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海马神经发生对抗抑郁药行为效应的需求。

Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants.

作者信息

Santarelli Luca, Saxe Michael, Gross Cornelius, Surget Alexandre, Battaglia Fortunato, Dulawa Stephanie, Weisstaub Noelia, Lee James, Duman Ronald, Arancio Ottavio, Belzung Catherine, Hen René

机构信息

Center for Neurobiology and Behavior, Columbia University, New York, NY 10032, USA.

出版信息

Science. 2003 Aug 8;301(5634):805-9. doi: 10.1126/science.1083328.

Abstract

Various chronic antidepressant treatments increase adult hippocampal neurogenesis, but the functional importance of this phenomenon remains unclear. Here, using genetic and radiological methods, we show that disrupting antidepressant-induced neurogenesis blocks behavioral responses to antidepressants. Serotonin 1A receptor null mice were insensitive to the neurogenic and behavioral effects of fluoxetine, a serotonin selective reuptake inhibitor. X-irradiation of a restricted region of mouse brain containing the hippocampus prevented the neurogenic and behavioral effects of two classes of antidepressants. These findings suggest that the behavioral effects of chronic antidepressants may be mediated by the stimulation of neurogenesis in the hippocampus.

摘要

各种慢性抗抑郁治疗可增加成年海马体神经发生,但这一现象的功能重要性仍不清楚。在此,我们使用基因和放射学方法表明,破坏抗抑郁药诱导的神经发生会阻断对抗抑郁药的行为反应。血清素1A受体缺失小鼠对血清素选择性再摄取抑制剂氟西汀的神经发生和行为效应不敏感。对小鼠大脑中包含海马体的受限区域进行X射线照射可阻止两类抗抑郁药的神经发生和行为效应。这些发现表明,慢性抗抑郁药的行为效应可能是由海马体神经发生的刺激介导的。

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