Abstract

Aim:Trypanosomosis is a vital protozoan disease of man and animals with devastating consequences in the tropical parts of the world, necessitating the investigation of the effects of diminazene aceturate (DA) and arteether (AR) on Trypanosoma brucei brucei experimental infection in rats.Materials and Methods:We used a total of 98 rats, which were divided into 14 groups (A-N) of seven rats each over 36 days after acclimatizing them. We administered 1×106 trypanosomes to the infected groups (B-N) with Group A as the unexposed control rats. Groups C-F became the infected and treated rats with 3.5 mg/kg, 7.0 mg/kg, 10.5 mg/kg, and 14.0 mg/kg of DA while Groups G-J became the infected and treated rats with 0.01 ml/kg, 0.02 ml/kg, 0.03 ml/kg, and 0.04 ml/kg of AR. Groups K-N became infected and treated rats with DA and AR combinations at similar doses.Results:Parasitemia suppression occurred in Groups G-J only but became cleared in Groups C-F and K-N. Survival time varied significantly (p<0.05) between Group B and the other infected groups. We recorded anemia in all the infected rats while significant (p<0.05) splenomegaly and hepatomegaly occurred in Groups G-J only compared to the other groups.Conclusion:AR did not inhibit or potentiate the anti-trypanosomal efficacy of DA, and therefore, it is comparatively less effective in combating T. brucei infection at the present doses and treatment regimen.

Highlights

  • Trypanosomosis is a serious tsetse fly-borne protozoan parasite disease that affects humans and animals [1]

  • We observed a gradual rise in parasitemia in the infected rats (B-N) from day 6 Pi until it peaked on day 12 Pi before the treatment commenced

  • We recorded a decreased level of parasitemia in Groups G-J from days 14 to 22 Pi before rising again from day 24 Pi

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Summary

Introduction

Trypanosomosis is a serious tsetse fly-borne protozoan parasite disease that affects humans and animals [1]. African animal trypanosomosis reportedly causes poor milk yield, poor hair coat, emaciation, anemia, anorexia, intermittent fever, lethargy, infertility, ascites, abortion, and death of the affected animal if it is not correctly treated [2]. There are many species of trypanosomes, but the dominant pathogenic species affecting animals are Trypanosoma vivax, Trypanosoma congolense, Trypanosoma simiae, Trypanosoma godfreyi, and Trypanosoma brucei brucei [3]. Trypanosoma brucei rhodesiense, and Trypanosoma brucei gambiense cause human African trypanosomosis or sleeping sickness [4]. The control of animal trypanosomosis has become a major problem as the parasites exhibit antigenic variation, thereby posing a significant threat to livestock

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