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三种倍半萜类化合物对 I 型旋毛虫 L(3)幼虫的体内外活性。

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

机构信息

Department of Pharmacology, Pharmacy Faculty, University of Granada, Granada 18071, Spain.

出版信息

Exp Parasitol. 2011 Feb;127(2):405-8. doi: 10.1016/j.exppara.2010.09.008. Epub 2010 Oct 20.

Abstract

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.

摘要

为了研究萜烯衍生物在治疗由海兽胃线虫 L(3)幼虫引起的异尖线虫病中的可能用途,我们研究了三种倍半萜(橙花叔醇、法呢醇和艾罗莫)的体外和体内杀幼虫活性。体外实验包括幼虫损伤的组织学研究,体内实验则是在给予倍半萜后测量大鼠胃肠道髓过氧化物酶活性。在体外检测中,对 L(3)幼虫最具活性的化合物是橙花叔醇,其次是法呢醇;两者均导致所有线虫死亡,表现为角质层变化和肠壁破裂。在体内检测中,与对照组动物的 86.6%相比,仅 20%用橙花叔醇或法呢醇治疗的感染大鼠出现胃壁损伤。根据这些结果,橙花叔醇和法呢醇是作为抗海兽胃线虫 I 型 L(3)幼虫的杀生物剂进一步研究的良好候选物。

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