Whittle N, Lubec G, Singewald N
Department of Pharmacology and Toxicology, Institute of Pharmacy, Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innsbruck, Austria.
Amino Acids. 2009 Jan;36(1):147-58. doi: 10.1007/s00726-008-0195-6. Epub 2008 Oct 31.
A relationship between zinc (Zn)-deficiency and mood disorders has been suspected. Here we examined for the first time whether experimentally-induced Zn-deficiency in mice would alter depression- and anxiety-related behaviour assessed in established tests and whether these alterations would be sensitive to antidepressant treatment. Mice receiving a Zn-deficient diet (40% of daily requirement) had similar homecage and open field activity compared to normally fed mice, but displayed enhanced depression-like behaviour in both the forced swim and tail suspension tests which was reversed by chronic desipramine treatment. An anxiogenic effect of Zn-deficiency prevented by chronic desipramine and Hypericum perforatum treatment was observed in the novelty suppressed feeding test, but not in other anxiety tests performed. Zn-deficient mice showed exaggerated stress-evoked immediate-early gene expression in the amygdala which was normalised following DMI treatment. Taken together these data support the link between low Zn levels and depression-like behaviour and suggest experimentally-induced Zn deficiency as a putative model of depression in mice.
锌(Zn)缺乏与情绪障碍之间的关系一直受到怀疑。在此,我们首次研究了实验诱导的小鼠锌缺乏是否会改变在既定测试中评估的抑郁和焦虑相关行为,以及这些改变是否对抗抑郁治疗敏感。与正常喂养的小鼠相比,接受缺锌饮食(每日需求量的40%)的小鼠在笼内和旷场活动方面相似,但在强迫游泳和悬尾试验中均表现出增强的抑郁样行为,慢性地昔帕明治疗可逆转这种行为。在新奇抑制摄食试验中观察到慢性地昔帕明和贯叶连翘治疗可预防锌缺乏的致焦虑作用,但在其他进行的焦虑试验中未观察到。缺锌小鼠在杏仁核中表现出应激诱发的即刻早期基因表达过度,DMI治疗后恢复正常。综上所述,这些数据支持低锌水平与抑郁样行为之间的联系,并表明实验诱导的锌缺乏是小鼠抑郁症的一种假定模型。