| Autor: |
Hémelin R, Farias, Joice R, Gabriel, Maria Laura, Cecconi, Isabela S, Lemos, Victoria L, de Rezende, Letícia B, Wessler, Mariane B, Duarte, Giselli, Scaini, Jade, de Oliveira, Emilio L, Streck |
| Rok vydání: |
2020 |
| Předmět: |
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| Zdroj: |
Metabolic brain disease. 36(1) |
| ISSN: |
1573-7365 |
| Popis: |
Maple syrup urine disease (MSUD) is characterized by a deficiency in the mitochondrial branched-chain α-keto acid dehydrogenase complex activity and, consequently, accumulation of the branched-chain amino acids and their respective branched-chain α-keto acids in fluids and the tissue. MSUD clinical symptoms include neurological alterations. KIC is considered one of the significant neurotoxic metabolites since its increased plasma concentrations are associated with neurological symptoms. We evaluated the effect of KIC intracerebroventricular (ICV) injection in hippocampal mitochondria function in rats. We also investigated the impact of KIC in cells' metabolic activity (using MTT assay) and reactive species (RS) production in HT-22 cells. For this, thirty-day-old male rats were bilaterally ICV injected with KIC or aCSF. Thus, 1 hour after the administration, animals were euthanized, and the hippocampus was harvested for measured the activities of mitochondrial respiratory chain enzymes and RS production. Furthermore, HT-22 cells were incubated with KIC (1-10 mM) in 6, 12, and 24 h. Mitochondrial complexes activities were reduced, and the formation of RS was increased in the hippocampus of rats after KIC administration. Moreover, KIC reduced the cells' metabolic ability to reduce MTT and increased RS production in hippocampal neurons. Impairment in hippocampal mitochondrial function seems to be involved in the neurotoxicity induced by KIC. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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