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Synaptic plasticity and depression: New insights from stress and rapid-acting antidepressants

机译:突触可塑性和抑郁:来自压力和速效抗抑郁药的新见解

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摘要

Depression is a common, devastating illness. Current pharmacotherapies help many patients, but there are high rates of partial- or non-response and the delayed onset of the effects of antidepressant leave many patients inadequately treated. However, new insights into the neurobiology of stress and human mood disorders have shed light on mechanisms underlying the vulnerability of individuals to depression and have pointed to novel antidepressants. Environmental events and other risk factors contribute to depression through converging molecular and cellular mechanisms that disrupt neuronal function and morphology, resulting in dysfunction of the circuitry essential for mood regulation and cognitive function. Although current antidepressants such as serotonin reuptake inhibitors produce subtle changes that take effect in weeks or months, new agents have recently shown improvement in mood ratings within hours of dosing in patients resistant to typical antidepressants. These new agents have also been shown to reverse the synaptic deficits caused by stress within a similar time scale.
机译:抑郁症是一种常见的破坏性疾病。当前的药物疗法对许多患者有帮助,但是部分或无反应的发生率很高,抗抑郁药作用的延迟发作使许多患者没有得到充分的治疗。然而,对压力和人类情绪障碍的神经生物学的新见解揭示了个体易患抑郁症的潜在机制,并指出了新型抗抑郁药。环境事件和其他危险因素通过会破坏神经元功能和形态的分子和细胞融合机制而导致抑郁,导致情绪调节和认知功能必不可少的电路功能障碍。尽管目前的抗抑郁药(例如5-羟色胺再摄取抑制剂)会产生细微的变化,这些变化会在数周或数月内生效,但新药已显示出在对典型抗抑郁药耐药的患者给药后数小时内的情绪等级有所改善。这些新的药物还被证明可以在相似的时间范围内逆转由压力引起的突触缺陷。

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