Pharmacological profiles of benzodiazepinergic hypnotics and correlations with receptor subtypes

Mitsuru Yasui, Akira Kato, Toshiyuki Kanemasa, Shunji Murata, Kohei Nishitomi, Katsumi Koike, Nobuyuki Tai, Shunji Shinohara, Miwa Tokumura, Masahito Horiuchi, Kohji Abe


15 被引用数 (Scopus)


We examined the behavioral pharmacological properties of six benzodiazepine (ω) receptor ligands including brotizoram, nitrazepam, quazepam, rilmazafone, zolpidem and zopiclone and the binding of these drugs with ω receptor subtypes. Behavioral tests were performed at the time of the maximal effects induced by each drug following its oral administration to mice. All of these drugs dose-dependently induced impairment of motor coordination as rotarod performance and potentiation of thiopental-induced anesthesia as hypnotic effect. The hypnotic effects of rilmazafone, whose major metabolites were bound to both ω1 and ω2 receptors with high affinity, and ω1 selective quazepam were about 20 times more effective than the induction of motor impairments when compared with ED 50 values. However, there was no difference between the ED 50 values of ω1 selective zolpidem alone in these two tests. An antianxiety efficacy of zolpidem was relatively weak unlike that of other drugs in the elevated plus-maze. It has been reported that ω1, but not ω1, receptors are associated with motor impairment and anxiolytic effect. The weak anxiolytic effect of zolpidem supports the previous hypothesis. However, the strong motor incoordination of zolpidem suggests that not only ω2 but also ω1 receptors are related to motor impairment unlike the previous hypothesis.

ジャーナルJapanese Journal of Neuropsychopharmacology
出版ステータスPublished - 7月 1 2005

ASJC Scopus subject areas

  • 臨床心理学
  • 薬理学
  • 精神医学および精神衛生
  • 薬理学(医学)


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