml:lang="ru"><p>кандидат медицинских наук, доцент кафедры фармакологии и биоинформатики ФГБОУ ВО ВолгГМУ Минздрава России; младший научный сотрудник лаборатории экспериментальной фармакологии ГБУ ВМНЦ</p></bio><email>a.brigadirova@gmail.com</email><xref ref-type="aff" rid="aff5"/><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0162-0653</contrib-id><name-alternatives><name xml:lang="en"><surname>Litvinov</surname><given-names>Roman A.</given-names></name><name xml:lang="ru"><surname>Литвинов</surname><given-names>Роман Александрович</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Candidate of Sciences (Medicine), Senior researcher of the Metabotropic drugs Laboratory, Volgograd State Medical University; Researcher of the Laboratory of Experimental Pharmacology, Volgograd Medical Research Center</p></bio><bio xml:lang="ru"><p>кандидат медицинских наук, старший научный сотрудник лаборатории метаботропных лекарственных средств НЦИЛС, ФГБОУ ВО ВолгГМУ Минздрава России; научный сотрудник лаборатории экспериментальной фармакологии ГБУ ВМНЦ</p></bio><email>litvinov.volggmu@mail.ru</email><xref ref-type="aff" rid="aff5"/><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-0670-1444</contrib-id><name-alternatives><name xml:lang="en"><surname>Gurova</surname><given-names>Natalia A.</given-names></name><name xml:lang="ru"><surname>Гурова</surname><given-names>Наталия Алексеевна</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Doctor of Sciences (Medicine), Professor of the Pharmacology and Bioinformatics Department</p></bio><bio xml:lang="ru"><p>доктор медицинских наук, профессор кафедры фармакологии и биоинформатики</p></bio><email>gurova.vlgmed@mail.ru</email><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-5351-6105</contrib-id><name-alternatives><name xml:lang="en"><surname>Smirnov</surname><given-names>Alexey V.</given-names></name><name xml:lang="ru"><surname>Смирнов</surname><given-names>Алексей Владимирович</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Doctor of Sciences (Medicine), Head of the Pathological Anatomy Department, Volgograd State Medical University</p></bio><bio xml:lang="ru"><p>доктор медицинских наук, заведующий кафедрой патологической анатомии ФГБОУ ВО ВолгГМУ Минздрава России</p></bio><email>alexey-smirnov@rambler.ru</email><xref ref-type="aff" rid="aff5"/><xref ref-type="aff" rid="aff4"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4035-4108</contrib-id><name-alternatives><name xml:lang="en"><surname>Pan’shin</surname><given-names>Nicolay G.</given-names></name><name xml:lang="ru"><surname>Паньшин</surname><given-names>Николай Геннадьевич</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Candidate of Sciences (Medicine), Associate Professor, Pathological Anatomy Department</p></bio><bio xml:lang="ru"><p>кандидат медицинских наук, доцент кафедры патологической анатомии</p></bio><email>panshin.nickolay@gmail.com</email><xref ref-type="aff" rid="aff5"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Abbas</surname><given-names>Haider S.A.</given-names></name><name xml:lang="ru"><surname>Аббас</surname><given-names>Хайдер Сабри Аббас</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Master’s student of the Organic Synthesis Laboratory</p></bio><bio xml:lang="ru"><p>магистрант лаборатории органического синтеза</p></bio><email>vip.haider89@gmail.ru</email><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9182-6101</contrib-id><name-alternatives><name xml:lang="en"><surname>Morkovnik</surname><given-names>Anatoliy S.</given-names></name><name xml:lang="ru"><surname>Морковник</surname><given-names>Анатолий Савельевич</given-names></name><name xml:lang="zh"><surname></surname><given-names></given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Doctor of Sciences (Chemistry), Chief Researcher, Organic Synthesis Laboratory</p></bio><bio xml:lang="ru"><p>доктор химических наук, главный научный сотрудник лаборатории органического синтеза</p></bio><email>asmork@mail.ru</email><xref ref-type="aff" rid="aff6"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Volgograd State Medical University</institution></aff><aff><institution xml:lang="ru">Федеральное государственное бюджетное образовательное учреждение высшего образования «Волгоградский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution></aff><aff><institution xml:lang="zh"></institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Volgograd Medical Research Center</institution></aff><aff><institution xml:lang="ru">Государственное бюджетное учреждение «Волгоградский медицинский научный центр»</institution></aff><aff><institution xml:lang="zh"></institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Institute of Physical and Organic Chemistry, Southern Federal University</institution></aff><aff><institution xml:lang="ru">Научно-исследовательский институт физической и органической химии федеральное государственное автономное образовательное учреждение высшего профессионального образования «Южный федеральный университет»</institution></aff><aff><institution xml:lang="zh"></institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">Volgograd Medical Research Center</institution></aff><aff><institution xml:lang="ru">Государственное бюджетное учреждение «Волгоградский медицинский научный центр»</institution></aff></aff-alternatives><aff-alternatives id="aff5"><aff><institution xml:lang="en">Volgograd State Medical University</institution></aff><aff><institution xml:lang="ru">Федеральное государственное бюджетное образовательное учреждение высшего образования «Волгоградский государственный медицинский университет» Министерства здравоохранения Российской Федерации</institution></aff></aff-alternatives><aff-alternatives id="aff6"><aff><institution xml:lang="en">Institute of Physical and Organic Chemistry, Southern Federal University</institution></aff><aff><institution xml:lang="ru">Научно-исследовательский институт физической и органической химии федеральное государственное автономное образовательное учреждение высшего профессионального образования «Южный федеральный университет»</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2022-12-02" publication-format="electronic"><day>02</day><month>12</month><year>2022</year></pub-date><volume>10</volume><issue>6</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><issue-title xml:lang="zh"/><fpage>549</fpage><lpage>561</lpage><history><date date-type="received" iso-8601-date="2023-04-27"><day>27</day><month>04</month><year>2023</year></date><date date-type="accepted" iso-8601-date="2023-04-27"><day>27</day><month>04</month><year>2023</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2022, Spasov A.A., Zhukovskaya O.N., Rashchenko A.I., Brigadirova A.A., Litvinov R.A., Gurova N.A., Smirnov A.V., Pan’shin N.G., Abbas H.S., Morkovnik A.S.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2022, Спасов А.А., Жуковская О.Н., Ращенко А.И., Бригадирова А.А., Литвинов Р.А., Гурова Н.А., Смирнов А.В., Паньшин Н.Г., Аббас Х.С., Морковник А.С.</copyright-statement><copyright-statement xml:lang="zh">Copyright ©; 2022, Spasov A., Zhukovskaya O., Rashchenko A., Brigadirova A., Litvinov R., Gurova N., Smirnov A., Pan’shin N., Abbas H., Morkovnik A.</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="en">Spasov A.A., Zhukovskaya O.N., Rashchenko A.I., Brigadirova A.A., Litvinov R.A., Gurova N.A., Smirnov A.V., Pan’shin N.G., Abbas H.S., Morkovnik A.S.</copyright-holder><copyright-holder xml:lang="ru">Спасов А.А., Жуковская О.Н., Ращенко А.И., Бригадирова А.А., Литвинов Р.А., Гурова Н.А., Смирнов А.В., Паньшин Н.Г., Аббас Х.С., Морковник А.С.</copyright-holder><copyright-holder xml:lang="zh">Spasov A., Zhukovskaya O., Rashchenko A., Brigadirova A., Litvinov R., Gurova N., Smirnov A., Pan’shin N., Abbas H., Morkovnik A.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://journals.eco-vector.com/2307-9266/article/view/352579">https://journals.eco-vector.com/2307-9266/article/view/352579</self-uri><abstract xml:lang="en"><p>Advanced glycation end-products play an important role in the development of diabetic complications, so slowing down of glycated proteins’ cross-links formation have been suggested as a potential therapeutic option for the treatment of vascular diabetic complications and preventing their progression.</p> <p><bold>The aim </bold>of the work was to assess the influence of novel anticrosslinking agent DF-5 on the renal advanced glycation end-products and collagen contents, body weight, blood glucose and glycated hemoglobin levels and the development of early renal disease in streptozotocin-induced diabetic rats.</p> <p><bold>Materials and methods.</bold> 40 male Sprague-Dawley rats were used in the study. Two months after inducing diabetes, the study substance was administered intragastrically once a day for 28 days (12.5 mg/kg). Measurements included the assessment of blood glucose and HbA1c levels, the evaluation of the renal function, and the results of histology and immunohistochemical staining of kidneys.</p> <p><bold>Results. </bold>A repeated intragastric administration of DF-5 for 30 days significantly reduced the level of HbA1c in the blood, but did not affect the level of fasting blood glucose. DF-5 compound significantly reduced proteinuria and prevented kidney damage in experimental animals by limiting damage of the glomeruli and tubules. It was found that DF-5 inhibits the progression of an early renal dysfunction in rats with streptozotocin-induced diabetic nephropathy. This was associated with a decreased accumulation of advanced glycation end-products in the kidney, accompanied by the improvement of both renal morphology and function.</p> <p><bold>Conclusion. </bold>The results obtained provide investigators with additional therapeutic options for the treatment of diabetic nephropathy and possibly other complications of diabetes.</p></abstract><trans-abstract xml:lang="ru"><p>Конечные продукты гликирования играют важную роль в развитии осложнений сахарного диабета. По этой причине замедление образования поперечных сшивок гликированных белков, как предполагается, является потенциальным терапевтическим подходом к лечению и профилактике осложнений заболевания, связанных с поражением сосудов.</p> <p><bold>Цель. </bold>Оценка способности нового антисшивающего соединения ДФ-5 влиять на количество конечных продуктов гликирования и коллагена в почках, на массу тела, уровни глюкозы и гликированного гемоглобина, а также на развитие ранних проявлений поражения почек у крыс со стрептозотоциновым сахарным диабетом.</p> <p><bold>Материалы и методы. </bold>Работа проведена на 40 самцах крыс Sprague-Dawley. Через 2 месяца после индукции диабета исследуемое вещество вводили внутрижелудочно (12,5 мг/кг) 1 р/сут в течение 28 дней с помощью зонда. Определяли уровень глюкозы и гликированного гемоглобина в крови, оценивали функцию почек, а также проводили гистологическое и иммуногистохимическое исследования тканей почек.</p> <p><bold>Результаты.</bold> Регулярное внутрижелудочное введение ДФ-5 в течение 30 сут статистически значимо снижало уровень HbA1c в крови, но не влияло на уровень глюкозы в крови натощак. Соединение ДФ-5 существенно уменьшало протеинурию и предотвращало повреждение почек у экспериментальных животных за счет ограничения повреждений клубочков и канальцев. Было установлено, что соединение ДФ-5 замедляет повреждение почек на ранней стадии диабетической нефропатии, что сопровождается снижением количества конечных продуктов гликирования в ткани почек, улучшением их морфологической картины и функции.</p> <p><bold>Заключение.</bold> Полученные результаты открывают возможность для разработки дополнительного терапевтического подхода к лечению диабетической нефропатии и, возможно, других осложнений сахарного диабета.</p></trans-abstract><trans-abstract xml:lang="zh"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>advanced glycation endproducts</kwd><kwd>cross-links</kwd><kwd>ALT-711 (alagebrium)</kwd><kwd>diabetes mellitus</kwd><kwd>diabetic kidney disease (nephropathy)</kwd><kwd>streptozotocin-induced diabetes</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>конечные продукты гликирования</kwd><kwd>поперечные сшивки</kwd><kwd>ALT-711 (алагебриум)</kwd><kwd>сахарный диабет</kwd><kwd>диабетическая болезнь почек (нефропатия)</kwd><kwd>стрептозотоцин-индуцированный диабет</kwd></kwd-group><funding-group><funding-statement xml:lang="en">The chemical part of this work was carried out in the Institute of Organic and Physical Chemistry, Southern Federal University with a financial support by the Ministry of Science and Higher Education of the Russian Federation in the framework of the state task, grant FENW-2020-0031 (0852-2020-0031). The biological part of this work was financially supported by the Russian Science Foundation (Project 14-25-00139)</funding-statement><funding-statement xml:lang="ru">Химическая часть исследования выполнена в Институте органической и физической химии ФГАОУ ВПО «Южный федеральный университет» при финансовой поддержке Министерства науки и высшего образования Российской Федерации в рамках государственного задания, грант ФЕНВ-2020-0031 (0852-2020-0031). Биологическая часть исследования проведена при финансовой поддержке Российского научного фонда (проект 14-25-00139)</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Silva JAD, Souza ECF, Echazú Böschemeier AG, Costa CCMD, Bezerra HS, Feitosa EELC. Diagnosis of diabetes mellitus and living with a chronic condition: participatory study. BMC Public Health. 2018 Jun 5;18(1):699. DOI:10.1186/s12889-018-5637-9</mixed-citation><mixed-citation xml:lang="ru">Silva J.A.D., Souza E.C.F., Echazú Böschemeier A.G., Costa C.C.M.D., Bezerra H.S., Feitosa E.E.L.C. Diagnosis of diabetes mellitus and living with a chronic condition: participatory study // BMC Public Health. – 2018. – Vol. 18, No. 1. – Art. ID: 699. DOI:10.1186/s12889-018-5637-9</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Singh VP, Bali A, Singh N, Jaggi AS. Advanced glycation end products and diabetic complications. Korean J Physiol Pharmacol. 2014 Feb;18(1):1–14. DOI:10.4196/kjpp.2014.18.1.1</mixed-citation><mixed-citation xml:lang="ru">Singh V.P., Bali A., Singh N., Jaggi A.S. Advanced Glycation End Products and Diabetic Complications // Korean J. Physiol. Pharmacol. – 2014. – Vol. 18, No. 1. – P. 1–14. DOI:10.4196/kjpp.2014.18.1.1</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Rhee SY, Kim YS. The Role of Advanced Glycation End Products in Diabetic Vascular Complications. Diabetes Metab J. 2018 Jun;42(3):188–95. DOI:10.4093/dmj.2017.0105</mixed-citation><mixed-citation xml:lang="ru">Rhee S.Y., Kim Y.S. The Role of Advanced Glycation End Products in Diabetic Vascular Complications // Diabetes Metab. J. – 2018. – Vol. 42, No. 3. – P. 188–195. DOI:10.4093/dmj.2017.0105</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Chaudhuri J, Bains Y, Guha S, Kahn A, Hall D, Bose N, Gugliucci A, Kapahi P. The Role of Advanced Glycation End Products in Aging and Metabolic Diseases: Bridging Association and Causality. Cell Metab. 2018 Sep 4;28(3):337–52. DOI:10.1016/j.cmet.2018.08.014</mixed-citation><mixed-citation xml:lang="ru">Chaudhuri J., Bains Y., Guha S., Kahn A., Hall D., Bose N., et al. The Role of Advanced Glycation End Products in Aging and Metabolic Diseases: Bridging Association and Causality // Cell Metab. – 2018. – Vol .28, No. 3. – P. 337–352. DOI:10.1016/j.cmet.2018.08.014</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Bodiga VL, Eda SR, Bodiga S. Advanced glycation end products: role in pathology of diabetic cardiomyopathy. Heart Fail Rev. 2014 Jan;19(1):49–63. DOI:10.1007/s10741-013-9374-y</mixed-citation><mixed-citation xml:lang="ru">Bodiga V.L., Eda S.R., Bodiga S. Advanced glycation end products: role in pathology of diabetic cardiomyopathy // Heart Fail Rev. – 2014. – Vol. 19, No. 1. – P. 49–63. DOI:10.1007/s10741-013-9374-y</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Bhat S, Mary S, Giri AP, Kulkarni MJ. Advanced Glycation End Products (AGEs) in Diabetic Complications. In: Kartha CC, Ramachandran S, Pillai RM, editors. Mechanisms of Vascular Defects in Diabetes Mellitus, Cham: Springer International Publishing; 2017, p. 423–49. DOI:10.1007/978-3-319-60324-7_19</mixed-citation><mixed-citation xml:lang="ru">Bhat S., Mary S., Giri A.P., Kulkarni M.J. Advanced Glycation End Products (AGEs) in Diabetic Complications / Mechanisms of Vascular Defects in Diabetes Mellitus. Advances in Biochemistry in Health and Disease // Edited by Kartha C.C., Ramachandran S., Pillai R.M. Cham: Springer International Publishing, 2017. – P. 423–449. DOI:10.1007/978-3-319-60324-7_19</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Rabbani N, Thornalley PJ. Advanced glycation end products in the pathogenesis of chronic kidney disease. Kidney Int. 2018 Apr;93(4):803–13. DOI:10.1016/j.kint.2017.11.034</mixed-citation><mixed-citation xml:lang="ru">Rabbani N., Thornalley P.J. Advanced glycation end products in the pathogenesis of chronic kidney disease // Kidney Int. – 2018. – Vol. 93, No. 4 – P. 803–813. DOI:10.1016/j.kint.2017.11.034</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Nabi R, Alvi SS, Saeed M, Ahmad S, Khan MS. Glycation and HMG-CoA Reductase Inhibitors: Implication in Diabetes and Associated Complications. Curr Diabetes Rev. 2019;15(3):213–23. DOI:10.2174/1573399814666180924113442</mixed-citation><mixed-citation xml:lang="ru">Nabi R., Alvi S.S., Saeed M., Ahmad S., Khan M.S. Glycation and HMG-CoA Reductase Inhibitors: Implication in Diabetes and Associated Complications // Curr. Diabetes Rev. – 2019. – Vol. 15, No. 3. – P. 213–223. DOI:10.2174/1573399814666180924113442</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Nabi R, Alvi SS, Khan RH, Ahmad S, Ahmad S, Khan MS. Antiglycation study of HMG-R inhibitors and tocotrienol against glycated BSA and LDL: A comparative study. Int J Biol Macromol. 2018 Sep;116:983–92. DOI:10.1016/j.ijbiomac.2018.05.115</mixed-citation><mixed-citation xml:lang="ru">Nabi R., Alvi S.S., Khan R.H., Ahmad S., Ahmad S., Khan M.S. Antiglycation study of HMG-R inhibitors and tocotrienol against glycated BSA and LDL: A comparative study // Int. J. Biol. Macromol. – 2018. – Vol. 116. – P. 983–992. DOI:10.1016/j.ijbiomac.2018.05.115</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Rahbar S, Figarola JL. Novel inhibitors of advanced glycation endproducts. Arch Biochem Biophys. 2003 Nov 1;419(1):63–79. DOI:10.1016/j.abb.2003.08.009</mixed-citation><mixed-citation xml:lang="ru">Rahbar S., Figarola J.L. Novel inhibitors of advanced glycation endproducts // Arch. Biochem. Biophys. – 2003. – Vol. 419, No. 1. – P. 63–79. DOI:10.1016/j.abb.2003.08.009</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Akhter F, Khan MS, Ahmad S. Acquired immunogenicity of calf thymus DNA and LDL modified by D-ribose: a comparative study. Int J Biol Macromol. 2015 Jan;72:1222-7. DOI:10.1016/j.ijbiomac.2014.10.034</mixed-citation><mixed-citation xml:lang="ru">Akhter F., Khan M.S., Ahmad S. Acquired immunogenicity of calf thymus DNA and LDL modified by D-ribose: a comparative study // Int. J. Biol. Macromol. – 2015. – Vol. 72. – P. 1222–1227. DOI:10.1016/j.ijbiomac.2014.10.034</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Jabir NR, Ahmad S, Tabrez S. An insight on the association of glycation with hepatocellular carcinoma. Semin Cancer Biol. 2018 Apr;49:56–63. DOI:10.1016/j.semcancer.2017.06.005</mixed-citation><mixed-citation xml:lang="ru">Jabir N.R., Ahmad S., Tabrez S. An insight on the association of glycation with hepatocellular carcinoma // Semin. Cancer. Biol. – 2018. – Vol. 49. – P. 56–63. DOI:10.1016/j.semcancer.2017.06.005</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Brings S, Fleming T, Freichel M, Muckenthaler MU, Herzig S, Nawroth PP. Dicarbonyls and Advanced Glycation End-Products in the Development of Diabetic Complications and Targets for Intervention. Int J Mol Sci. 2017 May 5;18(5):984. DOI:10.3390/ijms18050984</mixed-citation><mixed-citation xml:lang="ru">Brings S., Fleming T., Freichel M., Muckenthaler M.U., Herzig S., Nawroth P.P. Dicarbonyls and Advanced Glycation End-Products in the Development of Diabetic Complications and Targets for Intervention // Int. J. Mol. Sci. – 2017. – Vol. 18, No. 5. – Art. ID: 984. DOI:10.3390/ijms18050984</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Vasan S, Foiles P, Founds H. Therapeutic potential of breakers of advanced glycation end product-protein crosslinks. Arch Biochem Biophys. 2003 Nov 1;419(1):89–96. DOI:10.1016/j.abb.2003.08.016</mixed-citation><mixed-citation xml:lang="ru">Vasan S., Foiles P., Founds H. Therapeutic potential of breakers of advanced glycation end product–protein crosslinks // Arch. Biochem. Biophys. – 2003. – Vol. 419, No. 1. – P. 89–96. DOI:10.1016/j.abb.2003.08.016</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Zuehlke CW. Methods of Organic Elemental Microanalysis. J Am Chem Soc. 1963;85(16):2536. DOI:10.1021/ja00899a055</mixed-citation><mixed-citation xml:lang="ru">Zuehlke C.W. Methods of Organic Elemental Microanalysis // J. Am. Chem. Soc. – 1963. – Vol. 85, No. 16. – Art. ID: 2536. DOI:10.1021/ja00899a055</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">Vasan S, Zhang X, Zhang X, Kapurniotu A, Bernhagen J, Teichberg S, Basgen J, Wagle D, Shih D, Terlecky I, Bucala R, Cerami A, Egan J, Ulrich P. An agent cleaving glucose-derived protein crosslinks in vitro and in vivo. Nature. 1996 Jul 18;382(6588):275–8. DOI:10.1038/382275a0</mixed-citation><mixed-citation xml:lang="ru">Vasan S., Zhang X., Zhang X., Kapurniotu A., Bernhagen J., Teichberg S., Basgen J., Wagle D., Shih D., Terlecky I., Bucala R., Cerami A., Egan J., Ulrich P. An agent cleaving glucose-derived protein crosslinks in vitro and in vivo // Nature. – 1996. – Vol. 382, No. 6588. – P. 275–278. DOI:10.1038/382275a0</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">Zhukovskaya ON, Anisimova VA, Morkovnik AS, Petrov VI, Spasov AA, Rashchenko AI, Brigadirova AA, Abbas HSA. 9-Benzyl-2-biphenylimidazo[1,2-a]benzimidazole and pharmaceutically acceptable salts thereof that express properties of destroyers of transversal cross-links of glycosylated proteins. RU 2627769 C1, 2017.</mixed-citation><mixed-citation xml:lang="ru">Жуковская О.Н., Анисимова В.А., Морковник А.С., Петров В.И., Спасов А.А., Ращенко А.И., Бригадирова А.А., Аббас Х.С.А. 9-бензил-2-бифенилимидазо[1,2-а]бензимидазол и его фармацевтически приемлемые соли, проявляющие свойства разрушителей поперечных сшивок гликированных белков. RU 2627769 C1, 2017.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">Zhang B, He K, Chen W, Cheng X, Cui H, Zhong W, Li S, Wang L. Alagebrium (ALT-711) improves the anti-hypertensive efficacy of nifedipine in diabetic-hypertensive rats. Hypertens Res. 2014 Oct;37(10):901–7. DOI: 10.1038/hr.2014.98</mixed-citation><mixed-citation xml:lang="ru">Zhang B., He K., Chen W., Cheng X., Cui H., Zhong W., Li S., Wang L. Alagebrium (ALT-711) improves the anti-hypertensive efficacy of nifedipine in diabetic-hypertensive rats // Hypertens. Res. – 2014. – Vol. 37, No. 10. – P. 901–907. DOI:10.1038/hr.2014.98</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">Cheng G, Wang LL, Qu WS, Long L, Cui H, Liu HY, Cao YL, Li S. C16, a novel advanced glycation endproduct breaker, restores cardiovascular dysfunction in experimental diabetic rats. Acta Pharmacol Sin. 2005 Dec; 26(12):1460–6. DOI:10.1111/j.1745-7254.2005.00240.x</mixed-citation><mixed-citation xml:lang="ru">Cheng G., Wang L.L., Qu W.S., Long L., Cui H., Liu H.Y., Cao Y.L., Li S. C16, a novel advanced glycation endproduct breaker, restores cardiovascular dysfunction in experimental diabetic rats // Acta Pharmacol. Sin. – 2005. – Vol. 26, No. 12. – P. 1460–1466. DOI:10.1111/j.1745-7254.2005.00240.x</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">Cheng G, Wang LL, Long L, Liu HY, Cui H, Qu WS, Li S. Beneficial effects of C36, a novel breaker of advanced glycation endproducts cross-links, on the cardiovascular system of diabetic rats. Br J Pharmacol. 2007 Dec;152(8):1196–206. DOI:10.1038/sj.bjp.0707533</mixed-citation><mixed-citation xml:lang="ru">Cheng G., Wang L.L., Long L., Liu H.Y., Cui H., Qu W.S., Li S. Beneficial effects of C36, a novel breaker of advanced glycation endproducts cross-links, on the cardiovascular system of diabetic rats // Br. J. Pharmacol. – 2007. – Vol. 152, No. 8. – P. 1196–1206. DOI:10.1038/sj.bjp.0707533</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">Spasov AA, Zhukovskaya ON, Brigadirova AA, Abbas HSA, Anisimova VA, Sysoeva VA, Rashchenko AI, Litvinov RA, Mayka OYu, Babkov DA, Morkovnik AS. Synthesis and pharmacological activity of 2-(biphenyl-4-yl)imidazo[1,2-a]benzimidazoles. Russ Chem Bull. 2017;66:1905–1912. DOI: 10.1007/s11172-017-1965-7</mixed-citation><mixed-citation xml:lang="ru">Spasov A.A., Zhukovskaya O.N., Brigadirova A.A., Abbas H.S.A., Anisimova V.A., Sysoeva V.A., Rashchenko A.I., Litvinov R.A., Mayka O.Yu., Babkov D.A., Morkovnik A.S. Synthesis and pharmacological activity of 2-(biphenyl-4-yl)imidazo[1,2-a]benzimidazoles // Russ. Chem. Bull. – 2017. – Vol. 66. – P. 1905–1912. DOI:10.1007/s11172-017-1965-7</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Cho SJ, Roman G, Yeboah F, Konishi Y. The road to advanced glycation end products: a mechanistic perspective. Curr Med Chem. 2007;14(15):1653–71. DOI:10.2174/092986707780830989</mixed-citation><mixed-citation xml:lang="ru">Cho S.J., Roman G., Yeboah F., Konishi Y. The Road to Advanced Glycation End Products: A Mechanistic Perspective // Curr. Med. Chem. – 2007. – Vol. 14, No. 15. – P. 1653–1671. DOI:10.2174/092986707780830989</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">Tang SCW, Yiu WH. Innate immunity in diabetic kidney disease. Nat Rev Nephrol. 2020 Apr;16(4):206–22. DOI:10.1038/s41581-019-0234-4</mixed-citation><mixed-citation xml:lang="ru">Tang S.C.W., Yiu W.H. Innate immunity in diabetic kidney disease // Nat. Rev. Nephrol. 2020- Vol. 16. – P. 206–222. DOI:10.1038/s41581-019-0234-4</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">Yao D, Wang S, Wang M, Lu W. Renoprotection of dapagliflozin in human renal proximal tubular cells via the inhibition of the high mobility group box 1-receptor for advanced glycation end products-nuclear factor-κB signaling pathway. Mol Med Rep. 2018 Oct;18(4):3625–30. DOI:10.3892/mmr.2018.9393</mixed-citation><mixed-citation xml:lang="ru">Yao D., Wang S., Wang M., Lu W. Renoprotection of dapagliflozin in human renal proximal tubular cells via the inhibition of the high mobility group box 1receptor for advanced glycation end productsnuclear factorκB signaling pathway // Mol. Med. Rep. – 2018. – Vol. 18, No. 4. – P. 3625–3630. DOI:10.3892/mmr.2018.9393.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">Kolset SO, Reinholt FP, Jenssen T. Diabetic nephropathy and extracellular matrix. J Histochem Cytochem. 2012 Dec;60(12):976–86. DOI:10.1369/0022155412465073</mixed-citation><mixed-citation xml:lang="ru">Kolset S.O., Reinholt F.P., Jenssen T. Diabetic Nephropathy and Extracellular Matrix // J. Histochem. Cytochem. – 2012. – Vol. 60, No. 12. – P. 976–986. DOI: 10.1369/0022155412465073</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">Dalla Vestra M, Saller A, Mauer M, Fioretto P. Role of mesangial expansion in the pathogenesis of diabetic nephropathy. J Nephrol. 2001 Nov-Dec;14 Suppl 4:S51-7.</mixed-citation><mixed-citation xml:lang="ru">Dalla Vestra M., Saller A., Mauer M., Fioretto P. Role of mesangial expansion in the pathogenesis of diabetic nephropathy // J. Nephrol. – 2001. – Vol. 14, Suppl 4. – P. 51–57.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">Amorim RG, Guedes GDS, Vasconcelos SML, Santos JCF. Kidney Disease in Diabetes Mellitus: Cross-Linking between Hyperglycemia, Redox Imbalance and Inflammation. Arq Bras Cardiol. 2019 Jun 6;112(5):577–87. DOI:10.5935/abc.20190077. Erratum in: Arq Bras Cardiol. 2019 Aug 08;113(1):182.</mixed-citation><mixed-citation xml:lang="ru">Amorim R.G., Guedes G. da S., Vasconcelos S.M. de L., Santos J.C. de F. Kidney Disease in Diabetes Mellitus: Cross-Linking between Hyperglycemia, Redox Imbalance and Inflammation // Arq. Bras. Cardiol. – 2019. – Vol. 112, No. 5. – P. 577-587. DOI: 10.5935/abc.20190077. Erratum in: Arq. Bras. Cardiol. – 2019. – Vol. 113, No. 1. – Art. ID: 182.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">Vasan S, Foiles PG, Founds HW. Therapeutic potential of AGE inhibitors and breakers of AGE protein cross-links. Expert Opin Investig Drugs. 2001 Nov;10(11):1977–87. DOI:10.1517/13543784.10.11.1977</mixed-citation><mixed-citation xml:lang="ru">Vasan S., Foiles P.G., Founds H.W. Therapeutic potential of AGE inhibitors and breakers of AGE protein cross-links // Expert Opin. Investig. Drugs. – 2001. – Vol. 10, No. 11. – P. 1977–1987. DOI:10.1517/13543784.10.11.1977</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">Forbes JM, Thallas V, Thomas MC, Founds HW, Burns WC, Jerums G, Cooper ME. The breakdown of preexisting advanced glycation end products is associated with reduced renal fibrosis in experimental diabetes. FASEB J. 2003 Sep;17(12):1762–4. DOI:10.1096/fj.02-1102fje</mixed-citation><mixed-citation xml:lang="ru">Forbes J.M., Thallas V., Thomas M.C., Founds H.W., Burns W.C., Jerums G., Cooper ME. The breakdown of preexisting advanced glycation end products is associated with reduced renal fibrosis in experimental diabetes // FASEB J. – 2003. – Vol. 17, No. 12. – P. 1762–1764. DOI:10.1096/fj.02-1102fje</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">Kim YS, Kim J, Kim CS, Sohn EJ, Lee YM, Jeong IH, Kim H, Jang DS, Kim JS. KIOM-79, an Inhibitor of AGEs-Protein Cross-linking, Prevents Progression of Nephropathy in Zucker Diabetic Fatty Rats. Evid Based Complement Alternat Med. 2011;2011:761859. DOI:10.1093/ecam/nep078</mixed-citation><mixed-citation xml:lang="ru">Kim Y.S., Kim J., Kim C.S., Sohn E.J., Lee Y.M., Jeong I.H., Kim H., Jang D.S., Kim J.S. KIOM-79, an Inhibitor of AGEs–Protein Cross-linking, Prevents Progression of Nephropathy in Zucker Diabetic Fatty Rats // Evid. Based Complement. Alternat. Med. – 2011. – Vol. 2011. – P. 1–10. DOI:10.1093/ecam/nep078</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">Jung E, Park SB, Jung WK, Kim HR, Kim J. Antiglycation Activity of Aucubin In Vitro and in Exogenous Methylglyoxal Injected Rats. Molecules. 2019 Oct 10;24(20):3653. DOI:10.3390/molecules24203653</mixed-citation><mixed-citation xml:lang="ru">Jung E., Park S.B., Jung W.K., Kim H.R., Kim J. Antiglycation Activity of Aucubin In Vitro and in Exogenous Methylglyoxal Injected Rats // Molecules. – 2019. – Vol. 24, No. 20. – Art. ID: 3653. DOI:10.3390/molecules24203653</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">Kim J, Kim CS, Kim YS, Lee IS, Kim JS. Jakyakgamcho-tang and Its Major Component, Paeonia Lactiflora, Exhibit Potent Anti-glycation Properties. J Exerc Nutrition Biochem. 2016 Dec 31;20(4):60–4. DOI:10.20463/jenb.2016.0049</mixed-citation><mixed-citation xml:lang="ru">Kim J., Kim C.S., Kim Y.S., Lee I.S., Kim J.S. Jakyakgamcho-tang and Its Major Component, Paeonia Lactiflora, Exhibit Potent Anti-glycation Properties // J. Exerc. Nutrition Biochem. – 2016. – Vol. 20, No. 4. – P. 60–64. DOI:10.20463/jenb.2016.0049</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">Kim CS, Jo K, Pyo MK, Kim JS, Kim J. Pectin lyase-modified red ginseng extract exhibits potent anti-glycation effects in vitro and in vivo. J Exerc Nutrition Biochem. 2017 Jun 30;21(2):56–62. DOI:10.20463/jenb.2017.0011</mixed-citation><mixed-citation xml:lang="ru">Kim C.S., Jo K., Pyo M.K., Kim J.S., Kim J. Pectin lyase-modified red ginseng extract exhibits potent anti-glycation effects in vitro and in vivo // J. Exerc. Nutrition Biochem. – 2017. – Vol. 21, No. 2. – P. 56–62. DOI:10.20463/jenb.2017.0011</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">Coughlan MT, Forbes JM, Cooper ME. Role of the AGE crosslink breaker, alagebrium, as a renoprotective agent in diabetes. Kidney International. 2007;72(Suppl 106): 54–60. DOI:doi.org/10.1038/sj.ki.5002387</mixed-citation><mixed-citation xml:lang="ru">Coughlan M.T., Forbes J.M., Cooper M.E. Role of the AGE crosslink breaker, alagebrium, as a renoprotective agent in diabetes // Kidney International. – 2007. – Vol. 72, Suppl. 106. – P. 54–60. DOI:10.1038/sj.ki.5002387</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">Thallas-Bonke V, Lindschau C, Rizkalla B, Bach LA, Boner G, Meier M, Haller H, Cooper ME, Forbes JM. Attenuation of Extracellular Matrix Accumulation in Diabetic Nephropathy by the Advanced Glycation End Product Cross-Link Breaker ALT-711 via a Protein Kinase C- -Dependent Pathway. Diabetes. 2004;53:2921–30. DOI:10.2337/diabetes.53.11.2921</mixed-citation><mixed-citation xml:lang="ru">Thallas-Bonke V., Lindschau C., Rizkalla B., Bach L.A., Boner G., Meier M., Haller H., Cooper M.E., Forbes J.M. Attenuation of Extracellular Matrix Accumulation in Diabetic Nephropathy by the Advanced Glycation End Product Cross-Link Breaker ALT-711 via a Protein Kinase C- -Dependent Pathway // Diabetes. – 2004. – Vol. 53. – P. 2921–2930. DOI:10.2337/diabetes.53.11.2921</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">Yang S, Litchfield JE, Baynes JW. AGE-breakers cleave model compounds, but do not break Maillard crosslinks in skin and tail collagen from diabetic rats. Arch Biochem Biophys. 2003 Apr 1;412(1):42–6. DOI:10.1016/s0003-9861(03)00015-8</mixed-citation><mixed-citation xml:lang="ru">Yang S., Litchfield J.E., Baynes J.W. AGE-breakers cleave model compounds, but do not break Maillard crosslinks in skin and tail collagen from diabetic rats // Arch. Biochem. Biophys. – 2003. – Vol. 412, No. 1. – P. 42–46. DOI:10.1016/S0003-9861(03)00015-8</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">Nasiri R, Field MJ, Zahedi M, Moosavi-Movahedi AA. Cross-linking mechanisms of arginine and lysine with α,β-dicarbonyl compounds in aqueous solution. J Phys Chem A. 2011 Nov 24;115(46):13542–55. DOI:10.1021/jp205558d</mixed-citation><mixed-citation xml:lang="ru">Nasiri R., Field M.J., Zahedi M., Moosavi-Movahedi A.A. Cross-Linking Mechanisms of Arginine and Lysine with α,β-Dicarbonyl Compounds in Aqueous Solution // J. Phys. Chem. A. – 2011. – Vol. 115, No. 46. – P. 13542–13555. DOI:10.1021/jp205558d</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">Nasiri R, Field MJ, Zahedi M, Moosavi-Movahedi AA. Comparative DFT Study To Determine if α-Oxoaldehydes are Precursors for Pentosidine Formation. J Phys Chem A 2012;116(11):2986–96. DOI:10.1021/jp2104165</mixed-citation><mixed-citation xml:lang="ru">Nasiri R., Field M.J., Zahedi M., Moosavi-Movahedi A.A. Comparative DFT Study To Determine if α-Oxoaldehydes are Precursors for Pentosidine Formation // J. Phys. Chem. A. – 2012. – Vol. 116, No. 11. – P. 2986–2996. DOI:10.1021/jp2104165</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">Nobécourt E, Zeng J, Davies MJ, Brown BE, Yadav S, Barter PJ, Rye KA. Effects of cross-link breakers, glycation inhibitors and insulin sensitisers on HDL function and the non-enzymatic glycation of apolipoprotein A-I. Diabetologia. 2008 Jun;51(6):1008–17. DOI:10.1007/s00125-008-0986-z</mixed-citation><mixed-citation xml:lang="ru">Nobécourt E., Zeng J., Davies M.J., Brown B.E., Yadav S., Barter P.J., Rye K.A. Effects of cross-link breakers, glycation inhibitors and insulin sensitisers on HDL function and the non-enzymatic glycation of apolipoprotein A-I // Diabetologia. – 2008. – Vol. 51, No. 6. – P. 1008–1017. DOI:10.1007/s00125-008-0986-z</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">Kim T, Spiegel DA. The unique reactivity of N-phenacyl-derived thiazolium salts toward α-dicarbonyl compounds. Rejuvenation Res. 2013 Feb;16(1):43–50. DOI:10.1089/rej.2012.1370</mixed-citation><mixed-citation xml:lang="ru">Kim T., Spiegel D.A. The Unique Reactivity of N-Phenacyl-Derived Thiazolium Salts Toward α-Dicarbonyl Compounds // Rejuvenation Res. – 2013. – Vol. 16, No. 1. – P. 43–50. DOI:10.1089/rej.2012.1370</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">Sherwani SI, Khan HA, Ekhzaimy A, Masood A, Sakharkar MK. Significance of HbA1c Test in Diagnosis and Prognosis of Diabetic Patients. Biomark Insights. 2016 Jul 3;11: 95–104. DOI:10.4137/BMI.S38440</mixed-citation><mixed-citation xml:lang="ru">Sherwani S.I., Khan H.A., Ekhzaimy A., Masood A., Sakharkar M.K. Significance of HbA1c Test in Diagnosis and Prognosis of Diabetic Patients // Biomark Insights. – 2016. – Vol. 11. – P. 95–104. DOI:10.4137/BMI.S38440</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">Nagai R, Murray DB, Metz TO, Baynes JW. Chelation: a fundamental mechanism of action of AGE inhibitors, AGE breakers, and other inhibitors of diabetes complications. Diabetes. 2012 Mar;61(3):549–59. DOI:10.2337/db11-1120</mixed-citation><mixed-citation xml:lang="ru">Nagai R., Murray D.B., Metz T.O., Baynes J.W. Chelation: A Fundamental Mechanism of Action of AGE Inhibitors, AGE Breakers, and Other Inhibitors of Diabetes Complications // Diabetes. 2012. – Vol. 61, No. 3. – P. 549–559. DOI:10.2337/db11-1120</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">Toprak C, Yigitaslan S. Alagebrium and Complications of Diabetes Mellitus. Eurasian J Med. 2019 Oct;51(3): 285–92. DOI:10.5152/eurasianjmed.2019.18434</mixed-citation><mixed-citation xml:lang="ru">Toprak C., Yigitaslan S. Alagebrium and Complications of Diabetes Mellitus // Eurasian J. Med. – 2019. – Vol. 51, No. 3. – P. 285–292. DOI:10.5152/eurasianjmed.2019.18434</mixed-citation></citation-alternatives></ref></ref-list></back></article>
