脒类化合物抗锥虫活性:最新进展。
Diamidine activity against trypanosomes: the state of the art.
机构信息
Laboratory Biologia Celular, Instituto Oswaldo Cruz, FIOCRUZ, Avenida Brasil 4365, Manguinhos, 21045-900, Rio de Janeiro, RJ, Brazil.
出版信息
Curr Mol Pharmacol. 2008 Jun;1(2):151-61. doi: 10.2174/1874467210801020151.
Aromatic diamidines and related compounds are DNA minor groove binders that have been screened against a variety of pathogenic microorganisms such as bacteria, fungi and protozoa and show promising results. Parasitic infections are widespread in developing countries and are major contributors to human mortality and morbidity, causing considerable economic hardship. Trypanosomes are unicellular protozoan organisms that cause serious public health problems in developing countries: African trypanosomiasis (sleeping sickness) in Africa, and Chagas' disease, in Latin America. Sleeping sickness, caused by sub-species of Trypanosome brucei (T. brucei gambiense and T. brucei rhodesiense), is a fatal disease if left untreated, with about 60 million people currently at risk. Trypanosoma cruzi is the etiological agent of Chagas' disease, an important parasitic illness that affects nearly 17 million individuals in endemic areas. The fact that the available clinical drugs are expensive, toxic, require long treatment periods, frequently exhibit reduced activity towards certain parasite strains and evolutive stages, and are beginning to show development of resistance, demonstrates the urgent need for the development of new drugs for both pathologies. For some time much attention has been focused on the effect of diamidines (and related compounds) on African trypanosomes. However more recent studies have pointed to their potential activity against T.cruzi. In this review the current therapeutic state of the art of aromatic diamidines and related compounds used against T.brucei and T.cruzi is reviewed with a focus on their potential use as antiparasitic drugs for the treatment of both these important neglected diseases.
芳香二脒类化合物和相关化合物是 DNA 小沟结合物,已针对多种致病微生物(如细菌、真菌和原生动物)进行了筛选,显示出有希望的结果。寄生虫感染在发展中国家广泛存在,是导致人类死亡率和发病率的主要原因,造成了相当大的经济困难。锥虫是单细胞原生动物,在发展中国家引起严重的公共卫生问题:非洲锥虫病(昏睡病)在非洲,和恰加斯病,在拉丁美洲。如果不治疗,由锥虫亚种(布氏锥虫冈比亚亚种和布氏锥虫罗得西亚亚种)引起的昏睡病是一种致命疾病,目前约有 6000 万人面临风险。克氏锥虫是恰加斯病的病原体,这是一种重要的寄生虫病,在流行地区影响近 1700 万人。现有的临床药物昂贵、有毒、需要长期治疗、对某些寄生虫株和进化阶段的活性常常降低,而且开始出现耐药性的发展,这表明迫切需要开发针对这两种疾病的新药。一段时间以来,人们一直关注二脒类化合物(和相关化合物)对非洲锥虫的作用。然而,最近的研究指出,它们对 T.cruzi 可能具有潜在的活性。在这篇综述中,回顾了用于治疗布氏锥虫和 T.cruzi 的芳香二脒类化合物和相关化合物的当前治疗现状,重点关注它们作为抗寄生虫药物治疗这两种重要的被忽视疾病的潜在用途。