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首页> 外文期刊>Brain research >Hypothalamic-pituitary-adrenal axis responsivity to an acute novel stress in female rats subjected to the chronic mild stress paradigm
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Hypothalamic-pituitary-adrenal axis responsivity to an acute novel stress in female rats subjected to the chronic mild stress paradigm

机译:丘脑 - 垂体 - 肾上腺轴对慢性轻度胁迫范例进行慢性轻度胁迫范例的雌性大鼠急性新胁迫的反应性

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摘要

The chronic mild stress (CMS) paradigm is the most frequently investigated animal model for major depression. The hypothalamic-pituitary-adrenal (HPA) axis participates in the generation of depressive symptomatology. We examined whether the depression-like state induced by CMS is associated with immediate changes in HPA axis activation in response to a novel acute stress and whether this response could be modified by hormonal status. Adult female Wistar rats were ovariectomized and received estrogen or vehicle pellets. After 2 weeks, rats were subjected to CMS (or control) conditions for 2.5 or 4.5 weeks. Rats were subsequently subjected to restraint stress for 1 h, and plasma corticosterone (CT) levels were determined before (2:00 p.m.) and after acute stress induction (3:00 and 4:00 p.m.). CT levels and FOS expression were measured in the medial parvocellular subdivision of the PVN (PaMP), central (CeA) and medial amygdala (MeA) and ventral subiculum of the hippocampus (vSub). Plasma CT levels in animals treated with 6.5 weeks of estrogen were elevated before and 1 h after restraint stress induction. Results indicate that the estrogen chronicity and CMS exposure impacted CT secretion. Neuronal PaMP, CeA, MeA and vSub activity decreased after 4.5 weeks of CMS in all groups. No differences were detected between CMS and non-CMS groups. These data suggest that the HPA central hyporesponsiveness observed in the experimental groups subjected to a longer protocol period was independent to CMS paradigm and estrogen treatment restored partially its activity. These data suggest that additional stressors could be responsible for the observed alterations of the HPA axis.
机译:慢性轻度压力​​(CMS)范式是主要抑郁症最常见的动物模型。下丘脑 - 垂体 - 肾上腺(HPA)轴参与抑郁症状的产生。我们检查了CMS诱导的抑郁状状态是否与HPA轴激活的立即变化相关,响应于新型急性应力,以及是否可以通过激素状态修改该响应。成年女性Wistar大鼠是卵巢切除和接受雌激素或载体颗粒。 2周后,对大鼠进行CMS(或对照)条件2.5或4.5周。随后对大鼠进行约束应激1小时,并且在(下午2:00)和急性应激诱导(下午4:00)之后测定血浆皮质酮(CT)水平。在PVN(PAMP),中央(CEA)和中介杏仁肽(MEA)和海马(VSUB)的腹侧腹部的内侧细胞细胞细胞细胞细胞细胞细胞细胞下测量CT水平和FOS表达。用6.5周雌激素治疗的动物中的血浆CT水平在约束应激诱导后升高至1小时。结果表明,雌激素慢性和CMS暴露受到CT分泌。在所有组中CMS 4.5周后,神经元PAMP,CEA,MEA和VSUB活性降低。 CMS和非CMS组之间没有检测到差异。这些数据表明,在经过较长的协议期间观察到的HPA中央低反向性是独立于CMS范例和雌激素治疗的部分恢复活性。这些数据表明,额外的压力源可能负责HPA轴的改变。

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