16p11.2 deletion mice exhibit compromised fronto-temporal connectivity, GABAergic dysfunction, and enhanced attentional ability
Openshaw, Rebecca L. and Thomson, David M. and Bristow, Greg C. and Mitchell, Emma J. and Pratt, Judith A. and Morris, Brian J. and Dawson, Neil (2023) 16p11.2 deletion mice exhibit compromised fronto-temporal connectivity, GABAergic dysfunction, and enhanced attentional ability. Communications Biology, 6. 557. ISSN 2399-3642 (https://doi.org/10.1038/s42003-023-04891-2)
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Abstract
Autism spectrum disorders are more common in males, and have a substantial genetic component. Chromosomal 16p11.2 deletions in particular carry strong genetic risk for autism, yet their neurobiological impact is poorly characterised, particularly at the integrated systems level. Here we show that mice reproducing this deletion (16p11.2 DEL mice) have reduced GABAergic interneuron gene expression (decreased parvalbumin mRNA in orbitofrontal cortex, and male-specific decreases in Gad67 mRNA in parietal and insular cortex and medial septum). Metabolic activity was increased in medial septum, and in its efferent targets: mammillary body and (males only) subiculum. Functional connectivity was altered between orbitofrontal, insular and auditory cortex, and between septum and hippocampus/subiculum. Consistent with this circuit dysfunction, 16p11.2 DEL mice showed reduced prepulse inhibition, but enhanced performance in the continuous performance test of attentional ability. Level 1 autistic individuals show similarly heightened performance in the equivalent human test, also associated with parietal, insular-orbitofrontal and septo-subicular dysfunction. The data implicate cortical and septal GABAergic dysfunction, and resulting connectivity changes, as the cause of pre-attentional and attentional changes in autism.
ORCID iDs
Openshaw, Rebecca L., Thomson, David M. ORCID: https://orcid.org/0000-0002-0356-3525, Bristow, Greg C., Mitchell, Emma J., Pratt, Judith A., Morris, Brian J. and Dawson, Neil;-
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Item type: Article ID code: 85624 Dates: DateEvent24 May 2023Published1 May 2023Accepted6 December 2022SubmittedSubjects: Medicine > Internal medicine > Neuroscience. Biological psychiatry. Neuropsychiatry Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 26 May 2023 13:49 Last modified: 12 Dec 2024 14:45 URI: https://strathprints.strath.ac.uk/id/eprint/85624