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2-(三氟甲基)-1H-苯并咪唑衍生物对旋毛虫肌幼虫的作用分析

Analysis of the effect of a 2-(trifluoromethyl)-1H-benzimidazole derivative on Trichinella spiralis muscle larvae.

作者信息

Matadamas-Martínez Félix, Nogueda-Torres Benjamín, Hernández-Campos Alicia, Hernández-Luis Francisco, Castillo Rafael, Mendoza Guillermo, Ambrosio Javier R, Andrés-Antonio Gabriela, Yépez-Mulia Lilián

机构信息

UIMEIP-Pediatría, Centro Médico Nacional Siglo XXI, IMSS, México, DF 06720, Mexico.

出版信息

Vet Parasitol. 2013 May 20;194(2-4):193-7. doi: 10.1016/j.vetpar.2013.01.054. Epub 2013 Feb 5.

Abstract

Albendazole and mebendazole are widely used in the treatment of trichinellosis; however, chemotherapy failure has been reported. In an effort to develop new anthelminthic compounds, we examined a previously synthesized 2-(trifluoromethyl)-1H-benzimidazole derivative (1) that showed good in vitro activity against Trichinella spiralis muscle larvae but low in vivo efficacy. In order to improve the solubility of compound 1, an inclusion complex with 2-hydroxypropyl-β-cyclodextrin (1/HP-βCD) was prepared. When 1/HP-βCD was tested in vivo, it significantly reduced the ML burden (84%). In addition, a proteomic analysis of T. spiralis ML treated with 1 revealed significant changes in the expression levels of proteins involved in energy metabolism and the cytoskeleton of the parasite. Compound (1) also induced extensive ultrastructural changes in the cuticle, hypodermis and midgut of the parasite.

摘要

阿苯达唑和甲苯达唑被广泛用于治疗旋毛虫病;然而,化疗失败的情况已有报道。为了开发新的驱虫化合物,我们研究了一种先前合成的2-(三氟甲基)-1H-苯并咪唑衍生物(1),该衍生物对旋毛虫肌幼虫显示出良好的体外活性,但体内疗效较低。为了提高化合物1的溶解度,制备了与2-羟丙基-β-环糊精的包合物(1/HP-βCD)。当在体内测试1/HP-βCD时,它显著降低了肌幼虫负担(84%)。此外,对用1处理的旋毛虫肌幼虫进行的蛋白质组学分析显示,参与寄生虫能量代谢和细胞骨架的蛋白质表达水平发生了显著变化。化合物(1)还引起了寄生虫角质层、皮下组织和中肠广泛的超微结构变化。

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