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首页> 外文期刊>Journal of neurotrauma >Endoplasmic Reticulum Stress and Disrupted Neurogenesis in the Brain Are Associated with Cognitive Impairment and Depressive-Like Behavior after Spinal Cord Injury
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Endoplasmic Reticulum Stress and Disrupted Neurogenesis in the Brain Are Associated with Cognitive Impairment and Depressive-Like Behavior after Spinal Cord Injury

机译:脊髓损伤后内质网应激和大脑神经发生紊乱与认知障碍和抑郁样行为相关

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摘要

Clinical and experimental studies show that spinal cord injury (SCI) can cause cognitive impairment and depression that can significantly impact outcomes. Thus, identifying mechanisms responsible for these less well-examined, important SCI consequences may provide targets for more effective therapeutic intervention. To determine whether cognitive and depressive-like changes correlate with injury severity, we exposed mice to sham, mild, moderate, or severe SCI using the Infinite Horizon Spinal Cord Impactor and evaluated performance on a variety of neurobehavioral tests that are less dependent on locomotion. Cognitive impairment in Y-maze, novel objective recognition, and step-down fear conditioning tasks were increased in moderate-and severe-injury mice that also displayed depressive-like behavior as quantified in the sucrose preference, tail suspension, and forced swim tests. Bromo-deoxyuridine incorporation with immunohistochemistry revealed that SCI led to a long-term reduction in the number of newly-generated immature neurons in the hippocampal dentate gyrus, accompanied by evidence of greater neuronal endoplasmic reticulum (ER) stress. Stereological analysis demonstrated that moderate/severe SCI reduced neuronal survival and increased the number of activated microglia chronically in the cerebral cortex and hippocampus. The potent microglial activator cysteine-cysteine chemokine ligand 21 (CCL21) was elevated in the brain sites after SCI in association with increased microglial activation. These findings indicate that SCI causes chronic neuroinflammation that contributes to neuronal loss, impaired hippocampal neurogenesis and increased neuronal ER stress in important brain regions associated with cognitive decline and physiological depression. Accumulation of CCL21 in brain may subserve a pathophysiological role in cognitive changes and depression after SCI.
机译:临床和实验研究表明,脊髓损伤(SCI)会导致认知障碍和抑郁,从而可能严重影响预后。因此,确定引起这些未经充分检查的重要SCI后果的机制可能为更有效的治疗干预提供目标。为了确定认知和抑郁样变化是否与损伤严重程度相关,我们使用无限视野脊髓撞击器将小鼠暴露于假,轻度,中度或重度SCI,并评估了对运动的依赖性较小的各种神经行为测试的性能。在中度和重度损伤的小鼠中,Y迷宫的认知障碍,新颖的客观识别和逐步降低恐惧的调节任务增加,这些小鼠还表现出像蔗糖偏爱,尾巴悬吊和强迫游泳测试中所表现出的抑郁样行为。溴脱氧尿苷与免疫组织化学的结合显示,SCI导致海马齿状回中新生成的未成熟神经元的数量长期减少,同时伴随着更大的神经元内质网(ER)应激的证据。体视学分析表明,中度/重度SCI会长期降低大脑皮层和海马的神经元存活率,并增加活化小胶质细胞的数量。 SCI后,与小胶质细胞活化增加有关,大脑中的有效小胶质细胞活化剂半胱氨酸-半胱氨酸趋化因子配体21(CCL21)升高。这些发现表明,SCI引起慢性神经发炎,导致与认知能力下降和生理抑郁相关的重要脑区域的神经元丢失,海马神经发生受损和神经元ER应激增加。大脑中CCL21的积累可能在SCI后的认知变化和抑郁中发挥了病理生理作用。

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