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Beneficial effect of Punica granatum peel extract on murine malaria-induced spleen injury

BACKGROUND: Multiple drug-resistant malaria parasites have been widely detected, which has encouraged research studies focused on discovering alternative therapies. Medicinal plants such as pomegranate, Punica granatum, have been proven to exhibit antiprotozoal effects and therefore, we examined its...

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Autores principales: Mubaraki, Murad A., Hafiz, Taghreed A., Dkhil, Mohamed A., Al-Quraishy, Saleh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947305/
https://www.ncbi.nlm.nih.gov/pubmed/27422638
http://dx.doi.org/10.1186/s12906-016-1207-9
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author Mubaraki, Murad A.
Hafiz, Taghreed A.
Dkhil, Mohamed A.
Al-Quraishy, Saleh
author_facet Mubaraki, Murad A.
Hafiz, Taghreed A.
Dkhil, Mohamed A.
Al-Quraishy, Saleh
author_sort Mubaraki, Murad A.
collection PubMed
description BACKGROUND: Multiple drug-resistant malaria parasites have been widely detected, which has encouraged research studies focused on discovering alternative therapies. Medicinal plants such as pomegranate, Punica granatum, have been proven to exhibit antiprotozoal effects and therefore, we examined its effects on murine malaria-induced splenic injury and oxidative stress in this study. METHODS: Mice were divided into three groups, a vehicle control and two groups that were infected with 10(6)Plasmodium chabaudi-parasitized red blood cells (RBCs). The third group was gavaged with 100 μL of 300 mg/kg pomegranate peel extract for 6 days. All mice were euthanized on day 6 post-infection. RESULTS: The results revealed the potential antimalarial, antioxidant, and anti-inflammatory effects of pomegranate. Furthermore, pomegranate peel extracts significantly reduced parasitemia and spleen index of the treated mice compared to the untreated group. Additionally, the spleen histology score supported the findings by showing better amelioration in the pomegranate-treated mice than in the untreated mice. Concomitantly, the spleen capsule thickness showed clear evidence of splenomegaly in the untreated mice, as evidenced by the reduced spleen capsule. However, pomegranate peel extract exhibited a remarkable restorative effect on the spleen capsules of the treated mice. Moreover, the extract significantly reduced the expression levels of the proinflammatory cytokines interleukin (IL)-1β, tumor necrosis factor (TNF)-α, and interferon (IFN)-γ as well as inducible nitric oxide synthase (iNOS). Moreover, our study showed that pomegranate extract profoundly affected oxidative stress levels by reducing the oxidant molecules, nitric oxide (NO) and malondialdehyde (MDA). CONCLUSION: This study showed that pomegranate clearly induced antimalarial activity in the host by attenuating inflammatory and oxidative stress responses. Furthermore, pomegranate enhanced the innate immune responses and, therefore, could serve an alternative therapy to control clinical malaria episodes and may protect against malaria infection.
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spelling pubmed-49473052016-07-17 Beneficial effect of Punica granatum peel extract on murine malaria-induced spleen injury Mubaraki, Murad A. Hafiz, Taghreed A. Dkhil, Mohamed A. Al-Quraishy, Saleh BMC Complement Altern Med Research Article BACKGROUND: Multiple drug-resistant malaria parasites have been widely detected, which has encouraged research studies focused on discovering alternative therapies. Medicinal plants such as pomegranate, Punica granatum, have been proven to exhibit antiprotozoal effects and therefore, we examined its effects on murine malaria-induced splenic injury and oxidative stress in this study. METHODS: Mice were divided into three groups, a vehicle control and two groups that were infected with 10(6)Plasmodium chabaudi-parasitized red blood cells (RBCs). The third group was gavaged with 100 μL of 300 mg/kg pomegranate peel extract for 6 days. All mice were euthanized on day 6 post-infection. RESULTS: The results revealed the potential antimalarial, antioxidant, and anti-inflammatory effects of pomegranate. Furthermore, pomegranate peel extracts significantly reduced parasitemia and spleen index of the treated mice compared to the untreated group. Additionally, the spleen histology score supported the findings by showing better amelioration in the pomegranate-treated mice than in the untreated mice. Concomitantly, the spleen capsule thickness showed clear evidence of splenomegaly in the untreated mice, as evidenced by the reduced spleen capsule. However, pomegranate peel extract exhibited a remarkable restorative effect on the spleen capsules of the treated mice. Moreover, the extract significantly reduced the expression levels of the proinflammatory cytokines interleukin (IL)-1β, tumor necrosis factor (TNF)-α, and interferon (IFN)-γ as well as inducible nitric oxide synthase (iNOS). Moreover, our study showed that pomegranate extract profoundly affected oxidative stress levels by reducing the oxidant molecules, nitric oxide (NO) and malondialdehyde (MDA). CONCLUSION: This study showed that pomegranate clearly induced antimalarial activity in the host by attenuating inflammatory and oxidative stress responses. Furthermore, pomegranate enhanced the innate immune responses and, therefore, could serve an alternative therapy to control clinical malaria episodes and may protect against malaria infection. BioMed Central 2016-07-16 /pmc/articles/PMC4947305/ /pubmed/27422638 http://dx.doi.org/10.1186/s12906-016-1207-9 Text en © The Author(s). 2016 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
Mubaraki, Murad A.
Hafiz, Taghreed A.
Dkhil, Mohamed A.
Al-Quraishy, Saleh
Beneficial effect of Punica granatum peel extract on murine malaria-induced spleen injury
title Beneficial effect of Punica granatum peel extract on murine malaria-induced spleen injury
title_full Beneficial effect of Punica granatum peel extract on murine malaria-induced spleen injury
title_fullStr Beneficial effect of Punica granatum peel extract on murine malaria-induced spleen injury
title_full_unstemmed Beneficial effect of Punica granatum peel extract on murine malaria-induced spleen injury
title_short Beneficial effect of Punica granatum peel extract on murine malaria-induced spleen injury
title_sort beneficial effect of punica granatum peel extract on murine malaria-induced spleen injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947305/
https://www.ncbi.nlm.nih.gov/pubmed/27422638
http://dx.doi.org/10.1186/s12906-016-1207-9
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