Artículo

In vitro and in vivo efficacy of carvacrol against Echinococcus granulosus

Fabbri, Julia Icon; Maggiore, Marina Alejandra Icon; Pensel, Patricia Eugenia Icon; Denegri, Guillermo Maria Icon; Gende, Liesel Brenda Icon; Elissondo, María Celina Icon

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Fecha

12/2016

Editorial

Elsevier Science

Revista

Acta Tropica

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ISSN

0001-706X

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Inglés

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Resumen

Currently, benzimidazoles are used as chemotherapeutic agents and as a complement to surgery and PAIR in the treatment of cystic echinococcosis (CE). They are generally applied at high doses causing side effects and, 50% of cases do not respond favorably to such chemotherapy. The use of essential oils obtained by distillation from aromatic plants would be an effective alternative or complementary to the synthetic compounds, because would not bring the appearance of side effects. Carvacrol and his isomer thymol are the main phenolic components from essential oils of Origanum vulgare (oregano) and Thymus vulgaris (thyme). The aim of the present work was to evaluate the in vitro and in vivo efficacy of carvacrol against Echinococcus granulosus metacestodes. For the in vitro assay, protoscoleces and cysts of E. granulosus were incubated with carvacrol at the following final concentrations: 10, 5 and 1 μg/ml of carvacrol. The maximum protoscolicidal effect was found with 10 μg/ml of carvacrol. Results of viability tests were consistent with the structural and ultrastructural damage observed in protoscoleces. Ultrastructural studies revealed that the germinal layer of cysts treated with carvacrol lost the multicellular structure feature. In the clinical efficacy study, a reduction in cyst weight was observed after the administration of 40 mg/kg of carvacrol during 20 days in mice with cysts developed during 4 months, compared to that of those collected from control mice. Given that the in vivo effect of carvacrol was comparable with the treatment of reference with ABZ and the fact that is a safe compound, we postulated that carvacrol may be an alternative option for treatment of human CE.

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