Effect of aqueous moringa seed extract on oxidative stress in Alloxan- induced gestational diabetic rats

Main Article Content

Festus Adu Yusuf J Ajao F O Odedele L O

Abstract

ABSTRACTS

The mechanistic pathway for the antioxidant efficacy of the aqueous Moringa oleifera seed extract in gestational diabetes was investigated by evaluating five  antioxidant parameters, three (MDA,GSH and GST) of which were done from the uterus and two (CAT  and SOD) from the serum using a pregnant diabetic animal model. Pregnant Wistar rats were divided into four groups of 8 each made up of Normal control untreated, Non-diabetic treated, Diabetic treated and  Diabetic untreated. The four groups of animals were used to evaluate the effect of the extract on the biochemical parameters and the level of antioxidants in the uterus and the serum. The level of significance of the level of biochemical parameters were determined respectively using the Analysis of variance(ANOVA).

The administration of 300mg/kg body weight of Moringa oleifera seed extract produced significant increase in Catalase and SOD levels in the serum. However, there was a significant decrease in the uterus of MDA and a significant increase in the uterus of GSH and GST when compared with the normal untreated group and the untreated diabetic groups.

These observations support the hypothesis that aqueous Moringa oleifera seed extract possesses antioxidant parameters that are able to counter or revert the effect of gestational diabetes induced by oxidative stress.    

Article Details

How to Cite
ADU, Festus et al. Effect of aqueous moringa seed extract on oxidative stress in Alloxan- induced gestational diabetic rats. Medical Research Archives, [S.l.], v. 5, n. Issue 9, sep. 2017. ISSN 2375-1924. Available at: <https://esmed.org/MRA/mra/article/view/1554>. Date accessed: 22 dec. 2024.
Keywords
Key Words: Gestational diabetes, Moringa, Antioxidants, Oxidative Stress, Alloxan
Section
Research Articles

References

References
1. Davies, KJ. Oxidative stress: The paradox of aerobic life. Biochemical Society symposia 61: 1995; 1-31.
2. Sies, H. Oxidative stress: Oxidants and antioxidants. Experimental Physiology 1997; 82(2): 291-295.
3. Vertuani, S; Angusti, A; Manfredini, S. The antioxidants and Pro-Antioxidants Network: An overview. Current Pharmaceutical Design. 2004, vol 10(14) : 1677-1694.
4. Christen, Y. Oxidative stress and Alzheimer disease. Amer Jour Clin Nutr. 2000;71(2) ;621S-629S
5. Davi, G, Falco A., Patrono C. Lipid peroxidation in diabetes mellitus. Anatioxid Redox Signal. 2005; 71(1-2) :2
6. Al-Gubory, KH, Fowler PA, Garrel C. The roles of cellular reactive oxygen species, oxidative stress and antioxidants in pregnancy outcomes. Int J Biochem Cell Biol. 2010 Oct;42(10):1634-50.
7. Agarwal A1, Gupta S, Sharma RK. Role of oxidative stress in female reproduction. Reprod Biol Endocrinol. 2005 Jul 14;3:28
8. Kristina, B., Nanmi S., Kota, MK, and Kristina Rao RV. Evaluation of antihyperglycemic effects of Datura metal lim seeds in normal and alloxan induced rats. Journal of Ethnopharmacol. 2004; 9:95-98.
9. World Health Organization. Dept of non-communicable disease surveillance. Definition and classification of diabetes mellitus and its complications. Reports. 1999.WHO. Geneva.pp. 1-33.
10. DeSmet, PAGM and D’Arcy, PF. Drug interaction with herbal anad non orthordox remedies. In: D’Arcy PF, McElna JC, Welling PG, eds Mechanism of drug interactions New York NY: Springer-Verlag:327-352.
11. Kar, A.Chouldhary BK, Bandyopadhyay NG. comparative evaluation of hypoglycemic activity of some indian medicinal plants in alloxan diabetic rats. Jour. Ethnophaarmacol. 2003; 84: 105-108.
12. Aebi, HE. Catalase:In Bergmeyer HU. Ed. Methods of enzymatic analysis. Verlag Chemie, Weinhem, 1983; 273-286.
13. Misral, HP and Fridovich, I. The role of superoxide dismutase in the anti-oxidation of epinephrine and a simple assay for superoxide dismutase. Jour Biol Chem 1982; 247(10):3171-3175.
14. Varshney, R. and Kale, RK. Effect of Calmodulin Antagonist on Radiation-Induced Lipid Peroxidation in Microsomes. International Journal of Radiation Biology,1990; 58, 733-743.
15. Vashney,R. and Kale, R.K. Effects of calmodulin Antagoniss. Int. J Rad.Biol.1990. 58:733-743
16. Habig, WH., Pabst, MJ., Jacoby, WB. Glutathion-stransferase. The first step in mercapturic acid formation. Bio chem. 1974. 249: 7130-7139
17. Siddhuraju P and Becker K. Antioxidant properties of various solvent extracts of total henolic constituents from different agroclimatic origin of Moringa oleifera. Jour of Agric food chem. 2003; 51, (18):2144-2155.
18. Gomez-Zubeldia, MA, Arbues, J., Corrales, S; Millan, JS, and Nogales, AG. Gynecologic Oncology 2000; 86:250-258.
19. Guney M, Oral B, Demirin H, Karahan N, Mungan T, Delibas N. Protective effect of vitamin C and E against against endometrial damage and oxidative stress in fluoride intoxication. 2007; 34(5-6):467-475.
20. Singhal SS, Yallampalli C, Singhal J, Piper JT, Awasthi S. Purification and Gluthatione -S- Transferases of rat uterus. 1996; 11: 1271-1283.
21. White V, Jawerbaum A, Sinner D, Pustovrh C, Capubianco E, Gonzales E. Oxidative stress and altered prostanoid production in the placenta of streptozotocin-induced diabetic rat. Reprod Fertil Dev 2002; 14:117-123.
22. Cederberg J, Siman CM, Erikson UJ Combined treatment with vitamin E and vitamin decreases oxidative stress and improves fetal outcome in experimental diabetic pregnancy. Pediatr Res 2001; 49:755-762.