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首页> 外文期刊>Cellular and Molecular Neurobiology >Sodium Phenylbutyrate and Edaravone Abrogate Chronic Restraint Stress-Induced Behavioral Deficits: Implication of Oxido-Nitrosative, Endoplasmic Reticulum Stress Cascade, and Neuroinflammation
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Sodium Phenylbutyrate and Edaravone Abrogate Chronic Restraint Stress-Induced Behavioral Deficits: Implication of Oxido-Nitrosative, Endoplasmic Reticulum Stress Cascade, and Neuroinflammation

机译:苯基丁酯和赤纬慢性抑制应激诱导的行为缺陷:氧化亚硝化,内质网应激级联和神经素炎症的含义

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摘要

Chronic stress exposure can produce deleterious effects on the hippocampus (HC) which eventually leads to cognitive impairment and depression. Endoplasmic reticulum (ER) stress has been reported as one of the major culprits in the development of stress-induced cognitive impairment and depression. We investigated the neuroprotective efficacy of sodium phenylbutyrate (SPB), an ER stress inhibitor, and edaravone, a free radical scavenger, against chronic restraint stress (CRS)-induced cognitive deficits and anxiety- and depressive-like behavior in mice. Adult male Swiss albino mice were restrained for 6 h/day for 28 days and injected (i.p.) with SPB (40 and 120 mg/kg) or edaravone (3 and 10 mg/kg) for the last seven days. After stress cessation, the anxiety- and depressive-like behavior along with spatial learning and memory were examined. Furthermore, oxido-nitrosative stress, proinflammatory cytokines, and gene expression level of ER stress-related genes were assessed in HC and prefrontal cortex (PFC). CRS-exposed mice showed anxiety- and depressive-like behavior, which was significantly improved by SPB and edaravone treatment. In addition, SPB and edaravone treatment significantly alleviated CRS-induced spatial learning and memory impairment. Furthermore, CRS-evoked oxido-nitrosative stress, neuroinflammation, and depletion of Brain-derived neurotrophic factor were significantly ameliorated by SPB and edaravone treatment. We found significant up-regulation of ER stress-related genes in both HC and PFC regions, which were suppressed by SPB and edaravone treatment in CRS mice. Our study provides evidence that SPB and edaravone exerted neuroprotective effects on CRS-induced cognitive deficits and anxiety- and depressive-like behavior, which is possibly coupled with inhibition of oxido-nitrosative stress, neuroinflammation, and ER stress cascade.
机译:慢性应激暴露会对最终导致认知障碍和抑郁症的海马(HC)产生有害影响。内质网(ER)压力被报告为强调诱发的认知障碍和抑郁症的主要罪魁祸首之一。我们研究了苯基丁酸钠(SPB),ER应激抑制剂和埃及龙酮,自由基清除剂的神经保护效果,反对慢性约束应激(CRS) - 诱导小鼠中的认知缺陷和焦虑和抑郁的行为。将成年雄性瑞士白化小鼠约束为6小时/天28天,并在过去的七天内用SPB(40和120mg / kg)或埃达伐(3和10mg / kg)注射(I.P.)。在应力停止后,检查了焦虑和抑郁的行为以及空间学习和记忆。此外,在HC和前额叶皮质(PFC)中评估ER应激相关基因的氧化 - 亚硝酸盐应激,促炎细胞因子和基因表达水平。 CRS暴露的小鼠表现出焦虑和抑郁的行为,通过SPB和赤纬治疗显着改善。此外,SPB和赤纬治疗显着缓解了CRS引起的空间学习和记忆障碍。此外,通过SPB和埃达拉夫酮治疗,CRS诱发的氧化氧化胁迫,神经炎炎症和脑衍生的神经营养因子的消耗显着改善。我们发现HC和PFC区域中的ER应激相关基因的显着上调,这些基因在CRS小鼠中被SPB和Edaravone治疗抑制。我们的研究提供了证据表明,SPB和Edaravone对CRS引起的认知缺陷和焦虑和抑郁样行为施加了神经保护作用,这可能与氧化氮磷胁迫,神经炎炎症和ER应激级联的抑制相结合。

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