The metabolic impact of β-hydroxybutyrate on neurotransmission: Reduced glycolysis mediates changes in calcium responses and KATPchannel receptor sensitivity
| Autor: | Trine Meldgaard Lund, Inger Jansen-Olesen, Kenneth Beri Ploug, Anne Iversen, Anders A. Jensen |
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| Rok vydání: | 2015 |
| Předmět: |
Male
medicine.medical_specialty Blotting Western chemistry.chemical_element Carbohydrate metabolism Calcium Neurotransmission Polymerase Chain Reaction Synaptic Transmission Biochemistry Glibenclamide Mice Cellular and Molecular Neuroscience KATP Channels Internal medicine medicine Animals Glycolysis Cells Cultured Neurons 3-Hydroxybutyric Acid Chemistry Metabolism Cell biology Endocrinology Ketone bodies NMDA receptor Female Energy Metabolism medicine.drug |
| Zdroj: | Lund, T M, Ploug, K B, Iversen, A, Jensen, A A & Jansen-Olesen, I 2015, ' The metabolic impact of β-hydroxybutyrate on neurotransmission: Reduced glycolysis mediates changes in calcium responses and KATP channel receptor sensitivity ', Journal of Neurochemistry, vol. 132, no. 5, pp. 520-531 . https://doi.org/10.1111/jnc.12975 |
| ISSN: | 0022-3042 |
| DOI: | 10.1111/jnc.12975 |
| Popis: | Glucose is the main energy substrate for neurons, and ketone bodies are known to be alternative substrates. However, the capacity of ketone bodies to support different neuronal functions is still unknown. Thus, a change in energy substrate from glucose alone to a combination of glucose and β-hydroxybutyrate might change neuronal function as there is a known coupling between metabolism and neurotransmission. The purpose of this study was to shed light on the effects of the ketone body β-hydroxybutyrate on glycolysis and neurotransmission in cultured murine glutamatergic neurons. Previous studies have shown an effect of β-hydroxybutyrate on glucose metabolism, and the present study further specified this by showing attenuation of glycolysis when β-hydroxybutyrate was present in these neurons. In addition, the NMDA receptor-induced calcium responses in the neurons were diminished in the presence of β-hydroxybutyrate, whereas a direct effect of the ketone body on transmitter release was absent. However, the presence of β-hydroxybutyrate augmented transmitter release induced by the KATP channel blocker glibenclamide, thus giving an indirect indication of the involvement of KATP channels in the effects of ketone bodies on transmitter release.Energy metabolism and neurotransmission are linked and involve ATP-sensitive potassium (KATP) channels. However, it is still unclear how and to what degree available energy substrate affects this link. We investigated the effect of changing energy substrate from only glucose to a combination of glucose and R-β-hydroxybutyrate in cultured neurons. Using the latter combination, glycolysis was diminished, NMDA receptor-induced calcium responses were lower, and the KATP channel blocker glibenclamide caused a higher transmitter release. |
| Databáze: | OpenAIRE |
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