首页> 外文期刊>Behavioural Brain Research: An International Journal >Long-term effects of early adolescent stress: dysregulation of hypothalamic-pituitary-adrenal axis and central corticotropin releasing factor receptor 1 expression in adult male rats
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Long-term effects of early adolescent stress: dysregulation of hypothalamic-pituitary-adrenal axis and central corticotropin releasing factor receptor 1 expression in adult male rats

机译:早期青春期应激的长期影响:丘脑垂体 - 肾上腺轴和中枢性皮质甾醇释放因子受体1在成年雄性大鼠中表达的缺陷

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摘要

Post-traumatic stress disorder (PTSD) is a stress-related mental disorder caused by traumatic experiences. Studies have found that exposure to early stressful events is a risk factor for developing PTSD. However, a limited number of studies have explored the effects of traumatic stress in early adolescence on behavior, hypothalamic-pituitary-adrenal (HPA) axis function, central corticotropin releasing factor receptor 1 (CRER1) expression and the relative vulnerability of PTSD in adulthood. The current study aims to explore these issues using inescapable electric foot shock to induce a PTSD model in early adolescent rats. Meanwhile, running on a treadmill for six weeks and administration of the antagonist with 3.2 mg/kg/day of CP-154, 526 for 14 consecutive days were used as therapeutic measures. Presently, the stress (S) group showed more anxiety and depression in the open field (OF) test and elevated plus maze (EPM) test, memory damage in the Y maze test, decreased basal CORT level, increased DEX negative feedback inhibition and exacerbated and longer-lasting reaction to CRH challenge in the DEX/CRH test compared with the control group. Central CRER1 expression was also changed in the S group, as evidenced by the increased CRER1 expression in the hypothalamus, amygdala and the prefrontal cortex (PFC). However, treadmill exercise alleviated early adolescent stress-induced behavior abnormalities and improved the functional state of the HPA axis, performing a more powerful effect than the CRER1 antagonist CP-154, 526. Additionally, this study revealed that the alteration of central CRER1 expression might play an important role in etiology of PTSD in adulthood. (C) 2015 Elsevier B.V. All rights reserved.
机译:创伤后应激障碍(PTSD)是由创伤体验引起的应激相关的精神障碍。研究发现暴露于早期压力事件是开发应激障碍的危险因素。然而,有限数量的研究已经探讨了创伤性应激在早期青春期的影响,下丘脑 - 垂体 - 肾上腺(HPA)轴函数,中央皮质甾醇释放因子受体1(CRER1)表达以及PTSD在成年中的相对脆弱性。目前的研究旨在探讨使用不可避免的电脚冲击来诱导早期青少年大鼠的PTSD模型。同时,在跑步机上运行六周并用3.2mg / kg / kg / kg / kg / kg / kg / p-154,526连续14天施用拮抗剂作为治疗措施。目前,应力在张田(OF)测试和升高的Plus迷宫(EPM)测试中表现出更多的焦虑和抑郁症,Y迷宫试验中的记忆损伤,增加了基础树皮水平,增加了DEX负反馈抑制和加剧与对照组相比,对DEX / CRH试验中CRH攻击的更长持久反应。在S组中也改变了中央Crer1表达,如下丘脑,Amygdala和前额叶皮质(PFC)中增加的Crer1表达所证明。然而,跑步机运动缓解了早期的青少年应激诱导的行为异常并改善了HPA轴的功能状态,表现比CRER1对拮抗剂CP-154,526更强大的效果。此外,该研究表明,中央CRER1表达的改变可能在成年前期目标的病因中发挥重要作用。 (c)2015 Elsevier B.v.保留所有权利。

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