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首页> 外文期刊>Molecular brain >The BDNF-FoxO1 Axis in the medial prefrontal cortex modulates depressive-like behaviors induced by chronic unpredictable stress in postpartum female mice
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The BDNF-FoxO1 Axis in the medial prefrontal cortex modulates depressive-like behaviors induced by chronic unpredictable stress in postpartum female mice

机译:内侧前额叶皮质中的BDNF-FOXO1轴调节产后女性小鼠慢性不可预测应力诱导的抑郁样行列

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摘要

Postpartum depression (PPD) is a serious psychiatric disorder, affecting not only the childbearing women but also the health of their offsprings. The brain-derived neurotrophic factor (Bdnf) gene is an important target gene for the study of depression and antidepressant therapy. FoxO1, belonging to the FoxO subfamily is involved in the development of major depressive disorders. However, the role of BDNF and its functional brain regions involved in PPD remains unknown. Here, we report that chronic unpredictable stress (CUS) can produce depression-associated behaviors in postpartum female mice. CUS can decrease total Bdnf mRNA and exon specific mRNAs in the medial prefrontal cortex (mPFC), accompanied by reduced protein levels, that were correlated with depression-related behaviors. Moreover, postpartum, not virgin female mice showed increased susceptibility to subthreshold stress-induced depression-related behaviors. Selective deletion of BDNF in the mPFC induced anhedonia as indicated by reduced sucrose preference and increased latency to food in the novelty suppressed food test in postpartum, but not in virgin female mice. Furthermore, we found that FoxO1 is also decreased in CUS-treated postpartum female mice with a significant correlation with depression-related behaviors. BDNF-specific knockout in the mPFC decreased FoxO1 expression in female mice. Our results indicate that the BDNF-FoxO1 axis in mPFC?can regulate depression-related behaviors and stress vulnerability in postpartum female mice.
机译:产后抑郁症(PPD)是一种严重的精神疾病,不仅影响了生育的女性,而且影响了他们的后代的健康。脑衍生的神经营养因子(BDNF)基因是研究抑郁症和抗抑郁疗法的重要靶基因。 FOXO1,属于Foxo亚家族参与了主要抑郁症的发展。然而,BDNF及其在PPD中的功能性脑区域的作用仍然未知。在这里,我们报告说,慢性不可预测的压力(CUS)可以在产后女性小鼠中产生抑郁相关的行为。 CU可以在内侧前额叶皮质(MPFC)中减少总BDNF mRNA和外显子特异性mRNA,伴随着减少的蛋白质水平,与抑郁相关的行为相关。此外,产后,不是原始的雌性小鼠对亚阈值应激引起的抑郁症相关行为的敏感性增加。在MPFC诱导的Anhedonia中选择性缺失BDNF,如在产后的新颖性抑制食物试验中的降低,但在原始女鼠中增加了食物中的食物等潜伏期。此外,我们发现FOXO1在CUS治疗的产后女鼠中也降低了与抑郁相关行为显着相关的雌性小鼠。 MPFC中的BDNF特异性敲除降低了雌性小鼠的FoxO1表达。我们的结果表明,MPFC中的BDNF-FOXO1轴?可以调节产后雌性小鼠的抑郁相关行为和压力脆弱性。

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