The Polyamine Pathway as a Potential Target for Leishmaniases Chemotherapy

J. I. Aoki, S. Muxel, Juliane Cristina RibeiroFernandes, L. Floeter-Winter
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引用次数: 2

Abstract

Considering the limitations of the current leishmaniases chemotherapy and the lack of effective vaccines, the identification of novel drugs and/or vaccine approaches for the leishmaniases treatment and control is urgently required. In fact, a rational strategy for the parasite control can be based on the identification of essential metabolic pathways of the parasite. One of the most important pathways is the polyamine biosynthesis. Leishmania is auxotrophic for many amino acids, such as l-arginine, a precursor of orni -thine, putrescine, and spermidine. These metabolites are essential for parasite replication and establishment of infection in the mammalian host. In addition, Leishmania has a specific and complex machinery to uptake and metabolize exogenous sources of those mol - ecules. In this chapter, we will focus on the main aspects of the polyamine pathway as a potential target for infection control aiming for new targets for Leishmania chemotherapy.
多胺途径作为利什曼病化疗的潜在靶点
考虑到目前利什曼病化疗的局限性和缺乏有效的疫苗,迫切需要确定治疗和控制利什曼病的新药和/或疫苗方法。事实上,合理的寄生虫控制策略可以建立在寄生虫基本代谢途径的识别基础上。其中最重要的途径是多胺生物合成。利什曼原虫对许多氨基酸缺乏营养,如l-精氨酸,鸟氨酸、腐胺和亚精胺的前体。这些代谢物对寄生虫在哺乳动物宿主中的复制和感染的建立至关重要。此外,利什曼原虫有一种特殊而复杂的机制来吸收和代谢外源的这些分子。在本章中,我们将重点介绍多胺途径作为感染控制的潜在靶点的主要方面,旨在为利什曼原虫化疗提供新的靶点。
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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