Abstract

Fast neuronal network oscillations in the gamma-frequency band (30–−100 Hz) provide a fundamental mechanism of complex neuronal information processing in the hippocampus and neocortex of mammals. Gamma oscillations have been implicated in higher brain functions such as sensory perception, motor activity, and memory formation. The oscillations emerge from precise synapse interactions between excitatory principal neurons such as pyramidal cells and inhibitory GABAergic interneurons, and they are associated with high energy expenditure. However, both energy substrates and metabolic pathways that are capable to power cortical gamma oscillations have been less defined. Here, we investigated the energy sources fueling persistent gamma oscillations in the CA3 subfield of organotypic hippocampal slice cultures of the rat. This preparation permits superior oxygen supply as well as fast application of glucose, glycolytic metabolites or drugs such as glycogen phosphorylase inhibitor during extracellular recordings of the local field potential. Our findings are: (i) gamma oscillations persist in the presence of glucose (10 mmol/L) for greater than 60 min in slice cultures while (ii) lowering glucose levels (2.5 mmol/L) significantly reduces the amplitude of the oscillation. (iii) Gamma oscillations are absent at low concentration of lactate (2 mmol/L). (iv) Gamma oscillations persist at high concentration (20 mmol/L) of either lactate or pyruvate, albeit showing significant reductions in the amplitude. (v) The breakdown of glycogen significantly delays the decay of gamma oscillations during glucose deprivation. However, when glucose is present, the turnover of glycogen is not essential to sustain gamma oscillations. Our study shows that fast neuronal network oscillations can be fueled by different energy-rich substrates, with glucose being most effective.

Highlights

  • The mammalian brain is a highly oxidative organ owing to the disproportionately large fraction of oxygen consumption compared with the small fraction of the total body mass (Rolfe and Brown, 1997; Erecinska and Silver, 2001)

  • Glucose enters the extracellular space of the brain parenchyma based on a large concentration gradient (5–7 mmol/L in the blood and 1–2 mmol/L in the extracellular space) via glucose transporters (GLUTs) that are located on endothelial cells of the blood-brain-barrier as well as astrocytes (Roberts, 2007; Hertz et al, 2014)

  • Slice cultures were used after 7–21 days in vitro (DIV), when the tissue had recovered from the slice preparation and damaged cut surfaces were re-organized (Kann and Kovács, 2007)

Read more

Summary

Introduction

The mammalian brain is a highly oxidative organ owing to the disproportionately large fraction of oxygen consumption compared with the small fraction of the total body mass (in humans about 20% and 2%, respectively) (Rolfe and Brown, 1997; Erecinska and Silver, 2001). This suggests that complex neuronal information processing is associated with high energy expenditure and requires continuous delivery of glucose from the blood (Shulman et al, 2001; Attwell et al, 2010; Kann, 2012). Neurons are able to utilize exogenous and endogenous energy substrates other than glucose in certain physiological and pathophysiological conditions (Roberts, 2007)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call