Fast inhibition of glutamate-activated currents by caffeine

Nicholas P. Vyleta, Stephen Smith

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Background: Caffeine stimulates calcium-induced calcium release (CICR) in many cell types. In neurons, caffeine stimulates CICR presynaptically and thus modulates neurotransmitter release. Methodology/Principal Findings: Using the whole-cell patch-clamp technique we found that caffeine (20 mM) reversibly increased the frequency and decreased the amplitude of miniature excitatory postsynaptic currents (mEPSCs) in neocortical neurons. The increase in mEPSC frequency is consistent with a presynaptic mechanism. Caffeine also reduced exogenously applied glutamate-activated currents, confirming a separate postsynaptic action. This inhibition developed in tens of milliseconds, consistent with block of channel currents. Caffeine (20 mM) did not reduce currents activated by exogenous NMDA, indicating that caffeine block is specific to non-NMDA type glutamate receptors. Conclusions/Significance: Caffeine-induced inhibition of mEPSC amplitude occurs through postsynaptic block of non-NMDA type ionotropic glutamate receptors. Caffeine thus has both pre and postsynaptic sites of action at excitatory synapses.

Original languageEnglish (US)
Article numbere3155
JournalPLoS One
Volume3
Issue number9
DOIs
StatePublished - Sep 10 2008

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caffeine
Caffeine
glutamates
Glutamic Acid
Excitatory Postsynaptic Potentials
Calcium
calcium
Neurons
neurons
Ionotropic Glutamate Receptors
patch-clamp technique
Clamping devices
Glutamate Receptors
Patch-Clamp Techniques
N-Methylaspartate
synapse
neurotransmitters
Synapses
Neurotransmitter Agents
cells

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Fast inhibition of glutamate-activated currents by caffeine. / Vyleta, Nicholas P.; Smith, Stephen.

In: PLoS One, Vol. 3, No. 9, e3155, 10.09.2008.

Research output: Contribution to journalArticle

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