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From bench to bedside: The mGluR5 system in people with and without Autism Spectrum Disorder and animal model systems

Abstract:
F] FPEB binding (t (13) = -2.86, p = 0.047) in the left striatum/thalamus region of interest as compared to controls. Within this region, there was a strong negative correlation between GABA + and mGluR5 density across the entire cohort (Pearson's correlation: r (14) = -0.763, p = 0.002). Cntnap2 KO mice had significantly higher mGlu5 receptor binding in the striatum (caudate-putamen) as compared to wild-type (WT) mice (n = 15, p = 0.03). There were no differences in mGluR5 binding for mice with the Shank3 knockout or 16p11.2 deletion. Given that Cntnap2 is associated with a specific striatal deficit of parvalbumin positive GABA interneurons and 'autistic' features, our findings suggest that an increase in mGluR5 in ASD may relate to GABAergic interneuron abnormalities.
Publication status:
Published
Peer review status:
Peer reviewed

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Role:
Author
ORCID:
0000-0001-7128-7246
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-1312-688X
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Role:
Author
ORCID:
0000-0002-0936-9993
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Role:
Author
ORCID:
0000-0002-0680-0135
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Role:
Author
ORCID:
0000-0002-7052-8623


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Funder identifier:
10.13039/501100000764
Grant:
115300


Publisher:
Springer Nature [academic journals on nature.com]
Journal:
Translational Psychiatry More from this journal
Volume:
12
Issue:
1
Pages:
395-395
Article number:
395
Publication date:
2022-09-20
DOI:
EISSN:
2158-3188
ISSN:
2158-3188


Language:
English
Keywords:
Pubs id:
1286037
Local pid:
pubs:1286037
Source identifiers:
W4296483653
Deposit date:
2026-04-29
ARK identifier:
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