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磷酸化蛋白质组学揭示阿片类药物的作用机制。

Phosphoproteomics Illuminates Opioid Actions.

作者信息

Che Tao, Roth Bryan L

机构信息

Department of Pharmacology , University of North Carolina School of Medical , Chapel Hill , North Carolina 27514 , United States.

出版信息

Biochemistry. 2018 Sep 25;57(38):5505-5506. doi: 10.1021/acs.biochem.8b00809. Epub 2018 Sep 13.

Abstract

Opioids are widely used analgesic medications with a high potential for tolerance and dependence and represent a frequent cause of death due to overdose. Opioids mediate their actions via a family of opioid G protein coupled receptors. Elucidating the biochemical mechanism(s) responsible for both the therapeutic and deleterious side effects of opioids could provide a biochemical roadmap for selectively targeting therapeutic signaling pathways. Here we provide a perspective on emerging findings, which illuminate these signaling pathways via unbiased and quantitative phosphoproteomic analysis. What emerged from these studies is the discovery that certain deleterious actions mediated by the κ opioid receptors appear due to specific activation of mTOR pathways. The findings imply that designing drugs, which bypass mTOR signaling, could yield safer and more effective analgesics.

摘要

阿片类药物是广泛使用的镇痛药,具有很高的耐受性和依赖性,并且是过量用药导致死亡的常见原因。阿片类药物通过阿片类G蛋白偶联受体家族介导其作用。阐明导致阿片类药物治疗作用和有害副作用的生化机制,可为选择性靶向治疗信号通路提供生化路线图。在此,我们对新出现的研究结果进行了展望,这些结果通过无偏倚的定量磷酸化蛋白质组学分析阐明了这些信号通路。这些研究中出现的发现是,κ阿片受体介导的某些有害作用似乎是由于mTOR通路的特定激活所致。这些发现意味着,设计绕过mTOR信号传导的药物可能会产生更安全、更有效的镇痛药。

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