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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:青春期早期应激的长期影响:成年雄性大鼠下丘脑-垂体-肾上腺轴和中央促肾上腺皮质激素释放因子受体1表达异常

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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)是由创伤经历引起的与压力相关的精神障碍。研究发现,暴露于早期压力事件是发展PTSD的危险因素。然而,有限的研究已经探索了青春期早期创伤性应激对行为,下丘脑-垂体-肾上腺(HPA)轴功能,中枢促肾上腺皮质激素释放因子受体1(CRER1)表达以及成年后PTSD相对脆弱性的影响。当前的研究旨在利用不可避免的脚底电击在青春期早期大鼠中诱发PTSD模型来探索这些问题。同时,在跑步机上跑步六周并以3.2mg / kg /天的CP-154、526连续14天施用拮抗剂连续14天作为治疗措施。目前,压力(S)组在开放视野(OF)测试和高迷迷宫(EPM)测试中表现出更多的焦虑和抑郁感,在Y迷宫测试中表现为记忆力受损,基础CORT水平降低,DEX负反馈抑制作用增加并且加剧与对照组相比,DEX / CRH测试中对CRH激发的反应持续时间更长。 S组中CRER1的中央表达也发生了改变,下丘脑,杏仁核和前额叶皮层(PFC)中CRER1表达的增加证明了这一点。但是,跑步机锻炼减轻了青少年早期应激引起的行为异常,并改善了HPA轴的功能状态,比CRER1拮抗剂CP-154、526发挥了更强大的作用。此外,这项研究表明,中央CRER1表达的改变可能在成年后PTSD的病因中起重要作用。 (C)2015 Elsevier B.V.保留所有权利。

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