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The Protective Effect of Artemisia spicigera Ethanolic Extract against Cryptosporidium parvum Infection in Immunosuppressed Mice
BACKGROUND: A specific treatment has not yet developed for cryptosporidiosis, and some of the used drugs had side effects in immunodeficient patients. The goal of an appropriate remedy is to remove symptoms and improve immune responses in hosts. The current study was designed to evaluate the therape...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Tehran University of Medical Sciences
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418654/ https://www.ncbi.nlm.nih.gov/pubmed/34557243 http://dx.doi.org/10.18502/ijpa.v16i2.6318 |
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author | Shahbazi, Parisa Nematollahi, Ahmad Arshadi, Sanaz Farhang, Hosein Hashemzadeh Shahbazfar, Amir Ali |
author_facet | Shahbazi, Parisa Nematollahi, Ahmad Arshadi, Sanaz Farhang, Hosein Hashemzadeh Shahbazfar, Amir Ali |
author_sort | Shahbazi, Parisa |
collection | PubMed |
description | BACKGROUND: A specific treatment has not yet developed for cryptosporidiosis, and some of the used drugs had side effects in immunodeficient patients. The goal of an appropriate remedy is to remove symptoms and improve immune responses in hosts. The current study was designed to evaluate the therapeutic efficacy of Artemisia spicigera ethanolic extract in experimentally infected immunosuppressed mice. METHODS: Thirty six NMRI mice, 4–6 wk old, were randomly divided into six equal groups. C1: uninfected, treated control; C2: infected, untreated control; T1, T2, T3, and P: infected, treated with 0.2, 2, and 20 mg/ml extract, and 5mg/ml paromomycin, respectively. Mice were experimentally infected by oral administration of 10(4) oocysts/animal of Cryptosporidium parvum and treated orally for eight days per 12h, starting 12h before experimental infection. The presence of oocyst shedding, weight gain/loss, and the histopathology of ileum sections were examined. RESULTS: Results revealed that oocyst shedding was significantly (P<0.05) reduced in treatment groups. There was no significant difference between the mean of weight gain/loss in the infected control and treated groups. Histopathological analysis of ileum sections further supported the parasitological findings. CONCLUSION: Artemisia spicigera had acceptable efficacy as a therapeutic agent for cryptosporidiosis. |
format | Online Article Text |
id | pubmed-8418654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Tehran University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-84186542021-09-22 The Protective Effect of Artemisia spicigera Ethanolic Extract against Cryptosporidium parvum Infection in Immunosuppressed Mice Shahbazi, Parisa Nematollahi, Ahmad Arshadi, Sanaz Farhang, Hosein Hashemzadeh Shahbazfar, Amir Ali Iran J Parasitol Original Article BACKGROUND: A specific treatment has not yet developed for cryptosporidiosis, and some of the used drugs had side effects in immunodeficient patients. The goal of an appropriate remedy is to remove symptoms and improve immune responses in hosts. The current study was designed to evaluate the therapeutic efficacy of Artemisia spicigera ethanolic extract in experimentally infected immunosuppressed mice. METHODS: Thirty six NMRI mice, 4–6 wk old, were randomly divided into six equal groups. C1: uninfected, treated control; C2: infected, untreated control; T1, T2, T3, and P: infected, treated with 0.2, 2, and 20 mg/ml extract, and 5mg/ml paromomycin, respectively. Mice were experimentally infected by oral administration of 10(4) oocysts/animal of Cryptosporidium parvum and treated orally for eight days per 12h, starting 12h before experimental infection. The presence of oocyst shedding, weight gain/loss, and the histopathology of ileum sections were examined. RESULTS: Results revealed that oocyst shedding was significantly (P<0.05) reduced in treatment groups. There was no significant difference between the mean of weight gain/loss in the infected control and treated groups. Histopathological analysis of ileum sections further supported the parasitological findings. CONCLUSION: Artemisia spicigera had acceptable efficacy as a therapeutic agent for cryptosporidiosis. Tehran University of Medical Sciences 2021 /pmc/articles/PMC8418654/ /pubmed/34557243 http://dx.doi.org/10.18502/ijpa.v16i2.6318 Text en Copyright © 2021 Shahbazi et al. Published by Tehran University of Medical Sciences https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited. |
spellingShingle | Original Article Shahbazi, Parisa Nematollahi, Ahmad Arshadi, Sanaz Farhang, Hosein Hashemzadeh Shahbazfar, Amir Ali The Protective Effect of Artemisia spicigera Ethanolic Extract against Cryptosporidium parvum Infection in Immunosuppressed Mice |
title | The Protective Effect of Artemisia spicigera Ethanolic Extract against Cryptosporidium parvum Infection in Immunosuppressed Mice |
title_full | The Protective Effect of Artemisia spicigera Ethanolic Extract against Cryptosporidium parvum Infection in Immunosuppressed Mice |
title_fullStr | The Protective Effect of Artemisia spicigera Ethanolic Extract against Cryptosporidium parvum Infection in Immunosuppressed Mice |
title_full_unstemmed | The Protective Effect of Artemisia spicigera Ethanolic Extract against Cryptosporidium parvum Infection in Immunosuppressed Mice |
title_short | The Protective Effect of Artemisia spicigera Ethanolic Extract against Cryptosporidium parvum Infection in Immunosuppressed Mice |
title_sort | protective effect of artemisia spicigera ethanolic extract against cryptosporidium parvum infection in immunosuppressed mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418654/ https://www.ncbi.nlm.nih.gov/pubmed/34557243 http://dx.doi.org/10.18502/ijpa.v16i2.6318 |
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