Impaired social interaction and reduced anxiety-related behavior in vasopressin V1a receptor knockout mice

被引:140
|
作者
Egashira, Nobuaki
Tanoue, Akito
Matsuda, Tomomi
Koushi, Emi
Harada, Satoko
Takano, Yukio
Tsujimoto, Gozoh
Mishima, Kenichi
Iwasaki, Katsunori
Fujiwara, Michihiro
机构
[1] Fukuoka Univ, Fac Pharmaceut Sci, Dept Neuropharmacol, Fukuoka 8140180, Japan
[2] Natl Res Inst Child Hlth & Dev, Dept Mol Cell Pharmacol, Tokyo 1578535, Japan
[3] Fukuoka Univ, Fac Pharmaceut Sci, Dept Pharmacol, Fukuoka 8140180, Japan
[4] Kyoto Univ, Fac Pharmaceut Sci, Grad Sch Pharmaceut Sci, Dept Genom Drug Discovery Sci, Kyoto 6068501, Japan
关键词
vasopressin; V1a receptor; knockout; social interaction; anxiety; mice;
D O I
10.1016/j.bbr.2006.12.009
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The arginine vasopressin (AVP) system plays an important role in social behavior. Autism, with its hallmark disturbances in social behavior, has been associated with the V1a receptor (V1aR) gene. Furthermore, impairments of social function are often observed in symptoms of schizophrenia. Subchronic phencyclidine (PCP) produces behaviors relating to certain aspects of schizophrenic symptoms such as impairing social interaction in animals and it reduces the density of V1aR binding sites in several brain regions. Here, we report that V1aR knockout (KO) mice exhibited impairment of social behavior in a social interaction test, and showed reduced anxiety-related behavior in elevated plus-maze and marble-burying behavior tests. Given the current findings, the V1aR may be involved in the regulation of social interaction, and V1aR KO mice could be used as an animal model of psychiatric disorders associated with social behavior deficits, such as autism and schizophrenia. (c) 2007 Published by Elsevier B.V.
引用
收藏
页码:123 / 127
页数:5
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