Metformin Accelerates Glycolytic Lactate Production in Cultured Primary Cerebellar Granule Neurons.
Eva-Maria BlumrichRalf DringenPublished in: Neurochemical research (2017)
Metformin is the most frequently used drug for the treatment of type-II diabetes. As metformin has been reported to cross the blood-brain barrier, brain cells will encounter this drug. To test whether metformin may affect the metabolism of neurons, we exposed cultured rat cerebellar granule neurons to metformin. Treatment with metformin caused a time- and concentration-dependent increase in glycolytic lactate release from viable neurons as demonstrated by the three-to fivefold increase in extracellular lactate concentration determined after exposure to metformin. Half-maximal stimulation of lactate production was found after incubation of neurons for 4 h with around 2 mM or for 24 h with around 0.5 mM metformin. Neuronal cell viability was not affected by millimolar concentrations of metformin during acute incubations in the hour range nor during prolonged incubations, although alterations in cell morphology were observed during treatment with 10 mM metformin for days. The acute stimulation of neuronal lactate release by metformin was persistent upon removal of metformin from the medium and was not affected by the presence of modulators of adenosine monophosphate activated kinase activity. In contrast, rabeprazole, an inhibitor of the organic cation transporter 3, completely prevented metformin-mediated stimulation of neuronal lactate production. In summary, the data presented identify metformin as a potent stimulator of glycolytic lactate production in viable cultured neurons and suggest that organic cation transporter 3 mediates the uptake of metformin into neurons.
Keyphrases
- spinal cord
- stem cells
- mesenchymal stem cells
- endothelial cells
- intensive care unit
- oxidative stress
- cell proliferation
- induced apoptosis
- small molecule
- metabolic syndrome
- liver failure
- computed tomography
- brain injury
- multiple sclerosis
- artificial intelligence
- adipose tissue
- machine learning
- bone marrow
- ionic liquid
- endoplasmic reticulum stress
- signaling pathway
- resistance training
- drug induced
- anti inflammatory
- cell cycle arrest