大麻酚
大麻素受体
GPR18
大麻素
受体
大麻素受体2型
药理学
小胶质细胞
神经科学
化学
生物
炎症
医学
内科学
生物化学
大麻
精神科
兴奋剂
出处
期刊:Central nervous system agents in medicinal chemistry
[Bentham Science]
日期:2012-08-01
卷期号:12 (3): 233-239
被引量:26
标识
DOI:10.2174/187152412802430156
摘要
O-1602 is a cannabidiol analogue that does not bind with high affinity to either the cannabinoid CB1 receptor or CB2 receptor. However, there is evidence that O-1602 has significant effects in the central nervous system as well as other parts of the body. Depending upon the model, O-1602 has anti-inflammatory or pronociceptive effects, mediated through a number of distinct receptors. This article reviews the evidence for functional effects of O-1602, particularly in the CNS, and describes its known targets as they relate to these effects. These include the abnormal cannabidiol (Abn- CBD) receptor and GPR55. The GPR18 receptor has been identified with the Abn-CBD receptor, and therefore the evidence that O-1602 also acts at GPR18 is also reviewed. Finally, the evidence that these receptor targets are expressed in the CNS and the phenotypes of cells expressing these targets is discussed, concluding with a discussion of the prospects for O-1602 as a therapeutic agent in the CNS.
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