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首页> 外文期刊>Neuroimmunomodulation >Delayed effects of brain irradiation - part 1: adrenocortical axis dysfunction and hippocampal damage in an adult rat model.
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Delayed effects of brain irradiation - part 1: adrenocortical axis dysfunction and hippocampal damage in an adult rat model.

机译:脑照射的延迟作用-第1部分:成年大鼠模型中的肾上腺皮质轴功能障碍和海马损伤。

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摘要

Background: Brain irradiation (BI) in humans may cause behavioral changes, cognitive impairment and neuroendocrine dysfunction. The effect of BI on the hypothalamic-pituitary-adrenal (HPA) axis is not fully understood. Objectives: To evaluate the effect of BI on HPA axis responses under basal and stressful conditions as well as following pretreatment with dexamethasone (Dex). Methods: Adult male rats were exposed to whole BI. HPA axis responses were examined at 2, 4, 9 and 20 weeks after BI. Histological evaluations of the irradiated rats and matched controls were conducted at 4 and 20 weeks after BI. Results: In contrast to the control group, the basal and stress-induced corticosterone levels were enhanced at 9 and 20 weeks after BI and the inhibitory effect of Dex was reduced. BI also caused hyposuppression of the adrenocortical response to stress. Histological assessment of the irradiated brains revealed hippocampal atrophy at 20 weeks after BI. The neuronal counts were lower only in the CA1 region of the irradiated brains. BI caused a decrease in the binding capacity of Dex to the hippocampal cytosolic fraction. Conclusions: Enhanced stress-induced HPA axis responses and the reduced effect of Dex suggest that BI has delayed effects on HPA axis responses as manifested by impairment of the negative feedback exerted by glucocorticoids (GCs). The mechanisms underlying these effects of BI are unknown. It is possible that the marked BI-induced damage in the hippocampus, which plays an important role in the regulation of the feedback effect of GCs, may cause abnormal HPA axis responses following BI.
机译:背景:人类的脑部辐射(BI)可能会导致行为改变,认知障碍和神经内分泌功能障碍。 BI对下丘脑-垂体-肾上腺(HPA)轴的影响尚不完全清楚。目的:评估基础和压力条件下以及地塞米松(Dex)预处理后BI对HPA轴反应的影响。方法:成年雄性大鼠暴露于整个BI。在BI后第2、4、9和20周检查HPA轴反应。在BI后4周和20周对受辐照的大鼠和相匹配的对照进行组织学评估。结果:与对照组相比,BI后9周和20周,基础和应激诱导的皮质酮水平升高,而Dex的抑制作用降低。 BI还引起对压力的肾上腺皮质反应的抑制。放疗后20周,对受辐照的大脑进行的组织学评估显示海马萎缩。仅在受辐照的大脑的CA1区神经元计数较低。 BI导致Dex与海马胞质部分的结合能力降低。结论:应激诱导的HPA轴反应增强,而Dex的作用降低,表明BI对HPA轴反应的延迟作用表现为糖皮质激素(GCs)产生的负反馈受损。 BI的这些作用的潜在机制尚不清楚。可能由BI引起的海马中显着的BI诱导的损伤在调节GC的反馈作用中起重要作用,可能会导致BI后出现异常的HPA轴反应。

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