Enhanced GABA(A) inhibition enhances synchrony coding in human perception

M. A. Elliot, C. Becker, M. Boucart, H. J. Muller

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

21 Citations (Scopus)

Abstract

The benzodiazepine, lorazepam enhances the efficiency of local, inhibitory GABA(A) synapses in the cortex, which stabilize postsynaptic, excitatory activity by synchronizing their own discharges at around 40 Hz. Treatment with lorazepam has also been shown to adversely influence detection performance in perceptual tasks, suggesting a role for GABA(A)-mediated synchronization during visuo-perceptual organization. Consistent with these findings we report that reaction times to target stimuli were slower following lorazepam treatment. However, when targets followed presentation of a synchronized prime, presented within a flickering 40-Hz display matrix, the effects of priming were amplified relative to baseline and control conditions. We conclude that enhanced GABA(A)-induced inhibition enhances stimulus-evoked synchronization with differential effects upon mechanisms of perceptual segmentation and grouping. (C) 2000 Lippincott Williams and Wilkins.

Original languageEnglish
Pages (from-to)3403-3407
Number of pages5
JournalNeuroReport
Volume11
Issue number15
Publication statusPublished - 2000
Externally publishedYes

Keywords

  • 40 Hz
  • Benzodiazepine
  • GABA(A)
  • Grouping
  • Lorazepam
  • Priming
  • Segmentation
  • Synchroniza tion
  • Vision

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