探索Zexie Tang调控阿尔茨海默病的机制:多组学分析的启示

IF 6.7 1区 医学 Q1 CHEMISTRY, MEDICINAL Phytomedicine Pub Date : 2025-02-07 DOI:10.1016/j.phymed.2025.156453
Shijie Su , Kongli Huang , Han Cai , Dongyun Wei , Haixia Ding , Liejie Lin , Yuting Wang , Jihong Gu , Qi Wang
{"title":"探索Zexie Tang调控阿尔茨海默病的机制:多组学分析的启示","authors":"Shijie Su ,&nbsp;Kongli Huang ,&nbsp;Han Cai ,&nbsp;Dongyun Wei ,&nbsp;Haixia Ding ,&nbsp;Liejie Lin ,&nbsp;Yuting Wang ,&nbsp;Jihong Gu ,&nbsp;Qi Wang","doi":"10.1016/j.phymed.2025.156453","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Neurodegenerative disorders, such as Alzheimer's disease (AD), are characterized by a progressive decline in cognitive function. Modulating microglial metabolic reprogramming presents a promising therapeutic avenue for AD. Previous studies have shown that Zexie Tang (ZXT) possesses neuroprotective properties and can ameliorate cognitive impairment, but the underlying mechanisms remain unclear.</div></div><div><h3>Purpose</h3><div>This study aimed to investigate the efficacy of ZXT in improving cognitive function in AD mice using a multi-omics approach and to explore its potential role in modulating microglial metabolic reprogramming.</div></div><div><h3>Methods</h3><div>Behavioral assessments were conducted to evaluate the effects of ZXT on cognitive function in APP/PS1 mice. H&amp;E, Nissl, and Thioflavin S staining were performed to assess the impact of ZXT on brain pathology. A multi-omics approach, including transcriptomics, gut microbiota analysis, and metabolomics, was employed to elucidate the mechanisms of action of ZXT. RT-qPCR, immunoblotting, and immunofluorescence were used to validate the effects of ZXT on glycolipid metabolism, neuroinflammation, and the AMPK-mTOR-HIF1α pathway.</div></div><div><h3>Results</h3><div>ZXT effectively protected against cognitive deficits, reduced hippocampal neuronal apoptosis, and decreased Aβ plaque deposition. Transcriptomics analysis revealed that ZXT was involved in immune system processes and metabolic processes and had a specific cellular response with microglia. Additionally, ZXT regulated the composition and functions of brain metabolites and gut microbiota. Our study demonstrated that ZXT positively influenced glucolipid metabolism and attenuated neuroinflammation, which were linked to the AMPK-mTOR-HIF1α pathway in the brain.</div></div><div><h3>Conclusion</h3><div>Our findings suggested that ZXT may mitigate cognitive deficits in APP/PS1 mice by modulating gut microbiota and enhancing brain energy metabolism. ZXT regulated glucolipid metabolism and neuroinflammation by modulating microglial metabolic reprogramming involving the AMPK-mTOR-HIF1α pathway.</div></div>","PeriodicalId":20212,"journal":{"name":"Phytomedicine","volume":"139 ","pages":"Article 156453"},"PeriodicalIF":6.7000,"publicationDate":"2025-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Exploring the mechanism by which Zexie Tang regulates Alzheimer's disease: Insights from multi-omics analysis\",\"authors\":\"Shijie Su ,&nbsp;Kongli Huang ,&nbsp;Han Cai ,&nbsp;Dongyun Wei ,&nbsp;Haixia Ding ,&nbsp;Liejie Lin ,&nbsp;Yuting Wang ,&nbsp;Jihong Gu ,&nbsp;Qi Wang\",\"doi\":\"10.1016/j.phymed.2025.156453\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>Neurodegenerative disorders, such as Alzheimer's disease (AD), are characterized by a progressive decline in cognitive function. Modulating microglial metabolic reprogramming presents a promising therapeutic avenue for AD. Previous studies have shown that Zexie Tang (ZXT) possesses neuroprotective properties and can ameliorate cognitive impairment, but the underlying mechanisms remain unclear.</div></div><div><h3>Purpose</h3><div>This study aimed to investigate the efficacy of ZXT in improving cognitive function in AD mice using a multi-omics approach and to explore its potential role in modulating microglial metabolic reprogramming.</div></div><div><h3>Methods</h3><div>Behavioral assessments were conducted to evaluate the effects of ZXT on cognitive function in APP/PS1 mice. H&amp;E, Nissl, and Thioflavin S staining were performed to assess the impact of ZXT on brain pathology. A multi-omics approach, including transcriptomics, gut microbiota analysis, and metabolomics, was employed to elucidate the mechanisms of action of ZXT. RT-qPCR, immunoblotting, and immunofluorescence were used to validate the effects of ZXT on glycolipid metabolism, neuroinflammation, and the AMPK-mTOR-HIF1α pathway.</div></div><div><h3>Results</h3><div>ZXT effectively protected against cognitive deficits, reduced hippocampal neuronal apoptosis, and decreased Aβ plaque deposition. Transcriptomics analysis revealed that ZXT was involved in immune system processes and metabolic processes and had a specific cellular response with microglia. Additionally, ZXT regulated the composition and functions of brain metabolites and gut microbiota. Our study demonstrated that ZXT positively influenced glucolipid metabolism and attenuated neuroinflammation, which were linked to the AMPK-mTOR-HIF1α pathway in the brain.</div></div><div><h3>Conclusion</h3><div>Our findings suggested that ZXT may mitigate cognitive deficits in APP/PS1 mice by modulating gut microbiota and enhancing brain energy metabolism. ZXT regulated glucolipid metabolism and neuroinflammation by modulating microglial metabolic reprogramming involving the AMPK-mTOR-HIF1α pathway.</div></div>\",\"PeriodicalId\":20212,\"journal\":{\"name\":\"Phytomedicine\",\"volume\":\"139 \",\"pages\":\"Article 156453\"},\"PeriodicalIF\":6.7000,\"publicationDate\":\"2025-02-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytomedicine\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0944711325000947\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytomedicine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0944711325000947","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
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
Exploring the mechanism by which Zexie Tang regulates Alzheimer's disease: Insights from multi-omics analysis

Background

Neurodegenerative disorders, such as Alzheimer's disease (AD), are characterized by a progressive decline in cognitive function. Modulating microglial metabolic reprogramming presents a promising therapeutic avenue for AD. Previous studies have shown that Zexie Tang (ZXT) possesses neuroprotective properties and can ameliorate cognitive impairment, but the underlying mechanisms remain unclear.

Purpose

This study aimed to investigate the efficacy of ZXT in improving cognitive function in AD mice using a multi-omics approach and to explore its potential role in modulating microglial metabolic reprogramming.

Methods

Behavioral assessments were conducted to evaluate the effects of ZXT on cognitive function in APP/PS1 mice. H&E, Nissl, and Thioflavin S staining were performed to assess the impact of ZXT on brain pathology. A multi-omics approach, including transcriptomics, gut microbiota analysis, and metabolomics, was employed to elucidate the mechanisms of action of ZXT. RT-qPCR, immunoblotting, and immunofluorescence were used to validate the effects of ZXT on glycolipid metabolism, neuroinflammation, and the AMPK-mTOR-HIF1α pathway.

Results

ZXT effectively protected against cognitive deficits, reduced hippocampal neuronal apoptosis, and decreased Aβ plaque deposition. Transcriptomics analysis revealed that ZXT was involved in immune system processes and metabolic processes and had a specific cellular response with microglia. Additionally, ZXT regulated the composition and functions of brain metabolites and gut microbiota. Our study demonstrated that ZXT positively influenced glucolipid metabolism and attenuated neuroinflammation, which were linked to the AMPK-mTOR-HIF1α pathway in the brain.

Conclusion

Our findings suggested that ZXT may mitigate cognitive deficits in APP/PS1 mice by modulating gut microbiota and enhancing brain energy metabolism. ZXT regulated glucolipid metabolism and neuroinflammation by modulating microglial metabolic reprogramming involving the AMPK-mTOR-HIF1α pathway.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
期刊最新文献
Novel anti-inflammatory compounds that alleviate experimental autoimmune encephalomyelitis Hua Zheng San Ji Fang suppresses liver cancer progression by inhibiting TYRO3 expression via the ERK signaling pathway Exploring the therapeutic potential of HAPC in COVID-19-induced acute lung injury Efficacy and safety of Shexiang Baoxin Pill in patients with angina and non-obstructive coronary arteries: A multicenter, randomized, double-blind, placebo-controlled, phase Ⅳ clinical trial Allicin alleviates traumatic brain injury-induced neuroinflammation by enhancing PKC-δ-mediated mitophagy
×
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