THE CORRECTIVE EFFECT OF PEPTIDES ON THE PRO- AND ANTIOXIDANT SYSTEM INDICATORS' CHANGES IN RATS OF DIFFERENT AGES AFFECTED BY HEAVY METALS AND GLYPHOSATE

Authors

  • Ye. B. Dmukhalska I. HORBACHEVSKY TERNOPIL NATIONAL MEDICAL UNIVERSITY
  • M. M. Korda I. HORBACHEVSKY TERNOPIL NATIONAL MEDICAL UNIVERSITY
  • T. Ya. Yaroshenko I. HORBACHEVSKY TERNOPIL NATIONAL MEDICAL UNIVERSITY

DOI:

https://doi.org/10.11603/mcch.2410-681X.2024.i2.14769

Keywords:

Lead acetate, Copper sulfate, glyphosate, oxidative stress, antioxidant systems

Abstract

Introduction. It is known that the effects of various environmental pollutants, such as heavy metals and organophosphorus compounds, cause various changes in the human body, accompanied by imbalances between oxidation and reduction, the formation of reactive oxygen species, which explains the development of oxidative stress. Heavy metals and organophosphorus compounds used in agriculture cause diseases of the liver and other organs, which contributes to the formation of reactive oxygen species (ROS), which can induce lipid peroxidation and inhibit the antioxidant system. The basis of the action of heavy metals is the blocking of functionally active groups of structural proteins, enzyme proteins, the blocking of sulfhydryl (thiol, SH) groups is of greatest importance. Under the action of heavy metals, most proteins lose their physicochemical and biological properties, which leads to disruption of protein and other metabolism. To date, the correction of violations of free radical and antioxidant processes by the combined action of heavy metals and organophosphorus pesticides remains incompletely studied.

The aim of the study – to study the antioxidant activity (AOA) of the peptides in virto and iv vivo in rats of various ages affected by lead acetate, cuprum sulfate, and glyphosate (in the form of roundup herbicide).

Research Methods. Experiments were conducted on laboratory non-linear white male rats of three age groups (sexually immature, sexually mature and old), which were administered intragastrically for 30 days with aqueous solutions of lead acetate, copper sulfate and glyphosate. For the purpose of correction, on the 21st day, 6 hours after the introduction of toxicants, peptides were administered for 10 days. Glutathione peroxidase, glutathione reductase, catalase, superoxide dismutase activity and the content of SH-groups, ROS, TBA-active products (TBA-AP) and diene conjugates (DC) were determined spectrophotometrically in blood serum and liver homogenate of affected and treated animals.

Results and Discussion. Heavy metals and organophosphorus compounds caused the formation of ROS, such as superoxide ions, hydrogen peroxide and hydroxyl radicals. With the combined action of lead acetate, copper sulfate, and glyphosate, the processes of free radical oxidation of lipids and the generation of ROS in rats were activated with age, which was evidenced by the increase in the content of DC, TBA-AP, superoxide anion radical, and hydroxyl radical. As our studies showed, the introduction of toxicants led to a decrease in glutathione peroxidase, glutathione reductase, catalase, superoxide dismutase activity, the level of SH-groups in blood serum and liver homogenate of affected animals. The use of peptides as correction factors contributed to a decrease towards the norm in the content of ROS and products of lipid peroxidation and normalization of the activity of enzymes of the antioxidant system, which obviously indicates the antioxidant and chelating properties of peptides.

Conclusion. Exposure of rats to lead acetate, copper sulfate and glyphosate at a dose of 1/20 LD50 leads to an increase in the content of TBA-AP, DC, ROS and a decrease in the activity of enzymes of the antioxidant system in blood serum and liver homogenate. Administration of peptides as corrective factors to animals of various ages with toxic liver damage increases glutathione peroxidase, glutathione reductase, catalase, and superoxide dismutase activity toward normal levels and reduces the content of lipid free radical oxidation products and ROS.

References

Netiykhailo, L.H., & Kharchenko, S.V. (2014). Aktyvni formy kysniu (ohliad literatury) [Active forms of oxygen (Literature overview)]. Molodyi vchenyi – Young Scientist, 9 (12), 131-135 [in Ukrainian].

Ray, P.D., Huang, B.W., Tsuji, Y. (2012). Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling. Cell Signal. 24, 981-990. DOI: 10. 1016/j.cellsig.2012.01.008.

Mut-Salud, N., Álvarez, P.J., Garrido, J.M., & Rodríguez-Serrano, F. (2016) Antioxidant intake and antitumor therapy: Toward nutritional recommendations for optimal results. Oxid. Med. Cell. Longev. 2016, 6719534. DOI: 10.1155/2016/6719534.

Di Meo, S., Reed, T.T., Venditti, P., Victor, V.M. (2016). Role of ROS and RNS sources in physiological and pathological conditions. Oxid Med Cell Longev. 2016, 1245049. DOI: 10.1155/2016/1245049 1245049.

Ahamed, M., Siddiqui, M.K.J. (2007). Environmental lead toxicity and nutritional factors. Environmental lead toxicity and nutritional factors. Clin. Nutr., 26 (4), 400-408.

Marushko, Iu.V. (2013). Significance of insufficient copper content in the body for clinical practice. Children's Doctor, 2 (23), 11-16 [in Ukrainian].

Arena, M., Auteri, D., Barmaz, S. & Villamar-Bouza, L. (2018). Peer review of the pesticide risk assessment of the active substance copper compounds copper(I), copper(II) variants namely copper hydroxide, copper oxychloride, tribasic copper sulfate, copper(I) oxide, Bordeaux mixture. EFSA Journal, 16 (1), 1-25. DOI: 10.2903/j.efsa.2018.5152.

Prasher, D. (2009). Heavy metals and noise exposure: health effects. Noise Health, 11, 141-144.

Karrari, P., Mehrpour, O., Abdollahi, M. (2012). A systematic review on status of lead pollution and toxicity in Iran; Guidance for preventive measures. Daru. 20, 1, 2-12.

Dietert, R.R., & Piepenbrink, M.S. (2006) Lead and immune function. Crit. Rev. Toxicol., 36, 359-385.

Ostrovska, S.S., Shatorna, V.F., & Slesarenko, O.H. (2021). The influence of lead on the reproductive health of men. Ukrainian Journal of Medicine, Biology and Sports, 6, 4 (32), 193-198 [in Ukrainian].

Mishra, D. (2008). Quercetin administration during chelation therapy protects arsenic induced oxi­dative stress in mouse. Biological Trace Element Re­search, 122, 137-147.

Blanusa, M. (2005). Chelators as antidotes of metal toxicity: therapeutic and experimental aspects. Current Medicinal Chemistry, 12, 2771-2794.

Pachauri, P. (2009). Combinational chelation therapy abrogates lead induced neurodegeneration in rats. Toxicology and Applied Pharmacology, 240, 255-265.

Guzmán, F., Aróstica, M., & Román, T. (2023) Peptides, solid-phase synthesis and characterization: Tailor-made methodologies. Electron J Biotechnol. 64. DOI: 10.1016/j.ejbt.2023.01.005.

Hubskyi, Yu.I., Dunaiev, V.V., & Bielenichev, I.F. (2002) Metody otsinky antyoksydantnykh vlastyvostei fiziolohichno aktyvnykh spoluk pry initsiiuvanni vilno­radykalnykh protsesiv u doslidakh in vitro: Metod. rekom. Kyiv: DFTs MOZ Ukrainy, Methodical recommend. Kyiv: State Department of the Ministry of Health of Ukraine, 26 [in Ukrainian].

Guo, J., Huang, X., & Dou, L. (2022) Aging and aging-related diseases: from molecular mechanisms to interventions and treatments. Sig Transduct Target Ther 7, 391, DOI: 10.1038/s41392-022-01251-0.

Meschyshen, I.F., & Hryhorieva, N.P. (2002). Method for quantitative determination of HS groups in the blood. Bukovyna Medical Bulletin, 6 (2), 190-192 [in Ukrainian].

Herush, I.V., & Meschyshen, I.F. (1998). The effect of alcohol tincture of Echinacea purpurea on the state of the antioxidant system of the liver in experimental erosive-ulcerative lesions of the gastroduodenal zone. Pharma-cological Bulletin, 5, 34-37 [in Ukrainian].

Vlizlo, V.V., Fedorchuk, R.S., & Ratych, I.B. (2012). Laboratory research methods in biology, animal husbandry and veterinary medicine: Handbook. Lviv: SPOLOM [in Ukrainian].

Sheng, Y., Abreu, I.A., & Cabelli, D.E. (2014). Superoxide dismutases and superoxide reductases. Chem. Rev., 114, 3854-3918.

Goth, L. (1991). A simple method for determination of serum catalase activity and revision of reference range. Clinica Chimica Acta., 196 (2-3), 143-151.

The Law of Ukraine “On the Protection of animals from ill-treatment” of 02.21. 006, No. 3447 [in Ukrainian].

Kozhemiakin, Yu.M., Khromova, O.S., & Filo­nenko, M.A. (2002). Scientific and practical recommen­dations for the maintenance of laboratory animals and work with them. Kyiv: Avitsena [in Ukrainian].

(1986). European convention for the protection of vertebrate animals used for experimental and other scientific purposes Council of Europe. Strasbourg.

Rosner, B. (2010). Fundamentals of Biostatistics. Boston, USA.

Omobowale, T.O, Oyagbemi, A.A, & Olopade, J.O. (2014). Failure of recovery from lead induced hepatoxicity and disruption of erythrocyte antioxidant defence system in Wistar rats. Environ. Toxicol. Pharm., 37 (3), 1202-1211.

Ahamed, M., & Siddiqui, M.K.J. (2007) Envi­ronmental lead toxicity and nutritional factors. Clin. Nutr., 26 (4), 400-408.

Published

2024-07-19

How to Cite

Dmukhalska, Y. B., Korda, M. M., & Yaroshenko, T. Y. (2024). THE CORRECTIVE EFFECT OF PEPTIDES ON THE PRO- AND ANTIOXIDANT SYSTEM INDICATORS’ CHANGES IN RATS OF DIFFERENT AGES AFFECTED BY HEAVY METALS AND GLYPHOSATE . Medical and Clinical Chemistry, (2), 65–74. https://doi.org/10.11603/mcch.2410-681X.2024.i2.14769

Issue

Section

ORIGINAL INVESTIGATIONS