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设计生物可利用促黑素的新方法。

Novel approaches to the design of bioavailable melanotropins.

作者信息

Zhou Yang, Cai Minying

机构信息

a Department of Chemistry and Biochemistry , University of Arizona , Tucson , AZ USA.

出版信息

Expert Opin Drug Discov. 2017 Oct;12(10):1023-1030. doi: 10.1080/17460441.2017.1351940. Epub 2017 Jul 12.

Abstract

The melanocortin system is a primordial and critical system for survival, involved in a wide variety of physiological functions. It includes melanocortin receptors (MCRs) and melanotropin ligands (MCLs). MCRs are important drug targets that can regulate several key physiological processes. Extensive efforts have been made to develop peptide and peptidomimetics targeting melanocortin receptors including MC1R, MC3R, MC4R and MC5R. Most research is focused on developing potent and selective melanotropins. However, developing bioavailable melanotropins remains challenging. Areas covered: Herein, the authors summarize promising strategies for developing bioavailable MCLs by using cyclized N-methylated melanotropins, and using cyclotide and tetrapeptide as templates. They discuss their unique advantages in oral availability and targeting MCRs in the central nervous system or in peripheral tissues. Finally, they discuss the observed differences in thepharmacology of MCRs between in vitro and in vivo tests. Expert opinion: N-methylated cyclized melanotropins have great potential to become bio- available drugs targeting MCRs in the brain, while MCR-grafted cyclotides tend to target MCRs in peripheral tissue. A better understanding of the biased signaling process is a new challenge and opportunity for the future discovery of bioavailable MCLs.

摘要

黑皮质素系统是一个对生存至关重要的原始系统,参与多种生理功能。它包括黑皮质素受体(MCRs)和促黑素配体(MCLs)。MCRs是重要的药物靶点,可调节多个关键生理过程。人们已付出大量努力来开发靶向黑皮质素受体(包括MC1R、MC3R、MC4R和MC5R)的肽和肽模拟物。大多数研究集中在开发强效且选择性的促黑素上。然而,开发具有生物利用度的促黑素仍然具有挑战性。涵盖领域:在此,作者总结了通过使用环化N-甲基化促黑素以及以环肽和四肽为模板来开发具有生物利用度的MCLs的有前景的策略。他们讨论了这些策略在口服可用性以及靶向中枢神经系统或外周组织中的MCRs方面的独特优势。最后,他们讨论了在体外和体内试验中观察到的MCRs药理学差异。专家观点:N-甲基化环化促黑素极有可能成为靶向大脑中MCRs的具有生物利用度的药物,而MCR嫁接环肽倾向于靶向外周组织中的MCRs。更好地理解偏向性信号传导过程是未来发现具有生物利用度的MCLs的新挑战和机遇。

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