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The potential role and apoptotic profile of three medicinal plant extracts on Leishmania tropica by MTT assay, macrophage model and flow cytometry analysis

INTRODUCTION: Treatment of leishmaniasis with conventional synthetic drugs is a major global challenge. This study was designed to explore the leishmanicidal activity and apoptotic profile of three leaf extracts on Leishmania tropica stages. METHODS: The plants of Quercus velutina, Calotropis procer...

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Autores principales: Ilaghi, Mozhde, Sharifi, Iraj, Sharififar, Fariba, Sharifi, Fatemeh, Oliaee, Razieh Tavakoli, Babaei, Zahra, Meimamandi, Manzume Shamsi, Keyhani, Alireza, Bamorovat, Mehdi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817489/
https://www.ncbi.nlm.nih.gov/pubmed/33511293
http://dx.doi.org/10.1016/j.parepi.2021.e00201
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author Ilaghi, Mozhde
Sharifi, Iraj
Sharififar, Fariba
Sharifi, Fatemeh
Oliaee, Razieh Tavakoli
Babaei, Zahra
Meimamandi, Manzume Shamsi
Keyhani, Alireza
Bamorovat, Mehdi
author_facet Ilaghi, Mozhde
Sharifi, Iraj
Sharififar, Fariba
Sharifi, Fatemeh
Oliaee, Razieh Tavakoli
Babaei, Zahra
Meimamandi, Manzume Shamsi
Keyhani, Alireza
Bamorovat, Mehdi
author_sort Ilaghi, Mozhde
collection PubMed
description INTRODUCTION: Treatment of leishmaniasis with conventional synthetic drugs is a major global challenge. This study was designed to explore the leishmanicidal activity and apoptotic profile of three leaf extracts on Leishmania tropica stages. METHODS: The plants of Quercus velutina, Calotropis procera and Nicotiana tabacum were gathered from Anbarabbad county, in the southeastern part of Kerman province and extracted by maceration method using methanol alcohol. Various concentrations of the extracts (1, 10, 100 and 1000 μg/mL) were used against L. tropica stages to evaluate the inhibitory effect by colorimetric assay, macrophage model and flow cytometry. The MTT assay was conducted to determine the IC(50) and CC(50) values in promastigotes and J774-A1 macrophages, respectively. For intra-macrophage amastigotes, the leishmanicidal activity was evaluated by calculating the mean number of amastigotes in each macrophage and also IC(50) values. The promastigote or amastigote stages with no drug and complete medium without organisms were considered as positive and negative controls, respectively. Meglumine antimoniate (Glucantime) was also used as standard drug. Also, annexin V was used to assess the apoptotic profile. All treatment settings were incubated for a standard time of 72 h in triplicates. Data were analyzed by t-test and ANOVA. RESULTS: The findings showed that all plant extracts inhibited the proliferation rate of promastigotes and amastigotes (P ˂ 0.001); especially, Q. velutina represented the lowest IC(50) in both stages. Besides, Q. velutina showed the least number of amastigotes in each macrophage compared to the other groups (4.5 μg/mL). The percentage of parasitic apoptosis at 1000 μg/mL of Q. velutina, C. procera, N. tabacum and Glucantime® were 37.4, 18.6, 8.5 and 52.4, respectively. Amastigotes (clinical stage) were significantly more susceptible to extracts and also Glucantime® than promastigotes (P < 0.001). CONCLUSIONS: This study revealed that all three extracts of Q. velutina, C. procera and N. tabacum exhibited an effective antileishmanial activity and induced apoptosis against the L. tropica promastigotes. Further investigations are essential to isolate and analyze the chemical compositions and their biological properties.
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spelling pubmed-78174892021-01-27 The potential role and apoptotic profile of three medicinal plant extracts on Leishmania tropica by MTT assay, macrophage model and flow cytometry analysis Ilaghi, Mozhde Sharifi, Iraj Sharififar, Fariba Sharifi, Fatemeh Oliaee, Razieh Tavakoli Babaei, Zahra Meimamandi, Manzume Shamsi Keyhani, Alireza Bamorovat, Mehdi Parasite Epidemiol Control Original Research article INTRODUCTION: Treatment of leishmaniasis with conventional synthetic drugs is a major global challenge. This study was designed to explore the leishmanicidal activity and apoptotic profile of three leaf extracts on Leishmania tropica stages. METHODS: The plants of Quercus velutina, Calotropis procera and Nicotiana tabacum were gathered from Anbarabbad county, in the southeastern part of Kerman province and extracted by maceration method using methanol alcohol. Various concentrations of the extracts (1, 10, 100 and 1000 μg/mL) were used against L. tropica stages to evaluate the inhibitory effect by colorimetric assay, macrophage model and flow cytometry. The MTT assay was conducted to determine the IC(50) and CC(50) values in promastigotes and J774-A1 macrophages, respectively. For intra-macrophage amastigotes, the leishmanicidal activity was evaluated by calculating the mean number of amastigotes in each macrophage and also IC(50) values. The promastigote or amastigote stages with no drug and complete medium without organisms were considered as positive and negative controls, respectively. Meglumine antimoniate (Glucantime) was also used as standard drug. Also, annexin V was used to assess the apoptotic profile. All treatment settings were incubated for a standard time of 72 h in triplicates. Data were analyzed by t-test and ANOVA. RESULTS: The findings showed that all plant extracts inhibited the proliferation rate of promastigotes and amastigotes (P ˂ 0.001); especially, Q. velutina represented the lowest IC(50) in both stages. Besides, Q. velutina showed the least number of amastigotes in each macrophage compared to the other groups (4.5 μg/mL). The percentage of parasitic apoptosis at 1000 μg/mL of Q. velutina, C. procera, N. tabacum and Glucantime® were 37.4, 18.6, 8.5 and 52.4, respectively. Amastigotes (clinical stage) were significantly more susceptible to extracts and also Glucantime® than promastigotes (P < 0.001). CONCLUSIONS: This study revealed that all three extracts of Q. velutina, C. procera and N. tabacum exhibited an effective antileishmanial activity and induced apoptosis against the L. tropica promastigotes. Further investigations are essential to isolate and analyze the chemical compositions and their biological properties. Elsevier 2021-01-10 /pmc/articles/PMC7817489/ /pubmed/33511293 http://dx.doi.org/10.1016/j.parepi.2021.e00201 Text en © 2021 Published by Elsevier Ltd on behalf of World Federation of Parasitologists. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research article
Ilaghi, Mozhde
Sharifi, Iraj
Sharififar, Fariba
Sharifi, Fatemeh
Oliaee, Razieh Tavakoli
Babaei, Zahra
Meimamandi, Manzume Shamsi
Keyhani, Alireza
Bamorovat, Mehdi
The potential role and apoptotic profile of three medicinal plant extracts on Leishmania tropica by MTT assay, macrophage model and flow cytometry analysis
title The potential role and apoptotic profile of three medicinal plant extracts on Leishmania tropica by MTT assay, macrophage model and flow cytometry analysis
title_full The potential role and apoptotic profile of three medicinal plant extracts on Leishmania tropica by MTT assay, macrophage model and flow cytometry analysis
title_fullStr The potential role and apoptotic profile of three medicinal plant extracts on Leishmania tropica by MTT assay, macrophage model and flow cytometry analysis
title_full_unstemmed The potential role and apoptotic profile of three medicinal plant extracts on Leishmania tropica by MTT assay, macrophage model and flow cytometry analysis
title_short The potential role and apoptotic profile of three medicinal plant extracts on Leishmania tropica by MTT assay, macrophage model and flow cytometry analysis
title_sort potential role and apoptotic profile of three medicinal plant extracts on leishmania tropica by mtt assay, macrophage model and flow cytometry analysis
topic Original Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817489/
https://www.ncbi.nlm.nih.gov/pubmed/33511293
http://dx.doi.org/10.1016/j.parepi.2021.e00201
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