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阿魏酸和芥子酸对人兽共患绦虫(Rudolphi,1819)的体外驱虫效果

In vitro anthelmintic efficacy of Ferulic and Sinapic acid against zoonotic cestode (Rudolphi, 1819).

作者信息

Saha Samiparna, Mondal Chandrani, Mandal Sudeshna, Ray Mou Singha, Lyndem Larisha M

机构信息

Parasitology Research Laboratory, Department of Zoology, Visva-Bharati, Santiniketan, West Bengal 731235 India.

出版信息

J Parasit Dis. 2024 Sep;48(3):501-513. doi: 10.1007/s12639-024-01689-9. Epub 2024 May 22.

Abstract

The present study is aimed to investigate potential in vitro anthelmintic efficacy of two phenolic compounds Ferulic acid and Sinapic acid against the parasite . Adult parasites collected from infected rat's intestine (maintained in our laboratory) were treated with 1, 2.5, 5, 10 and 20 mg/mL concentrations of both the compounds in RPMI-1640 media containing 1% Tween 20. Further, one group was treated in Praziquantel as a reference drug and another group of parasites were kept as control. The efficacy was evaluated on the basis of motility and mortality of the parasites. The paralyzed worms were further processed for the morphological and ultrastructural studies and observed through light and scanning electron microscopy. A significant dose-dependent efficacy was found in all treatment and decrease in relative movability value was also recorded in all the concentrations of two compounds treated parasites. The time taken for paralysis in 5 mg/mL of Ferulic acid and 10 mg/mL of Sinapic acid were 1.47 ± 0.04 h and 0.88 ± 0.03 h respectively which is accorded with the standard concentration of Praziquantel. Morphological micrographs revealed pronounced distortion and altered topography of scolex and tegument while histological study showed loss of uniform tegumental integrity with folds and cracks in the treated parasites. Further, extensive alteration in the scolex and irrevocable disruption all over the body surface with loss of trapezoid shape, shrinkage of tegument and sloughing off microtriches were observed in electron microscopic study. The study indicated that both the compounds possess strong activity against and further studies are required to understand their detailed mode of action to exploit them as potential alternative candidates for curing helminthiases.

摘要

本研究旨在探讨两种酚类化合物阿魏酸和芥子酸对该寄生虫的体外驱虫效果。从感染大鼠肠道(在我们实验室饲养)收集的成虫寄生虫,在含有1%吐温20的RPMI - 1640培养基中,用两种化合物浓度分别为1、2.5、5、10和20mg/mL进行处理。此外,一组用吡喹酮作为参考药物处理,另一组寄生虫作为对照。根据寄生虫的活力和死亡率评估疗效。对麻痹的蠕虫进一步进行形态学和超微结构研究,并通过光学显微镜和扫描电子显微镜观察。在所有处理中均发现显著的剂量依赖性疗效,并且在两种化合物处理的寄生虫的所有浓度下,相对活动值也有所降低。5mg/mL阿魏酸和10mg/mL芥子酸使寄生虫麻痹的时间分别为1.47±0.04小时和0.88±0.03小时,这与吡喹酮的标准浓度相符。形态学显微照片显示头节和体表有明显的变形和地形改变,而组织学研究表明处理后的寄生虫体表完整性丧失,出现褶皱和裂缝。此外,在电子显微镜研究中观察到头节有广泛改变,全身表面不可逆转地破坏,梯形形状丧失,体表收缩,微毛脱落。该研究表明这两种化合物对该寄生虫均具有强大活性,需要进一步研究以了解它们的详细作用方式,从而将它们开发为治疗蠕虫病的潜在替代候选药物。

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