Trichomonas vaginalis Drug Targets and Their Role in Drug Discovery and Development.

IF 4.3 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Mirna Samara Dié Alves, Ângela Sena-Lopes, Luiza Domingues Moron, Bárbara da Rocha Fonseca, Sibele Borsuk
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引用次数: 0

Abstract

Trichomonas vaginalis is the causative agent of trichomoniasis, the most common and prevalent sexually transmitted infection (STI) globally, with about 156 million cases annually. Trichomoniasis is a critical public health problem, and it is aggravated due to its association with a higher risk of HIV-1 acquisition and transmission and complications such as preterm delivery and pelvic inflammatory disease. This STI is treated mainly through the 5-nitroimidazole class, specifically metronidazole and tinidazole. However, drug resistance, which can represent between 5 and 20% of clinical cases, and hypersensitivity reactions are a general concern. In this context, drug development for trichomoniasis is an ever-growing research field. Therefore, considering how important drug targets and the mechanism of action of compounds can be to drug discovery, there is a growing interest in better understanding how some molecules can be used as targets. This article offers an overview of T. vaginalis drug targets, their significance in metabolism, pathogenesis, or survival, and their contribution to drug development for trichomoniasis.

阴道毛滴虫药物靶点及其在药物发现和开发中的作用。
阴道毛滴虫是滴虫病的病原体,滴虫病是全球最常见和流行的性传播感染,每年约有1.56亿例。滴虫病是一个严重的公共卫生问题,由于它与艾滋病毒-1感染和传播的高风险以及早产和盆腔炎等并发症有关,因此问题更加严重。这种STI主要通过5-硝基咪唑类药物治疗,特别是甲硝唑和替硝唑。然而,耐药(占临床病例的5%至20%)和过敏反应是一个普遍关注的问题。在此背景下,滴虫的药物开发是一个不断发展的研究领域。因此,考虑到药物靶点和化合物的作用机制对药物发现的重要性,人们对更好地了解如何将某些分子用作靶点越来越感兴趣。本文综述了阴道滴虫的药物靶点,它们在代谢、发病机制或生存中的意义,以及它们对滴虫病药物开发的贡献。
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
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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