Left ventricular remodeling in normotensive Wistar rats exposed to intermittent hypoxia of different duration

Authors

DOI:

https://doi.org/10.14739/2310-1237.2023.1.277406

Keywords:

myocardial remodeling, left ventricular, markers of myocardial remodeling, cardiotrophin-1, intermittent hypoxic hypoxia, rats

Abstract

Intermittent hypoxia has been studied for many years as a promising non-pharmacological method of cardiovascular disease prevention. Hypoxic effects are accompanied by structural and functional changes in the myocardium. There is a direct link between the duration of hypoxic exposures and the severity of left ventricular myocardial remodeling. A range of histochemical markers of myocardial remodeling (cardiotrophin-1, titin, collagen type 1, annexin V) characterizing parenchymal-stromal relationships in the myocardium has shown high informativeness and prognostic value.

The aim of the study was to examine cardiotrophin-1, titin, collagen type 1, annexin V and the morphofunctional state of the left ventricle of the heart in experimental rats exposed to intermittent 15-day (IH15) and 60-day hypoxia (IH60).

Materials and methods. Intermittent hypoxia was modeled using 30 normotensive male Wistar rats, 7–8 months old, which were randomly assigned to 3 experimental groups of 10 animals each: 1) INT – a control group – intact animals (196.3 ± 6.8 g); 2) IH15 – 15-day hypoxia (205.6 ± 4.1 g); 3) IH60 – 60-day hypoxia (201.1 ± 5.5 g). The study compared the effects of intermittent hypoxia of varying duration: 15-day and 60-day hypoxia. Experimental modeling of intermittent hypoxia of 2 terms revealed a number of differences between the effects dependent on this factor duration through functional (blood pressure measurement, echocardiography) and immunofluorescent studies.

Results. Blood pressure in rats of both groups was in the normotensive range, but an increase in systolic by 10 % and diastolic by 19 % was found in IH60 group compared to IH15 group (p < 0.05). In IH15 group, there was a significant decrease in end-diastolic dimension by 20 %, end-systolic dimension by 22 %, an increase in the thickness of left ventricular posterior wall by 44 % and interventricular septum by 33 % as well as left ventricular mass by 12 %, indicating concentric remodeling of the left ventricle, the development of which was confirmed by a 76 % increase in relative wall thickness compared to that in the control group (p < 0.05). Along with these changes, a decrease in end-diastolic volume by 47 %, end-systolic volume by 48 %, stroke volume by 49 % and cardiac output by 50 % with preserved ejection fraction was revealed (p < 0.05). While the parameters of IH60 rats were characterized by an increase in the thickness of interventricular septum by 33 % and left ventricular posterior wall by 17 %, as well as left ventricle mass by 23 %, relative left ventricular wall thickness was 15 % higher than the control value (p < 0.05). At the same time, diastolic volume was 9 % decreased and systolic volume was 24 % increased (p < 0.05). Also, cardiac output was increased by 58 % compared to that in 15-day hypoxic rats with an 8 % decrease in ejection fraction (p < 0.05). The concentrations of markers in IH60 group exceeded those in IH15, namely: cardiotrophin-1 by 39 %, titin by 70 %, collagen type 1 by 60 % and annexin V by 130 % (p < 0.05).

Conclusions. 15-day hypoxia forms concentric left ventricular hypertrophy according to echocardiography findings; the study of marker profile of myocardial remodeling has revealed the development of moderate hypertrophy with increased resilient-elastic properties and decreased intensity of cardiomyocyte death. Remodeling caused by 60-day hypoxia is characterized by the eccentric pattern of changes with severe hypertrophy, significant fibrosis associated with apoptosis of cardiomyocytes. Such morphofunctional state of the myocardium may indicate the initial stages of maladaptation, increasing the risk of heart failure development.

Author Biographies

Yu. M. Kolesnyk, Zaporizhzhia State Medical University, Ukraine

MD, PhD, DSc, Honorary Scientist and Engineering Worker of Ukraine, Professor, Rector

M. Yu. Kolesnyk, Zaporizhzhia State Medical University, Ukraine

MD, PhD DSc, Professor of the Department of Family Medicine, Therapy, Cardiology and Neurology, Faculty of Postgraduate Education, EACVI HIT Ambassador.

O. V. Hancheva, Zaporizhzhia State Medical University, Ukraine

MD, PhD, DSc, Professor, Head of the Department of Pathological Physiology with the Course of Normal Physiology

M. I. Isachenko, Zaporizhzhia State Medical University, Ukraine

MD, PhD, Аssociate Professor of the Department of Pathological Physiology with the Course of Normal Physiology

References

  1. Luo, B., Li, Y., Zhu, M., Cui, J., Liu, Y., & Liu, Y. (2022). Intermittent Hypoxia and Atherosclerosis: From Molecular Mechanisms to the Therapeutic Treatment. Oxidative medicine and cellular longevity, 2022, 1438470. https://doi.org/10.1155/2022/1438470
  2. Mallet, R. T., Burtscher, J., Pialoux, V., Pasha, Q., Ahmad, Y., Millet, G. P., & Burtscher, M. (2023). Molecular Mechanisms of High-Altitude Acclimatization. International journal of molecular sciences, 24(2), 1698. https://doi.org/10.3390/ijms24021698
  3. Bourdier, G., Détrait, M., Bouyon, S., Lemarié, E., Brasseur, S., Doutreleau, S., Pépin, J. L., Godin-Ribuot, D., Belaidi, E., & Arnaud, C. (2020). Intermittent Hypoxia Triggers Early Cardiac Remodeling and Contractile Dysfunction in the Time-Course of Ischemic Cardiomyopathy in Rats. Journal of the American Heart Association, 9(16), e016369. https://doi.org/10.1161/JAHA.120.016369
  4. Schüttler, D., Clauss, S., Weckbach, L. T., & Brunner, S. (2019). Molecular Mechanisms of Cardiac Remodeling and Regeneration in Physical Exercise. Cells, 8(10), 1128. https://doi.org/10.3390/cells8101128
  5. Ping, Y., Wang, X., Dai, Y., Wang, D., Liu, W., Yu, P., & Tao, Z. (2021). A quantitative detection of Cardiotrophin-1 in chronic heart failure by chemiluminescence immunoassay. Journal of clinical laboratory analysis, 35(4), e23570. https://doi.org/10.1002/jcla.23570
  6. Kellermayer, D., Smith, J. E., 3rd, & Granzier, H. (2019). Titin mutations and muscle disease. Pflugers Archiv : European journal of physiology, 471(5), 673-682. https://doi.org/10.1007/s00424-019-02272-5
  7. Yin, X., Yin, X., Pan, X., Zhang, J., Fan, X., Li, J., Zhai, X., Jiang, L., Hao, P., Wang, J., & Chen, Y. (2023). Post-myocardial infarction fibrosis: Pathophysiology, examination, and intervention. Frontiers in pharmacology, 14, 1070973. https://doi.org/10.3389/fphar.2023.1070973
  8. Zhang, J. (2022). Biomarkers of endothelial activation and dysfunction in cardiovascular diseases. Reviews in cardiovascular medicine, 23(2), 73. https://doi.org/10.31083/j.rcm2302073
  9. Nikolov, A., & Popovski, N. (2022). Extracellular Matrix in Heart Disease: Focus on Circulating Collagen Type I and III Derived Peptides as Biomarkers of Myocardial Fibrosis and Their Potential in the Prognosis of Heart Failure: A Concise Review. Metabolites, 12(4), 297. https://doi.org/10.3390/metabo12040297
  10. European Commission. (2010). Directive 2010/63/EU of the European Parliament and of the Council of 22 September 2010 on the protection of animals used for scientific purposes. Official Journal of the European Union. http://data.europa.eu/eli/dir/2010/63/oj
  11. Kolesnyk, Yu. M., & Isachenko, M. I. (2020). Pathogenetic features of morphodensitometric characteristics of cardiomyocytes and marker profile of the left ventricular remodeling in rats with experimental intermittent hypoxia of different duration. Journal of Education, Health and Sport, 10(9), 752-762. https://doi.org/10.12775/JEHS.2020.10.09.091
  12. Meerson, F. Z., & Pshennikova, M. G. (1988). Adaptatsiya k stressornyim situatsiyam i fizicheskim nagruzkam [Adaptatsiya k stressornym situatsiyam i fizicheskim nagruzkam]. Meditsina. [in Russian].
  13. Kolesnyk, Yu. M., Hancheva, O. V., Abramov, A. V., Ivanenko, T. V., Fedotova, M. I., & Danukalo, M. V. (2016). Sposib modeliuvannia fiziolohichnoho remodeliuvannia miokarda u dribnykh hryzuniv [Method for modeling physiological myocardial remodeling in small rodents]. Ukraine Patent UA 112290. https://sis.ukrpatent.org/uk/search/detail/824086/
  14. Kolesnyk, Yu. M., Isachenko, M. I., & Melnikova, O. V. (2019). The features of the nitric oxide system in the left ventricle myocardium in the rats with experimental intermittent hypoxia of different duration. Pathologia, 16(3), 308-314. https://doi.org/10.14739/2310-1237.2019.3.188783
  15. Ribeiro, S., Pereira, A. R. S., Pinto, A. T., Rocha, F., Ministro, A., Fiuza, M., Pinto, F., & Santos, S. C. R. (2019). Echocardiographic Assessment of Cardiac Anatomy and Function in Adult Rats. Journal of visualized experiments : JoVE, (154), 10.3791/60404. https://doi.org/10.3791/60404
  16. Saeed, A., Bashir, K., Shah, A. J., Qayyum, R., & Khan, T. (2022). Antihypertensive Activity in High Salt-Induced Hypertensive Rats and LC-MS/MS-Based Phytochemical Profiling of Melia azedarach L. (Meliaceae) Leaves. BioMed research international, 2022, 2791874. https://doi.org/10.1155/2022/2791874
  17. Papoušek, F., Sedmera, D., Neckář, J., Ošťádal, B., & Kolář, F. (2020). Left ventricular function and remodelling in rats exposed stepwise up to extreme chronic intermittent hypoxia. Respiratory physiology & neurobiology, 282, 103526. https://doi.org/10.1016/j.resp.2020.103526
  18. Rodríguez, A., Becerril, S., Hernández-Pardos, A. W., & Frühbeck, G. (2020). Adipose tissue depot differences in adipokines and effects on skeletal and cardiac muscle. Current opinion in pharmacology, 52, 1-8. https://doi.org/10.1016/j.coph.2020.04.003
  19. Matokhniuk, M. O., Limanskiy, O. V., Maiko, O. V., Zhebel, V., Shevchuk, O. K., & Palii, I. K. (2021). Prognostic significance of blood marker of hypertrophy- cardiotrophin-1 when carrying different variants of its gene in men with essential hypertension. Wiadomosci lekarskie, 74(2), 273-277.
  20. Polat, U., Aydinlar, A., Caliskan, S., Boyuk, F., & Unal, O. (2021). The correlation between cardiac enzymes and cardiotrophin-1 levels in patients with acute coronary syndrome. International Journal of Cardiovascular Sciences, 34, 12-21.
  21. Martínez-Martínez, E., Brugnolaro, C., Ibarrola, J., Ravassa, S., Buonafine, M., López, B., Fernández-Celis, A., Querejeta, R., Santamaria, E., Fernández-Irigoyen, J., Rábago, G., Moreno, M. U., Jaisser, F., Díez, J., González, A., & López-Andrés, N. (2019). CT-1 (Cardiotrophin-1)-Gal-3 (Galectin-3) Axis in Cardiac Fibrosis and Inflammation. Hypertension, 73(3), 602-611. https://doi.org/10.1161/HYPERTENSIONAHA.118.11874
  22. Raso, A., Dirkx, E., Philippen, L. E., Fernandez-Celis, A., De Majo, F., Sampaio-Pinto, V., Sansonetti, M., Juni, R., El Azzouzi, H., Calore, M., Bitsch, N., Olieslagers, S., Oerlemans, M. I. F. J., Huibers, M. M., de Weger, R. A., Reckman, Y. J., Pinto, Y. M., Zentilin, L., Zacchigna, S., Giacca, M., … De Windt, L. J. (2019). Therapeutic Delivery of miR-148a Suppresses Ventricular Dilation in Heart Failure. Molecular therapy, 27(3), 584-599. https://doi.org/10.1016/j.ymthe.2018.11.011
  23. Venugopal, H., Hanna, A., Humeres, C., & Frangogiannis, N. G. (2022). Properties and Functions of Fibroblasts and Myofibroblasts in Myocardial Infarction. Cells, 11(9), 1386. https://doi.org/10.3390/cells11091386
  24. Cziraki, A., Nemeth, Z., Szabados, S., Nagy, T., Szántó, M., Nyakas, C., & Koller, A. (2023). Morphological and Functional Remodeling of the Ischemic Heart Correlates with Homocysteine Levels. Journal of cardiovascular development and disease, 10(3), 122. https://doi.org/10.3390/jcdd10030122
  25. Czubryt, M. P. (2019). Cardiac Fibroblast to Myofibroblast Phenotype Conversion-An Unexploited Therapeutic Target. Journal of cardiovascular development and disease, 6(3), 28. https://doi.org/10.3390/jcdd6030028
  26. Pach, E., Kümper, M., Fromme, J. E., Zamek, J., Metzen, F., Koch, M., Mauch, C., & Zigrino, P. (2021). Extracellular Matrix Remodeling by Fibroblast-MMP14 Regulates Melanoma Growth. International journal of molecular sciences, 22(22), 12276. https://doi.org/10.3390/ijms222212276
  27. Shi, X., Dorsey, A., & Qiu, H. (2022). New Progress in the Molecular Regulations and Therapeutic Applications in Cardiac Oxidative Damage Caused by Pressure Overload. Antioxidants, 11(5), 877. https://doi.org/10.3390/antiox11050877
  28. Horowitz, M., & Hasin, Y. (2023). Vascular compliance and left ventricular compliance cross talk: Implications for using long-term heat acclimation in cardiac care. Frontiers in physiology, 14, 1074391. https://doi.org/10.3389/fphys.2023.1074391
  29. Koser, F., Loescher, C., & Linke, W. A. (2019). Posttranslational modifications of titin from cardiac muscle: how, where, and what for?. The FEBS journal, 286(12), 2240-2260. https://doi.org/10.1111/febs.14854
  30. Kötter, S., & Krüger, M. (2022). Protein Quality Control at the Sarcomere: Titin Protection and Turnover and Implications for Disease Development. Frontiers in physiology, 13, 914296. https://doi.org/10.3389/fphys.2022.914296
  31. Sharma, S., Sharma, P., Subedi, U., Bhattarai, S., Miller, C., Manikandan, S., Batinic-Haberle, I., Spasojevic, I., Sun, H., Panchatcharam, M., & Miriyala, S. (2023). Mn(III) Porphyrin, MnTnBuOE-2-PyP5+, Commonly Known as a Mimic of Superoxide Dismutase Enzyme, Protects Cardiomyocytes from Hypoxia/Reoxygenation Induced Injury via Reducing Oxidative Stress. International journal of molecular sciences, 24(7), 6159. https://doi.org/10.3390/ijms24076159
  32. Ji, H., Xiao, F., Li, S., Wei, R., Yu, F., & Xu, J. (2021). GRP78 effectively protect hypoxia/reperfusion-induced myocardial apoptosis via promotion of the Nrf2/HO-1 signaling pathway. Journal of cellular physiology, 236(2), 1228-1236. https://doi.org/10.1002/jcp.29929
  33. Méndez-Barbero, N., San Sebastian-Jaraba, I., Blázquez-Serra, R., Martín-Ventura, J. L., & Blanco-Colio, L. M. (2022). Annexins and cardiovascular diseases: Beyond membrane trafficking and repair. Frontiers in cell and developmental biology, 10, 1000760. https://doi.org/10.3389/fcell.2022.1000760

Downloads

Published

2023-04-28

How to Cite

1.
Kolesnyk YM, Kolesnyk MY, Hancheva OV, Isachenko MI. Left ventricular remodeling in normotensive Wistar rats exposed to intermittent hypoxia of different duration. Pathologia [Internet]. 2023Apr.28 [cited 2026May12];20(1):5-13. Available from: https://pat.zsmu.edu.ua/article/view/277406

Issue

Section

Original research