Nao Tan Qing ameliorates Alzheimer's disease-like pathology by regulating glycolipid metabolism and neuroinflammation: A network pharmacology analysis and biological validation

IF 9.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmacological research Pub Date : 2022-11-01 DOI:10.1016/j.phrs.2022.106489
Qianqian Li , Caixia Jia , Hongxing Wu , Yajin Liao , Ke Yang , Shuoshuo Li , Jing Zhang , Jinlei Wang , Guo Li , Fangxia Guan , Elaine Leung , Zengqiang Yuan , Qian Hua , Rui-Yuan Pan
{"title":"Nao Tan Qing ameliorates Alzheimer's disease-like pathology by regulating glycolipid metabolism and neuroinflammation: A network pharmacology analysis and biological validation","authors":"Qianqian Li ,&nbsp;Caixia Jia ,&nbsp;Hongxing Wu ,&nbsp;Yajin Liao ,&nbsp;Ke Yang ,&nbsp;Shuoshuo Li ,&nbsp;Jing Zhang ,&nbsp;Jinlei Wang ,&nbsp;Guo Li ,&nbsp;Fangxia Guan ,&nbsp;Elaine Leung ,&nbsp;Zengqiang Yuan ,&nbsp;Qian Hua ,&nbsp;Rui-Yuan Pan","doi":"10.1016/j.phrs.2022.106489","DOIUrl":null,"url":null,"abstract":"<div><p><span>Alzheimer's disease<span> (AD) is a neurodegenerative disorder characterized by progressive cognitive decline and currently there are no available treatments. Alongside the conventional Aβ and tau hypotheses, neuroinflammation and metabolism disruption have also been regarded as crucial hallmarks of AD. In this study, a novel Chinese formula Nao Tan Qing (NTQ) was developed and shown to improve AD. </span></span><em>In vivo</em><span><span><span> experiments showed that NTQ significantly mitigated cognitive impairment, Aβ burden and neuroinflammation in a transgenic AD mouse model (5×FAD). </span>Network pharmacology results revealed that the active components of NTQ could target inflammatory and metabolic pathways. In addition, hippocampal transcriptomics suggested that NTQ regulated signaling pathways related to inflammation and lipid metabolism. Consistently, serum metabolomics further indicated that NTQ could modulate </span>glycolipid metabolism. In summary, a combination of systems pharmacology analysis and biological validation study demonstrates that NTQ could alleviate behavioral abnormality and pathological alterations of AD by targeting glycolipid metabolism and neuroinflammation, and is accordingly a potential therapeutic agent for AD.</span></p></div>","PeriodicalId":19918,"journal":{"name":"Pharmacological research","volume":"185 ","pages":"Article 106489"},"PeriodicalIF":9.1000,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacological research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1043661822004352","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 5

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by progressive cognitive decline and currently there are no available treatments. Alongside the conventional Aβ and tau hypotheses, neuroinflammation and metabolism disruption have also been regarded as crucial hallmarks of AD. In this study, a novel Chinese formula Nao Tan Qing (NTQ) was developed and shown to improve AD. In vivo experiments showed that NTQ significantly mitigated cognitive impairment, Aβ burden and neuroinflammation in a transgenic AD mouse model (5×FAD). Network pharmacology results revealed that the active components of NTQ could target inflammatory and metabolic pathways. In addition, hippocampal transcriptomics suggested that NTQ regulated signaling pathways related to inflammation and lipid metabolism. Consistently, serum metabolomics further indicated that NTQ could modulate glycolipid metabolism. In summary, a combination of systems pharmacology analysis and biological validation study demonstrates that NTQ could alleviate behavioral abnormality and pathological alterations of AD by targeting glycolipid metabolism and neuroinflammation, and is accordingly a potential therapeutic agent for AD.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
脑炎清通过调节糖脂代谢和神经炎症改善阿尔茨海默病样病理:网络药理学分析和生物学验证
阿尔茨海默病(AD)是一种以进行性认知能力下降为特征的神经退行性疾病,目前尚无有效的治疗方法。除了传统的Aβ和tau假设外,神经炎症和代谢紊乱也被认为是AD的关键标志。本研究开发了一种新型中药脑痰清(NTQ),并证明其具有改善AD的作用。体内实验表明,NTQ可显著减轻转基因AD小鼠模型的认知障碍、a β负担和神经炎症(5×FAD)。网络药理学结果显示,NTQ的活性成分可以靶向炎症和代谢途径。此外,海马转录组学表明NTQ调节与炎症和脂质代谢相关的信号通路。与此一致,血清代谢组学进一步表明NTQ可以调节糖脂代谢。综上所述,系统药理学分析和生物学验证相结合的研究表明,NTQ可以通过靶向糖脂代谢和神经炎症来缓解AD的行为异常和病理改变,因此是一种潜在的AD治疗药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Pharmacological research
Pharmacological research 医学-药学
CiteScore
18.70
自引率
3.20%
发文量
491
审稿时长
8 days
期刊介绍: Pharmacological Research publishes cutting-edge articles in biomedical sciences to cover a broad range of topics that move the pharmacological field forward. Pharmacological research publishes articles on molecular, biochemical, translational, and clinical research (including clinical trials); it is proud of its rapid publication of accepted papers that comprises a dedicated, fast acceptance and publication track for high profile articles.
期刊最新文献
Comparative effectiveness and safety of imported and domestic immune checkpoint inhibitors in China: A systematic review and pairwise and network meta-analyses Corrigendum to "Overcoming limitations and advancing the therapeutic potential of antibody-oligonucleotide conjugates (AOCs): Current status and future perspectives" [Pharmacol. Res. 209 (2024) 107469]. Effect of anthocyanins on metabolic syndrome through interacting with gut microbiota PPARβ/δ prevents inflammation and fibrosis during diabetic cardiomyopathy Role for the F-box proteins in heart diseases
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1