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Evaluation of the in vitro and in vivo inhibitory effect of thymoquinone on piroplasm parasites
BACKGROUND: Developing new antibabesial drugs with a low toxic effect to the animal and with no resistance from Babesia parasites is in urgent demand. In this concern, the antimalarial, anticancer and antioxidant effect of thymoquinone (TQ), a phytochemical compound found in the plant Nigella sativa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335684/ https://www.ncbi.nlm.nih.gov/pubmed/30651142 http://dx.doi.org/10.1186/s13071-019-3296-z |
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author | El-Sayed, Shimaa Abd El-Salam Rizk, Mohamed Abdo Yokoyama, Naoaki Igarashi, Ikuo |
author_facet | El-Sayed, Shimaa Abd El-Salam Rizk, Mohamed Abdo Yokoyama, Naoaki Igarashi, Ikuo |
author_sort | El-Sayed, Shimaa Abd El-Salam |
collection | PubMed |
description | BACKGROUND: Developing new antibabesial drugs with a low toxic effect to the animal and with no resistance from Babesia parasites is in urgent demand. In this concern, the antimalarial, anticancer and antioxidant effect of thymoquinone (TQ), a phytochemical compound found in the plant Nigella sativa, has been reported. Therefore, in the present study, the antibabesial effect of this compound was evaluated on the growth of piroplasm parasites. RESULTS: Significant inhibition (P < 0.05) of the in vitro growth of piroplasm parasites were observed after treatment by TQ with IC(50) values of 35.41 ± 3.60, 7.35 ± 0.17, 0.28 ± 0.016, 74.05 ± 4.55 and 67.33 ± 0.94 μM for Babesia bovis, Babesia bigemina, Babesia divergens, Theileria equi and Babesia caballi, respectively. The in vitro inhibitory effect of TQ was significantly enhanced (P < 0.05) when used in combination with either diminazene aceturate on bovine Babesia and equine Babesia and Theileria cultures. In B. microti-infected mice, oral and intraperitoneal administrations of TQ showed significant (P < 0.05) inhibition of parasite growth at a dose of 70 mg/kg and 50 mg/kg, respectively, compared to the control group. CONCLUSIONS: The obtained results indicate that thymoquinone might be a promising medicinal compound for use in the treatment of animal piroplasmosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-019-3296-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6335684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63356842019-01-23 Evaluation of the in vitro and in vivo inhibitory effect of thymoquinone on piroplasm parasites El-Sayed, Shimaa Abd El-Salam Rizk, Mohamed Abdo Yokoyama, Naoaki Igarashi, Ikuo Parasit Vectors Research BACKGROUND: Developing new antibabesial drugs with a low toxic effect to the animal and with no resistance from Babesia parasites is in urgent demand. In this concern, the antimalarial, anticancer and antioxidant effect of thymoquinone (TQ), a phytochemical compound found in the plant Nigella sativa, has been reported. Therefore, in the present study, the antibabesial effect of this compound was evaluated on the growth of piroplasm parasites. RESULTS: Significant inhibition (P < 0.05) of the in vitro growth of piroplasm parasites were observed after treatment by TQ with IC(50) values of 35.41 ± 3.60, 7.35 ± 0.17, 0.28 ± 0.016, 74.05 ± 4.55 and 67.33 ± 0.94 μM for Babesia bovis, Babesia bigemina, Babesia divergens, Theileria equi and Babesia caballi, respectively. The in vitro inhibitory effect of TQ was significantly enhanced (P < 0.05) when used in combination with either diminazene aceturate on bovine Babesia and equine Babesia and Theileria cultures. In B. microti-infected mice, oral and intraperitoneal administrations of TQ showed significant (P < 0.05) inhibition of parasite growth at a dose of 70 mg/kg and 50 mg/kg, respectively, compared to the control group. CONCLUSIONS: The obtained results indicate that thymoquinone might be a promising medicinal compound for use in the treatment of animal piroplasmosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-019-3296-z) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-16 /pmc/articles/PMC6335684/ /pubmed/30651142 http://dx.doi.org/10.1186/s13071-019-3296-z Text en © The Author(s). 2019 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 El-Sayed, Shimaa Abd El-Salam Rizk, Mohamed Abdo Yokoyama, Naoaki Igarashi, Ikuo Evaluation of the in vitro and in vivo inhibitory effect of thymoquinone on piroplasm parasites |
title | Evaluation of the in vitro and in vivo inhibitory effect of thymoquinone on piroplasm parasites |
title_full | Evaluation of the in vitro and in vivo inhibitory effect of thymoquinone on piroplasm parasites |
title_fullStr | Evaluation of the in vitro and in vivo inhibitory effect of thymoquinone on piroplasm parasites |
title_full_unstemmed | Evaluation of the in vitro and in vivo inhibitory effect of thymoquinone on piroplasm parasites |
title_short | Evaluation of the in vitro and in vivo inhibitory effect of thymoquinone on piroplasm parasites |
title_sort | evaluation of the in vitro and in vivo inhibitory effect of thymoquinone on piroplasm parasites |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335684/ https://www.ncbi.nlm.nih.gov/pubmed/30651142 http://dx.doi.org/10.1186/s13071-019-3296-z |
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