PT - JOURNAL ARTICLE AU - Ruiqing Ni AU - Adrienne Müller Herde AU - Ahmed Haider AU - Claudia Keller AU - Georgios Louloudis AU - Markus Vaas AU - Roger Schibli AU - Simon M. Ametamey AU - Jan Klohs AU - Linjing Mu TI - <em>In vivo</em> imaging of cannabinoid type 2 receptors, functional and structural alterations in mouse model of cerebral ischemia by PET and MRI AID - 10.1101/2021.05.08.441033 DP - 2021 Jan 01 TA - bioRxiv PG - 2021.05.08.441033 4099 - http://biorxiv.org/content/early/2021/05/10/2021.05.08.441033.short 4100 - http://biorxiv.org/content/early/2021/05/10/2021.05.08.441033.full AB - Background and purpose Brain ischemia is one of the most important pathologies of the central nervous system. Non-invasive molecular imaging methods have the potential to provide critical insights into the temporal dynamics and follow alterations of receptor expression and metabolism in ischemic stroke. The aim of this study was to assess the cannabinoid type 2 receptors (CB2R) levels in transient middle cerebral artery occlusion (tMCAO) mouse models at subacute stage using positron emission tomography (PET) with our novel tracer [18F]RoSMA-18-d6, and structural imaging by magnetic resonance imaging (MRI).Methods Our recently developed CB2R PET tracer [18F]RoSMA-18-d6 was used for imaging the neuroinflammation at 24 h after reperfusion in tMCAO mice. The RNA expression levels of CB2R and other inflammatory markers were analyzed by quantitative real-time polymerase chain reaction using brain tissues from tMCAO (1 h occlusion) and sham-operated mice. [18F]fluorodeoxyglucose (FDG) was included for evaluation of the cerebral metabolic rate of glucose (CMRglc). In addition, diffusion-weighted imaging and T2-weighted imaging were performed for anatomical reference and delineating the lesion in tMCAO mice.Results mRNA expressions of inflammatory markers TNF-α, Iba1, MMP9 and GFAP, CNR2 were increased at 24 h after reperfusion in the ipsilateral compared to contralateral hemisphere of tMCAO mice, while mRNA expression of the neuronal marker MAP-2 was markedly reduced. Reduced [18F]FDG uptake was observed in the ischemic striatum of tMCAO mouse brain at 24 h after reperfusion. Although higher activity of [18F]RoSMA-18-d6 in ex-vivo biodistribution studies and higher standard uptake value ratio (SUVR) were detected in the ischemic ipsilateral compared to contralateral striatum in tMCAO mice, the in-vivo specificity of [18F]RoSMA-18-d6 was confirmed only in the CB2R-rich spleen.Conclusions This study revealed an increased [18F]RoSMA-18-d6 measure of CB2R and a reduced [18F]FDG measure of CMRglc in ischemic striatum of tMCAO mice at subacute stage. [18F]RoSMA-18-d6 might be a promising PET tracer for detecting CB2R alterations in animal models of neuroinflammation without neuronal loss.Competing Interest StatementThe authors have declared no competing interest.ADCApparent diffusion coefficientCB2RCannabinoid type 2 receptorsCBFCerebral blood flowCMRglcCerebral metabolic rate of glucoseCTcomputed tomographyDWDiffusion weightedFDGfluorodeoxyglucose% ID/g tissueInjected dose per gram tissueMRIMagnetic resonance imagingPETPositron emission tomographySUVStandardized uptake valueSUVRStandard uptake value ratiotMCAOtransient middle cerebral artery occlusionTSPOTranslocator proteinTTCTriphenyltetrazolium chloride