Anti-toxoplasmosis activity evaluation of Artemisia vulgaris L. extract and its subfractions in vitro and in vivo
Background and objectives: Toxoplasma gondii affects almost one-third of people worldwide, causing disorders such as abortion or congenital disease in its intermediate hosts. This is while the current available medications are limited in terms of efficacy and side effects. Previous researches have s...
Format: | Article |
---|---|
Language: | English |
Published: |
Iranian Society of Pharmacognosy
2017-11-01
|
Series: | Research Journal of Pharmacognosy |
Subjects: | |
Online Access: | http://www.rjpharmacognosy.ir/article_53363_838230485a9a012eb180e99e918b5001.pdf |
_version_ | 1818051384381014016 |
---|---|
collection | DOAJ |
description | Background and objectives: Toxoplasma gondii affects almost one-third of people worldwide, causing disorders such as abortion or congenital disease in its intermediate hosts. This is while the current available medications are limited in terms of efficacy and side effects. Previous researches have shown Artemisia annua to be highly effective on this parasite. The aim of this study was to evaluate the antitoxoplasma effects of A. vulgaris. Methods: Anti toxoplasmosis activity was evaluated in vitro using different concentrations of A. vulgaris total extract and the petroleum ether, chloroform, ethyl acetate and n-butanol fractions. After 2 h of incubation, flow cytometry method was applied to determine the anti-parasitic activity. Phytochemical profiles of these extracts were developed by HPTLC. For the in vivo experiment, toxoplasmosis was induced by intradermal injection of the parasite tachyzoites into the rats. Average survival time of the rats treated with 16-128 mg/kg of the total extract was compared with the control groups. Results: In vitro evaluation of A. vulgaris extracts revealed that the petroleum ether fraction was the most active by IC50 of 8.31 µg/mL and the n-butanol fraction didn’t exhibit any significant activity. In in vivo tests, all concentrations of the total extract led to an increase in the average survival time. HPTLC analysis of the crude extract and its fractions revealed the presence of terpenoids in the non-polar phase. Conclusion: According to the data and statistical analysis, A. vulgaris and particularly its petroleum ether fraction exhibit significant anti-toxoplasmosis activity, suggesting that the non-polar terpenoids could be responsible for this effect. |
first_indexed | 2024-12-10T11:08:31Z |
format | Article |
id | doaj.art-3726903f536b4f16853d86f2825293f9 |
institution | Directory Open Access Journal |
issn | 2345-4458 2345-5977 |
language | English |
last_indexed | 2024-12-10T11:08:31Z |
publishDate | 2017-11-01 |
publisher | Iranian Society of Pharmacognosy |
record_format | Article |
series | Research Journal of Pharmacognosy |
spelling | doaj.art-3726903f536b4f16853d86f2825293f92022-12-22T01:51:29ZengIranian Society of PharmacognosyResearch Journal of Pharmacognosy2345-44582345-59772017-11-014Supplement11511553363Anti-toxoplasmosis activity evaluation of Artemisia vulgaris L. extract and its subfractions in vitro and in vivoBackground and objectives: Toxoplasma gondii affects almost one-third of people worldwide, causing disorders such as abortion or congenital disease in its intermediate hosts. This is while the current available medications are limited in terms of efficacy and side effects. Previous researches have shown Artemisia annua to be highly effective on this parasite. The aim of this study was to evaluate the antitoxoplasma effects of A. vulgaris. Methods: Anti toxoplasmosis activity was evaluated in vitro using different concentrations of A. vulgaris total extract and the petroleum ether, chloroform, ethyl acetate and n-butanol fractions. After 2 h of incubation, flow cytometry method was applied to determine the anti-parasitic activity. Phytochemical profiles of these extracts were developed by HPTLC. For the in vivo experiment, toxoplasmosis was induced by intradermal injection of the parasite tachyzoites into the rats. Average survival time of the rats treated with 16-128 mg/kg of the total extract was compared with the control groups. Results: In vitro evaluation of A. vulgaris extracts revealed that the petroleum ether fraction was the most active by IC50 of 8.31 µg/mL and the n-butanol fraction didn’t exhibit any significant activity. In in vivo tests, all concentrations of the total extract led to an increase in the average survival time. HPTLC analysis of the crude extract and its fractions revealed the presence of terpenoids in the non-polar phase. Conclusion: According to the data and statistical analysis, A. vulgaris and particularly its petroleum ether fraction exhibit significant anti-toxoplasmosis activity, suggesting that the non-polar terpenoids could be responsible for this effect.http://www.rjpharmacognosy.ir/article_53363_838230485a9a012eb180e99e918b5001.pdfArtemisia vulgarisHPTLCToxoplasma gondii |
spellingShingle | Anti-toxoplasmosis activity evaluation of Artemisia vulgaris L. extract and its subfractions in vitro and in vivo Research Journal of Pharmacognosy Artemisia vulgaris HPTLC Toxoplasma gondii |
title | Anti-toxoplasmosis activity evaluation of Artemisia vulgaris L. extract and its subfractions in vitro and in vivo |
title_full | Anti-toxoplasmosis activity evaluation of Artemisia vulgaris L. extract and its subfractions in vitro and in vivo |
title_fullStr | Anti-toxoplasmosis activity evaluation of Artemisia vulgaris L. extract and its subfractions in vitro and in vivo |
title_full_unstemmed | Anti-toxoplasmosis activity evaluation of Artemisia vulgaris L. extract and its subfractions in vitro and in vivo |
title_short | Anti-toxoplasmosis activity evaluation of Artemisia vulgaris L. extract and its subfractions in vitro and in vivo |
title_sort | anti toxoplasmosis activity evaluation of artemisia vulgaris l extract and its subfractions in vitro and in vivo |
topic | Artemisia vulgaris HPTLC Toxoplasma gondii |
url | http://www.rjpharmacognosy.ir/article_53363_838230485a9a012eb180e99e918b5001.pdf |