4.6 Article

Sensory encoding in Neuregulin 1 mutants

Journal

BRAIN STRUCTURE & FUNCTION
Volume 221, Issue 2, Pages 1067-1081

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00429-014-0955-x

Keywords

Schizophrenia; Neuregulin 1; Signal-to-noise ratio; Gamma oscillations; Somatosensory cortex; Endophenotypes

Funding

  1. German Research Foundation (Deutsche Forschungsgemeinschaft, DFG) [IRTG 1328]
  2. Interdisciplinary Center for Clinical Research (IZKF Aachen) within the Faculty of Medicine at the RWTH Aachen University
  3. Fondation pour la Recherche Medicale [SPE20070709864]
  4. Barrel Cortex Function (BaCoFun) research group of the DFG
  5. Helmholtz association
  6. National Institute of Health (NIH) [MH064045, P50-MH096891, R01 EY020765]

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Schizophrenic patients show altered sensory perception as well as changes in electrical and magnetic brain responses to sustained, frequency-modulated sensory stimulation. Both the amplitude and temporal precision of the neural responses differ in patients as compared to control subjects, and these changes are most pronounced for stimulation at gamma frequencies (20-40 Hz). In addition, patients display enhanced spontaneous gamma oscillations, which has been interpreted as 'neural noise' that may interfere with normal stimulus processing. To investigate electrophysiological markers of aberrant sensory processing in a model of schizophrenia, we recorded neuronal activity in primary somatosensory cortex of mice heterozygous for the schizophrenia susceptibility gene Neuregulin 1. Sensory responses to sustained 20-70 Hz whisker stimulation were analyzed with respect to firing rates, spike precision (phase locking) and gamma oscillations, and compared to baseline conditions. The mutants displayed elevated spontaneous firing rates, a reduced gain in sensory-evoked spiking and gamma activity, and reduced spike precision of 20-40 Hz responses. These findings present the first in vivo evidence of the linkage between a genetic marker and altered stimulus encoding, thus suggesting a novel electrophysiological endophenotype of schizophrenia.

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