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KATP-dependent neurotransmitter release in the neuronal network of the rat caudate nucleus

Mirja Steinkamp, Tianlang Li, Henriette Fuellgraf, Andreas Moser*

*Corresponding author for this work

Abstract

KATP channels can couple the bioenergetic metabolism of the cell to membrane excitability. Here, we show γ-aminobutyric acid (GABA) mediated inhibition of dopamine outflow from slices of the rat caudate nucleus that is regulated by extracellular glucose via high- and low-affinity KATP channels. During glucose reduction, a biphasic dopamine effect could be observed with first a dopamine increase followed by a decline at low glucose concentrations. Both phases were inhibited by glibenclamide. Pinacidil decreased DA outflow without an effect of glucose reduction implying an overall activation of KATP channels. The first phase with dopamine increase was related to reduced GABAergic activity and could be blocked by bicuculline. Our results may be explained by different types of KATP channels with low affinity of ATP and glibenclamide on inhibitory GABAergic and high-affinity on excitatory DAergic neurons. This led us to suggest a biological principle through which neuronal networks are functioning.

Original languageEnglish
JournalNeurochemistry International
Volume50
Issue number1
Pages (from-to)159-163
Number of pages5
ISSN0197-0186
DOIs
Publication statusPublished - 01.01.2007

Funding

This study was supported by the Deutsche Forschungsgemeinschaft (Mo 473, KFO 126) and by research funds from the Deutsche Akademisches Auslandsdienst (TL). We would like to thank Katharina Schnackenberg for her excellent technical assistance.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 10 - Reduced Inequalities
    SDG 10 Reduced Inequalities

Research Areas and Centers

  • Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)

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