Unraveling Spatiotemporal Metabolic Perturbation of Amino Acids Associated with Ischemia-Reperfusion Injury by MALDI MS Imaging.

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-05-01 Epub Date: 2024-12-02 DOI:10.1007/s12035-024-04649-9
Kening Li, Yingying Gong, Wenqiao Chang, Jieping Yan, Ying Hu, Zongfu Pan, Ping Huang
{"title":"Unraveling Spatiotemporal Metabolic Perturbation of Amino Acids Associated with Ischemia-Reperfusion Injury by MALDI MS Imaging.","authors":"Kening Li, Yingying Gong, Wenqiao Chang, Jieping Yan, Ying Hu, Zongfu Pan, Ping Huang","doi":"10.1007/s12035-024-04649-9","DOIUrl":null,"url":null,"abstract":"<p><p>Various complex metabolic perturbations are involved in cerebral ischemia-reperfusion (I/R) injury. However, limited data have been reported on dynamic spatiotemporal metabolic perturbations of amino acids (AAs) in I/R injured rat brains. In this work, a combination of laser-assisted chemical transfer (LACT) and hexafluoroisopropanol (HFIP) was applied to the enhancement of on-tissue derivatization of AAs for matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) of their dynamic spatiotemporal changes during I/R injury. The spatiotemporal distribution patterns of 15 derivatized AAs in the rat subjected to middle cerebral artery occlusion (MCAO) followed by different periods of reperfusion were unraveled by using MALDI MSI, including excitatory amino acids (e.g., Glu, Asp), inhibitory amino acids (e.g., GABA, Gly) and the other amino acids (e.g., Val, Pro, Gln, Phe). The metabolic perturbations of AAs showed similarities and differences in cerebral cortex (CTX) and striatum (STR) of MCAO rat brains at different periods of I/R injury. Generally, in 0.5-1.5 h of ischemia followed by 1-6 h of reperfusion, I/R triggered a dramatic increase in the levels of some AAs such as Glu, Asp, Gly, GABA, Gln, and Phe in both CTX and STR. After 6 h of reperfusion, AA levels gradually decreased. Immunohistochemistry (IHC) assay further showed that the immunoreactivities of selected enzymes related to Glu and GABA metabolism increased at the later stage of reperfusion. This present work provided spatiotemporal metabolic perturbations of AAs, which will further help us understand the mechanisms of I/R injury and also have great significance in developing region-specific therapeutic drugs and diagnostic markers.</p>","PeriodicalId":18762,"journal":{"name":"Molecular Neurobiology","volume":" ","pages":"5744-5757"},"PeriodicalIF":4.6000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Neurobiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s12035-024-04649-9","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/2 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Various complex metabolic perturbations are involved in cerebral ischemia-reperfusion (I/R) injury. However, limited data have been reported on dynamic spatiotemporal metabolic perturbations of amino acids (AAs) in I/R injured rat brains. In this work, a combination of laser-assisted chemical transfer (LACT) and hexafluoroisopropanol (HFIP) was applied to the enhancement of on-tissue derivatization of AAs for matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) of their dynamic spatiotemporal changes during I/R injury. The spatiotemporal distribution patterns of 15 derivatized AAs in the rat subjected to middle cerebral artery occlusion (MCAO) followed by different periods of reperfusion were unraveled by using MALDI MSI, including excitatory amino acids (e.g., Glu, Asp), inhibitory amino acids (e.g., GABA, Gly) and the other amino acids (e.g., Val, Pro, Gln, Phe). The metabolic perturbations of AAs showed similarities and differences in cerebral cortex (CTX) and striatum (STR) of MCAO rat brains at different periods of I/R injury. Generally, in 0.5-1.5 h of ischemia followed by 1-6 h of reperfusion, I/R triggered a dramatic increase in the levels of some AAs such as Glu, Asp, Gly, GABA, Gln, and Phe in both CTX and STR. After 6 h of reperfusion, AA levels gradually decreased. Immunohistochemistry (IHC) assay further showed that the immunoreactivities of selected enzymes related to Glu and GABA metabolism increased at the later stage of reperfusion. This present work provided spatiotemporal metabolic perturbations of AAs, which will further help us understand the mechanisms of I/R injury and also have great significance in developing region-specific therapeutic drugs and diagnostic markers.

MALDI MS成像揭示与缺血再灌注损伤相关的氨基酸时空代谢扰动。
脑缺血再灌注(I/R)损伤涉及多种复杂的代谢扰动。然而,关于I/R损伤大鼠脑中氨基酸(AAs)动态时空代谢扰动的数据报道有限。在这项工作中,激光辅助化学转移(LACT)和六氟异丙醇(HFIP)的组合应用于增强组织上衍生化的AAs,用于基质辅助激光解吸/电离(MALDI)质谱成像(MSI)它们在I/R损伤期间的动态时空变化。应用MALDI MSI分析了大脑中动脉闭塞(MCAO)后不同再灌注期大鼠体内15种衍生氨基酸的时空分布规律,包括兴奋性氨基酸(如Glu、Asp)、抑制性氨基酸(如GABA、Gly)和其他氨基酸(如Val、Pro、Gln、Phe)。不同时期MCAO大鼠脑皮层(CTX)和纹状体(STR)的AAs代谢扰动表现出相似性和差异性。一般在缺血0.5 ~ 1.5 h,再灌注1 ~ 6 h时,I/R触发CTX和STR中Glu、Asp、Gly、GABA、Gln、Phe等部分AAs水平急剧升高,再灌注6 h后,AA水平逐渐下降。免疫组化(IHC)进一步显示,在再灌注后期,与Glu和GABA代谢相关的部分酶的免疫反应性升高。本研究提供了AAs的时空代谢扰动,这将进一步帮助我们了解I/R损伤的机制,并对开发区域特异性治疗药物和诊断标志物具有重要意义。
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 求助全文
来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信