Laxman Sunil, Beavo Joseph A
Department of Pharmacology, University of Washington School of Medicine, Seattle, WA 98105, USA.
Mol Interv. 2007 Aug;7(4):203-15. doi: 10.1124/mi.7.4.7.
Trypanosome infections cause several major human diseases, including sleeping sickness and Chagas disease, which affect millions of people in Africa and South America, respectively. Although adenosine 3',5'-monophosphate (cAMP) signaling and regulation have been widely studied in mammalian systems, and these pathways provide targets for the treatment of numerous pathologies, a molecular understanding of cAMP signaling in trypanosomes remains incomplete. Recent studies in these parasites, however, have revealed diverse families of adenylyl cyclase and phosphodiesterase that regulate cAMP concentrations. Importantly, these enzymes differ pharmacologically and biochemically from their mammalian counterparts. In this review, we discuss recent developments, emerging ideas, and gaps in knowledge in this area of research, highlighting aspects of enzymes in the cAMP signaling pathway that may be good targets for antitrypanosomal drug therapy.
锥虫感染会引发几种主要的人类疾病,包括昏睡病和恰加斯病,分别影响着非洲和南美洲的数百万人。尽管3',5'-环磷酸腺苷(cAMP)信号传导和调节在哺乳动物系统中已得到广泛研究,并且这些途径为众多疾病的治疗提供了靶点,但对锥虫中cAMP信号传导的分子理解仍不完整。然而,最近对这些寄生虫的研究揭示了调节cAMP浓度的腺苷酸环化酶和磷酸二酯酶的不同家族。重要的是,这些酶在药理学和生物化学性质上与它们的哺乳动物对应物不同。在这篇综述中,我们讨论了该研究领域的最新进展、新出现的观点以及知识空白,重点介绍了cAMP信号通路中可能成为抗锥虫药物治疗良好靶点的酶的各个方面。