基于结构的阿片类止痛药与减少副作用的发现
Aashish Manglik1, Henry Lin2, Dipendra K Aryal3
1Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, California 94305, USA.
Nature
|August 18, 2016
概括
研究人员发现了PZM21,一种激活片受体 (μOR) 缓解疼痛的新化合物. 不同于吗啡,PZM21提供强大的止痛药,
科学领域:
- 药理学
- 神经科学
- 医学化学
背景情况:
- 吗啡是一种μ-阿片类受体 (μOR) 激动剂,有效治疗疼痛,但引起危险的副作用.
- 片类药物的副作用与β- 停滞信号通路有关,而G- 蛋白信号通路则调解疼痛.
研究的目的:
- 确定针对μOR的新型非阿片类支架.
- 与传统阿片类药物相比,开发一种具有 μOR 选择性的化合物.
主要方法:
- 超过300万个分子与μOR结构的计算对接.
- 基于结构的优化创建PZM21.
- 在小鼠中评估PZM21的G蛋白和β- 止蛋白信号传递,止痛效果和副作用概况.
主要成果:
- 发现了与已知阿片类药物无关的新架.
- 开发了PZM21,一种强大的Gi激活剂,对μOR具有最小的β-arrestin-2招募.
- 在小鼠中,PZM21在疼痛缓解的情感成分中表现出有效性,没有呼吸抑制或强化作用.
结论:
- PZM21作为一个有价值的探测器来剖析μOR信号通路.
- PZM21代表了阿片类药物治疗疼痛的有希望的治疗方法,其安全性更好.
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