Department of Physiology, University of Tartu Tartu, Estonia ; Centre for Excellence in Translational Medicine, University of Tartu Tartu, Estonia.
Front Neurosci. 2013 Jul 31;7:132. doi: 10.3389/fnins.2013.00132. eCollection 2013.
It has been shown that mutations in the WFS1 gene make humans more susceptible to mood disorders. Besides that, mood disorders are associated with alterations in the activity of serotonergic and noradrenergic systems. Therefore, in this study, the effects of imipramine, an inhibitor of serotonin (5-HT) and noradrenaline (NA) reuptake, and paroxetine, a selective inhibitor of 5-HT reuptake, were studied in tests of behavioral despair. The tail suspension test (TST) and forced swimming test (FST) were performed in Wfs1-deficient mice. Simultaneously, gene expression and monoamine metabolism studies were conducted to evaluate changes in 5-HT- and NA-ergic systems of Wfs1-deficient mice. The basal immobility time of Wfs1-deficient mice in TST and FST did not differ from that of their wild-type littermates. However, a significant reduction of immobility time in response to lower doses of imipramine and paroxetine was observed in homozygous Wfs1-deficient mice, but not in their wild-type littermates. In gene expression studies, the levels of 5-HT transporter (SERT) were significantly reduced in the pons of homozygous animals. Monoamine metabolism was assayed separately in the dorsal and ventral striatum of naive mice and mice exposed for 30 min to brightly lit motility boxes. We found that this aversive challenge caused a significant increase in the levels of 5-HT and 5-hydroxyindoleacetic acid (5-HIAA), a metabolite of 5-HT, in the ventral and dorsal striatum of wild-type mice, but not in their homozygous littermates. Taken together, the blunted 5-HT metabolism and reduced levels of SERT are a likely reason for the elevated sensitivity of these mice to the action of imipramine and paroxetine. These changes in the pharmacological and neurochemical phenotype of Wfs1-deficient mice may help to explain the increased susceptibility of Wolfram syndrome patients to depressive states.
已经表明,WFS1 基因突变使人类更容易患情绪障碍。此外,情绪障碍与 5-羟色胺(5-HT)和去甲肾上腺素(NA)系统活性的改变有关。因此,在这项研究中,研究了三环抗抑郁药丙咪嗪(一种 5-HT 和 NA 再摄取的抑制剂)和帕罗西汀(一种 5-HT 再摄取的选择性抑制剂)在行为绝望测试中的作用。在 Wfs1 缺陷小鼠中进行了悬尾试验(TST)和强迫游泳试验(FST)。同时,进行了基因表达和单胺代谢研究,以评估 Wfs1 缺陷小鼠 5-HT 和 NA 能系统的变化。TST 和 FST 中 Wfs1 缺陷小鼠的基础不动时间与野生型同窝仔鼠无差异。然而,在纯合 Wfs1 缺陷小鼠中,观察到较低剂量的丙咪嗪和帕罗西汀反应性不动时间明显减少,但在野生型同窝仔鼠中未观察到。在基因表达研究中,5-HT 转运体(SERT)的水平在纯合动物的脑桥中显著降低。单独测定了去甲肾上腺素代谢物的水平,并在暴露于明亮光照运动箱 30 分钟的幼稚小鼠和小鼠的背侧和腹侧纹状体中进行了测定。我们发现,这种厌恶刺激导致野生型小鼠腹侧和背侧纹状体中 5-HT 和 5-羟吲哚乙酸(5-HIAA)(5-HT 的代谢产物)的水平显著增加,但在纯合子同窝仔鼠中没有。总之,5-HT 代谢的钝化和 SERT 水平的降低可能是这些小鼠对丙咪嗪和帕罗西汀作用敏感性增加的原因。Wfs1 缺陷小鼠的药理学和神经化学表型的这些变化可能有助于解释 Wolfram 综合征患者对抑郁状态的易感性增加。