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“墨西哥山金车花”菊科异叶泽兰属天然产物及其某些衍生物对肠贾第鞭毛虫的体外活性。

In vitro activity of 'Mexican Arnica' Heterotheca inuloides Cass natural products and some derivatives against Giardia intestinalis.

作者信息

Rodríguez-Chávez José Luis, Rufino-González Yadira, Ponce-Macotela Martha, Delgado Guillermo

机构信息

Instituto de Química, Universidad Nacional Autónoma de México,04510 México, D. F.,México.

Laboratorio de Parasitología Experimental, Instituto Nacional de Pediatría,Insurgentes Sur 3700-C, 04530 México, D. F.,México.

出版信息

Parasitology. 2015 Apr;142(4):576-84. doi: 10.1017/S0031182014001619. Epub 2014 Nov 3.

DOI:10.1017/S0031182014001619
PMID:25363565
Abstract

Giardiasis is a gastrointestinal disease that affects humans and other animals caused by parasitic protists of the genus Giardia. Giardia intestinalis (Syn. Giardia lamblia; Giardia duodenalis) infections can cause acute or chronic diarrhoea, dehydration, abdominal discomfort and weight loss. Metronidazole is the most widely used drug for treating giardiasis. Although effective, metronidazol has undesirable secondary effects. Plants used in traditional medicine as antidiarrhoeals or antiparasitics may represent alternative sources for new compounds to treat giardiasis. Heterotheca inuloides Cass. (Asteraceae/Compositae) plant is widely used in Mexican traditional medicine. The following secondary metabolites were isolated from H. inuloides flowers: 7-hydroxy-3,4-dihydrocadalene (1), 7-hydroxycadalene (2), 3,7-dihydroxy-3(4H)-isocadalen-4-one (3), 1R,4R-hydroxy-1,2,3,4-tetrahydrocadalen-15-oic acid (4), quercetin (5), quercetin-3,7,3'-trimethyl ether (6), quercetin-3,7,3',4'-tetramethyl ether (7) and eriodictyol-7,4'-dimethyl ether (8). The activity of these compounds against Giardia intestinalis trophozoites was assessed in vitro as was the activity of the semisynthetic compounds 7-acetoxy-3,4-dihydrocadalene (9), 7-benzoxy-3,4-dihydrocadalene (10), 7-acetoxycadalene (11), 7-benzoxycadalene (12), quercetin pentaacetate (13) and 7-hydroxycalamenene (14). Among these, 7-hydroxy-3,4-dihydrocadalene (1) and 7-hydroxycalamenene (14) were the most active, whereas the remaining compounds showed moderate or no activity. The G. intestinalis trophozoites exposed to compound 1 showed marked changes in cellular architecture along with ultrastructural disorganization. The aim of this study was to evaluate the giardicidal activity of selected H. inuloides metabolites and some semisynthetic derivatives using an in vitro experimental model of giardiasis.

摘要

贾第虫病是一种影响人类和其他动物的胃肠道疾病,由贾第虫属的寄生原生生物引起。肠贾第虫(同义词:蓝氏贾第虫;十二指肠贾第虫)感染可导致急性或慢性腹泻、脱水、腹部不适和体重减轻。甲硝唑是治疗贾第虫病最广泛使用的药物。尽管有效,但甲硝唑有不良副作用。在传统医学中用作止泻药或抗寄生虫药的植物可能是治疗贾第虫病新化合物的替代来源。异叶泽兰(菊科)植物在墨西哥传统医学中广泛使用。从异叶泽兰花中分离出以下次生代谢产物:7-羟基-3,4-二氢卡达烯(1)、7-羟基卡达烯(2)、3,7-二羟基-3(4H)-异卡达烯-4-酮(3)、1R,4R-羟基-1,2,3,4-四氢卡达烯-15-酸(4)、槲皮素(5)、槲皮素-3,7,3'-三甲醚(6)、槲皮素-3,7,3',4'-四甲醚(7)和圣草酚-7,4'-二甲醚(8)。评估了这些化合物对肠贾第虫滋养体的体外活性以及半合成化合物7-乙酰氧基-3,4-二氢卡达烯(9)、7-苄氧基-3,4-二氢卡达烯(10)、7-乙酰氧基卡达烯(11)、7-苄氧基卡达烯(12)、槲皮素五乙酸酯(13)和7-羟基卡拉烯(14)的活性。其中,7-羟基-3,4-二氢卡达烯(1)和7-羟基卡拉烯(14)活性最强,而其余化合物显示出中等活性或无活性。暴露于化合物1的肠贾第虫滋养体在细胞结构上出现明显变化,同时伴有超微结构紊乱。本研究的目的是使用贾第虫病的体外实验模型评估所选异叶泽兰代谢产物和一些半合成衍生物的杀贾第虫活性。

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