Department of Neurobiology, Care Sciences and Society, Division of Neurogeriatrics, Center for Alzheimer Research, Karolinska Institutet, Stockholm, Sweden.
Neuroscience Center of Excellence, School of Medicine, Louisiana State University Health New Orleans, New Orleans, LA, USA.
Commun Biol. 2022 Mar 21;5(1):245. doi: 10.1038/s42003-022-03169-3.
Sustained microglial activation and increased pro-inflammatory signalling cause chronic inflammation and neuronal damage in Alzheimer's disease (AD). Resolution of inflammation follows neutralization of pathogens and is a response to limit damage and promote healing, mediated by pro-resolving lipid mediators (LMs). Since resolution is impaired in AD brains, we decided to test if intranasal administration of pro-resolving LMs in the App mouse model for AD could resolve inflammation and ameliorate pathology in the brain. A mixture of the pro-resolving LMs resolvin (Rv) E1, RvD1, RvD2, maresin 1 (MaR1) and neuroprotectin D1 (NPD1) was administered to stimulate their respective receptors. We examined amyloid load, cognition, neuronal network oscillations, glial activation and inflammatory factors. The treatment ameliorated memory deficits accompanied by a restoration of gamma oscillation deficits, together with a dramatic decrease in microglial activation. These findings open potential avenues for therapeutic exploration of pro-resolving LMs in AD, using a non-invasive route.
持续的小胶质细胞激活和促炎信号增加导致阿尔茨海默病 (AD) 的慢性炎症和神经元损伤。炎症的消退遵循病原体的中和,是限制损伤和促进愈合的反应,由促解决脂质介质 (LM) 介导。由于 AD 大脑中的炎症消退受损,我们决定测试 AD 的 App 小鼠模型中鼻内给予促解决 LM 是否可以解决炎症并改善大脑中的病理。混合了促解决 LMs resolvin (Rv) E1、RvD1、RvD2、maresin 1 (MaR1) 和神经保护素 D1 (NPD1),以刺激它们各自的受体。我们检查了淀粉样蛋白负荷、认知、神经元网络振荡、神经胶质激活和炎症因子。该治疗改善了记忆缺陷,同时恢复了γ振荡缺陷,并显著减少了小胶质细胞激活。这些发现为 AD 中使用非侵入性途径探索促解决 LM 的治疗方法开辟了潜在途径。