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Anisakis simplex s.l.: Larvicidal activity of various monoterpenic derivatives of natural origin against L3 larvae in vitro and in vivo

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Identificadores
URI: https://hdl.handle.net/10481/101086
DOI: https://doi.org/10.1016/j.exppara.2008.07.014
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Autor
Navarro, M.C.; Noguera, M.A.; Romero, M.C.; Montilla, M.P.; González de Selga, J.M.; Valero, A
Editorial
Experimental Parasitology
Materia
Anisakis simplex s.l.
 
Larvicidal activity
 
Monoterpenic derivatives
 
α-Pinene
 
Ocimene
 
nutrition education
 
Fecha
2008-07-31
Referencia bibliográfica
M.C. Navarro, M.A. Noguera, M.C. Romero, M.P. Montilla, J.M. González de Selgas, A. Valero, Anisakis simplex s.l.: Larvicidal activity of various monoterpenic derivatives of natural origin against L3 larvae in vitro and in vivo, Experimental Parasitology, Volume 120, Issue 4, 2008, Pages 295-299,
Patrocinador
This work was partly funded by the Research Groups grant from the Junta de Andalucía, Spain
Resumen
This paper describes the activity against Anisakis simplex s.l. L3 larvae of six monoterpenic derivatives obtained from different essential oils, (α-pinene, β-pinene, ocimene, myrcene, geranyl acetate, and cineole). In in vitro assays, α-pinene, ocimene and cineole showed high activity at a concentration of 125 μg/mL (48 h) but only α-pinene and ocimene were active at 62.5 μg/mL. In in vivo assays, L3 larvae and study compounds were simultaneously administered per os to Wistar rats. The most active compound was α-pinene, finding lesions in only 20% of treated rats versus 98% of controls. Further in vivo studies are required to investigate whether addition of these compounds to food could have a prophylactic effect, reducing the pathogenicity of A. simplex s.l. L3 in humans, and to explore any possible synergy among compounds.
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