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Experimental therapeutic assays of tephrosia vogelii against leishmania major infection in murine model: in vitro and in vivo

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dc.contributor.author Marango, Sylvia N
dc.contributor.author Wandabwa, Christopher K
dc.contributor.author Makwali, Judith A
dc.contributor.author Jumba, Bernard N
dc.contributor.author Choge, Joseph K
dc.contributor.author Adino, Eric O
dc.contributor.author Anjili, Christopher O
dc.date.accessioned 2022-01-28T13:35:15Z
dc.date.available 2022-01-28T13:35:15Z
dc.date.issued 2017-12-06
dc.identifier.citation Marango, S. N., Khayeka-Wandabwa, C., Makwali, J. A., Jumba, B. N., Choge, J. K., Adino, E. O., & Anjili, C. O. (2017). Experimental therapeutic assays of Tephrosia vogelii against Leishmania major infection in murine model: in vitro and in vivo. BMC research notes, 10(1), 1-12. en_US
dc.identifier.uri https://doi.org/10.1186/s13104-017-3022-x
dc.identifier.uri http://ir-library.kabianga.ac.ke/handle/123456789/290
dc.description Research paper of biological science en_US
dc.description.abstract Background: Conventional targeted leishmanicidal chemotherapy has persistently remained prohibitive for most economically deprived communities due to costs, associated time to accessing health services and duration for suc‑ cessful treatment programme. Alternatives are bound to be incorporated in rational management of leishmaniasis by choice or default due to accessibility and cultural beliefs. Therefore, there is need to rigorously investigate and appraise the activity of medicinal compounds that may have anti-leishmanicidal activity especially in the context of products that are already being utilized by the populations for other ailments but have limited information on their therapeutic value and possible cytoxicity. Hence, the study examined both in vivo and in vitro response of L. major infection to Tephrosia vogelii extracts in BALB/c mice as the mouse model. Methods: A comparative study design was applied for the in vivo and in vitro assays of the extract with Pentostam (GlaxoSmithKline, UK) and Amphotericin B [Fungizone™, X-Gen Pharmaceuticals (US)] as standard drugs. Results: In BALB/c mice where the chemotherapeutic extract was administered intraperitoneally, there was sig‑ nifcantly (p < 0.05) larger reduction in lesion size and optimal control of parasite burden than those treated orally. However, standard drugs showed better activity. Tephrosia vogelii had 50% inhibitory concentration (IC50) and IC90 of 12 and 68.5 μg/ml respectively, while the standard drugs had IC50 and IC90 of 5.5 and 18 μg/ml for Pentostam and 7.8 and 25.5 μg/ml for Amphotericin B in that order. In the amastigote assay, the infection rates decreased with increase in chemotherapeutic concentration. The multiplication indices for L. major amastigotes in macrophages treated with 200 µg/ml of the standard drugs and extract were signifcantly diferent (p < 0.05). 200 µg/ml of T. vogelii extract showed a multiplication index of 20.57, 5.65% for Amphotericin B and 9.56% for Pentostam. There was also signifcant diference (p < 0.05) in levels of Nitric oxide produced in the macrophages. Conclusions: The fndings demonstrated that T. vogelii extract has anti-leishmanial ac en_US
dc.language.iso en en_US
dc.publisher BMC research notes en_US
dc.subject Leishmaniasis en_US
dc.subject Leishmania major en_US
dc.subject Tephrosia vogeli en_US
dc.subject Pentostam en_US
dc.subject Amphotericin B en_US
dc.subject 50% inhibitory concentration en_US
dc.subject Toxicity en_US
dc.subject Effcacy en_US
dc.title Experimental therapeutic assays of tephrosia vogelii against leishmania major infection in murine model: in vitro and in vivo en_US
dc.type Article en_US


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