{"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.
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.