Mice lacking the norepinephrine transporter ave supersensitive to psychostimulants

被引:322
作者
Xu, F
Gainetdinov, RR
Wetsel, WC
Jones, SR
Bohn, LM
Miller, GW
Wang, YM
Caron, MG [1 ]
机构
[1] Duke Univ, Med Ctr, Howard Hughes Med Inst Labs, Dept Cell Biol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Howard Hughes Med Inst Labs, Dept Med, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Psychiat, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Med Endocrinol, Durham, NC 27710 USA
[5] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
关键词
D O I
10.1038/74839
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The action of norepinephrine (NE) is terminated, in part, by its uptake into presynaptic noradrenergic neurons by the plasma-membrane NE transporter (NET), which is a target for antidepressants and psychostimulants. Disruption of the NET gene in mice prolonged the clearance of NE and elevated extracellular levels of this catecholamine. In a classical test for antidepressant drugs, the NET-deficient (NET-/-) animals behaved like antidepressant-treated wild-type mice. Mutants were hyper-responsive to locomotor stimulation by cocaine or amphetamine. These responses were accompanied by dopamine D-2/D-3 receptor supersensitivity. Thus altering NET expression significantly modulates midbrain dopaminergic function, an effect that may be an important component of the actions of antidepressants and psychostimulants.
引用
收藏
页码:465 / 471
页数:7
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