Premium
Brain histamine H1 receptor occupancy of loratadine measured by positron emission topography: comparison of H1 receptor occupancy and proportional impairment ratio
Author(s) -
Kubo Nobuo,
Senda Michio,
Ohsumi Yasunori,
Sakamoto Setsu,
Matsumoto Keiichi,
Tashiro Manabu,
Okamura Nobuyuki,
Yanai Kazuhiko
Publication year - 2011
Publication title -
human psychopharmacology: clinical and experimental
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.461
H-Index - 78
eISSN - 1099-1077
pISSN - 0885-6222
DOI - 10.1002/hup.1184
Subject(s) - occupancy , loratadine , histamine h1 receptor , histamine , positron emission tomography , receptor , medicine , nuclear medicine , pharmacology , biology , antagonist , ecology
Aims We have evaluated the sedative properties of H1‐antihistamines by using positron emission tomography (PET) and 11 C‐doxepin. The purpose of the present study was to measure histamine H1 receptor occupancy (H1RO) of loratadine 10 mg in patients with allergic rhinitis and to compare this occupancy with that of d ‐chlorpheniramine 2 mg, a first‐generation antihistamine. We also compared our PET findings with the proportional impairment ratio reported by McDonald et al.Methods The H1RO of loratadine 10 mg and d ‐chlorpheniramine 2 mg were evaluated in human brains in a double‐blind and crossover design using 11 C‐doxepin PET. Eleven young male patients with allergic rhinitis were examined by PET following oral single administration of loratadine 10 mg and d ‐chlorpheniramine 2 mg. Results Loratadine 10 mg occupied 11.7 ± 19.5% of histamine H1 receptors in the cortex, whereas d ‐chlorpheniramine 2 mg occupied 53.0 ± 33.2% in the same area, suggesting a non‐sedating property of loratadine at a dose of 10 mg. The H1RO values of loratadine and d ‐chlorpheniramine as well as those of previous studies were found to be significantly proportional to the proportional impairment ratio ( r = 0.899). Conclusion Measurement of H1RO is a sensitive and absolute method to characterize the non‐sedating property of drugs with H1 antagonistic activity. Copyright © 2011 John Wiley & Sons, Ltd.