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ABSTRACT: Introduction
Altered metabolic pathways are critical in the progression of traumatic brain injury (TBI). Identifying differentially abundant metabolites (DAMs) from specific cell types can offer valuable diagnostic and prognostic insights.Objective
This study aimed to characterize the metabolomic profile of injured human brain microvascular endothelial cells (hBMEC) at 2-, 12-, 24-, and 48 h post-injury.Methods
Using an in vitro TBI model, we analyzed metabolites in cell culture media through a combination of direct injection mass spectrometry and a custom reverse-phase LC-MS/MS assay. We evaluated 644 metabolites at each time point.Results
Phosphatidylcholines were significantly upregulated across all time intervals. At 2- and 12 h post-injury, the most sig
SUBMITTER: Cela E
PROVIDER: S-EPMC12204887 | biostudies-literature | 2025 Jun
REPOSITORIES: biostudies-literature