首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >The alpha(2a)-adrenergic receptor plays a protective role in mouse behavioral models of depression and anxiety.
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The alpha(2a)-adrenergic receptor plays a protective role in mouse behavioral models of depression and anxiety.

机译:alpha(2a)-肾上腺素受体在抑郁和焦虑的小鼠行为模型中起保护作用。

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摘要

The noradrenergic system is involved in the regulation of many physiological and psychological processes, including the modulation of mood. The alpha(2)-adrenergic receptors (alpha(2)-ARs) modulate norepinephrine release, as well as the release of serotonin and other neurotransmitters, and are therefore potential targets for antidepressant and anxiolytic drug development. The current studies were undertaken to examine the role of the alpha(2A) subtype of alpha(2)-AR in mouse behavioral models of depression and anxiety. We have observed that the genetic knock-out of the alpha(2A)-AR makes mice less active in a modified version of Porsolt's forced swim test and insensitive to the antidepressant effects of the tricyclic drug imipramine in this paradigm. Furthermore, alpha(2A)-AR knock-out mice appear more anxious than wild-type C57 Bl/6 mice in the rearing and light-dark models of anxiety after injection stress. These findings suggest that the alpha(2A)-AR may play a protective role in some forms of depression and anxiety and that the antidepressant effects of imipramine may be mediated by the alpha(2A)-AR.
机译:去甲肾上腺素能系统参与许多生理和心理过程的调节,包括情绪调节。 alpha(2)-肾上腺素受体(alpha(2)-ARs)调节去甲肾上腺素的释放以及5-羟色胺和其他神经递质的释放,因此是抗抑郁药和抗焦虑药开发的潜在目标。当前的研究进行以检查alpha(2A)亚型的alpha(2)-AR在小鼠抑郁和焦虑行为模型中的作用。我们已经观察到,α(2A)-AR的基因敲除使小鼠在Porsolt强迫游泳试验的改良版中活性降低,并且对这种范例中的三环药物丙咪嗪的抗抑郁作用不敏感。此外,在注射应激后,在饲养和光暗焦虑模型中,alpha(2A)-AR基因敲除小鼠比野生型C57 Bl / 6小鼠显得更焦虑。这些发现表明,α(2A)-AR在某些形式的抑郁和焦虑中可能起保护作用,而丙咪嗪的抗抑郁作用可能由α(2A)-AR介导。

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