Diagnosis of myocardial fibrosis in arterial hypertension: An experimental study
Abstract. Myocardial fibrosis is a global medical problem, as far as it is associated with almost all forms of cardiovascular disease, including arterial hypertension (AH). The aim: to determine the development of myocardial fibrosis in an experiment on laboratory animals using morphological and biochemical research methods. Material and methods. The study included 24 Wistar rats aged 13–14 weeks, in which hypertension was modeled by removing one of their kidneys (experimental group). The control group consisted of sham-operated rats, which underwent a translumbar approach without kidney removal, followed by wound closure (n = 6). Blood for the study was collected from the inferior vena cava after euthanasia of the animals and subjected to enzyme-linked immunosorbent assay using kits for transforming growth factor beta (TGF-β) level determination. Results. The average systolic blood pressure in the experimental group in the first month of the experiment was 167 mmHg, diastolic – 89 mmHg. In the 2nd month, similar indexes were 178 and 95 mm Hg, in the 3rd – 152 and 92.6 mm Hg, in the 4th – 173.3 and 98.6 mm Hg, in the 5th – 180.6 and 102 mm Hg, in the 6th month – 161.3 and 90.6 mm Hg. When analyzing plasma TGF-β levels, the average TGF-β level in the control group was 7.4 ng/ml at month 2, 9.13 at month 4, and 8.57 ng/ml at month 6. In the experimental group, the average TGF-β concentrations at the same time points were 20.48, 18.24, and 15.6 ng/ml, respectively (p <0.05). Conclusion. The development of myocardial fibrosis in rats from the experimental group with arterial hypertension was confirmed by a significant increase in plasma TGF-β levels comparatively to animals in the control group. Using of this biomarker may be promising for predicting the development of hypertension complications, such as myocardial infarction, cardiac rhythm and conduction disorder, acute cerebrovascular accident.Bushmanov P.A., Filippov E.V., Sinyaeva A.S., Shelomentsev V.V., Nekrasova M.S., Cherdantseva T.M.
Keywords
References
1. Global Burden of Metabolic Risk Factors for Chronic Diseases Collaboration. Cardiovascular disease, chronic kidney disease, and diabetes mortality burden of cardiometabolic risk factors from 1980 to 2010: A comparative risk assessment. Lancet Diabetes Endocrinol. 2014;2(8):634–47.
PMID: 24842598. PMCID: PMC4572741. https://doi.org/10.1016/S2213-8587(14)70102-0
2. Миклишанская С.В., Мазур Н.А., Шестакова Н.В. Механизмы формирования миокардиального фиброза в норме и при некоторых сердечно-сосудистых заболеваниях. Методы его диагностики. Медицинский совет. 2017;(12):75–81. (Miklishanskaya SV, Mazur NA, Shestakova NV. Mechanisms for the formation myocardial fibrosis in norm and in certain cardiovascular diseases, how to diagnose it. Meditsinskiy sovet = Medical Council. 2017;(12):75–81 (In Russ.)).
EDN: PKBFUX. https://doi.org/10.21518/2079-701X-2017-12-75-81
3. Сержантова Н.А. Обзор методов диагностики фиброза миокарда. Измерение. Мониторинг. Управление. Контроль. 2023;(2):104–115. (Serzhantova NA. Diagnostic methods for myocardial fibrosis. Izmerenie. Monitoring. Upravlenie. Kontrol’ = Measuring. Monitoring. Management. Control. 2023;(2):104–115 (In Russ.)).
EDN: GDEHDE. https://doi.org/10.21685/2307-5538-2023-2-13
4. Yi H, Liu C, Shi J, Wang S, Zhang H, He Y et al. EGCG alleviates obesity-induced myocardial fibrosis in rats by enhancing expression of SCN5A. Front Cardiovasc Med. 2022;9:869279.
PMID: 35571212. PMCID: PMC9098820. https://doi.org/10.3389/fcvm.2022.869279
5. Мазитов Т.М., Нигматуллина Р.Р., Исламов Р.Р. Морфофункциональные показатели левого желудочка сердца крыс в изопротеренол-флуоксетиновой модели хронической сердечной недостаточности. Успехи современного естествознания. 2013;(6):44–49. (Mazitov TM, Nigmatullina RR, Islamov RR. Morfufunctional indices of left ventricular isoproterenolfluoxetin rat chronic heart failure model. Uspekhi sovremennogo yestestvoznaniya = Advances in Current Natural Sciences. 2013;(6):44–49 (In Russ.)). EDN: QBSHTX.
6. Таримов К.О., Субботкин М.В., Куланова А.А., Петренко В.И., Кубышкин А.В., Фомочкина И.И. с соавт. Сравнительный анализ коррекции морфофункциональных нарушений в сердечно-сосудистой системе при моделированном метаболическом синдроме. Ожирение и метаболизм. 2020;17(2):208–219. (Tarimov CO, Subbotkin MV, Kulanova AA, Petrenko VI, Kubyshkin AV, Fomochkina II et al. Comparative analysis of cardiovascular system morphofunctional disorders’ correction in a simulated metabolic syndrome. Ozhireniye i metabolizm = Obesity and Metabolism. 2020;17(2):208–219 (In Russ.)).
EDN: FGUANT. https://doi.org/10.14341/omet12296
7. Pollak WM, Simmons JD, Interian A Jr, Atapattu SA, Castellanos A, Myerburg RJ, Mitrani RD. Clinical utility of intraatrial pacemaker stored electrograms to diagnose atrial fibrillation and flutter. Pacing Clin Electrophysiol. 2001;24(4):424–29.
PMID: 11341078. https://doi.org/10.1046/j.1460-9592.2001.00424.x
8. Nagao K, Inada T, Tamura A, Kajitani K, Shimamura K, Yukawa H et al. Circulating markers of collagen types I, III, and IV in patients with dilated cardiomyopathy: Relationships with myocardial collagen expression. ESC Heart Fail. 2018;5(6):1044–51.
PMID: 30273997. PMCID: PMC6301156. https://doi.org/10.1002/ehf2.12360
9. Ma ZG, Yuan YP, Wu HM, Zhang X, Tang QZ. Cardiac fibrosis: New insights into the pathogenesis. Int J Biol Sci. 2018;14(12):1645–57.
PMID: 30416379. PMCID: PMC6216032. https://doi.org/10.7150/ijbs.28103
About the Authors
Pavel A. Bushmanov, MD, postgraduate student of the Department of outpatient therapy, preventive medicine, and general medical practice, Academician I.P. Pavlov Ryazan State Medical University of the Ministry of Healthcare of Russia. Address: 390026, Ryazan, 9 Vysokovoltnaya St.E-mail: pawel.buschmanov@yandex.ru
ORCID: https://orcid.org/0009-0004-4279-7991. eLibrary SPIN: 5412-0295
Evgeny V. Filippov, MD, Dr. Sci. (Medicine), professor, head of the Department of outpatient therapy, preventive medicine, and general medical practice, Academician I.P. Pavlov Ryazan State Medical University of the Ministry of Healthcare of Russia. Address: 390026, Ryazan, 9 Vysokovoltnaya St.
E-mail: dr.philippov@vk.com
ORCID: https://orcid.org/0000-0002-7688-7176. eLibrary SPIN: 2809-2781. Scopus Author ID: 56699755400
Anna S. Sinyaeva, MD, assistant at the Department of outpatient therapy, preventive medicine, and general medical practice, Academician I.P. Pavlov Ryazan State Medical University of the Ministry of Healthcare of Russia. Address: 390026, Ryazan, 9 Vysokovoltnaya St.
E-mail: anya.anyuta-07@yandex.ru
ORCID: https://orcid.org/0000-0002-7205-5321. eLibrary SPIN: 1345-4520
Viktor V. Shelomentsev, MD, assistant at the Department of histology, pathological anatomy, and medical genetics, Academician I.P. Pavlov Ryazan State Medical University of the Ministry of Healthcare of Russia. Address: 390026, Ryazan, 9 Vysokovoltnaya St.
E-mail: shelvit94@gmail.com
ORCID: https://orcid.org/0000-0003-2617-8707. eLibrary SPIN: 8499-0269
Marina S. Nekrasova, MD, assistant at the Department of histology, pathological anatomy, and medical genetics, Academician I.P. Pavlov Ryazan State Medical University of the Ministry of Healthcare of Russia. Address: 390026, Ryazan, 9 Vysokovoltnaya St.
E-mail: marinanekrasova555@gmail.com
ORCID: https://orcid.org/0000-0001-8178-6014. eLibrary SPIN: 2035-8060
Tatiana M. Cherdantseva, MD, Dr. Sci. (Medicine), professor, head of the Department of histology, pathological anatomy, and medical genetics, Academician I.P. Pavlov Ryazan State Medical University of the Ministry of Healthcare of Russia. Address: 390026, Ryazan, 9 Vysokovoltnaya St.
E-mail: cherdan.morf@yandex.ru
ORCID: https://orcid.org/0000-0002-7292-4996. eLibrary SPIN: 3773-8785



