Annona muricata Polyphenols Induce Cytoskeletal Alterations and Predicted Aldose Reductase Binding in Giardia lamblia.

IF 2.9 Q3 PHARMACOLOGY & PHARMACY
Advances in Pharmacological and Pharmaceutical Sciences Pub Date : 2026-08-25 eCollection Date: 2026-01-01 DOI:10.1155/adpp/4133207
Diana Valeria Govea-Flores, Mariana Garza-Ontiveros, Filiberto Gutiérrez-Gutiérrez, Ana Gabriela Gómez-Ibarra, Sendar Daniel Nery-Flores, Juan Alberto Ascacio-Valdés, Lizeth Guadalupe Campos-Múzquiz, Raúl Rodríguez-Herrera, Lissethe Palomo-Ligas
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引用次数: 0

Abstract

Giardiasis has been classified as a neglected disease by the World Health Organization since 2004. Despite ongoing efforts, challenges such as drug resistance and treatment failures continue to hinder effective management. In recent years, the exploration of plant-derived compounds as antiparasitic agents has emerged as a promising strategy. This is supported by the discovery of plant-derived compounds such as quinine and artemisinin in antiparasitic pharmacology. The identification of specific molecular targets in Giardia lamblia, a protozoan with unique cytoskeletal and metabolic features, has further advanced drug discovery efforts. In this study, we evaluated the in vitro and in silico effects of a polyphenol-enriched extract from Annona muricata (soursop) leaves against G. lamblia trophozoites. The extract had a noticeable impact on parasite growth, cell adhesion, and morphology. Ultrastructural analyses revealed elongation, flagellar abnormalities, and damage to the ventral disk. Western blot and immunofluorescence assays demonstrated reduced α-tubulin expression and altered localization, indicating cytoskeletal alterations in treated trophozoites. Molecular docking analyses predicted favorable interactions between soursop polyphenols and Giardia aldose reductase, particularly involving the catalytic residues Y40 and K71. Collectively, these findings suggest that A. muricata polyphenols exert antigiardial effects through multiple cellular alterations and support the hypothesis that metabolic and cytoskeletal processes may both contribute to the observed biological effects. Further studies are required to experimentally validate the role of aldose reductase and its relationship with cytoskeletal disruption.

茉莉多酚诱导蓝氏贾第鞭毛虫细胞骨架改变并预测醛糖还原酶结合。
自2004年以来,贾第虫病一直被世界卫生组织列为被忽视的疾病。尽管正在进行努力,但耐药性和治疗失败等挑战继续阻碍有效管理。近年来,探索植物源化合物作为抗寄生虫剂已成为一种很有前途的策略。在抗寄生虫药理学中发现的植物衍生化合物,如奎宁和青蒿素,支持了这一点。兰氏贾第鞭毛虫是一种具有独特细胞骨架和代谢特征的原生动物,其特异性分子靶点的鉴定进一步推进了药物发现工作。在本研究中,我们评估了番荔枝叶多酚提取物对蓝氏滋养体的体外和室内作用。提取物对寄生虫生长、细胞粘附和形态有显著影响。超微结构分析显示延长、鞭毛异常和腹盘损伤。Western blot和免疫荧光分析显示α-微管蛋白表达降低,定位改变,表明处理过的滋养体细胞骨架发生改变。分子对接分析预测了刺果多酚与贾第鞭草醛糖还原酶之间有利的相互作用,特别是涉及催化残基Y40和K71。综上所述,这些发现表明,muricata多酚通过多种细胞改变发挥抗心绞痛作用,并支持代谢和细胞骨架过程可能都有助于观察到的生物学效应的假设。需要进一步的研究来实验验证醛糖还原酶的作用及其与细胞骨架破坏的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.30
自引率
3.60%
发文量
0
审稿时长
17 weeks
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