ACTIVITY OF LIPID PEROXIDATION PROCESSES IN THE HEART OF MALE RATS AFTER CASTRATION

Authors

  • M. S. Regeda DANYLO HALYTSKY LVIV NATIONAL MEDICAL UNIVERSITY
  • B. M. Verveha DANYLO HALYTSKY LVIV NATIONAL MEDICAL UNIVERSITY
  • Yu. M. Stepas DANYLO HALYTSKY LVIV NATIONAL MEDICAL UNIVERSITY
  • T. Ya. Yaroshenko I. HORBACHEVSKY TERNOPIL NATIONAL MEDICAL UNIVERSITY

DOI:

https://doi.org/10.11603/mcch.2410-681X.2022.i2.13209

Keywords:

lipid peroxidation, antioxidant system, heart, castration

Abstract

Introduction. Pathology of the cardiovascular system takes a leading place in the structure of morbidity and mortality. One of the reasons for its development is sex hormones.

The aim of the study – to evaluate the development of oxidative stress in the heart homogenate of male rats after castration and replacement therapy.

Research Methods. Experiments were performed on Wistar rats of 160–180 grams. The animals were divided into 5 groups – control, castration for 1 month, castration for 2 months, castration + replacement therapy for 1 month, castration + replacement therapy for 2 months. Hormone replacement therapy in castrated animals was reproduced with testosterone propionate ("Farmak") 1 mg/kg subcutaneously once a day throughout the experiment. The content of diene conjugates (DC), TBK-active products (TBK-ap), superoxide dismutase activity (SOD), catalase activi­ty was determined in the heart homogenate.

Results and Discussion. In the group of animals that were castrated a month ago, the content of DC and TBC-active products, compared to the control, decreased, and in rats that were castrated two months ago, they increased. Replacement therapy led to modulatory effects of the content of DC and TBA-active products: one-month therapy led to an increase, and two-month therapy led to a decrease in indicators. DC values during replacement therapy were not significantly different from controls, but were higher after a 2-month course of replacement therapy. The values of the index of TBC-active products during replacement therapy did not depend on the duration of the course and did not differ reliably from the control. The enzyme link of the antioxidant system increased 1 month after castration, and decreased 2 months later. Replacement therapy showed a modulating effect, causing the normalization of SOD and catalase activity.

Conclusion. Castration of male rats after 1 month causes an increase in SOD and catalase activity, a decrease in lipid peroxidation processes compared to the control. Castration of male rats after 2 months causes a decrease in SOD and catalase activity, an increase in lipid peroxidation processes compared to the control. Carrying out replacement therapy with sex hormones in castrated animals brings the studied biochemical indicators closer to the level of the control group of rats.

References

Bajelan, M., Etehad Roodi, N., Hasanzadeh Daloee, M., Farhangnia, M., & Samadi Kuchaksaraei, A. (2019). The effect of low testosterone and estrogen levels on progressive coronary artery disease in men. Reports of Biochemistry & Molecular Biology, 8 (2), 168-171.

Rosano, G.M., Sheiban, I., Massaro, R., Pagnotta, P., Marazzi, G., Vitale, C., Mercuro, G., et al. (2007). Low testosterone levels are associated with coronary artery disease in male patients with angina. International Journal of Impotence Research, 19 (2), 176-182.

Ueda, K., Fukuma, N., Adachi, Y., Numata, G., Tokiwa, H., Toyoda, M., Otani, A., et al. (2021). Sex differences and regulatory actions of estrogen in cardiovascular system. Frontiers in Physiology, 12, 738218.

Lucas-Herald, A.K., Alves-Lopes, R., Montezano, A.C., Ahmed, S.F., & Touyz, R.M. (2017). Genomic and non-genomic effects of androgens in the cardiovascular system: clinical implications. Clinical science (London, England: 1979), 131 (13), 1405-1418.

Tarhouni, K., Guihot, A.L., Freidja, M.L., Toutain, B., Henrion, B., Baufreton, C., Pinaud, F., et al. (2013). Key role of estrogens and endothelial estrogen receptor α in blood flow-mediated remodeling of resistance arteries. Arteriosclerosis, Thrombosis, and Vascular Biology, 33 (3), 605-611.

Melnik, A. (2017). Relations between sex hormones levels and sulfur amino acids and hydrogen sulfide in blood. Reports of Vinnytsia National Medical Univer­sity, 21 (1(1), 6-8 [in Ukrainian].

Sobrino, A., Oviedo, P.J., Novella, S., Laguna-Fernandez, A., Bueno, C., García-Pérez, M.A., et al. (2010). Estradiol selectively stimulates endothelial prostacyclin production through estrogen receptor-{alpha}. Journal of Molecular Endocrinology, 44 (4), 237-246.

Dubey, R.K., Jackson, E.K., Keller, P.J., Imthurn, B., & Rosselli, M. (2001). Estradiol metabolites inhibit endothelin synthesis by an estrogen receptor-independent mechanism. Hypertension (Dallas, Tex.: 1979), 37 (2 Pt 2), 640-644.

Akishita, M., & Yu, J. (2012). Hormonal effects on blood vessels. Hypertension research: official journal of the Japanese Society of Hypertension, 35 (4), 363-369.

Kibel, A., Lukinac, A.M., Dambic, V., Juric, I., & Selthofer-Relatic, K. (2020). Oxidative Stress in Ischemic Heart Disease. Oxidative Medicine and Cellular Longe­vity, 2020, 6627144.

Aloisi, A.M., Ceccarelli, I., & Fiorenzani, P. (2003). Gonadectomy affects hormonal and behavioral responses to repetitive nociceptive stimulation in male rats. Annals of the New York Academy of Sciences, 1007, 232-237.

Joshi, S.A., Shaikh, S., Ranpura, S., & Khole, V.V. (2003). Postnatal development and testosterone dependence of a rat epididymal protein identified by neonatal tolerization. Reproduction (Cambridge, England), 125 (4), 495-507.

Ali, B.H., Ismail, T.H.B., & Bashir, A.A. (2001). Sex difference in the susceptibility of rats to gentamicin nephrotoxicity: Influence of gonadectomy and hormonal replacement therapy. Indian Journal of Pharmacology, 33 (5), 369-373.

Yuzurihara, M., Ikarashi, Y., Noguchi, M., Kase, Y., Takeda, S., & Aburada, M. (2003). Involvement of calcitonin gene-related peptide in elevation of skin temperature in castrated male rats. Urology, 62 (5), 947-951

Khyshiktuev, B.S., Khyshiktueva, N.A., & Ivanov, V.N. (1996). Methods of measuring lipid peroxidation products in exhaled air condensate and their clinical significance. Clinical Laboratory Diagnostics, (3), 13-15 [in Russian].

Vladimirov, J.A., & Archakov, A.I. (1972). [Lipid peroxidation in biological membranes]. Moscow: Nauka [in Russian].

Chevari, S., Chaba, I., & Sekeĭ, I. (1985). Role of superoxide dismutase in cellular oxidative processes and method of its determination in biological materials. Laboratory Business, (11), 678-681 [in Russian].

Koroliuk, M.A., Ivanova, L.I., Maĭorova, I.G., & Tokarev, V.E. (1988). A method of determining catalase activity. Laboratory Business, (1), 16-19 [in Russian].

Melnyk, A.V., Zaichko, N.V., Kachula, S.O., & Strutyn, O.B. (2017). Analysis of the effect of sex hor­mones on the biochemical parameters of the heart of rats: the relationship with the level of hydrogen sulfide in the myocardium. Scientific Journal “ScienceRise: Medical Science”, 3 (11), 35-39 [in Ukrainian].

Published

2022-10-04

How to Cite

Regeda, M. S., Verveha, B. M., Stepas, Y. M., & Yaroshenko, T. Y. (2022). ACTIVITY OF LIPID PEROXIDATION PROCESSES IN THE HEART OF MALE RATS AFTER CASTRATION. Medical and Clinical Chemistry, (2), 75–79. https://doi.org/10.11603/mcch.2410-681X.2022.i2.13209

Issue

Section

ORIGINAL INVESTIGATIONS