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Evaluation of leishmanicidal activity and cytotoxicity of Ricinus communis and Azadirachta indica extracts from western Kenya: in vitro and in vivo assays

BACKGROUND: Despite advances to targeted leishmanicidal chemotherapy, defies around severe toxicity, recent emergence of resistant variants and absence of rational vaccine still persist. This necessitates search and/or progressive validation of accessible medicinal remedies including plant based. Th...

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Autores principales: Jumba, Bernard N., Anjili, Christopher O., Makwali, Judith, Ingonga, Johnstone, Nyamao, Rose, Marango, Sylvia, Choge, Joseph K., Khayeka-Wandabwa, Christopher
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635543/
https://www.ncbi.nlm.nih.gov/pubmed/26541197
http://dx.doi.org/10.1186/s13104-015-1605-y
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author Jumba, Bernard N.
Anjili, Christopher O.
Makwali, Judith
Ingonga, Johnstone
Nyamao, Rose
Marango, Sylvia
Choge, Joseph K.
Khayeka-Wandabwa, Christopher
author_facet Jumba, Bernard N.
Anjili, Christopher O.
Makwali, Judith
Ingonga, Johnstone
Nyamao, Rose
Marango, Sylvia
Choge, Joseph K.
Khayeka-Wandabwa, Christopher
author_sort Jumba, Bernard N.
collection PubMed
description BACKGROUND: Despite advances to targeted leishmanicidal chemotherapy, defies around severe toxicity, recent emergence of resistant variants and absence of rational vaccine still persist. This necessitates search and/or progressive validation of accessible medicinal remedies including plant based. The study examined both in vivo and in vitro response of L. major infection to combined therapy of Ricinus communis and Azadirachta indica extracts in BALB/c mice as the mouse model. A comparative study design was applied. RESULTS: BALB/c mice, treated with combination therapy resulted in significantly (p < 0.05) larger reduction of lesion than those treated with monotherapies. The spleno-somatic index was found to be significantly low with combination therapy than monotherapies. Antiparasitic effect of A. indica and R. communis on amastigote with a 50 % inhibitory concentration (IC(50)) was of 11.5 and 16.5 µg mL(−1) respectively while combination therapy gave 9.0 µg ml(−1) compared to the standard drugs, Pentostam and amphotericin B which had an IC(50) of 6.5 and 4.5 µg ml(−1) respectively. Optimal efficacy of A. indica and R. communis was 72 and 59.5 % respectively, combination therapy gave 88 %, while Pentostam and amphotericin B had 98 and 92 % respectively against amastigotes. Against promastigotes A. indica and R. Communis gave an IC(50) of 10.1, 25.5 µg mL(−1) respectively, while combination, 12.2 µg mL(−1) against 4.1 and 5.0 µg ml(−1) for Pentostam and amphotericin B respectively. The optimal efficacy of the compounds against promastigotes was 78.0, 61.5 and 91.2 % (A. indica, R. communis and A. indica + R. communis respectively) against 96.5 and 98 % for Pentostam and amphotericin B respectively. The concentrations at optimal efficacy were significantly different (p < 0.05) among the test compounds. An evaluation of the IC(50) values of the combination therapies clearly reveals synergistic effects. CONCLUSION: Combination therapy of A. indica and R. communis had best antileishmanial activity than the monotherapies. The active ingredients of both R. communis and A. indica need to be fractionated, and studied further for activity against Leishmania parasites.
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spelling pubmed-46355432015-11-07 Evaluation of leishmanicidal activity and cytotoxicity of Ricinus communis and Azadirachta indica extracts from western Kenya: in vitro and in vivo assays Jumba, Bernard N. Anjili, Christopher O. Makwali, Judith Ingonga, Johnstone Nyamao, Rose Marango, Sylvia Choge, Joseph K. Khayeka-Wandabwa, Christopher BMC Res Notes Research Article BACKGROUND: Despite advances to targeted leishmanicidal chemotherapy, defies around severe toxicity, recent emergence of resistant variants and absence of rational vaccine still persist. This necessitates search and/or progressive validation of accessible medicinal remedies including plant based. The study examined both in vivo and in vitro response of L. major infection to combined therapy of Ricinus communis and Azadirachta indica extracts in BALB/c mice as the mouse model. A comparative study design was applied. RESULTS: BALB/c mice, treated with combination therapy resulted in significantly (p < 0.05) larger reduction of lesion than those treated with monotherapies. The spleno-somatic index was found to be significantly low with combination therapy than monotherapies. Antiparasitic effect of A. indica and R. communis on amastigote with a 50 % inhibitory concentration (IC(50)) was of 11.5 and 16.5 µg mL(−1) respectively while combination therapy gave 9.0 µg ml(−1) compared to the standard drugs, Pentostam and amphotericin B which had an IC(50) of 6.5 and 4.5 µg ml(−1) respectively. Optimal efficacy of A. indica and R. communis was 72 and 59.5 % respectively, combination therapy gave 88 %, while Pentostam and amphotericin B had 98 and 92 % respectively against amastigotes. Against promastigotes A. indica and R. Communis gave an IC(50) of 10.1, 25.5 µg mL(−1) respectively, while combination, 12.2 µg mL(−1) against 4.1 and 5.0 µg ml(−1) for Pentostam and amphotericin B respectively. The optimal efficacy of the compounds against promastigotes was 78.0, 61.5 and 91.2 % (A. indica, R. communis and A. indica + R. communis respectively) against 96.5 and 98 % for Pentostam and amphotericin B respectively. The concentrations at optimal efficacy were significantly different (p < 0.05) among the test compounds. An evaluation of the IC(50) values of the combination therapies clearly reveals synergistic effects. CONCLUSION: Combination therapy of A. indica and R. communis had best antileishmanial activity than the monotherapies. The active ingredients of both R. communis and A. indica need to be fractionated, and studied further for activity against Leishmania parasites. BioMed Central 2015-11-05 /pmc/articles/PMC4635543/ /pubmed/26541197 http://dx.doi.org/10.1186/s13104-015-1605-y Text en © Jumba et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Jumba, Bernard N.
Anjili, Christopher O.
Makwali, Judith
Ingonga, Johnstone
Nyamao, Rose
Marango, Sylvia
Choge, Joseph K.
Khayeka-Wandabwa, Christopher
Evaluation of leishmanicidal activity and cytotoxicity of Ricinus communis and Azadirachta indica extracts from western Kenya: in vitro and in vivo assays
title Evaluation of leishmanicidal activity and cytotoxicity of Ricinus communis and Azadirachta indica extracts from western Kenya: in vitro and in vivo assays
title_full Evaluation of leishmanicidal activity and cytotoxicity of Ricinus communis and Azadirachta indica extracts from western Kenya: in vitro and in vivo assays
title_fullStr Evaluation of leishmanicidal activity and cytotoxicity of Ricinus communis and Azadirachta indica extracts from western Kenya: in vitro and in vivo assays
title_full_unstemmed Evaluation of leishmanicidal activity and cytotoxicity of Ricinus communis and Azadirachta indica extracts from western Kenya: in vitro and in vivo assays
title_short Evaluation of leishmanicidal activity and cytotoxicity of Ricinus communis and Azadirachta indica extracts from western Kenya: in vitro and in vivo assays
title_sort evaluation of leishmanicidal activity and cytotoxicity of ricinus communis and azadirachta indica extracts from western kenya: in vitro and in vivo assays
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635543/
https://www.ncbi.nlm.nih.gov/pubmed/26541197
http://dx.doi.org/10.1186/s13104-015-1605-y
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