Uridine is released by depolarization and inhibits unit activity in the rat hippocampus

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

Perfusion of 5 μM kainate through microdialysis probes induced >2-fold elevation of extracellular uridine and adenosine concentrations in the hippocampus and in the thalamus of anaesthetized rats. Administration of uridine via this route produced an estimated uridine concentration of 50-100 μM around the electrode surface. This markedly decreased the average firing rate of neurones in the hippocampus, but not in the thalamus. Activity of separated single hippocampal pyramidal cells was completely inhibited by uridine. The same amount of adenosine completely blocked neuronal activity in both hippocampus and thalamus. Uridine administration had no effect on extracellular adenosine concentration. These findings suggest an important neuromodulatory role for depolarization-released uridine in the CNS.

Original languageEnglish
Pages (from-to)3049-3053
Number of pages5
JournalNeuroReport
Volume10
Issue number14
Publication statusPublished - Sep 29 1999

Fingerprint

Uridine
Hippocampus
Thalamus
Adenosine
Pyramidal Cells
Kainic Acid
Microdialysis
Electrodes
Perfusion
Neurons

Keywords

  • Adenosine
  • Extracellular unit activity
  • Hippocampus
  • In vivo release
  • Neuromodulator
  • Uridine

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Uridine is released by depolarization and inhibits unit activity in the rat hippocampus. / Dobolyi, A.; Szikra, T.; Kékesi, K.; Kovács, Z.; Juhász, G.

In: NeuroReport, Vol. 10, No. 14, 29.09.1999, p. 3049-3053.

Research output: Contribution to journalArticle

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