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Biol Psychiatry. 2010 Dec 15;68(12):1100-6. doi: 10.1016/j.biopsych.2010.09.031.

Validating γ oscillations and delayed auditory responses as translational biomarkers of autism.

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Department of Psychiatry, University of Pennsylvania, Philadelphia, 19104, USA.



Difficulty modeling complex behavioral phenotypes in rodents (e.g., language) has hindered pathophysiological investigation and treatment development for autism spectrum disorders. Recent human neuroimaging studies, however, have identified functional biomarkers that can be more directly related to the abnormal neural dynamics of autism spectrum disorders. This study assessed the translational potential of auditory evoked-response endophenotypes of autism in parallel mouse and human studies of autism.


Whole-cortex magnetoencephalography was recorded in 17 typically developing and 25 autistic children during auditory pure-tone presentation. Superior temporal gyrus activity was analyzed in time and frequency domains. Auditory evoked potentials were recorded in mice prenatally exposed to valproic acid (VPA) and analyzed with analogous methods.


The VPA-exposed mice demonstrated selective behavioral alterations related to autism, including reduced social interactions and ultrasonic vocalizations, increased repetitive self-grooming, and prepulse inhibition deficits. Autistic subjects and VPA-exposed mice showed a similar 10% latency delay in the N1/M100 evoked response and a reduction in γ frequency (30-50 Hz) phase-locking factor. Electrophysiological measures were associated with mouse behavioral deficits. In mice, γ phase-locking factor was correlated with expression of the autism risk gene neuroligin-3 and neural deficits were modulated by the mGluR5-receptor antagonist MPEP.


Results demonstrate a novel preclinical approach toward mechanistic understanding and treatment development for autism.

[Indexed for MEDLINE]
Free PMC Article

Conflict of interest statement

Financial Disclosures Drs. Edgar and Roberts report no biomedical financial interests or potential conflicts of interest. Mr. Gandal and Mr. Ehrlichman report no biomedical financial interests or potential conflicts of interest. Ms Mehta reports no biomedical financial interests or potential conflicts of interest.

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