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3-碘甲状腺原氨酸及其衍生物:代谢综合征的新盟友?

3-Iodothyronamine and Derivatives: New Allies Against Metabolic Syndrome?

机构信息

Department of Pathology, University of Pisa, 56100 Pisa, Italy.

出版信息

Int J Mol Sci. 2020 Mar 15;21(6):2005. doi: 10.3390/ijms21062005.

Abstract

In the two decades since its discovery, a large body of evidence has amassed to highlight the potential of 3-iodothyronamine (T1AM) as an antiobesity drug, whose pleiotropic signaling actions profoundly impact energy metabolism. In the present review, we recapitulate the most relevant properties of T1AM, including its structural and functional relationship to thyroid hormone, its endogenous levels, molecular targets, as well as its genomic and non-genomic effects on metabolism elicited in experimental models after exogenous administration. The physiological and pathophysiological relevance of T1AM in the regulation of energy homeostasis and metabolism is also discussed, along with its potential therapeutic applications in metabolic disturbances. Finally, we examine a number of T1AM analogs that have been recently developed with the aim of designing novel pharmacological agents for the treatment of interlinked diseases, such as metabolic and neurodegenerative disorders, as well as additional synthetic tools that can be exploited to further explore T1AM-dependent mechanisms and the physiological roles of trace amine-associated receptor 1 (TAAR1)-mediated effects.

摘要

自发现以来的二十年中,大量证据表明 3-碘甲状腺原氨酸(T1AM)有作为一种抗肥胖药物的潜力,其多效性信号作用对能量代谢有深远影响。在本综述中,我们总结了 T1AM 的最相关特性,包括其与甲状腺激素的结构和功能关系、内源性水平、分子靶点,以及在外源给予后在实验模型中对代谢产生的基因组和非基因组效应。还讨论了 T1AM 在调节能量平衡和代谢中的生理和病理生理学相关性,以及它在代谢紊乱治疗中的潜在治疗应用。最后,我们研究了最近开发的一些 T1AM 类似物,旨在设计用于治疗代谢和神经退行性等相关疾病的新型药理学药物,以及可用于进一步探索 T1AM 依赖性机制和痕量胺相关受体 1(TAAR1)介导作用的生理作用的其他合成工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c85/7139928/86caec02315a/ijms-21-02005-g001.jpg

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