Evaluation of Histopathological Effect of Kaempferol in Trypanosoma brucei brucei Experimentally Infected Mice

Main Article Content

Muhammad Y
Jatau I.D
Tahir A. T
Dahiru M
Nasir S

Abstract

Kaempferol is a polyphenolic compound that is widely distributed in plants. It is used in the treatment of different immunocompromised disease conditions. Toxicity and development of resistance are two major setbacks associated withavilablesynthetic antitrypanosomal drugs, therefore, search for safer and more effective alternative therapy of trypanosomosis becomes paramount. This studywas aimed at evaluating the histopathological effect of kaempferol in mice with experimental Trypanosoma brucei bruceiinfection. Thirty-six adult Swiss albino mice of either sexes were randomly divided into six groups of six mice each. Mice in group I were untreated uninfected. Mice in group II were pre-treated with kaempferol (1 mg/kg) for 14 days. Mice in groups II to VI each were inoculated with blood containing Trypanosoma brucei brucei (106 trypanosomes/ml of blood/mouse) intraperitoneally. Histopathological examination was also conducted post-infection and post-treatment. Histopathological lesions observed were acute and are seen only in infected untreated groups, which involved the brain (slight necrosis), heart (slight myocardial necrosis s) and kidney (lymphocyte hyperplasia and tubular necrosis), liver (vascular congestion), lungs (perivascular lymphocyte infiltration) and alveolar congestion). Kaempferol treated mice showed no clear histopathological lesion. Therefore, treatment with kaempferol in mice with experimental Trypanosoma brucei brucei infection have prevented the parasite from reaching the selected organs being examined.  

Article Details

How to Cite
Y, M., I.D, J., A. T, T., M, D., & S, N. (2022). Evaluation of Histopathological Effect of Kaempferol in Trypanosoma brucei brucei Experimentally Infected Mice. International Journal of Pharmaceutical and Bio Medical Science, 2(01), 01–09. https://doi.org/10.47191/ijpbms/v2-i1-01
Section
Articles

References

Anosa, V.O. (1977). Studies on the Mechanism of Anaemia and the Pathology of Experimental Trypanosoma vivax (Zieman, 1905) Infection in Sheep and Goats. PhD Thesis,University of Ibadan, Ibadan, Nigeria.

Anosa, V.O. (1983). Mammalian blood: cells in health and in trypanosomiasis. Tropical Veterinary Journal, 1: 177-199.

Drury, R. and Wallington, E. A. (1976) Carteton’s Histological techniques (4th edn), Oxford University Press, London 21-70.

Ekanem, J.T. and Yusuf, O.K. (2008) Some biochemical and haematological effects of black seed (Nigella sativa) oil on T. brucei-infected rats. African Journal of Biomedical Research. 2008;11:79–85.

Ezeokonkwo, R.C., Ezeh, I.O., Onunkwo, J.I., Obi, P.O., Onyenwe, I.W. and Agu, W.E. (2010). Comparative haematological study of single and mixed infections of mongrel dogs with Trypanosoma congolenseand Trypanosoma brucei brucei. Journal of Veterinary Parasitology, 173: 48-54.

Garba, U. M., Sackey, A. K. B., Lawal, A. I., Esievo. K. A. N., Bisalla, M. and Sambo, J. S. (2017). Gross and Histopathological Alterations in Experimental Trypanosoma Evansi Infection in Donkeys and the Effect of Isometamidium Chloride Treatment. Journal of Veterinary Science & Animal Husbandry, Pp 1-10.

Geerts, S. and Holmes, P.H. (1998). Drug management and parasite resistance in animal trypanosomiasis in Africa. Programme Against African Trypanosomiasis (PAAT) Technical and Scientific Series 1, Food and Agriculture Organization of the United Nations (FAO), Rome, Italy.

Jean, R., Israel S., Peter, G. and Kennedy (2019). Generation of neuroinflammation in human African trypanosomiasis. Neurology, Neuroimmunology and Neuroinflammation, Volume (6), Pp: 1-9.

Karina, P., Jorge, M.A. and Marcelo, S.S. (2011) Induced cytokine network during experimental African trypanosomosis. International Journal of Interferon and Cytokine Mediator, Res., 3: 71-78.

Kobo, P. I., Erin, P. J., Suleiman, M. M., Aliyu, Tauheed, H. M., Muftau, and M. Mamman. M. (2014b). Antitrypanosomal effect of methanolic extract of Zingiber officinale (ginger) on Trypanosoma brucei brucei-infected Wistar mice. Veterinary World, 770-775.

Kobo, P.I., Ayo, J.O., Aluwong, A., Zezi, A.U., Maikai, V. and Ambali, S.F. (2014a) Flavonoid mixture ameliorates increase in erythrocyte osmotic fragility and malondialdehyde concentration induced by Trypanosoma brucei brucei-infection in Wistar rats. Reseach in Veterinary Science. 96: 139-142

Mahomoodally, M. F., Gurib-Fakim, A., and SubrattY, A.H. (2005). “Antimicrobial activities and phytochemical profiles of endemic medicinal plants of Mauritius,” Pharmaceutical Biology, 43(3): 237–242.

Masocha, W., and Kristensson, K. (2012). Passage of parasites across the blood-brain barrier. Virulence,3(2): 202–12.

McCarroll, C. S., Rossor, C. L., Morrison, L. R., Morrison, L. J. and Loughrey, CM (2015) A Pre-clinical Animal Model of Trypanosoma brucei Infection Demonstrating Cardiac Dysfunction.PLoS Neglected Tropical Disease, 9(5): e0003811. doi: 10.1371/journal.pntd.0003811.

Mott, F. W. (1911) The comparative neuropathology of trypanosome and spirochate infections, with a resume of our knowledge of human trypanosomiasis. Proceeding Research in Medicine, 4:1–40.

Pandey, A. K. (2007). “Anti-staphylococcal activity of a pan-tropical aggressive and obnoxious weed Pariheniumhisterophorus: an invitro study,” National Academy Science Letters, 30 (11-12): 383–386.

Saba, A.B., Adedapo, A.A., Oyagbemi, A.T. and Odudu, Z.K. (2007) Laboratory evaluation of senative pair of diminazene aceturate and isometamedium chloride as combination therapy for animal trypanosomosis. Folia Veterinary, 51(3-4): 169-174.

Shaba, P., Pandey, N.N., Sharma, O.P., Rao, J.R. and Singh, R.K. (2011) Anti-trypanosomal potential of methanolic extract of Calotropis gigantea leaves against Trypanosoma evansi and its cytotoxicity. International Journal of Biomedical Resource Stress Manage., 73: