化学
巴基斯坦卢比
药理学
大麻酚
体内
上瘾
有条件地点偏好
神经炎症
类阿片
吗啡
受体
生物化学
糖酵解
丙酮酸激酶
神经科学
医学
酶
大麻
免疫学
炎症
心理学
生物技术
精神科
生物
作者
Sha Jin,Cong Lin,Yibo Wang,Hongshuang Wang,Xin Wen,Peng Xiao,Xiaodong Li,Yinghua Peng,Jin‐Peng Sun,Yuyuan Lu,Xiaohui Wang
标识
DOI:10.1021/acs.jmedchem.3c01029
摘要
Opioid addiction is a chronically relapsing disorder that causes critical public health problems. Currently, there is a lack of effective drug treatment. Herein, one cannabidiol derivative, CIAC001, was discovered as an effective agent for treating morphine-induced addiction. In vitro, CIAC001 exhibited significantly improved anti-neuroinflammatory activity with lower toxicity. In vivo, CIAC001 ameliorated the morphine-induced withdrawal reaction, behavioral sensitization, and conditional position preference by inhibiting morphine-induced microglia activation and neuroinflammation. Target fishing for CIAC001 by activity-based protein profiling led to the identification of pyruvate kinase M2 (PKM2) as the target protein. CIAC001 bound to the protein-protein interface of the PKM2 dimer and promoted the tetramerization of PKM2. Moreover, CIAC001 exhibited an anti-neuroinflammatory effect by reversing the decrease of the PKM2 tetramer and inhibiting the nuclear translocation of PKM2. In summary, this study identified CIAC001 as a lead compound in targeting PKM2 to treat morphine-induced addiction.
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