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首页> 外文期刊>Brain, Behavior, and Immunity >Stress exacerbates neuron loss and microglia proliferation in a rat model of excitotoxic lower motor neuron injury
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Stress exacerbates neuron loss and microglia proliferation in a rat model of excitotoxic lower motor neuron injury

机译:压力加剧了神经元损失和微胶质细胞增殖在兴奋性毒性毒素下电动元损伤的大鼠模型中

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摘要

All individuals experience stress and hormones (e.g., glucocorticoids/GCs) released during stressful events can affect the structure and function of neurons. These effects of stress are best characterized for brain neurons; however, the mechanisms controlling the expression and binding affinity of glucocorticoid receptors in the spinal cord are different than those in the brain. Accordingly, whether stress exerts unique effects on spinal cord neurons, especially in the context of pathology, is unknown. Using a controlled model of focal excitotoxic lower motor neuron injury in rats, we examined the effects of acute or chronic variable stress on spinal cord motor neuron survival and glial activation. New data indicate that stress exacerbates excitotoxic spinal cord motor neuron loss and associated activation of microglia. In contrast, hypertrophy and hyperplasia of astrocytes and NG2+ glia were unaffected or were modestly suppressed by stress. Although excitotoxic lesions cause significant motor neuron loss and stress exacerbates this pathology, overt functional impairment did not develop in the relevant forelimb up to one week post-lesion. These data indicate that stress is a disease-modifying factor capable of altering neuron and glial responses to pathological challenges in the spinal cord. (C) 2015 Elsevier Inc. All rights reserved.
机译:所有人在压力事件中释放的所有个人体验压力和激素(例如,糖皮质激素/ GCS)可以影响神经元的结构和功能。这些应力的影响最佳地表征脑神经元;然而,控制糖皮质激素受体在脊髓中的表达和结合亲和力的机制不同于大脑中的机制。因此,压力是否对脊髓神经元的独特作用,特别是在病理学的背景下,是未知的。使用大鼠局灶性吞噬毒性下电机神经元损伤的受控模型,我们研究了急性或慢性可变胁迫对脊髓运动神经元生存和胶质激活的影响。新数据表明,压力加剧了兴奋毒性脊髓电机神经元损失和相关的微胶质细胞活化。相反,星形胶质细胞和NG2 +胶质胶质细胞的肥大和增生不受影响或受到压力的温和抑制。虽然兴奋毒性病变引起显着的运动神经元损失和压力加剧了这种病理学,但明显的功能障碍在相关的预防损失后未发生在病变后一周。这些数据表明,应力是能够改变神经元和脊髓病理挑战的神经元和胶质响应的疾病改性因素。 (c)2015 Elsevier Inc.保留所有权利。

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