Brain lipidomic profiles of sleep enhancement through co-administration of alprazolam and CGS21680

IF 3 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology FEBS Letters Pub Date : 2025-02-17 DOI:10.1002/1873-3468.70009
Yi Zhang, Xingle Xia, Qian Jin, Guixiang Yang, Manzhu Cao, Xingxing Zong, Jingjing Shi, Chen Wang, Liqin Li
{"title":"Brain lipidomic profiles of sleep enhancement through co-administration of alprazolam and CGS21680","authors":"Yi Zhang,&nbsp;Xingle Xia,&nbsp;Qian Jin,&nbsp;Guixiang Yang,&nbsp;Manzhu Cao,&nbsp;Xingxing Zong,&nbsp;Jingjing Shi,&nbsp;Chen Wang,&nbsp;Liqin Li","doi":"10.1002/1873-3468.70009","DOIUrl":null,"url":null,"abstract":"<p>Alprazolam and CGS21680 are both drugs known for their sleep and sedation effects. The study aimed to utilize mass spectrometry imaging to assess the regulatory changes in brain lipids of mice by the sleep-enhancing effects of the co-administration of alprazolam and CGS21680. A seven-day continuous administration mouse model was established using alprazolam and CGS21680. Glycerophosphoinositols were elevated in nine regions, glycerophosphoglycerols rising in six brain regions, and glycerophosphoserines increasing in six regions. Other lipid classes exhibited reductions, with fatty acids decreasing in 10 regions, carnitines in seven regions, ceramides in nine regions, and diacylglycerols in 10 regions. The research provides valuable insights into sleep-related regulation pathways by delineating the regulation of various lipid biomarkers in multiple brain regions.</p>","PeriodicalId":12142,"journal":{"name":"FEBS Letters","volume":"599 11","pages":"1556-1568"},"PeriodicalIF":3.0000,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"FEBS Letters","FirstCategoryId":"99","ListUrlMain":"https://febs.onlinelibrary.wiley.com/doi/10.1002/1873-3468.70009","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0

Abstract

Alprazolam and CGS21680 are both drugs known for their sleep and sedation effects. The study aimed to utilize mass spectrometry imaging to assess the regulatory changes in brain lipids of mice by the sleep-enhancing effects of the co-administration of alprazolam and CGS21680. A seven-day continuous administration mouse model was established using alprazolam and CGS21680. Glycerophosphoinositols were elevated in nine regions, glycerophosphoglycerols rising in six brain regions, and glycerophosphoserines increasing in six regions. Other lipid classes exhibited reductions, with fatty acids decreasing in 10 regions, carnitines in seven regions, ceramides in nine regions, and diacylglycerols in 10 regions. The research provides valuable insights into sleep-related regulation pathways by delineating the regulation of various lipid biomarkers in multiple brain regions.

Abstract Image

Abstract Image

Abstract Image

Abstract Image

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
通过阿普唑仑和CGS21680联合使用增强睡眠的脑脂质学特征。
阿普唑仑和CGS21680都是具有睡眠和镇静作用的药物。本研究旨在利用质谱成像技术,通过阿普唑仑与CGS21680共给药的促睡眠作用,评估小鼠脑脂质的调节变化。用阿普唑仑和CGS21680建立小鼠连续给药7 d模型。9个脑区甘油磷酸肌醇升高,6个脑区甘油磷酸甘油升高,6个脑区甘油磷酸丝氨酸升高。其他脂类也出现了减少,脂肪酸在10个区域减少,肉碱在7个区域减少,神经酰胺在9个区域减少,二酰基甘油在10个区域减少。该研究通过描述大脑多个区域中各种脂质生物标志物的调节,为睡眠相关的调节途径提供了有价值的见解。
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
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
期刊最新文献
The crystal structure of the TPR domain of the EccA5 ATPase and demonstration of its interaction with EspG5 from the mycobacterial ESX-5 pathway. Transferrin receptor 1-mediated iron uptake supports thermogenic activation in human cervical-derived adipocytes. Disrupted STIL-BRCA1 axis causes centrosome amplification and genomic instability. CPEB3 selectively inhibits α-synuclein aggregation without modulating TDP-43 pathology. Deciphering the signaling landscape of YAP in the tumor microenvironment-Insights into hepatocellular carcinoma progression.
×
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:604180095
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