Yoon Soojung, Iqbal Hamid, Kim Sun Mi, Jin Mirim
Department of Health Sciences and Technology, GAIHST, Gachon University, Incheon 21999, Republic of Korea.
Department of Microbiology, College of Medicine, Gachon University, Incheon 21999, Republic of Korea.
Biomol Ther (Seoul). 2023 Mar 1;31(2):148-160. doi: 10.4062/biomolther.2022.116. Epub 2023 Jan 25.
Depression is a neuropsychiatric disorder associated with persistent stress and disruption of neuronal function. Persistent stress causes neuronal atrophy, including loss of synapses and reduced size of the hippocampus and prefrontal cortex. These alterations are associated with neural dysfunction, including mood disturbances, cognitive impairment, and behavioral changes. Synaptic plasticity is the fundamental function of neural networks in response to various stimuli and acts by reorganizing neuronal structure, function, and connections from the molecular to the behavioral level. In this review, we describe the alterations in synaptic plasticity as underlying pathological mechanisms for depression in animal models and humans. We further elaborate on the significance of phytochemicals as bioactive agents that can positively modulate stress-induced, aberrant synaptic activity. Bioactive agents, including flavonoids, terpenes, saponins, and lignans, have been reported to upregulate brain-derived neurotrophic factor expression and release, suppress neuronal loss, and activate the relevant signaling pathways, including TrkB, ERK, Akt, and mTOR pathways, resulting in increased spine maturation and synaptic numbers in the neuronal cells and in the brains of stressed animals. In clinical trials, phytochemical usage is regarded as safe and well-tolerated for suppressing stress-related parameters in patients with depression. Thus, intake of phytochemicals with safe and active effects on synaptic plasticity may be a strategy for preventing neuronal damage and alleviating depression in a stressful life.
抑郁症是一种与持续应激和神经元功能紊乱相关的神经精神疾病。持续应激会导致神经元萎缩,包括突触丧失以及海马体和前额叶皮质体积减小。这些改变与神经功能障碍有关,包括情绪障碍、认知损害和行为变化。突触可塑性是神经网络对各种刺激作出反应的基本功能,它通过在分子水平到行为水平上重组神经元结构、功能和连接来发挥作用。在本综述中,我们描述了突触可塑性的改变作为动物模型和人类抑郁症潜在病理机制的情况。我们进一步阐述了植物化学物质作为生物活性剂的重要性,这些生物活性剂可以积极调节应激诱导的异常突触活动。据报道,包括黄酮类化合物、萜类化合物、皂苷和木脂素在内的生物活性剂可上调脑源性神经营养因子的表达和释放,抑制神经元损失,并激活相关信号通路,包括TrkB、ERK、Akt和mTOR通路,从而导致应激动物的神经元细胞和大脑中树突棘成熟和突触数量增加。在临床试验中,植物化学物质的使用被认为对抑制抑郁症患者的应激相关参数是安全且耐受性良好的。因此,摄入对突触可塑性具有安全且积极作用的植物化学物质可能是在压力生活中预防神经元损伤和缓解抑郁症的一种策略。