Busca avançada
Ano de início
Entree
(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Glutamate reduces glucose utilization while concomitantly enhancing AQP9 and MCT2 expression in cultured rat hippocampal neurons

Texto completo
Autor(es):
Tescarollo, Fabio [1, 2] ; Covolan, Luciene [1] ; Pellerin, Luc [2]
Número total de Autores: 3
Afiliação do(s) autor(es):
[1] Univ Fed Sao Paulo, Dept Fisiol, Sao Paulo - Brazil
[2] Univ Lausanne, Dept Physiol, Lab Neuroenerget, Lausanne - Switzerland
Número total de Afiliações: 2
Tipo de documento: Artigo Científico
Fonte: FRONTIERS IN NEUROSCIENCE; v. 8, AUG 12 2014.
Citações Web of Science: 3
Resumo

The excitatory neurotransmitter glutamate has been reported to have a major impact on brain energy metabolism. Using primary cultures of rat hippocampal neurons, we observed that glutamate reduces glucose utilization in this cell type, suggesting alteration in mitochondrial oxidative metabolism. The aquaglyceroporin AQP9 and the monocarboxylate transporter MCT2, two transporters for oxidative energy substrates, appear to be present in mitochondria of these neurons. Moreover, they not only co-localize but they interact with each other as they were found to co-immunoprecipitate from hippocampal neuron homogenates. Exposure of cultured hippocampal neurons to glutamate 100 mu M for 1 h led to enhanced expression of both AQP9 and MCT2 at the protein level without any significant change at the mRNA level. In parallel, a similar increase in the protein expression of LDHA was evidenced without an effect on the mRNA level. These data suggest that glutamate exerts an influence on neuronal energy metabolism likely through a regulation of the expression of some key mitochondrial proteins. (AU)

Processo FAPESP: 10/50349-1 - Expressao mitocondrial da proteina aquaporina 9 em celulas hipocampais e sua possivel participacao nos mecanismos de lancadeira de lactato.
Beneficiário:Fábio Cesar Tescarollo
Modalidade de apoio: Bolsas no Brasil - Doutorado