Tiwari Neeraj, Gedda Mallikarjuna Rao, Tiwari Vinod K, Singh Surya P, Singh Rakesh K
Department of Biochemistry, Institute of Science, Banaras Hindu University, Varanasi - 221 005, India.
Department of Chemistry, Institute of Science, Banaras Hindu University, Varanasi - 221 005, India.
Mini Rev Med Chem. 2018;18(1):26-41. doi: 10.2174/1389557517666170425105129.
Soon after the identification of Leishmania parasite as a causative agent, the pentavalent antimony compounds have been the mainstay to treat all forms of leishmaniasis. Due to growing incidences of antimony resistant parasites and unavailability of true antileishmanial compounds, few drugs like pentamidine (antimicrobial), amphotericin B (antifungal) or miltefosine (antitumor) are currently being used but these are associated with serious side effects. Unfortunately, the emergence of amphotericin B and miltefosine resistant parasites in clinical settings has further questioned their sustained use in leishmanial control. Moreover, the parameters of protective immunity are not well understood in leishmanial pathogenesis therefore, a vaccine candidate, either prophylactic or preventive, is still an unrealized goal. In addition, the emergence of insecticide resistance sand flies in disease endemic regions also stance a big threat for the current elimination strategies. Therefore, in lieu of the limited drug regimen and unavailability of a vaccine, the necessity of a true antileishmanial agent is always there. Although, leishmanial infections have been neglected for many decades but recent studies have identified potential drug targets that could be targeted to control the growth of parasites. In recent past many compounds derived from natural sources have also been shown to possess excellent antiparasitic potential; however, most of these studies are limited to primary evaluation and only a few have reached to clinical levels. In this review, we discuss the limitations of current drug regimen, explore possible drug targets of Leishmania species and summarize wide range of compounds isolated from various natural sources that are worth screening as antileishmanial drug candidates.
在利什曼原虫被确认为致病因子后不久,五价锑化合物一直是治疗所有利什曼病的主要药物。由于抗锑寄生虫的发病率不断上升以及真正的抗利什曼原虫化合物的缺乏,目前正在使用一些药物,如喷他脒(抗菌药)、两性霉素B(抗真菌药)或米替福新(抗肿瘤药),但这些药物都有严重的副作用。不幸的是,临床环境中出现的对两性霉素B和米替福新耐药的寄生虫进一步质疑了它们在利什曼病防治中的持续使用。此外,在利什曼病发病机制中,保护性免疫的参数尚未得到很好的理解,因此,候选疫苗,无论是预防性还是治疗性的,仍然是一个未实现的目标。此外,疾病流行地区出现的对杀虫剂耐药的白蛉也对当前的消除策略构成了巨大威胁。因此,鉴于药物治疗方案有限且缺乏疫苗,真正的抗利什曼原虫药物一直是必要的。尽管利什曼病感染在过去几十年中一直被忽视,但最近的研究已经确定了潜在的药物靶点,可以针对这些靶点来控制寄生虫的生长。最近,许多天然来源的化合物也被证明具有优异的抗寄生虫潜力;然而,这些研究大多仅限于初步评估,只有少数达到了临床水平。在这篇综述中,我们讨论了当前药物治疗方案的局限性,探索了利什曼原虫物种可能的药物靶点,并总结了从各种天然来源分离出的、值得作为抗利什曼原虫候选药物进行筛选的广泛化合物。