| Literature DB >> 35348805 |
Sara de la Salle1, Joelle Choueiry1,2, Judy McIntosh1, Hayley Bowers3, Vadim Ilivitsky1, Verner Knott4,5.
Abstract
Deficits in early auditory sensory processing in schizophrenia have been linked to N-methyl-D-aspartate receptor (NMDAR) hypofunction, but the role of NMDARs in aberrant auditory sensory gating (SG) in this disorder is unclear. This study, conducted in 22 healthy humans, examined the acute effects of a subanesthetic dose of the NMDAR antagonist ketamine on SG as measured electrophysiologically by suppression of the P50 event-related potential (ERP) to the second (S2) relative to the first (S1) of two closely paired (500 ms) identical speech stimuli. Ketamine induced impairment in SG indices at sensor (scalp)-level and at source-level in the auditory cortex (as assessed with eLORETA). Together with preliminary evidence of modest positive associations between impaired gating and dissociative symptoms elicited by ketamine, tentatively support a model of NMDAR hypofunction underlying disturbances in auditory SG in schizophrenia.Entities:
Keywords: Auditory sensory gating; N-methyl-D-aspartate receptor (NMDAR); P50 event-related potential (ERP); Schizophrenia; Symptomatology
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Year: 2022 PMID: 35348805 DOI: 10.1007/s00213-022-06090-z
Source DB: PubMed Journal: Psychopharmacology (Berl) ISSN: 0033-3158 Impact factor: 4.530