Suppr超能文献

阿苯达唑和三氯苯达唑对肝片吸虫卵杀卵活性的比较评估

Comparative assessment of albendazole and triclabendazole ovicidal activity on Fasciola hepatica eggs.

作者信息

Alvarez L, Moreno G, Moreno L, Ceballos L, Shaw L, Fairweather I, Lanusse C

机构信息

Laboratorio de Farmacología, Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires (UNCPBA), Campus Universitario, 7000, Tandil, Argentina.

出版信息

Vet Parasitol. 2009 Oct 14;164(2-4):211-6. doi: 10.1016/j.vetpar.2009.05.014. Epub 2009 May 20.

Abstract

The benzimidazole compounds albendazole (ABZ) and triclabendazole (TCBZ) are both effective against Fasciola hepatica, although ABZ is only effective against adult flukes. Additionally, ABZ is a broad-spectrum nematodicidal compound with well-known ovicidal activity. However, no data on the ovicidal effect of TCBZ against F. hepatica eggs are available. The work reported here evaluated the comparative ovicidal effect of ABZ, TCBZ and their sulphoxide metabolites on F. hepatica eggs recovered from bile of sheep artificially infected with either a TCBZ-susceptible (Cullompton) or a TCBZ-resistant (Sligo) isolate of F. hepatica. Additionally, the effects of different non-flukicidal methylcarbamate benzimidazole compounds on the hatching of F. hepatica eggs were evaluated. Eggs (500 eggs/mL, n=4) were incubated for 12h either with TCBZ, TCBZ sulphoxide (TCBZ.SO), ABZ (5, 10 and 20 nmol/mL) or without drug (untreated control) (Experiment 1). Additionally, the effect of TCBZ and TCBZ.SO (5 nmol/mL) on egg hatchability was examined after a long (15 days) drug exposure (Experiment 2). Furthermore, the ovicidal effect of ABZ and ABZ.SO at different concentrations (5, 1, 0.5, 0.1 and 0.05 nmol/mL) (Experiment 3), and the effect of fenbendazole (FBZ), oxfendazole (OFZ), mebendazole (MBZ), flubendazole (FLBZ) (5 nmol/mL) and reduced-FLBZ (R-FLBZ) (2 microg/mL) on fluke eggs, were evaluated after a 12-h exposure (Experiment 4). Egg hatch was assessed by direct microscopic observation after incubation at 25 degrees C for 15 days. TCBZ and TCBZ.SO did not affect egg hatch after a 12-h incubation. A similar result was obtained after a much longer drug exposure (15 days) (Experiment 1 and 2). However, a significant (P<0.05) inhibition of egg hatch was observed in ABZ- and ABZ.SO-incubated eggs (Experiments 1 and 3). Additionally, the non-flukicidal compounds (Experiment 4) affected egg hatchability, particularly FLBZ and R-FLBZ. In conclusion, ABZ and ABZ.SO had a clear inhibitory effect on egg development of F. hepatica. However, the most extensively used flukicidal compound, TCBZ, and its main sulphoxide metabolite, did not affect egg hatch, even in TCBZ-susceptible flukes.

摘要

苯并咪唑类化合物阿苯达唑(ABZ)和三氯苯达唑(TCBZ)对肝片吸虫均有效,不过阿苯达唑仅对成虫有效。此外,阿苯达唑是一种具有众所周知的杀卵活性的广谱杀线虫化合物。然而,尚无关于三氯苯达唑对肝片吸虫虫卵杀卵作用的数据。本文报道的研究评估了阿苯达唑、三氯苯达唑及其亚砜代谢产物对从人工感染了对三氯苯达唑敏感(Cullompton)或耐药(Sligo)的肝片吸虫分离株的绵羊胆汁中收集的肝片吸虫虫卵的比较杀卵作用。此外,还评估了不同的非杀吸虫性氨基甲酸甲酯苯并咪唑化合物对肝片吸虫虫卵孵化的影响。将虫卵(500个虫卵/毫升,n = 4)与三氯苯达唑、三氯苯达唑亚砜(TCBZ.SO)、阿苯达唑(5、10和20纳摩尔/毫升)一起孵育12小时,或不添加药物(未处理对照)(实验1)。此外,在长时间(15天)药物暴露后,检测了三氯苯达唑和三氯苯达唑亚砜(5纳摩尔/毫升)对虫卵孵化率的影响(实验2)。此外,评估了不同浓度(5、1、0.5、0.1和0.05纳摩尔/毫升)的阿苯达唑和阿苯达唑亚砜的杀卵作用(实验3),以及芬苯达唑(FBZ)、奥芬达唑(OFZ)、甲苯达唑(MBZ)、氟苯达唑(FLBZ)(5纳摩尔/毫升)和还原氟苯达唑(R-FLBZ)(2微克/毫升)对吸虫虫卵的作用,在暴露12小时后进行评估(实验4)。在25℃孵育15天后,通过直接显微镜观察评估虫卵孵化情况。孵育12小时后,三氯苯达唑和三氯苯达唑亚砜不影响虫卵孵化。在更长时间的药物暴露(15天)后也得到了类似结果(实验1和2)。然而,在阿苯达唑和阿苯达唑亚砜孵育的虫卵中观察到了显著(P<0.05)的虫卵孵化抑制(实验1和3)。此外,非杀吸虫性化合物(实验4)影响虫卵孵化率,尤其是氟苯达唑和还原氟苯达唑。总之,阿苯达唑和阿苯达唑亚砜对肝片吸虫的虫卵发育有明显的抑制作用。然而,使用最广泛的杀吸虫化合物三氯苯达唑及其主要亚砜代谢产物,即使在对三氯苯达唑敏感的吸虫中,也不影响虫卵孵化。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验