Impaired locomotor activity and exploratory behavior in mice lacking histamine H1 receptors

Isao Inoue, Kazuhiko Yanai, Daisuke Kitamura, Ichiro Taniuchi, Takashi Kobayashi, Kaku Niimura, Takehiko Watanabe, Takeshi Watanabe

Research output: Contribution to journalArticle

253 Citations (Scopus)

Abstract

From pharmacological studies using histamine antagonists and agonists, it has been demonstrated that histamine modulates many physiological functions of the hypothalamus, such as arousal state, locomotor activity, feeding, and drinking. Three kinds of receptors (H1, H2, and H3) mediate these actions. To define the contribution of the histamine H1 receptors (H1R) to behavior, mutant mice lacking the H1R were generated by homologous recombination. In brains of homozygous mutant mice, no specific binding of [3H]pyrilamine was seen. [3H]Doxepin has two saturable binding sites with higher and lower affinities in brains of wild-type mice, but H1R-deficient mice showed only the weak labeling of [3H]doxepin that corresponds to lower- affinity binding sites. Mutant mice develop normally, but absence of H1R significantly increased the ratio of ambulation during the light period to the total ambulation for 24 hr in an accustomed environment. In addition, mutant mice significantly reduced exploratory behavior of ambulation and rearings in a new environment. These results indicate that through H1R, histamine is involved in circadian rhythm of locomotor activity and exploratory behavior as a neurotransmitter.

Original languageEnglish
Pages (from-to)13316-13320
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume93
Issue number23
DOIs
Publication statusPublished - 1996 Nov 12

ASJC Scopus subject areas

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