期刊
PSYCHOPHARMACOLOGY
卷 232, 期 19, 页码 3497-3505出版社
SPRINGER
DOI: 10.1007/s00213-015-4002-2
关键词
Histamine; Histamine H-1 receptor occupancy; Human brain; Antipsychotics; Olanzapine; PET; Quetiapine
资金
- Japan Society for the Promotion of Science [21650088, 26253016]
- Japan Society of Technology
- Grants-in-Aid for Scientific Research [25293257, 15K08127, 26830041, 21650088, 26253016, 25670525] Funding Source: KAKEN
Rationale Histamine H-1 antagonists have hypnotic, appetite-promoting, and sedative side effects. Most second-generation antipsychotics have potent antagonistic effects on histamine H-1 receptor (H1R). Positron emission tomography (PET) can measure the H1R occupancy (H1RO) in vivo, although there are no reports regarding antipsychotics. Objectives We studied the H1RO of olanzapine and quetiapine in vivo with respect to their plasma concentrations and subjective drowsiness by performing human PET imaging studies with [C-11]doxepin, a potent PET ligand of H1R. Methods Six healthy Japanese male volunteers were enrolled. Cross-randomized PET imaging was performed after a single oral administration of olanzapine (2.5 mg), quetiapine (25mg), or placebo. PET data were analyzed by region of interest and voxel-by-voxel analysis. We concurrently measured plasma drug concentrations by liquid chromatography/tandem mass spectrometry and evaluated subjective sleepiness. Results The binding potential ratios of olanzapine and quetiapine in the cerebral cortex were significantly lower than that of the placebo. The H1RO values of olanzapine and quetiapine in the cortex were approximately 61-80 and 56-81 %, respectively. The binding potential ratios of the drugs were significantly lower than that of the placebo in the dorsolateral prefrontal and lateral temporal cortices, and anterior and posterior cingulate gyri. The H1RO values in the cortex were significantly correlated with subjective sleepiness but not plasma drug concentrations. Conclusions Olanzapine and quetiapine have high H1RO values in the human brain under their clinical minimum doses. This study provides a foundation of the properties by which new-generation antipsychotics block the central histaminergic system in humans.
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