Evidence map›Paper›PMID 39090264›Full record

ArticleAnalytical and bioanalytical chemistry2024

Mapping small metabolite changes after traumatic brain injury using AP-MALDI MSI.

Angela Marika Siciliano, Federico Moro, Giulia De Simone, Francesca Pischiutta, Aurelia Morabito, Roberta Pastorelli, Laura Brunelli, Elisa R Zanier, Enrico Davoli

Abstract read
In one paragraph

Article in Analytical and bioanalytical chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Angela Marika SicilianoMass Spectrometry Research Centre for Health and Environment and Laboratory of Mass Spectrometry, Environmental Health Sciences Department, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, 20156, Milan, Italy.
Federico MoroLaboratory of Traumatic Brain Injury and Neuroprotection, Department of Acute Brain and Cardiovascular Injury, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Giulia De SimoneLaboratory of Protein and Metabolites in Translational Research, Environmental Health Sciences Department, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, 20156, Milan, Italy.
Francesca PischiuttaLaboratory of Traumatic Brain Injury and Neuroprotection, Department of Acute Brain and Cardiovascular Injury, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Aurelia MorabitoLaboratory of Protein and Metabolites in Translational Research, Environmental Health Sciences Department, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, 20156, Milan, Italy.
Roberta PastorelliLaboratory of Protein and Metabolites in Translational Research, Environmental Health Sciences Department, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, 20156, Milan, Italy.
Laura BrunelliLaboratory of Protein and Metabolites in Translational Research, Environmental Health Sciences Department, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, 20156, Milan, Italy.
Elisa R ZanierLaboratory of Traumatic Brain Injury and Neuroprotection, Department of Acute Brain and Cardiovascular Injury, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan, Italy.
Enrico DavoliMass Spectrometry Research Centre for Health and Environment and Laboratory of Mass Spectrometry, Environmental Health Sciences Department, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, 20156, Milan, Italy. enrico.davoli@marionegri.it.ORCID http://orcid.org/0000-0003-0933-1351

Funding

Paguni Lugli Family In memory of Rodolfo Paguni
6 · The paper itself

Abstract

Traumatic brain injury (TBI) is an alteration of brain function caused by a sudden transmission of an external force to the head. The biomechanical impact induces acute and chronic metabolic changes that highly contribute to injury evolution and outcome. TBI heterogeneity calls for approaches allowing the mapping of regional molecular and metabolic changes underpinning disease progression, with mass spectrometry imaging (MSI) as an efficient tool to study the spatial distribution of small metabolites. In this study, we applied an innovative targeted atmospheric pressure-MALDI mass spectrometry imaging (AP-MALDI MSI) approach, starting from an extensive list of metabolites, representative of different metabolic pathways, individually validated on the tissue under analysis with original standards using 2,5-dihydroxybenzoic acid (DHB), to characterize the impact of TBI on regional changes to small metabolites in the brain. Brains from sham and TBI mice obtained 21 days post-injury were analyzed to examine the spatial metabolic profile of small metabolites belonging to different metabolic pathways. By a whole brain analysis, we identified four metabolites (alanine, lysine, histidine, and inosine) with higher abundance in TBI than sham mice. Within the TBI group, lysine, histidine, and inosine were higher in the hemisphere ipsilateral to the biomechanical impact vs. the contralateral one. Images showed a major involvement of the ipsilateral thalamus characterized by the increase of arginine, lysine, histidine, and inosine and a significant reduction of glutamic acid, and N-acetylaspartic acid compared to the contralateral thalamus. These findings indicate high-resolution imaging mass spectrometry as a powerful tool to identify region-specific changes after a TBI to understand the metabolic changes underlying brain injury evolution.

Indexed as

Brain Injuries, TraumaticSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAnimalsBrainMaleMiceMice, Inbred C57BLAP-MALDIMass spectrometry imagingSmall metabolitesTraumatic brain injury

Identifiers

PMID39090264
PMCPMC11330407

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.