In vivo efficacy of uvangoletin from Piper aduncum (Piperaceae) against Schistosoma mansoni and in silico studies targeting SmNTPDases.

IF 1.4 4区 医学 Q3 PARASITOLOGY
Everton Allan Ferreira, Igor Moreira Campos, Rayssa A Cajas, Danilo de Souza Costa, Lara Soares Aleixo de Carvalho, Paula Fernandes da Costa Franklin, Nathália de Paula D de Nigro, Priscila de Faria Pinto, PriscilaV S Z Capriles, Josué de Moraes, Ademar A da Silva Filho
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Abstract

Schistosomiasis stands as one of the most significant parasitic diseases on a global scale, with approximately 250 million infections worldwide. It is imperative to address this pressing issue by developing new antischistosomal drugs. Chalcones have emerged as a promising class of natural compounds, demonstrating noteworthy effects observed in vitro experiments with Schistosoma mansoni, and demonstrating the ability to inhibit SmNTPDases and apyrase from potatoes. In this study, we focused on uvangoletin, a naturally occurring dihydrochalcone from Piper aduncum. We isolated uvangoletin from P. aduncum fruits and conducted in vivo experiments to evaluate the efficacy of uvangoletin against adult Schistosoma parasites. Furthermore, we explored the inhibitory effects of uvangoletin on potato apyrase and employed molecular docking analyses to investigate its interactions with apyrase from potato and the two isoforms SmNTPDase 1 and 2 through in silico studies. Uvangoletin (400 mg/kg, p. o.), exhibited significant in vivo antiparasitic effects against adult S. mansoni, leading to a decrease of 53.7% in worm burden and 54.3% in egg production. The treatment also reduced hepatomegaly and splenomegaly. In silico investigations and ADMET studies indicated that uvangoletin possesses favorable drug-like properties and may interact with key residues involved in apyrase and SmNTPDases activities. Furthermore, uvangoletin demonstrated a substantial reduction in potato apyrase activity. These results suggest the potential for exploring other dihydrochalcones as promising candidates for antischistosomal agents.

胡椒科植物紫万素抗曼氏血吸虫体内药效及针对smntpases的硅片研究。
血吸虫病是全球范围内最严重的寄生虫病之一,全世界约有2.5亿人感染。迫切需要开发新的抗血吸虫药物来解决这一紧迫问题。查尔酮已成为一类很有前途的天然化合物,在曼氏血吸虫的体外实验中显示出显著的效果,并显示出抑制马铃薯中smntpases和apyrase的能力。在这项研究中,我们重点研究了一种天然存在的二氢查尔酮。本研究从黄菖蒲果实中分离得到乌万素,并进行体内实验,评价乌万素对血吸虫成虫的抑制作用。此外,我们探索了uvangoletin对马铃薯apyrase的抑制作用,并通过分子对接分析研究了其与马铃薯apyrase以及smntpase 1和2两个异构体的相互作用。百万素(400mg /kg, p.o)对马氏夜蛾有显著的体内抗寄生作用,虫量减少53.7%,产蛋量减少54.3%。治疗还可减少肝和脾肿大。计算机研究和ADMET研究表明,uvangoltin具有良好的药物样性质,并可能与apyrase和smntpases活性的关键残基相互作用。此外,uvangoltin显示了马铃薯apyrase活性的显著降低。这些结果提示探索其他二氢查尔酮作为抗血吸虫药物的有希望的候选者的潜力。
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
Experimental parasitology
Experimental parasitology 医学-寄生虫学
CiteScore
3.10
自引率
4.80%
发文量
160
审稿时长
3 months
期刊介绍: Experimental Parasitology emphasizes modern approaches to parasitology, including molecular biology and immunology. The journal features original research papers on the physiological, metabolic, immunologic, biochemical, nutritional, and chemotherapeutic aspects of parasites and host-parasite relationships.
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