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基于 Tagetes patula L. (Asteraceae) 中鉴定出的噻吩的纳米制剂对小反刍动物线虫 Haemonchus contortus 的驱虫活性。

Anthelmintic activity of a nanoformulation based on thiophenes identified in Tagetes patula L. (Asteraceae) against the small ruminant nematode Haemonchus contortus.

机构信息

School of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara (SP), Brazil.

University of São Paulo (USP), Physics Institute of São Carlos (IFSC), São Carlos (SP), Brazil.

出版信息

Acta Trop. 2021 Jul;219:105920. doi: 10.1016/j.actatropica.2021.105920. Epub 2021 Apr 20.

Abstract

The synthesis of thiophenic compounds, previously identified in Tagetes patula, revealed that 4-(5'-(hydroxymethyl)-[2,2'-bithiophene]-5-yl)but-3-yn-1-ol), or simply Thio1, has a pronounced in vitro anthelmintic effect against Haemonchus contortus, showing 100% efficacy in the egg hatch and larval development tests presenting EC = 0.1731 mg.mL and EC = 0.3243 mg.mL, respectively. So, this compound was selected to preparation of a nanostructured formulation to be orally administered to Santa Inês sheep. In general, from the fecal egg count reduction test (FECRT), it was observed that the product kept the parasitic load in the digestive tract of the hosts stable, with eggs per gram of faeces (EPG) counts having a mean value < 3,000 (EPG = 2167.1, efficacy = 36,45%), thus protecting the animals from health risks caused by a massive nematode infestation. To better understand the mode of action of this thiophene derivative, in silico molecular modeling studies were carried out with the glutamate-activated chloride channel (GluCl), a well-known molecular target of anthelmintic compounds. Based on the affinity score (GlideScore = -5.7 kcal.mol) and the proposed binding mode, Thio1 could be classified as a potential GluCl ligand, justifying the promising results observed in the anthelmintic assays.

摘要

噻吩类化合物的合成,先前在 Tagetes patula 中被鉴定出来,结果表明 4-(5'-(羟甲基)-[2,2'-联噻吩]-5-基)丁-3-炔-1-醇), 简称 Thio1,对 Haemonchus contortus 具有显著的体外驱虫效果,在卵孵化和幼虫发育试验中表现出 100%的功效,EC = 0.1731 mg.mL 和 EC = 0.3243 mg.mL。因此,选择该化合物制备一种纳米结构制剂,以便口服给予 Santa Inês 绵羊。一般来说,从粪便虫卵减少试验(FECRT)中可以观察到,该产品使宿主消化道中的寄生虫负荷保持稳定,每克粪便中的虫卵数(EPG)平均值<3000(EPG = 2167.1,疗效 = 36.45%),从而保护动物免受大量线虫感染带来的健康风险。为了更好地了解这种噻吩衍生物的作用模式,我们进行了基于 GluCl 的分子模拟研究,GluCl 是驱虫化合物的一个众所周知的分子靶点。基于亲和力评分(GlideScore = -5.7 kcal.mol)和提出的结合模式,Thio1 可被归类为潜在的 GluCl 配体,这解释了在驱虫试验中观察到的有希望的结果。

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