Wang Pengwen, Su Caixin, Feng Huili, Chen Xiaopei, Dong Yunfang, Rao Yingxue, Ren Ying, Yang Jinduo, Shi Jing, Tian Jinzhou, Jiang Shucui
1 Key Laboratory of Chinese Internal Medicine of Ministry of Education and Beijing, Dongzhimen Hospital, Beijing University of Chinese Medicine (BUCM), Beijing, China.
2 Key Laboratory of Pharmacology of Dongzhimen Hospital (BUCM), State Administration of Traditional Chinese Medicine, Beijing, China.
Int J Immunopathol Pharmacol. 2017 Mar;30(1):25-43. doi: 10.1177/0394632016688025. Epub 2017 Jan 26.
Recent studies have shown the therapeutic potential of curcumin in Alzheimer's disease (AD). In 2014, our lab found that curcumin reduced Aβ40, Aβ42 and Aβ-derived diffusible ligands in the mouse hippocampus, and improved learning and memory. However, the mechanisms underlying this biological effect are only partially known. There is considerable evidence in brain metabolism studies indicating that AD might be a brain-specific type of diabetes with progressive impairment of glucose utilisation and insulin signalling. We hypothesised that curcumin might target both the glucose metabolism and insulin signalling pathways. In this study, we monitored brain glucose metabolism in living APPswe/PS1dE9 double transgenic mice using a micro-positron emission tomography (PET) technique. The study showed an improvement in cerebral glucose uptake in AD mice. For a more in-depth study, we used immunohistochemical (IHC) staining and western blot techniques to examine key factors in both glucose metabolism and brain insulin signalling pathways. The results showed that curcumin ameliorated the defective insulin signalling pathway by upregulating insulin-like growth factor (IGF)-1R, IRS-2, PI3K, p-PI3K, Akt and p-Akt protein expression while downregulating IR and IRS-1. Our study found that curcumin improved spatial learning and memory, at least in part, by increasing glucose metabolism and ameliorating the impaired insulin signalling pathways in the brain.
最近的研究表明姜黄素在阿尔茨海默病(AD)中具有治疗潜力。2014年,我们实验室发现姜黄素可降低小鼠海马体中的Aβ40、Aβ42和Aβ衍生的可扩散配体,并改善学习和记忆。然而,这种生物学效应背后的机制仅部分为人所知。脑代谢研究中有大量证据表明,AD可能是一种脑部特异性糖尿病,伴有葡萄糖利用和胰岛素信号传导的进行性损害。我们假设姜黄素可能靶向葡萄糖代谢和胰岛素信号传导途径。在本研究中,我们使用微型正电子发射断层扫描(PET)技术监测了活的APPswe/PS1dE9双转基因小鼠的脑葡萄糖代谢。研究表明AD小鼠的脑葡萄糖摄取有所改善。为了进行更深入的研究,我们使用免疫组织化学(IHC)染色和蛋白质印迹技术来检测葡萄糖代谢和脑胰岛素信号传导途径中的关键因子。结果表明,姜黄素通过上调胰岛素样生长因子(IGF)-1R、IRS-2、PI3K、p-PI3K、Akt和p-Akt蛋白表达,同时下调IR和IRS-1,改善了有缺陷的胰岛素信号传导途径。我们的研究发现,姜黄素至少部分地通过增加葡萄糖代谢和改善脑中受损的胰岛素信号传导途径来改善空间学习和记忆。