2017
DOI: 10.4314/ajcem.v18i2.11
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Comparative bone marrow responses of albino rats experimentally infected with single and mixed species of <i>Trypanosoma congolense</i> and <i>Trypanosoma brucei</i> and ability to control anaemia

Abstract: Effect of Trypanosoma congolence and T. brucei mixed infection on ability of the bone marrow to respond to anemia was investigated in albino rats. This was with the view of assessing the possible impact on recovery rate from anemia following chemotherapy of African trypanosomosis. The investigation involved descriptive evaluation of packed cell volume and corresponding bone marrow cytological changes associated with single and mixed infection of T. congolense and T. brucei. It involved laboratory based experim… Show more

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Cited by 3 publications
(2 citation statements)
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“…The myeloid: erythroid ratio by mean 0.91±0.03 indicates that dark erythrocytic cells are higher than faint myeloid cells found in the bone marrow smears, which was pointed out in normal animals (5,38). The young, healthy animals had the activity of erythroid division more than myeloid when suggesting a normal blood periphery status (39,40). The megakaryocyte, a progenitor cell for the platelets (41), was rarely seen in the present study, which explained that megakaryocytes are often not outwarded in bone marrow biopsy (5,42,43).…”
Section: Discussionmentioning
confidence: 85%
“…The myeloid: erythroid ratio by mean 0.91±0.03 indicates that dark erythrocytic cells are higher than faint myeloid cells found in the bone marrow smears, which was pointed out in normal animals (5,38). The young, healthy animals had the activity of erythroid division more than myeloid when suggesting a normal blood periphery status (39,40). The megakaryocyte, a progenitor cell for the platelets (41), was rarely seen in the present study, which explained that megakaryocytes are often not outwarded in bone marrow biopsy (5,42,43).…”
Section: Discussionmentioning
confidence: 85%
“…The mechanisms by which trypanosomes establish, multiply, and inundate the host with heavy parasitaemia is believed to involve the variable surface glycoprotein (VSG) genes which constitute about 10% of the trypanosome genome and of which only one is expressed at any given time (Igbokwe, 2018). This gene pool provides the molecular resources for antigenic variation which enables the parasite to discard the surface coat regularly, evade recognition by host immune system and endogenous trypanocidal factors (Abenga et al, 2017;Akinseye et al, 2020;Aresta-Blanco et al, 2019). In addition, trypanosomes utilize host nutrient supplies (carbohydrates, proteins, lipids, and micronutrients) for their metabolism (Igbokwe, 2018) and release metabolites some of which contribute to the pathogenesis of the disease (Mishra et al, 2017;Getahun et al, 2022).…”
Section: Introductionmentioning
confidence: 99%