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首页> 外文期刊>Journal of Alzheimer's disease: JAD >The Synergistic Roles of the Chronic Prenatal and Offspring Stress Exposures in Impairing Offspring Learning and Memory
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The Synergistic Roles of the Chronic Prenatal and Offspring Stress Exposures in Impairing Offspring Learning and Memory

机译:慢性产前和后代应激暴露在削弱后代学习和记忆中的协同作用

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In Alzheimer's disease (AD), extensive experimental studies have demonstrated a negative impact of chronic stress during various stages of life (including prenatal phase) on some aspects of AD pathology. Nevertheless, presently, few studies have been involved in the learning and memory impairments, as well as neuropathology elicited by the chronic prenatal stress (CPS) and the chronic offspring stress (COS) exposures simultaneously, particularly for the adult male APPswe/PS1dE9 murine offspring. Therefore, the aim of the present study was to investigate the influence of CPS on learning and memory impairments induced by COS in 6-month-old male APPswe/PS1dE9 offspring mice and the related mechanism. Our study firstly demonstrates that 14-day exposure to CPS could exacerbate the learning and memory impairments, as well as neuropathological damages in the CA3 regions of the hippocampus and cortex neurons, which is induced by the 28-day exposure to COS in 6-month-old male APPswe/PS1dE9 offspring mice. In addition, CPS could potentiate the production of A beta PP, A beta(42), and corticosterone in 6-month-old male APPswe/PS1dE9 offspring that also suffer COS. In conclusion, our novel findings strongly implicate the synergistic roles of the CPS and COS exposures in impairing offspring learning and memory. Moreover, CPS potentiating the production of A beta(42) might be mediated by glucocorticoids through increasing the expression of APP and BACE1 gene.
机译:在阿尔茨海默氏病(AD)中,广泛的实验研究表明,生命的各个阶段(包括产前阶段)的慢性应激对AD病理学的某些方面产生负面影响。然而,目前,很少有研究涉及学习和记忆障碍,以及同时暴露于慢性产前应激(CPS)和慢性后代应激(COS)引起的神经病理学,特别是对于成年男性APPswe / PS1dE9鼠后代。因此,本研究的目的是研究CPS对6月龄雄性APPswe / PS1dE9后代小鼠COS诱导的学习和记忆障碍的影响及其相关机制。我们的研究首先证明,暴露于CPS的14天可能加剧学习和记忆障碍,以及海马和皮层神经元CA3区的神经病理学损害,这是由暴露6个月的COS 28天引起的岁的雄性APPswe / PS1dE9后代小鼠。此外,CPS可以增强同样患有COS的6个月大的雄性APPswe / PS1dE9后代的A beta PP,A beta(42)和皮质酮的产生。 CPS和COS暴露会损害后代的学习和记忆能力。此外,通过增加APP和BACE1基因的表达,糖皮质激素可能介导增强Aβ(42)产生的CPS。

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