Compartments of Labeled and Endogenous γ-Aminobutyric Acid Giving Rise to Release Evoked by Potassium or Veratridine in Rat Cortical Slices |
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Authors: | John C Szerb T Elaine Ross Lea Gurevich |
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Institution: | Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia, Canada |
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Abstract: | Abstract— To establish compartments involved in depolarization-induced release of γ-aminobutyric acid (GABA) in rat brain slices, the amount of exogenous labeled and endogenous GABA released and retained was followed during 48 min exposure to 50 m m -K+ or to 50 μ m -veratridine. Endogenous GABA was measured with high performance liquid chromatography. The presence of 10 μ m -aminooxyacetic acid throughout prevented both the metabolism of GABA and the formation of endogenous GABA due to depolarization. During super-fusion with 50 m m -K+ and 2.6 m m -Ca2+ the efflux of labeled and endogenous GABA after an initial large increase declined to 10% of the highest value with constant and identical rates. Kinetic analysis of efflux showed that 10% of endogenous and 25% of labeled GABA present is available for release by high K+ and Ca2+. In the absence of Ca2+, release by high K+ of both labeled and endogenous GABA was nearly suppressed. Veratridine, unlike high K+, caused an efflux which declined with an initial fast and late very slow phase. The slow efflux by veratridine was doubled in the absence of Ca2+. Exposure to veratridine in the absence of Ca2+ during 120 min released nearly 70% of labeled and endogenous GABA present. Results suggest that only about 0.25 μmol g?1 endogenous GABA is the source of physiological Ca2+-dependent release, while much of the remaining GABA present is released only under unphysiological conditions. |
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Keywords: | Endogenous GABA compartments Elevated K+ Veratridine Ca2+ dependence |
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