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丝状线虫鹿丝状线虫的生化组成和代谢途径:寻找新的抗丝虫药物。

Biochemical composition and metabolic pathways of filarial worms Setaria cervi: search for new antifilarial agents.

作者信息

Ahmad Rumana, Srivastava Arvind K

机构信息

Division of Biochemistry, Po Box 173, Central Drug Research Institute, Chattar Manzil Palace, Lucknow-226001, India.

出版信息

J Helminthol. 2007 Sep;81(3):261-80. doi: 10.1017/S0022149X07799133.

Abstract

The main problem regarding the chemotherapy of filariasis is that no safe and effective drug is available yet to combat the adult human filarial worms. Setaria cervi, the causal organism of setariasis and lumbar paralysis in cattle, is routinely employed as a model organism for conducting biochemical and enzymatic studies on filarial parasites. In view of the practical difficulties in procuring human strains of Wuchereria bancrofti and Brugia malayi for drug screening, the bovine filarial parasite S. cervi, resembling the human species in having microfilarial periodicity and chemotherapeutic response to known antifilarial agents, is widely used as a model in such studies. For a rational approach to antifilarial chemotherapy, knowledge of the biochemical composition and metabolic pathways of this helminth parasite may be of paramount importance, so that more potent antifilarial agents based on specific drug targets can be identified in drug discovery programmes. The present review provides an update on the biochemistry of the important metabolic pathways functioning within this potentially important bovine parasite, that have so far been studied, and on those that need to be investigated further so as to identify novel drug targets that can be exploited for designing new antifilarial drugs.

摘要

丝虫病化疗的主要问题在于,目前尚无安全有效的药物来对抗人体中的成虫丝虫。牛腹腔丝虫是牛腹腔丝虫病和腰麻痹的病原体,常被用作对丝虫寄生虫进行生化和酶学研究的模式生物。鉴于获取班氏吴策线虫和马来布鲁线虫人体菌株用于药物筛选存在实际困难,牛丝虫寄生虫鹿腹腔丝虫在微丝蚴周期性和对已知抗丝虫药物的化疗反应方面与人类丝虫相似,因此在这类研究中被广泛用作模式生物。对于抗丝虫化疗的合理方法而言,了解这种蠕虫寄生虫的生化组成和代谢途径可能至关重要,以便在药物研发计划中确定基于特定药物靶点的更有效的抗丝虫药物。本综述提供了关于该潜在重要牛寄生虫内迄今已研究的重要代谢途径的生物化学的最新情况,以及关于那些需要进一步研究以确定可用于设计新抗丝虫药物的新药物靶点的代谢途径的最新情况。

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