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The content of malonic dialdehyde in the tissues of golden trout (Oncorchynchus mykiss) when foraging with organomineral chelate complexes

https://doi.org/10.52419/issn2072-2419.2025.3.411

Abstract

The activity of antioxidant enzymes depends on a number of variables, including the content of nutrients in the diet. To normalize the mineral component of diets, it is proposed to use various metal-containing preparations, including chelated (intracomplex) compounds. A number of studies have demonstrated that chelated compounds have greater bioavailability compared to inorganic sources of trace elements.

The aim of the study was to study the effect of the chelate complex on the processes of free radical oxidation in trout by determining the activity of catalase and the content of malonic aldehyde. An organomineral chelate complex (Jupiter LLC, Russia) was investigated. The active base of the mineral supplement is a complex of ethylenediaminediantharic acid and lysine with trace elements (Fe, Mn, Cu, Zn, Co, Se, I). Fish of the experimental groups (n=10) were given the supplement for 30 days; the data were compared with the control (n=10). The chelate complex was administered together with the feed once a day, at a concentration of 0.5 g/ kg (counting from the weight of the feed). The activity of catalase and the concentration of malonic aldehyde in the liver and muscles were determined. The use of organomineral chelate complexes led to a decrease in the content of malondialdehyde in the liver and skeletal muscles. A decrease in lipid peroxidation products was accompanied by a significant increase in catalase activity. The conducted studies suggest that metals in the composition of chelate complexes lead to an increase in the activity of antioxidant enzymes, resulting in a decrease in lipid peroxidation products. Thus, the results obtained serve as an indirect confirmation of the effectiveness of the use of organomineral chelate complexes in industrial aquaculture.

About the Authors

P. A. Polistovskaya
St. Petersburg State University of Veterinary Medicine
Russian Federation

PhD., associate Professor of the Department of Biochemistry and Physiology



L. Yu. Karpenko
St. Petersburg State University of Veterinary Medicine
Russian Federation

Doctor of Biological Sciences, Professor, Head of the Department. Biochemistry and physiology



I. A. Makhnin
St. Petersburg State University of Veterinary Medicine
Russian Federation

post-graduate student of the 2st year of study, assistant of the Department of Biochemistry and Physiology



References

1. Irina Sergeevna Marchenko Development of aquaculture as a factor of ensuring food security // The Eurasian Union of Scientists. 2015. №11-4 (20).

2. Martos-Sitcha, Juan Antonio et al. “Editorial: Welfare and Stressors in Fish: Challenges Facing Aquaculture.” Frontiers in physiology vol. 11 162. 25 Feb. 2020, doi:10.3389/fphys.2020.00162

3. Zengin, H. The effects of feeding and starvation on antioxidant defence, fatty acid composition and lipid peroxidation in reared Oncorhynchus mykiss fry. Sci Rep 11, 16716 (2021). https://doi.org/10.1038/s41598-021-96204-y

4. Karbyshev, M. S. Biochemistry of oxidative stress: an educational and methodical manual / M. S. Karbyshev, Sh. P. Abdullaev; under the general editorship of A.V. Shespopalov. - Moscow: Publishing House XX, 2018. - 60s.

5. Tunçelli G, Ertik O, Bayrak BB, Memiş D, Yanardag R. Effects of swimming activity and feed restriction on antioxidant and digestive enzymes in juvenile rainbow trout: Implications for nutritional and exercise strategies in aquaculture. Vet Med Sci. 2024 May;10(3):e1466. doi: 10.1002/vms3.1466.

6. Ludan V. V., Polskaya L. V. The role of antioxidants in the vital activity of the body. 2019. №3.).

7. Ivakhnenko, V. I. Investigation of the activity of metal-dependent enzymes of antioxidant protection and indicators of lipid peroxidation in rats under the action of nutritional factors: specialty 03.00.04 "Biochemistry" : Abstract for candidate of Biological Sciences / Ivakhnenko, V. I.; State Research Institute of Nutrition of the Russian Academy of Medical Sciences. — Moscow, 2008. — 23 p.

8. Ghasemi, H.A., Hajkhodadadi, I., Hafizi, M. et al. Effect of advanced chelate technology-based trace minerals on growth performance, mineral digestibility, tibia characteristics, and antioxidant status in broiler chickens. Nutr Metab (Lond) 17, 94 (2020). https://doi.org/10.1186/s12986-020-00520-5

9. Karkishchenko N. N., Karkishchenko V. N., Lyublinsky S. L., Kapanadze G. D., Shustov E. B., Revyakin A. O., Bolotskikh L. A., Kasinskaya N. V., Stankova N. V. The role of trace elements in sports nutrition and the safety of metallochelates // Biomedicine. 2013. №2.

10. Koshchaev A.G., Gorkovenko N.E., Kosykh A.V., Antipova D.V. Chelated compounds and their use for the correction of microelementosis in farm animals (literature review). Veterinary medicine today. 2024;13 (2):136-142.

11. Livshits, V. M. Biochemical analyses in the clinic: a handbook [Text] / V. M. Livshits, V. I. Sinelnikova. – M. : Medical Information Agency, 1998. – p. 303 (20).

12. Bogacheva E. V., Alabovsky V. V., Perov S. Yu. Determination of the concentration of malonic dialdehyde in the serum of rats irradiated with an electromagnetic field of the meter range // Izv. Sarath. University of Nov. ser. Ser. Chemistry. Biology. Ecology. 2016. No. 1.).

13. Yu, H., Zhang, C., Zhang, X., Wang, C., Li, P., Liu, G., et al. (2020). Dietary nanoselenium enhances antioxidant capacity and hypoxia tolerance of grass carp Ctenopharyngodon idella fed with high-fat diet. Aquac. Nutr. 26, 545–557. doi:10.1111/anu.13016

14. Liu, G. X., Jiang, G. Z., Lu, K. L., Li, X. F., Zhou, M., Zhang, D. D., et al. (2017). Effects of dietary selenium on the growth, selenium status, antioxidant activities, muscle composition and meat quality of blunt snout bream, Megalobrama amblycephala. Aquac. Nutr. 23, 777–787. doi:10.1111/anu.12444

15. Behera, T., Swain, P., Rangacharulu, P.V. et al. Nano-Fe as feed additive improves the hematological and immunological parameters of fish, Labeo rohita H. Appl Nanosci 4, 687 –694 (2014). https://doi.org/10.1007/s13204-013-0251-8

16. Kumar, N., Krishnani, K.K. & Singh, N.P. Effect of Dietary Zinc-Nanoparticles on Growth Performance, Anti-Oxidative and Immunological Status of Fish Reared Under Multiple Stressors. Biol Trace Elem Res 186, 267–278 (2018). https://doi.org/10.1007/s12011-018-1285-2

17. Tang, Q.Q., Feng, L., Jiang, W.D. et al. Effects of Dietary Copper on Growth, Digestive, and Brush Border Enzyme Activities and Antioxidant Defense of Hepatopancreas and Intestine for Young Grass Carp (Ctenopharyngodon idella). Biol Trace Elem Res 155, 370–380 (2013). https://doi.org/10.1007/s12011-013-9785-6

18. Hernroth B., Baden S. P., Holm K., André T., Söderhäll I. (2004). Manganese induced immune suppression of the lobster, nephrops norvegicus. Aquat. Toxicol. 70:3, 223–231. doi: 10.1016/j.aquatox.2004.09.004

19. Abarghoei S., Hedayati A., Ghorbani R., Miandareh H. K., Bagheri T. (2016). Histopathological effects of waterborne silver nanoparticles and silver salt on the gills and liver of goldfish carassius auratus. Int. J. Environ. Sci. Technol. 13 (7), 1753–1760. doi: 10.1007/s13762-016-0972-9

20. Liu X. F., Zhang L. M., Guan H. N., Zhang Z. W., Xu S. W. (2013). “Effects of oxidative stress on apoptosis in manganeseinduced testicular toxicity in cocks.” Food & Chemical Toxicology 60. Complete (2013), 168–176. doi: 10.1016/j.fct.2013.07.058


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For citations:


Polistovskaya P.A., Karpenko L.Yu., Makhnin I.A. The content of malonic dialdehyde in the tissues of golden trout (Oncorchynchus mykiss) when foraging with organomineral chelate complexes. International Journal of Veterinary Medicine. 2025;(3):411-418. (In Russ.) https://doi.org/10.52419/issn2072-2419.2025.3.411

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