ANTIOXIDANT EFFECT OF EXTRACT OF YELLOW FRUITS OF CORNELIAN CHERRY (CORNUS MAS L.) IN RATS’ LEUKOCYTES UNDER STREPTOZOTOCIN-INDUCED DIABETES MELLITUS

M. B. Seniv, O. V. Dzydzan, I. V. Brodyak, A. Z. Kucharska, N. O. Sybirna


DOI: http://dx.doi.org/10.30970/sbi.1501.645

Abstract


Background. The chronic hyperglycemia and intensified metabolic pathways of glucose conversion lead to the formation of excessive amounts of the reactive oxygen species and the development of oxidative stress under the condition of diabetes mellitus. In the recent decades, scientists have been searching for new drugs based on plant materials to prevent metabolic, structural and functional disorders in the body under diabetes. It has long been known that fruits and vegetables are sources of biologically active substances that have a beneficial effect on human health. The yellow fruits of the cornelian cherry (Cornus mas L.) contain a significant amount of substances (iridoids, phenolic acids and flavonoids), whose properties, biological effects and mechanism of action are not fully understood.
The aim of the study was to investigate the effect of the extract of yellow fruits of the cornelian cherry on the reactive oxygen species content and the activity of antioxidant enzymes in rats’ leukocytes with streptozotocin-induced diabetes mellitus.
Materials and Methods. Experimental diabetes mellitus in rats was induced by intraperitoneal administration of streptozotocin. The development of diabetes mellitus was monitored by blood glucose level. From the 10th day after the induction of diabetes, the animals were orally administered the extract of yellow fruits of the cornelian cherry at a dose of 20 mg/kg of the body weight for 14 days. On the last day of the experiment, we collected the blood into vials with heparin and isolated leukocytes to further determine the content of reactive oxygen species and the activity of antioxidant enzymes. Statistical analysis of the results was performed using MS Excel-2013.
Results. The content of the reactive oxygen species is increased and the activity of antioxidant enzymes is reduced in the rats’ leukocytes during streptozotocin-induced diabetes mellitus. Oral administration of the extract of yellow fruits of the cornelian cherry to diabetic animals improves the antioxidant status of leukocytes, which is manifested in an increased activity of superoxide dismutase, catalase and glutathione peroxidase along with a decrease in the level of intracellular reactive oxygen species.
Conclusions. The extract of yellow fruits of the cornelian cherry (Cornus mas L.) restores the balance between prooxidants and antioxidant defense system in leukocytes of rats with streptozotocin-induced diabetes mellitus. Such results suggest that the extract of yellow fruits of the cornelian cherry might be one of the plant components in the development of new drugs that will correct metabolic and functional disorders in leukocytes under diabetes.


Keywords


extract of yellow fruits, cornelian cherry, diabetes mellitus, reactive oxygen species, antioxidant enzymes, leukocytes

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References


1. Asgary S., Rafieian-Kopaei M., Shamsi F., Najafi S., Sahebkar A. Biochemical and histopathological study of the anti-hyperglycemic and anti-hyperlipidemic effects of cornelian cherry (Cornus mas L.) in alloxan-induced diabetic rats. Journal of Complementary and Integrative Medicine, 2014; 11(2): 63-69.
CrossrefPubMedGoogle Scholar

2. Bayram H.M., Ozturkcan Arda S. Bioactive components and biological properties of cornelian cherry (Cornus mas L.): A comprehensive review. Journal of Functional Foods, 2020; 75: 104252.
CrossrefGoogle Scholar

3. Bila I., Dzydzan O., Brodyak I., Sybirna N. Agmatine prevents oxidative-nitrative stress in blood leukocytes under streptozotocin-induced diabetes mellitus. Open Life Sciences, 2019; 14: 299-310.
CrossrefGoogle Scholar

4. Dzydzan O., Bila I., Kucharska A. Z., Brodyak I., Sybirna N. Antidiabetic effects of extracts of red and yellow fruits of cornelian cherries (Cornus mas L.) on rats with streptozotocin-induced diabetes mellitus. Food Funct., 2019; 10(10): 6459-6472.
CrossrefPubMedGoogle Scholar

5. Dzydzan O., Brodyak I., Sokół-Łętowska A., Kucharska A.Z., Sybirna N. Loganic acid, an iridoid glycoside extracted from Cornus mas L. fruits, reduces of carbonyl/oxidative stress biomarkers in plasma and restores antioxidant balance in leukocytes of rats with streptozotocin-induced diabetes mellitus. Life (Basel), 2020; 10(12): 349.
CrossrefPubMedPMCGoogle Scholar

6. Ferents I.V., Brodyak I.V., Lyuta M.Ya., Burda V.A., Sybirna N.O. Suppressive effect of agmatine on genetically programmed death of leukocytes in a diabetes model. Cytol. Genet., 2016; 50(4): 241-250.
CrossrefGoogle Scholar

7. Goldberg D.M., Spooner R.J. Glutathione Reductase. In methods of enzymatic analysis, 3rd ed.; Bergmeyer H.U., Bergmeyer J., GraBI M., Eds.; Verlag Chemie: Weinheim, Germany, 1983: 258-265.
Google Scholar

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

9. Graves D.T., Kayal R.A. Diabetic complications and dysregulated innate immunity. Frontiers in Bioscience, 2008; 13: 1227-1239.
CrossrefPubMedPMCGoogle Scholar

10. Ighodaro O.M., Akinloye O.A. First line defence antioxidants-superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX): Their fundamental role in the entire antioxidant defence grid. Alexandria Journal of Medicine, 2018; 54(4): 287-293.
CrossrefGoogle Scholar

11. Kakkar P., Das B., Viswanathan P.N. A modified spectrophotometric assay of superoxide dismutase. Indian Journal of Biochemistry & Biophysics, 1984; 21(2): 130-132.
PubMedGoogle Scholar

12. Limón-Pacheco J., Gonsebatt M.E. The role of antioxidants and antioxidant-related enzymes in protective responses to environmentally induced oxidative stress. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 2009; 674(1-2): 137-147.
CrossrefPubMedGoogle Scholar

13. Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry, 1951; 193(1): 265-275.
CrossrefPubMedGoogle Scholar

14. Marrocco I., Altieri F., Peluso I. Measurement and clinical significance of biomarkers of oxidative stress in humans. Oxidative Medicine and Cellular Longevity, 2017; 2017: 6501046.
CrossrefPubMedPMCGoogle Scholar

15. Matough F.A., Budin S.B., Hamid Z.A., Alwahaibi N., Mohamed J. The role of oxidative stress and antioxidants in diabetic complications. Sultan Qaboos University Medical Journal, 2012; 12(1): 5-18.
CrossrefPubMedPMCGoogle Scholar

16. Mclennan S.V., Heffernan S., Wright L., Rae C., Fisher E., Yue D.K., Turtle J.R. Changes in hepatic glutathione metabolism in diabetes. Diabetes, 1991; 40(3): 344-348.
CrossrefPubMedGoogle Scholar

17. Melekh B., Ilkiv I., Lozynskyi A., Sklyarov A. Antioxidant enzyme activity and lipid peroxidation in rat liver exposed to celecoxib and lansoprazole under epinephrine-induced stress. Journal of Applied Pharmaceutical Science, 2017; 7(10): 94-99.
CrossrefGoogle Scholar

18. Moldovan B., David L. Bioactive flavonoids from Cornus mas L. fruits. Mini-Reviews in Organic Chemistry, 2017; 14(6): 489-495.
CrossrefGoogle Scholar

19. Newsholme P., Cruzat V.F., Keane K.N., Carlessi R., De Bittencourt Jr P.I.H. Molecular mecha­nisms of ROS production and oxidative stress in diabetes. Biochemical Journal, 2016; 473(24): 4527-4550.
CrossrefPubMedGoogle Scholar

20. Nimse S.B., Pal D. Free radicals, natural antioxidants, and their reaction mechanisms. RSC Advances, 2015; 5: 27986-28006.
CrossrefGoogle Scholar

21. Ozougwu J.C., Obimba K.C., Belonwu C.D., Unakalamba C.B. The pathogenesis and pathophysiology of type 1 and type 2 diabetes mellitus. Journal of Physiology and Pathophysiology, 2013; 4(4): 46-57.
CrossrefGoogle Scholar

22. Patel H., Chen J., Das K.C., Kavdia M. Hyperglycemia induces differential change in oxidative stress at gene expression and functional levels in HUVEC and HMVEC. Cardiovasc Diabetol, 2013; 12: 142.
CrossrefPubMedPMCGoogle Scholar

23. Pavelescu L.A. On reactive oxygen species measurement in living systems. Journal of Medicine and Life, 2015; 8 (Spec Issue): 38-42.
PubMedPMCGoogle Scholar

24. Rains J.L., Jain S.K. Oxidative stress, insulin signaling and diabetes. Free Radical Biology and Medicine, 2011; 50(5): 567-575.
CrossrefPubMedPMCGoogle Scholar

25. Rolo A.P., Palmeira C.M. Diabetes and mitochondrial function: role of hyperglycemia and oxidative stress. Toxicology and Applied Pharmacology, 2006; 212(2): 167-178.
CrossrefPubMedGoogle Scholar

26. Rubattu S., Forte M., Raffa S. Circulating leukocytes and oxidative stress in cardiovascular disease: a state of the art. Oxidative Medicine and Cellular Longevity, 2019; 2019(16): 1-9.
CrossrefPubMedPMCGoogle Scholar

27. Schmoch T., Uhle F., Siegler B.H., Fleming T., Morgenstern J., Nawroth P.P., Weigand M.A., Brenner T. The glyoxalase system and methylglyoxal-derived carbonyl stress in sepsis: glycotoxic aspects of sepsis pathophysiology. Int J Mol Sci, 2017; 18(3): 657.
CrossrefPubMedPMCGoogle Scholar

28. Soltani R., Gorji A., Asgary S., Sarrafzadegan N., Siavash M. Evaluation of the effects of Cornus mas L. fruit extract on glycemic control and insulin level in type 2 diabetic adult patients: A randomized double-blind placebo-controlled clinical trial. Evidence-Based Complementary and Alternative Medicine, 2015; 2015: 740954.
CrossrefPubMedPMCGoogle Scholar

29. Sybirna N.O., Hachkova G.Ya., Brodyak I.V., Sybirna K.A., Khokhla M.R., Sabadashka M.V. Functional biochemistry. Ed. N.O. Sybirna. Lviv: Ivan Franko National University of Lviv, 2018. 644 p. (Series "Studia Biologica"). (In Ukrainian)

30. Zdioruk M., Barska M., Brodyak I., Vovk O., Urbanovich A., Sybirna N. Influence of wortmanin on agregation ability of neutrophylic granulocytes under type 1 diabetes mellitus. Studia Biologica, 2009; 3(2): 133-140. (In Ukrainian)
CrossrefGoogle Scholar

31. Zdioruk M., Brodyak I., Sybirna N. Participation of PI-3′-kinase signaling pathway in determining structural and functional state of leukocyte membranes under type 1 diabetes mellitus. Studia Biologica, 2011; 5(1): 85-96. (In Ukrainian)
CrossrefGoogle Scholar

32. Zhang P., Li T., Wu X., Nice E.C., Huang C., Zhang Y. Oxidative stress and diabetes: antioxidative strategies. Frontiers of Medicine, 2020; 14(5): 583-600.
CrossrefPubMedGoogle Scholar


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