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系统药理学将G蛋白偶联受体与视网膜退行性疾病联系起来。

Systems Pharmacology Links GPCRs with Retinal Degenerative Disorders.

作者信息

Chen Yu, Palczewski Krzysztof

机构信息

Yueyang Hospital and.

Clinical Research Institute of Integrative Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 200437, China.

出版信息

Annu Rev Pharmacol Toxicol. 2016;56:273-98. doi: 10.1146/annurev-pharmtox-010715-103033. Epub 2015 Mar 23.

Abstract

In most biological systems, second messengers and their key regulatory and effector proteins form links between multiple cellular signaling pathways. Such signaling nodes can integrate the deleterious effects of genetic aberrations, environmental stressors, or both in complex diseases, leading to cell death by various mechanisms. Here we present a systems (network) pharmacology approach that, together with transcriptomics analyses, was used to identify different G protein-coupled receptors that experimentally protected against cellular stress and death caused by linked signaling mechanisms. We describe the application of this concept to degenerative and diabetic retinopathies in appropriate mouse models as an example. Systems pharmacology also provides an attractive framework for devising strategies to combat complex diseases by using (repurposing) US Food and Drug Administration-approved pharmacological agents.

摘要

在大多数生物系统中,第二信使及其关键调节蛋白和效应蛋白在多个细胞信号通路之间形成联系。这些信号节点可整合复杂疾病中遗传畸变、环境应激源或两者的有害影响,通过多种机制导致细胞死亡。在此,我们提出一种系统(网络)药理学方法,该方法与转录组学分析一起,用于识别不同的G蛋白偶联受体,这些受体在实验中可保护细胞免受由相关信号机制引起的细胞应激和死亡。我们以在合适的小鼠模型中将这一概念应用于退行性和糖尿病性视网膜病变为例进行描述。系统药理学还为利用美国食品药品监督管理局批准的药物(重新利用)设计对抗复杂疾病的策略提供了一个有吸引力的框架。

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