Department of Pharmaceutical Pharmacology, College of Pharmaceutical Sciences, Matsuyama University 4-2 Bunkyo-cho, Matsuyama, Ehime 790-8578, Japan.
Eur J Pharmacol. 2013 Jan 15;699(1-3):118-23. doi: 10.1016/j.ejphar.2012.11.043. Epub 2012 Dec 5.
Cerebral ischemia causes delayed neuronal cell death in the hippocampus resulting in sequential cognitive impairments. Hyper-activated inflammation following ischemia is one of the etiologies for delayed neuronal cell death. In the present study, using a transient global ischemia mouse model, we showed that auraptene (AUR), a citrus coumarin, effectively inhibited microglia activation, cyclooxygenase-2 expression by astrocytes, and neuronal cell death in the hippocampus following ischemic insults. These results suggest that AUR acts as a neuroprotective agent in the ischemic brain, which may be mediated by suppression of the inflammatory response.
脑缺血导致海马区神经元延迟性死亡,进而导致认知功能障碍。缺血后继发的过度激活炎症反应是神经元延迟性死亡的一个病因。在本研究中,我们利用短暂性全脑缺血小鼠模型发现,柑橘香豆素佛手柑素(AUR)可有效抑制缺血性损伤后小胶质细胞的激活、星形胶质细胞中环氧化酶-2 的表达以及海马区神经元的死亡。这些结果表明,AUR 可作为缺血性脑损伤的神经保护剂,其作用机制可能与抑制炎症反应有关。