期刊
NEUROPSYCHOPHARMACOLOGY
卷 28, 期 4, 页码 675-682出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.npp.1300087
关键词
auditory evoked potentials; mouse; schizophrenia; ketamine; p300
资金
- NIMH NIH HHS [P50-MH64045] Funding Source: Medline
People with schizophrenia exhibit impaired ability to modify electroencephalographic event-related potential (FRP) responses to novel stimuli. These deficits serve as a window into the abnormalities of neuronal organization and function and are thought to reflect a component of genetic vulnerability for schizophrenia. We describe differences among inbred mouse strains for ERPs following a novelty detection paradigm, as a model for genetic contributions to disease vulnerability. Auditory-evoked potentials were recorded during an auditory oddball task in nonanesthetized C57BL/6J, C3H/HeJ, and DBA/2J mice prior to and following ketamine (10 mg/kg). Stimuli consisted of 80 sets of 24 standard tones followed by one novel tone. Principal component analysis yielded four temporal components that contribute to the auditory ERP responses to standard and novel stimuli. Two principal components that varied between standard and novel stimuli also differed among inbred mouse strains. Post hoc analyses indicate that strain effects on novelty detection are due to a significant difference between the response to novel and standard tones in C3H/HeJ mice that is absent in the other two strains. Inbred strains of mice vary in their ability to per-form neuronal detection of change in the auditory environment. The ability to model novelty detection deficits in mice will aid in identifying genetic contributions to abnormal neuronal organization in people with schizophrenia.
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