Merck
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  • In vitro and in vivo activity of three sesquiterpenes against L(3) larvae of Anisakis type I.

In vitro and in vivo activity of three sesquiterpenes against L(3) larvae of Anisakis type I.

Experimental parasitology (2010-10-12)
Ma Concepción Navarro-Moll, Ma Carmen Romero, Ma Pilar Montilla, Adela Valero
摘要

In order to investigate the possible use of terpenic derivatives to treat anisakiasis caused by L(3) larvae of Anisakis, we studied the in vitro and in vivo larvicidal activity of three sesquiterpenes (nerolidol, farnesol and elemol). In vitro experiments included the histological study of larval damage and in vivo studies the measurement of myeloperoxidase activity in rat gastrointestinal tract after administration of the sesquiterpenes. In the in vitro assays, the most active compound against the L(3) larvae was nerolidol, followed by farnesol; both caused the death of all nematodes, which showed cuticle changes and intestinal wall rupture. In the in vivo assays, only 20% of infected rats treated with nerolidol or farnesol showed gastric wall lesions in comparison to 86.6% of control animals. According to these results, nerolidol and farnesol are good candidates for further research as biocidal agents against L(3) larvae of Anisakis type I.

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Sigma-Aldrich
橙花叔醇, mixture of cis and trans, ≥97%, stabilized, FG
Sigma-Aldrich
橙花叔醇, 98%, Mixture of cis and trans
Supelco
反式-橙花叔醇, analytical standard