Laboratorio de Biotecnología Farmacéutica, Centro de Biotecnología Genómica, Instituto Politécnico Nacional, Reynosa 88710, Mexico.
Laboratorio de Estudios Epidemiológicos, Clínicos, Diseños Experimentales e Investigación, Facultad de Ciencias Químicas, Universidad Autónoma "Benito Juárez" de Oaxaca, Oaxaca 68120, Mexico.
Int J Mol Sci. 2024 Jun 5;25(11):6238. doi: 10.3390/ijms25116238.
Parasitic diseases, predominantly prevalent in developing countries, are increasingly spreading to high-income nations due to shifting migration patterns. The World Health Organization (WHO) estimates approximately 300 million annual cases of giardiasis. The emergence of drug resistance and associated side effects necessitates urgent research to address this growing health concern. In this study, we evaluated over eleven thousand pharmacological compounds sourced from the FDA database to assess their impact on the TATA-binding protein (TBP) of the early diverging protist , which holds medical significance. We identified a selection of potential pharmacological compounds for combating this parasitic disease through in silico analysis, employing molecular modeling techniques such as homology modeling, molecular docking, and molecular dynamics simulations. Notably, our findings highlight compounds DB07352 and DB08399 as promising candidates for inhibiting the TBP of Also, these compounds and DB15584 demonstrated high efficacy against trophozoites in vitro. In summary, this study identifies compounds with the potential to combat giardiasis, offering the prospect of specific therapies and providing a robust foundation for future research.
寄生虫病主要在发展中国家流行,但由于移民模式的改变,这些疾病正越来越多地传播到高收入国家。世界卫生组织(WHO)估计每年有大约 3 亿例贾第虫病。由于耐药性的出现以及相关的副作用,迫切需要进行研究来解决这一日益严重的健康问题。在这项研究中,我们评估了来自 FDA 数据库的超过一万一千种药理学化合物,以评估它们对早期分化原生动物 TATA 结合蛋白(TBP)的影响,这具有医学意义。我们通过计算机模拟分析,利用同源建模、分子对接和分子动力学模拟等分子建模技术,确定了一些具有治疗这种寄生虫病潜力的潜在药理学化合物。值得注意的是,我们的研究结果突出了化合物 DB07352 和 DB08399 作为抑制 TBP 的候选物的潜力,此外,这些化合物和 DB15584 在体外对滋养体显示出很高的疗效。总之,这项研究确定了具有抗贾第虫病潜力的化合物,为特定疗法提供了前景,并为未来的研究提供了坚实的基础。