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Hippocampal metabolic profile during epileptogenesis in the pilocarpine model of epilepsy.
Meier, Letícia; Bruginski, Estevan; Marafiga, Joseane Righes; Caus, Letícia Barbieri; Pasquetti, Mayara Vendramin; Calcagnotto, Maria Elisa; Campos, Francinete Ramos.
Afiliação
  • Meier L; Biosciences and Mass Spectrometry Laboratory, Department of Pharmacy, Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Bruginski E; Graduate Program in Pharmaceutical Science, Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Marafiga JR; Biosciences and Mass Spectrometry Laboratory, Department of Pharmacy, Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Caus LB; Graduate Program in Pharmaceutical Science, Universidade Federal do Paraná, Curitiba, PR, Brazil.
  • Pasquetti MV; Neurophysiology and Neurochemistry of Neuronal Excitability and Synaptic Plasticity Laboratory (NNNESP Lab.), Department of Biochemistry, ICBS, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
  • Calcagnotto ME; Graduate Program in Biological Science: Biochemistry, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
  • Campos FR; Neurophysiology and Neurochemistry of Neuronal Excitability and Synaptic Plasticity Laboratory (NNNESP Lab.), Department of Biochemistry, ICBS, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Biomed Chromatogr ; 38(4): e5820, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38154955
ABSTRACT
Temporal lobe epilepsy (TLE) is a common form of refractory epilepsy in adulthood. The metabolic profile of epileptogenesis is still poorly investigated. Elucidation of such a metabolic profile using animal models of epilepsy could help identify new metabolites and pathways involved in the mechanisms of epileptogenesis process. In this study, we evaluated the metabolic profile during the epileptogenesis periods. Using a pilocarpine model of epilepsy, we analyzed the global metabolic profile of hippocampal extracts by untargeted metabolomics based on ultra-performance liquid chromatography-high-resolution mass spectrometry, at three time points (3 h, 1 week, and 2 weeks) after status epilepticus (SE) induction. We demonstrated that epileptogenesis periods presented different hippocampal metabolic profiles, including alterations of metabolic pathways of amino acids and lipid metabolism. Six putative metabolites (tryptophan, N-acetylornithine, N-acetyl-L-aspartate, glutamine, adenosine, and cholesterol) showed significant different levels during epileptogenesis compared to their respective controls. These putative metabolites could be associated with the imbalance of neurotransmitters, mitochondrial dysfunction, and cell loss observed during both epileptogenesis and epilepsy. With these findings, we provided an overview of hippocampal metabolic profiles during different stages of epileptogenesis that could help investigate pathways and respective metabolites as predictive tools in epilepsy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / Epilepsia do Lobo Temporal Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epilepsia / Epilepsia do Lobo Temporal Limite: Animals Idioma: En Ano de publicação: 2024 Tipo de documento: Article