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脑源性神经营养因子在抑郁症发病机制中的作用:对药物治疗的启示。

Role of brain-derived neurotrophic factor in the aetiology of depression: implications for pharmacological treatment.

机构信息

Sigrid Jusélius Laboratory, Neuroscience Center, University of Helsinki, Helsinki, Finland.

出版信息

CNS Drugs. 2010 Jan;24(1):1-7. doi: 10.2165/11530010-000000000-00000.

Abstract

Brain-derived neurotrophic factor (BDNF) is a critical mediator of activity-dependent neuronal plasticity in the cerebral cortex. Deficits in neurotrophic factors have been proposed to underlie mood disorders. However, recent evidence suggests that mood disorders may be produced by abnormalities in the adaptation of neural networks to environmental conditions. Antidepressants may act by enhancing neuronal plasticity, which allows environmental inputs to modify the neuronal networks to better fine tune the individual to the outside world. Recent observations in the visual cortex directly support this idea. According to the network hypothesis of depression, changes in the levels of neurotrophins including BDNF may not directly produce depression or an antidepressant effect, but neurotrophins may act as critical tools in the process whereby environmental conditions guide neuronal networks to better adapt to the environment. This hypothesis suggests that antidepressant drugs should not be used alone but should always be combined with rehabilitation to guide the plastic networks within the brain.

摘要

脑源性神经营养因子(BDNF)是大脑皮层中活性依赖的神经元可塑性的关键介质。神经营养因子的缺乏被认为是导致情绪障碍的基础。然而,最近的证据表明,情绪障碍可能是由于神经网络对环境条件的适应异常而产生的。抗抑郁药可能通过增强神经元可塑性起作用,从而使环境输入能够改变神经元网络,使个体更好地适应外部世界。最近在视觉皮层中的观察结果直接支持了这一观点。根据抑郁症的网络假说,包括 BDNF 在内的神经营养因子水平的变化可能不会直接导致抑郁或抗抑郁作用,但神经营养因子可能是环境条件引导神经元网络更好地适应环境的过程中的关键工具。该假说表明,抗抑郁药物不应单独使用,而应始终与康复相结合,以引导大脑内的可塑性网络。

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