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老年神经肽Y(NPY)Y2基因敲除小鼠的情绪行为

Emotional behavior in aged neuropeptide Y (NPY) Y2 knockout mice.

作者信息

Carvajal Cristina, Dumont Yvan, Herzog Herbert, Quirion Rémi

机构信息

Douglas Hospital Research Centre, Department of Neurology and Neurosurgery, Department of Psychiatry, McGill University, Montréal QC, Canada H4H 1R3.

出版信息

J Mol Neurosci. 2006;28(3):239-45. doi: 10.1385/JMN:28:3:239.

Abstract

Neuropeptide Y (NPY) was shown to modulate anxiety- and depression-related behaviors in various animal models. Previous studies demonstrated that NPY Y2 receptor knockout (KO) mice display an anxiolytic- and antidepressant-like phenotype compared with control animals. However, the long-term effect of the deletion of this receptor in aged animals is unknown. Thus, anxiety- and depression-related behaviors were investigated in 2-yr-old NPY Y2 KO mice. Aged NPY Y2 KO mice display an anxiolytic-like profile as assessed in the elevated plus-maze and open field, providing further support for a role for Y2 receptors in anxiety-related behaviors. Furthermore, aged NPY Y2 KO mice have significantly lower immobility scores in the forced swim test; supporting the role for this receptor in antidepressant-like behaviors. These data provide further evidence that modulators of the NPY Y2 receptor subtype are drug targets for the treatment of anxiety and mood disorders in human subjects.

摘要

神经肽Y(NPY)已被证明可在多种动物模型中调节与焦虑和抑郁相关的行为。先前的研究表明,与对照动物相比,NPY Y2受体敲除(KO)小鼠表现出抗焦虑和抗抑郁样表型。然而,在老年动物中缺失该受体的长期影响尚不清楚。因此,对2岁的NPY Y2 KO小鼠的焦虑和抑郁相关行为进行了研究。在高架十字迷宫和旷场试验中评估,老年NPY Y2 KO小鼠表现出抗焦虑样特征,为Y2受体在焦虑相关行为中的作用提供了进一步支持。此外,老年NPY Y2 KO小鼠在强迫游泳试验中的不动时间显著降低;支持该受体在抗抑郁样行为中的作用。这些数据进一步证明,NPY Y2受体亚型的调节剂是治疗人类焦虑和情绪障碍的药物靶点。

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