GPR18
内大麻素系统
大麻素受体
神经炎症
大麻素
大麻素受体2型
神经科学
受体
去极化抑制抑制
神经退行性变
G蛋白偶联受体
免疫系统
生物
药理学
炎症
医学
免疫学
疾病
生物化学
内科学
兴奋剂
作者
Orla Haugh,June Penman,Andrew J. Irving,Veronica A. Campbell
出处
期刊:Current Drug Targets
[Bentham Science]
日期:2016-01-13
卷期号:17 (16): 1834-1840
被引量:23
标识
DOI:10.2174/1389450117666160112113703
摘要
The classical endogenous cannabinoid (CB) system is composed of the endocannabinoid signalling molecules, 2-arachidonoyl glycerol (2-AG) and anandamide (AEA) and their G-protein coupled receptors (GPCR), CB1 and CB2 which together constitutes the endocannabinoid system (ECS). However, putative, novel lipid-sensing CB receptors have recently been identified, including the orphan GPR55 and GPR18 receptors that are regulated by cannabinoid-like molecules and interact with CB system. CB receptors and associated orphan GPCRs are expressed at high levels in the immune and/or central nervous systems (CNS) and regulate a number of neurophysiological processes, including key events involved in neuroinflammation. As such, these receptors have been identified as emerging therapeutic targets for a number of brain disorders in which neuroinflammation is a key feature, including multiple sclerosis (MS) and Alzheimer's disease (AD). This review will consider the role of the wider cannabinoid receptor superfamily in mediating immune function with a focus on the immune processes that contribute to neuroinflammatory conditions.
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