In vitro and in vivo activity of three sesquiterpenes against L3 larvae of Anisakis type I

被引:15
作者
Concepcion Navarro-Moll, Ma [1 ]
Carmen Romero, Ma [2 ]
Pilar Montilla, Ma [1 ]
Valero, Adela [2 ]
机构
[1] Univ Granada, Fac Pharm, Dept Pharmacol, E-18071 Granada, Spain
[2] Univ Granada, Fac Pharm, Dept Parasitol, E-18071 Granada, Spain
关键词
Anisakis; Anisakiasis; Sesquiterpenes; Nerolidol; Farnesol; Elemol; MONOTERPENIC DERIVATIVES; STAPHYLOCOCCUS-AUREUS; GASTRIC ANISAKIASIS; LARVICIDAL ACTIVITY; ESSENTIAL OIL;
D O I
10.1016/j.exppara.2010.09.008
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
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. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:405 / 408
页数:4
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