Departamento de Ciencias Biomédicas, Facultad de Veterinaria, Universidad de León, Campus de Vegazana s/n, 24071 León, Spain.
Instituto de Biomedicina (IBIOMED), Universidad de León, Campus de Vegazana s/n, 24071 León, Spain.
Molecules. 2024 May 9;29(10):2214. doi: 10.3390/molecules29102214.
Infectious diseases caused by trypanosomatids, including African trypanosomiasis (sleeping sickness), Chagas disease, and different forms of leishmaniasis, are Neglected Tropical Diseases affecting millions of people worldwide, mainly in vulnerable territories of tropical and subtropical areas. In general, current treatments against these diseases are old-fashioned, showing adverse effects and loss of efficacy due to misuse or overuse, thus leading to the emergence of resistance. For these reasons, searching for new antitrypanosomatid drugs has become an urgent necessity, and different metabolic pathways have been studied as potential drug targets against these parasites. Considering that trypanosomatids possess a unique redox pathway based on the trypanothione molecule absent in the mammalian host, the key enzymes involved in trypanothione metabolism, trypanothione reductase and trypanothione synthetase, have been studied in detail as druggable targets. In this review, we summarize some of the recent findings on the molecules inhibiting these two essential enzymes for and viability.
由利什曼原虫和锥虫引起的传染病,包括非洲锥虫病(昏睡病)、恰加斯病和不同形式的利什曼病,是影响全球数百万人的被忽视的热带病,主要发生在热带和亚热带地区的脆弱领土上。一般来说,目前针对这些疾病的治疗方法已经过时,由于误用或滥用,出现了不良反应和疗效丧失,从而导致耐药性的出现。出于这些原因,寻找新的抗利什曼原虫药物已成为当务之急,不同的代谢途径已被研究作为针对这些寄生虫的潜在药物靶点。鉴于锥虫具有基于三肽硫醇分子的独特氧化还原途径,而哺乳动物宿主中不存在该分子,因此参与三肽硫醇代谢的关键酶,即三肽硫醇还原酶和三肽硫醇合成酶,已被详细研究为可成药的靶点。在这篇综述中,我们总结了一些关于抑制这两种对生存至关重要的酶的分子的最新发现。