Addiction to
morphine is a chronic
brain disease leading to compulsive abuse.
Drug addiction animal models with and without conditioned place preference (
CPP) training have been used to investigate cue-elicited drug craving. We used 18 F-fluorodeoxyglucose (18 F-FDG) and 11 C-2-β-carbomethoxy-3-β-(4-fluorophenyl)tropane (11 C-CFT) micro-PET/CT scans to examine the regional changes in brain
glucose metabolism and
dopamine transporter (DAT) availability to study their relationship underlying drug memory in
morphine-treated rat models with and without
CPP. Standardized uptake value ratio (SUVr) of 18 F-FDG significantly decreased in the medial prefrontal cortex (mPFC) and cingulate with short-term
morphine administration compared with the baseline condition. Voxelwise analysis indicated
glucose metabolism alterations in the somatosensory cortex, hippocampus and cingulate in
morphine-treated rats and in the striatum, thalamus, medial prefrontal cortex, primary motor cortex and many regions in the cortex in the
CPP group compared with the baseline condition. Alterative
glucose metabolism was also observed in the striatum, primary somatosensory cortex and some cortical regions in the
CPP group compared with
morphine alone group. DAT expression alterations were only observed in the long-term
morphine compared with the short-term
morphine group. This study shows that cerebral
glucose metabolism significantly altered during
morphine administration and
CPP process mainly in the mPFC, striatum and hippocampus, which indicates that the function of these brain regions is involved in cue-induced craving and memory retrieval.