Abstract
In this work, we specify potential elements of the brain to sense and regulate the energy metabolism of the organism. Our numerical investigations base on neurochemical experiments demonstrating a biphasic association between brain glucose level and neuronal activity. The dynamics of high and low affine KATP channels are most likely to play a decisive role in neuronal activity. We develop a coupled Hodgkin-Huxley model describing the interactive behavior of inhibitory GABAergic and excitatory dopaminergic neurons projecting into the caudate nucleus. The novelty in our approach is that we include the synaptic coupling of GABAergic and dopaminergic neurons as well as the interaction of high and low affine KATP channels. Both are crucial mechanisms described by kinetic models. Simulations demonstrate that our new model is coherent with neurochemical in vitro experiments. Even experimental interventions with glibenclamide and glucosamine are reproduced by our new model. Our results show that the considered dynamics of high and low affine KATP channels may be a driving force in energy sensing and global regulation of the energy metabolism, which supports central aspects of the new Selfish Brain Theory. Moreover, our simulations suggest that firing frequencies and patterns of GABAergic and dopaminergic neurons are correlated to their neurochemical outflow.
Highlights
Neurochemical experiments show that extracellular glucose level influences the neurochemical activity of neurons
We develop a coupled Hodgkin-Huxley model describing the interactive behavior of inhibitory GABAergic and excitatory dopaminergic neurons projecting into the caudate nucleus
The dopamine outflow rises with increasing glucose concentration at low glucose levels since the inhibitory effect of the GABAergic neuron is not effective enough to interfere with the dopaminergic neuron
Summary
Neurochemical experiments show that extracellular glucose level influences the neurochemical activity of neurons. Steinkamp and colleagues showed that decreasing glucose levels cause a neuronal biphasic response [1]. Slices of the rat caudate nucleus are examined in vitro in a superfusion chamber treated by artificial cerebrospinal fluid. The glucose level in the fluid varies from 0 to 10 mM while the dopamine outflow is measured concomitantly. The effect of different glucose concentrations on dopamine and GABA (γ-aminobutyric acid) outflow is investigated by means of high-performance liquid chromatography and electrochemical detection.
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