Fan Xiaorui, Liu Bin, Zhou Junyi, Gu Xinru, Zhou Yanyan, Yang Yifei, Guo Feifei, Wei Xiaolu, Wang Hongjie, Si Nan, Yang Jian, Bian Baolin, Zhao Haiyu
School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing, China.
Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
Front Aging Neurosci. 2021 Jun 8;13:658376. doi: 10.3389/fnagi.2021.658376. eCollection 2021.
Alzheimer's disease (AD) is a progressive neurodegenerative disease caused by the complex interaction of multiple mechanisms. Recent studies examining the effect of high-fat diet (HFD) on the AD phenotype have demonstrated a significant influence on both inflammation and cognition. However, different studies on the effect of high-fat diet on AD pathology have reported conflicting conclusions. To explore the involvement of HFD in AD, we investigated phenotypic and metabolic changes in an AD mouse model in response to HFD. The results indicated there was no significant effect on Aβ levels or contextual memory due to HFD treatment. Of note, HFD did moderate neuroinflammation, despite spurring inflammation and increasing cholesterol levels in the periphery. In addition, diet affected gut microbiota symbiosis, altering the production of bacterial metabolites. HFD created a favorable microenvironment for bile acid alteration and arachidonic acid metabolism in APP/PS1 mice, which may be related to the observed improvement in LXR/PPAR expression. Our previous research demonstrated that Huanglian Jiedu decoction (HLJDD) significantly ameliorated impaired learning and memory. Furthermore, HLJDD may globally suppress inflammation and lipid accumulation to relieve cognitive impairment after HFD intervention. It was difficult to define the effect of HFD on AD progression because the results were influenced by confounding factors and biases. Although there was still obvious damage in AD mice treated with HFD, there was no deterioration and there was even a slight remission of neuroinflammation. Moreover, HLJDD represents a potential AD drug based on its anti-inflammatory and lipid-lowering effects.
阿尔茨海默病(AD)是一种由多种机制复杂相互作用引起的进行性神经退行性疾病。最近关于高脂饮食(HFD)对AD表型影响的研究表明,其对炎症和认知均有显著影响。然而,关于高脂饮食对AD病理影响的不同研究报告了相互矛盾的结论。为了探究高脂饮食在AD中的作用,我们研究了AD小鼠模型对高脂饮食的表型和代谢变化。结果表明,高脂饮食处理对Aβ水平或情境记忆没有显著影响。值得注意的是,尽管高脂饮食会刺激外周炎症并增加胆固醇水平,但它确实减轻了神经炎症。此外,饮食影响肠道微生物群共生,改变细菌代谢产物的产生。高脂饮食为APP/PS1小鼠的胆汁酸改变和花生四烯酸代谢创造了有利的微环境,这可能与观察到的LXR/PPAR表达改善有关。我们之前的研究表明,黄连解毒汤(HLJDD)能显著改善受损的学习和记忆。此外,黄连解毒汤可能通过全面抑制炎症和脂质积累来缓解高脂饮食干预后的认知障碍。由于结果受到混杂因素和偏差的影响,很难确定高脂饮食对AD进展的影响。尽管高脂饮食处理的AD小鼠仍有明显损伤,但没有恶化,甚至神经炎症有轻微缓解。此外,基于其抗炎和降脂作用,黄连解毒汤是一种潜在的AD药物。