大麻素受体激动剂和拮抗剂对小胶质细胞的抑制作用涉及 ERK1/2、cPLA2 和 NF-κB。
Involvement of ERK1/2, cPLA2 and NF-κB in microglia suppression by cannabinoid receptor agonists and antagonists.
机构信息
Program in Neuroscience, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA.
出版信息
Prostaglandins Other Lipid Mediat. 2013 Jan;100-101:1-14. doi: 10.1016/j.prostaglandins.2012.11.003. Epub 2012 Dec 5.
Cannabinoids have been consistently shown to suppress microglia activation and the release of cytotoxic factors including nitric oxide, superoxide and proinflammatory cytokines. However, the underlying molecular mechanisms and whether the action of cannabinoids is coupled to the activation of cannabinoid type 1 (CB1) and type 2 (CB2) receptors are still poorly defined. In this study we observed that the CB1 and CB2 receptor non-selective or selective agonists dramatically attenuate iNOS induction and ROS generation in LPS-activated microglia. These effects are due to their reduction of phosphorylation of extracellular signal regulated kinase 1/2 (ERK1/2), cytosolic phospholipase A (cPLA) and activation of NF-κB. Surprisingly, instead of reversing the effect of the respective CB1 and CB2 receptor agonists, the antagonists also suppress iNOS induction and ROS generation in activated microglia by similar mechanisms. Taken together, these results indicate that both cannabinoid receptor agonists and antagonists might suppress microglia activation by CB1 and CB2 receptor independent mechanisms, and provide a new insight into the mechanisms of microglia inhibition by cannabinoids.
大麻素已被一致证明可抑制小胶质细胞的激活和细胞毒性因子的释放,包括一氧化氮、超氧化物和促炎细胞因子。然而,其潜在的分子机制以及大麻素的作用是否与大麻素 1 型 (CB1) 和 2 型 (CB2) 受体的激活有关仍未得到明确界定。在这项研究中,我们观察到 CB1 和 CB2 受体非选择性或选择性激动剂可显著抑制 LPS 激活的小胶质细胞中诱导型一氧化氮合酶 (iNOS) 的诱导和活性氧 (ROS) 的产生。这些作用是由于它们减少了细胞外信号调节激酶 1/2 (ERK1/2)、胞质型磷脂酶 A (cPLA) 的磷酸化和 NF-κB 的激活。令人惊讶的是,拮抗剂并没有逆转各自的 CB1 和 CB2 受体激动剂的作用,也通过类似的机制抑制激活的小胶质细胞中 iNOS 的诱导和 ROS 的产生。总之,这些结果表明,大麻素受体激动剂和拮抗剂可能通过 CB1 和 CB2 受体非依赖性机制抑制小胶质细胞的激活,并为大麻素抑制小胶质细胞的机制提供了新的见解。