Main Article Content

Abstract

The correlations of reduced glutathione (GSH) and glutathione peroxidase (GPx) levels with biochemical markers of liver and kidney damage in Trypanosoma brucei brucei infection were studied in rats. Forty adult male rats divided into 2 groups of control and infected were used. Infected rats were inoculated intraperitoneally with 1.0 ml of blood at concentration of 1 x 106 trypanosomes per ml. Serum and tissue samples were collected on days 0, 3, 5 and 7 post-infection (pi) for biochemical analyses. Serum GPx activity had a significant (p < 0.05) positive correlations with liver (r = 0.96) and kidney GSH (r = 0.93) levels. All the measured serum parameters had significant (p < 0.05) negative correlations with serum GPx activity. In conclusion infection of rats with T. brucei brucei caused a decrease in the serum GPx activities and organ GSH levels with increasing parasitaemia and duration of the infection.

Keywords

Trypanosoma brucei brucei; Oxidative stress; Glutathione peroxidase; Glutathione; Liver and kidney function

Article Details

Author Biographies

J. P. Erin, Department of Veterinary Pathology Ahmadu Bello University Zaria

Department of Veterinary Pathology

S. Y. Idris, Ahmadu Bello University, Zaria

Lecturer II Department of Veterinary Pathology ABU Zaria, Nigeria

B. J. Kolawole, Michael Okpara University of Agriculture, Umudike, Abia State.

Department of Veterinary Medicine

O. G. Fanaiye, Dept of Theriogenology and Production, ABU Zaria.

Dept of Theriogenology and Production

S. Adamu, Ahmadu Bello University Zaria

Department of Veterinary Pathology

K. A. N. Esievo, Ahmadu Bello University Zaria

Veterinary Pathology

How to Cite
Correlations of Reduced Glutathione and Glutathione Peroxidase Activities with Biochemical Markers of Liver and Kidney Damage in Trypanosoma brucei brucei Infected Rats. (2020). Sahel Journal of Veterinary Sciences, 17(2), 1-6. https://doi.org/10.54058/saheljvs.v17i2.95

How to Cite

Correlations of Reduced Glutathione and Glutathione Peroxidase Activities with Biochemical Markers of Liver and Kidney Damage in Trypanosoma brucei brucei Infected Rats. (2020). Sahel Journal of Veterinary Sciences, 17(2), 1-6. https://doi.org/10.54058/saheljvs.v17i2.95

References

  1. Adamu, S., Barde, N., Abenga, J. N., Useh, N. M., Ibrahim, N. D. G. and Esievo, K. A. N. (2009). Experimental Trypanosoma brucei infection – induced changes in the serum profiles of lipids and cholesterol and the clinical implications in pigs. J. Cell Anim. Biol., 3: 015-020.
  2. Ahmed, Y., Hagos, A., Merga, B., Van Soom, A., Duchateau, L. and Goddeeris, B. (2018). Trypanosoma equiperdum in the horse - a neglected threat? Vlaams Diergeneeskd Tijdschr. 87: 66 – 75.
  3. Akanji, M. A., Adeyemi, O. S., Oguntoye, S. O. and Suleiman, F. (2009).Psidium guavaja extract reduses trypanosomiasis associated lipid peroxdation and raised glutathione concentrations in infected animals. EXCLI Journal, 8: 148 - 154.
  4. Anosa, V. O. (1988). Haematological and biochemical changes in human and animal trypanosomiasis. Rev. Elev. Med. Vet. Pays Trop.,41(2): 151-164.
  5. Ayla, O. and Metin, O. (2015). Biochemistry of reactive oxygen and nitrogen species. Faculty of veterinary medicine, University of Kafkas, Turkey, Croatia, InTech, Pp 37-58.
  6. Baydas, G., Canatan, H. and Turkoglu, A. (2002). Comparative analysis of the protective effects of melatonin and vitamin E on streptozotocin-induced diabetes mellitus. J. Pineal Res., 32: 225-230.
  7. Bouayed, J. and Bohn, T. (2010). Exogenous antioxidants—double-edged swords in cellular redox state: health beneficial effects at physiologic doses versus deleterious effects at high doses. Oxid. Med. Cell Longev., 3(4): 228-237.
  8. Cooper, A. J. L., Pinto, J. T. and Callery, P. S. (2011). Reversible and irreversible protein glutathionylation: biological and clinical aspects. Exp. Opinion Drg. Metabol. Toxicol, 7(7); 891 – 910
  9. Duan, S. and Chen, C. (2007). S-nitrosylation/denitrosylation and apoptosis of immune cells. Cell Mol. Immunol., 4(5); 353 – 358.
  10. Duarte, J., Galisteo, M., Ocete, M. A., Pérez-Vizcaino, F., Zarzuelo, A. and Tamargo, J. (2001). Effects of chronic quercetin treatment on hepatic oxidative status of spontaneously hypertensive rats. Mol. Cell. Biochem., 221: 155-60.
  11. Ekanem, J. T. and Yusuf, O. K. (2008). Some biochemical and haematological effects of black seed (Nigella sativa) oil on T. brucei-infected rats. Afr. J. Biomed. Res., 11:79–85.
  12. Fawcett, J. K. and Scott, J. E., (1960). A rapid and precise method for the determination of urea. J. Clin. Pathol., 13: 156-159.
  13. Fossati, P., Prencipe, L., Berti, G. (1983). Enzymatic creatinine assay: a new colorimetric method based on hydrogen peroxide measurement. Clin. Chem., 29: 1494-1496.
  14. Gutteridge. J. M. C. (1995). Lipid peroxidation and antioxidants as biomarkers of tissue damage. Clin. Chem., 41: 1819 - 1828.
  15. Herbert, W. J. and Lumsden, W. H. R. (1976). Trypanosoma brucei: a rapid “matching” method for estimating the host's parasitemia. Exp. Parasitol., 40(3): 427-431.
  16. Igbokwe, I. O. (1994): Mechanism of cellular injury in African trypanosomiasis. Vet. Bulletin, 64: 611-620.
  17. Igbokwe, I. O., Umar, I. A., Omage, J. J., Ibrahim, N. D. G., Kadima, K. B., Obagaiye, O. K., Saror, D. I. and Esievo, K. A. N. (1996). Effect of acute Trypanosoma vivax infection on cattle erythrocyte glutathione and susceptibility to in vitro peroxidation. Vet. Parasitol., 63: 215-24.
  18. Jones, T. C., Hunt, R. D. and King, N. W. (2000). Moléstias causadas por protozoários. In: Jones TC, Hunt RD, King NW, editors. Patologia veterinária. 6th ed. São Paulo: Manole, pp. 559 - 610.
  19. Jones, D. P. Park, Y. and Gletsu-Miller, N. (2011). Dietary sulfur amino acid effects on fasting plasma cysteine/cystine redox potential in humans. Nutrition, 27(2); 199 – 205.
  20. Klein, B., Read, P. A., Babson, L. A. (1960). Phenolphthalein monosubstrate method for the evaluation of serum levels of alkaline phosphatase. Clin. Chem., 6: 269-275.
  21. Kobo P. I., Ayo, J. O., Aluwong, T., Zezi, A. U., Maikai, V. A. (2014). Haematological changes in Trypanosoma brucei brucei Infected Wistar Rats Treated with a Flavonoid Mixture and/or Diminazene aceturate. Biol. Med.,6: 213.
  22. Lee, J., Koo, N. and Min, D. B. (2004). Reactive oxygen species, aging, and antioxidative nutraceuticals. Compr. Rev. Food Sci. F., 3: 21-33.
  23. Murray, R. K., Granner, D. K., Mayes, P. A. and Rodwell, V. W. (2003). Harper’s Illustrated Biochemistry a Lange Medical Book, 26th ed. The McGraw-Hill Companies, Inc., United States of America. pp. 622 - 701.
  24. Nantulya, V. M. (1990). Trypanosomiasis in domestic animals: the problems of diagnosis. Rev. Sci. Tech., 9: 357-367.
  25. Ogunsanmi, A. O. and Taiwo, V. O. (2007). Pathobiochemical mechanism involved in the control of the disease caused by Trypanosoma congolense in African grey duiker (Sylvicapra grimmia). Vet. Parasitol. 96: 51 – 63.
  26. Omer, O. H., Mousa, H. M. and Al-Wabel, N. (2007). Study on the antioxidant status of rats experimentally infected with Trypanosoma evansi. Vet. Parasitol.,145: 142-145.
  27. Radostis, O. M., Gay, C. C., Blood, D. C. and Hinchcliff, K. W. (2003). Diseases of Cattle, Sheep, Pig, Goats and Horses (9thed Britain) pp. 1330-1334.
  28. Reitman, S. and Frankel, S. (1957). A colorimetric method for determination of serum glutamic oxaloacetic acid and glutamic pyruvate transaminases. Am. J. Clin. Pathol., 28: 56-63.
  29. Saleh, M. A, Bassam, M. A. and Sanousi, S. A. (2009). Oxidative stress in blood of camels (Camelus dromedaries) naturally infected with Trypanosoma evansi. Vet. Parasitol., 162: 192-199.
  30. Szkudeslski T. (2001). The Mechanism of alloxan and streptozotocin action in B cells of the rat pancreas. Physiol. Res., 50: 536-46.
  31. Toppo, S., Flohé, L., Ursini, F., Vanin, S. and Maiorino, M. (2009). Catalytic mechanisms and specificities of glutathione peroxidases: variations of a basic scheme. Biochimica Biophysica Acta, 1790(11); 1486 – 1500.
  32. Umar, I. A., Toh, Z. A., Igbalajobi, F. I., Igbokwe, I. O. and Gidado, A. (1999). The effect of orally administered vitamins C and E on severity of anaemia in T. brucei infected rats. Trop. Vet., 18: 71-77.
  33. Umar, I. A., Ogenyi, E., Okodaso, D., Kimeng, E., Stancheva, G. I., Omage, J. J., Isah S. and Ibrahim, M. A. (2007). Amelioration of anaemia and organ damage by combined intraperitoneal administration of vitamins A and C to Trypanosoma brucei brucei-infected rats. Afr. J. Biotechnol., 6: 2083-2086.
  34. Vivancos, P. D., Wolff, T., Markovic, J., Pallardó, F. V. and Foyer, C. H. (2010). A nuclear glutathione cycle within the cell cycle. Biochemic J., 431(2); 169 – 178.
  35. Woo, P. T. (1969). The haematocrit centrifuge for the detection of trypanosomes in blood. Can. J. Zool., 47(5): 921-923.
  36. Yusuf, A. B, Umar, I.A, Musa U. B. M. and Nok, A. J. (2012). Screening of Vernonia amygdalina and Hymenocardia acida extracts and 1-3-diaminopropane for antitrypanosomal activity: in vitro model. J. Med. Plant. Res., 6(19): 3573-3578.