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Quantification of Metabotropic Glutamate Receptor 5 Availability With Both [11C]ABP688 and [18F]FPEB Positron Emission Tomography in the Sapap3 Knockout Mouse Model for Obsessive-Compulsive-like Behavior.
Glorie, Dorien; Verhaeghe, Jeroen; Miranda, Alan; De Lombaerde, Stef; Stroobants, Sigrid; Staelens, Steven.
Affiliation
  • Glorie D; Molecular Imaging Center Antwerp, University of Antwerp, Wilrijk, Belgium.
  • Verhaeghe J; Molecular Imaging Center Antwerp, University of Antwerp, Wilrijk, Belgium.
  • Miranda A; Molecular Imaging Center Antwerp, University of Antwerp, Wilrijk, Belgium.
  • De Lombaerde S; Molecular Imaging Center Antwerp, University of Antwerp, Wilrijk, Belgium; Department of Nuclear Medicine, Antwerp University Hospital, Edegem, Belgium.
  • Stroobants S; Molecular Imaging Center Antwerp, University of Antwerp, Wilrijk, Belgium; Department of Nuclear Medicine, Antwerp University Hospital, Edegem, Belgium.
  • Staelens S; Molecular Imaging Center Antwerp, University of Antwerp, Wilrijk, Belgium. Electronic address: steven.staelens@uantwerpen.be.
Article in En | MEDLINE | ID: mdl-34856382
BACKGROUND: This study provides a first direct comparison between positron emission tomography radioligands targeting the allosteric site of the metabotropic glutamate receptor 5 (mGluR5): [11C]ABP688 and [18F]FPEB. A blocking paradigm was set up to substantiate the common binding site of both radioligands. Second, both radioligands were applied in Sapap3 knockout (KO) mice showing compulsive-like behavior characterized by a lower in vivo mGluR5 availability. METHODS: First, wild-type mice (n = 7) received four position emission tomography/computed tomography scans: a [11C]ABP688 scan, a [18F]FPEB scan, and two blocking scans using cold FPEB and cold ABP688, respectively. A second experiment compared both radioligands in wild-type (n = 7) and KO (n = 10) mice. The simplified reference tissue model was used to calculate the nondisplaceable binding potential representing the in vivo availability of mGluR5 in the brain. RESULTS: Using cold FPEB as a blocking compound for [11C]ABP688 micro-positron emission tomography and vice versa, we observed averaged global reductions in mGluR5 availability of circa 98% for [11C]ABP688 and 82%-96% for [18F]FPEB. For KOs, the [11C]ABP688 nondisplaceable binding potential was on average 25% lower compared with wild-type control mice (p < .0001-.001), while this was about 17% for [18F]FPEB (p < .05). CONCLUSIONS: The current findings substantiate a common binding site and suggest a strong relationship between mGluR5 availability levels measured with both radioligands. In Sapap3 KO mice, a reduced mGluR5 availability could therefore be demonstrated with both radioligands. With [11C]ABP688, higher significance levels were achieved in more brain regions. These findings suggest [11C]ABP688 as a preferable radiotracer to quantify mGluR5 availability, as exemplified here in a model for compulsive-like behavior.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptor, Metabotropic Glutamate 5 / Obsessive-Compulsive Disorder Type of study: Prognostic_studies Limits: Animals Language: En Journal: Biol Psychiatry Cogn Neurosci Neuroimaging Year: 2022 Document type: Article Affiliation country: Belgium Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptor, Metabotropic Glutamate 5 / Obsessive-Compulsive Disorder Type of study: Prognostic_studies Limits: Animals Language: En Journal: Biol Psychiatry Cogn Neurosci Neuroimaging Year: 2022 Document type: Article Affiliation country: Belgium Country of publication: United States