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Reduced aggression in mice lacking GABA transporter subtype 1
Author(s) -
Liu GuoXiang,
Liu Shuai,
Cai GuoQiang,
Sheng ZheJing,
Cai YouQing,
Jiang Jie,
Sun Xia,
Ma SunKai,
Wang Long,
Wang ZhuGang,
Fei Jian
Publication year - 2006
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.21148
Subject(s) - tiagabine , gaba transporter , bicuculline , gabaergic , gabaa receptor , medicine , gaba receptor antagonist , transporter , endocrinology , pharmacology , inhibitory postsynaptic potential , biology , neuroscience , receptor , epilepsy , anticonvulsant , biochemistry , gene
Dysregulation of the brain GABAergic system has been implicated in the pathophysiology of violence and aggression. As a key regulator of central GABAergic activity, dysfunction of the GABA transporter subtype 1 (GAT1) represents a potential mechanism mediating pathologic aggression. We provide evidence that GAT1−/− mice and GAT1+/− mice exhibit lower aggressive behavior both in home cage resident–intruder test and neutral arena resident–intruder test, compared to wild‐type mice (GAT1+/+). The pharmacologic effects of the GAT1 inhibitor, tiagabine and the GABA A receptor antagonist, bicuculline have been assessed in GAT1+/+ mice: tiagabine inhibits attacks but bicuculline induces attacks. Compared to GAT1+/− and +/+ mice, the GAT1−/− mice displayed a normal circadian pattern of home cage activity, but more activity overall. Meanwhile, reduced testosterone concentration was found in GAT1−/− mice compared to GAT1+/+ mice but not in GAT1+/+ mice treated with tiagabine, suggesting that testosterone is not directly involved in GAT1 mediated aggressive behavior regulation. These results showed that GAT1 is an important target involved in the regulation of aggressive behavior in mice, and long‐term dysfunction of GAT1 may also result in the alteration of testosterone secretion. © 2006 Wiley‐Liss, Inc.