Vulnerability to psychotogenic effects of ketamine is associated with elevated D2/3-receptor availability.

@article{Vernaleken2013VulnerabilityTP,
  title={Vulnerability to psychotogenic effects of ketamine is associated with elevated D2/3-receptor availability.},
  author={Ingo Vernaleken and Majken Klomp and Olaf Moeller and Mardjan Raptis and Arne Nagels and Frank R{\"o}sch and Wolfgang M. Schaefer and Paul Cumming and Gerhard Gr{\"u}nder},
  journal={The international journal of neuropsychopharmacology},
  year={2013},
  volume={16 4},
  pages={
          745-54
        }
}
Previous positron emission tomography (PET) studies employing competition paradigms have shown either no change or substantial declines in striatal [(11)C]-raclopride binding after challenge with psychotogenic doses of the N-methyl-D-aspartate antagonist ketamine. We sought to probe the relationship between the severity of ketamine-induced psychotic symptoms and altered dopamine D(2/3) receptor availability throughout brain using the high affinity ligand [(18)F]-fallypride (FP). PET recordings… 

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