首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Prophylactic Ketamine Treatment Promotes Resilience to Chronic Stress and Accelerates Recovery: Correlation with Changes in Synaptic Plasticity in the CA3 Subregion of the Hippocampus
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Prophylactic Ketamine Treatment Promotes Resilience to Chronic Stress and Accelerates Recovery: Correlation with Changes in Synaptic Plasticity in the CA3 Subregion of the Hippocampus

机译:预防性氯胺酮治疗可增强对慢性应激的抵抗力并加速恢复:与海马CA3区域突触可塑性变化相关

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摘要

Ketamine is an N-methyl-d-aspartate receptor antagonist that has gained wide attention as a potent antidepressant. It has also been recently reported to have prophylactic effects in animal models of depression and anxiety. Alterations of neuroplasticity in different brain regions; such as the hippocampus; prefrontal cortex; and amygdala; are a hallmark of stress-related disorders; and such changes may endure beyond the treatment of symptoms. The present study investigated whether a prophylactic injection of ketamine has effects on structural plasticity in the brain in mice that are subjected to chronic unpredictable stress followed by an 8-day recovery period. Ketamine administration (3 mg/kg body weight) 1 h before stress exposure increased the number of resilient animals immediately after the cessation of stress exposure and positively influenced the recovery of susceptible animals to hedonic deficits. At the end of the recovery period; ketamine-treated animals exhibited significant differences in dendritic spine density and dendritic spine morphology in brain regions associated with depression compared with saline-treated animals. These results confirm previous findings of the prophylactic effects of ketamine and provide further evidence of an association between the antidepressant-like effect of ketamine and alterations of structural plasticity in the brain
机译:氯胺酮是一种N-甲基-d-天冬氨酸受体拮抗剂,作为有效的抗抑郁药已引起广泛关注。最近还据报道在抑郁症和焦虑症的动物模型中具有预防作用。不同大脑区域神经可塑性的改变;如海马;前额叶皮层和杏仁核;是与压力有关的疾病的标志;并且这种变化可能会超出症状的治疗范围。本研究调查了预防性注射氯胺酮是否会对遭受长期不可预知的应激并随后为期8天的恢复期的小鼠的大脑结构可塑性产生影响。应激暴露前1小时服用氯胺酮(3 mg / kg体重),可在应激暴露停止后立即增加有弹性的动物的数量,并积极影响易患动物享乐缺陷的恢复。恢复期结束时;与盐水治疗的动物相比,氯胺酮治疗的动物在与抑郁症相关的大脑区域的树突棘密度和树突棘形态上表现出显着差异。这些结果证实了氯胺酮预防作用的先前发现,并为氯胺酮的抗抑郁样作用与大脑结构可塑性改变之间的联系提供了进一步的证据。

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