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首页> 外文期刊>Hormones and behavior >Prior stress followed by a novel stress challenge results in sex-specific deficits in behavioral flexibility and changes in gene expression in rat medial prefrontal cortex
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Prior stress followed by a novel stress challenge results in sex-specific deficits in behavioral flexibility and changes in gene expression in rat medial prefrontal cortex

机译:先前的压力,然后进行新的应力攻击导致大鼠内侧前额定皮层中的行为柔韧性和基因表达的变化产生性别特异性缺陷

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Chronic stress leads to sex-specific changes in the structure and function of rat medial prefrontal cortex (mPFC). Little is known about whether these effects persist following the cessation of chronic stress, or how these initial effects may impact responses to future stressors. Here we examined attentional set-shifting in male and female rats following chronic restraint stress, a post-chronic stress rest period, and an acute novel stress challenge. Chronic stress resulted in a reversible impairment in extradimensional set-shifting in males, but had no effect on attentional set-shifting in females. Surprisingly, chronically stressed female, but not male, rats had impaired extradimensional set-shifting following a novel stress challenge. Alterations in the balance of excitation and inhibition of mPFC have been implicated in behavioral deficits following chronic stress. Thus, in a separate group of rats, we examined changes in the expression of genes related to glutamatergic (NR1, NR2A, NR2B, GluR1) and GABAergic (Gad67, parvalbumin, somatostatin) neurotransmission in mPFC after acute and chronic stress, rest, and their combination. Stress significantly altered the expression of NR1, GluR1, Gad67, and parvalbumin. Notably, the pattern of stress effects on NR1, Gad67, and parvalbumin expression differed between males and females. In males, these genes were upregulated following the post-chronic stress rest period, while minimal changes were found in females. In contrast, both males and females had greater GluR1 expression following a rest period. These findings suggest that chronic stress leads to sex-specific stress adaptation mechanisms that may contribute to sex differences in response to subsequent stress exposure.
机译:慢性应激导致大鼠内侧前额叶皮质(MPFC)结构和功能的性别特异性变化。众所周知,这些效果是否持续存在于慢性应激之后,或这些初始效应如何影响对未来的压力源的影响。在这里,我们在慢性约束应力,慢性应激休息时间和急性新的压力挑战后检查了雄性和女性大鼠中的注意力设置。慢性胁迫导致雄性胎儿换档的可逆损伤,但对女性的注意力设定没有影响。令人惊讶的是,慢性强调的女性,但不是雄性,大鼠在新的压力攻击后已经受损了额外的设定换档。慢性胁迫后,MPFC的激发和抑制平衡的改变涉及行为缺陷。因此,在一组单独的大鼠中,我们检查急性和慢性应激后MPFC中与谷氨酰胺(NR1,NR2A,NR2B,GLUR1)和加巴能物质(GAD67,Parvalbumis,Somatostatin)神经递质的基因表达的变化。他们的组合。压力显着改变了NR1,Glur1,GAD67和Parvalbumin的表达。值得注意的是,对NR1,GAD67和Parvalbumin表达的应力效应的模式不同于雄性和女性。在雄性后,在慢性应激休息时间后上调这些基因,而在女性中发现了最小的变化。相比之下,休息时间后,男性和女性都有更大的Glur1表达。这些研究结果表明,慢性应激导致性别特异性应力适应机制,可能导致对后续压力暴露的响应性差异有助于性差异。

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