探索重度抑郁障碍的进展:关于氧化应激、血清素代谢、BDNF、HPA 轴功能障碍和药物疗法进展的见解

A. Correia, Nuno Vale
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摘要

重度抑郁障碍(MDD)是一种普遍存在的精神疾病,其特点是生物因素的复杂混合。本综述将重点讨论氧化应激、色氨酸-羟色胺代谢、脑源性神经营养因子(BDNF)和下丘脑-垂体-肾上腺(HPA)轴在 MDD 病理生理学中的作用。氧化应激被定义为促氧化剂和抗氧化剂之间的失衡,与 MDD 的神经生物学变化密切相关。色氨酸(TRP)-/羟色胺(5-HT)代谢途径在情绪调节中也至关重要,其失调是 MDD 的一个核心方面。此外,对神经元生长和可塑性起关键作用的 BDNF 也经常在 MDD 患者中发生改变,这支持了它在该疾病的发展过程中的作用。此外,管理应激反应的 HPA 轴也经常在 MDD 患者中受到破坏,这进一步加剧了其复杂的病理过程。除了探讨这些生物机制外,本综述还探讨了 MDD 的药物治疗,包括新的进展。这些治疗策略的进步对于有效控制 MDD 至关重要。了解这些机制和最新的药物干预对开发更有效的 MDD 治疗方法至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancements Exploring Major Depressive Disorder: Insights on Oxidative Stress, Serotonin Metabolism, BDNF, HPA Axis Dysfunction, and Pharmacotherapy Advances
Major depressive disorder (MDD), a prevalent mental illness, is marked by a complex mixture of biological factors. This review focuses on the roles of oxidative stress, tryptophan-serotonin metabolism, brain-derived neurotrophic factor (BDNF), and the hypothalamic–pituitary–adrenal (HPA) axis in MDD’s pathophysiology. Oxidative stress, defined as an imbalance between pro-oxidants and antioxidants, is closely linked to MDD’s neurobiological changes. The tryptophan (TRP)-/serotonin (5-HT) metabolic pathway is also known to be crucial in mood regulation, with its dysregulation being a central aspect of MDD. Additionally, BDNF, key for neuronal growth and plasticity, often shows alterations in MDD patients, supporting its role in the disorder’s progression. Furthermore, the HPA axis, which manages stress response, is frequently disrupted in MDD, further contributing to its complex pathology. In addition to exploring these biological mechanisms, this review also explores the pharmacotherapy of MDD, including new advances. These advancements in treatment strategies are crucial for managing MDD effectively. Understanding these mechanisms and the latest pharmacological interventions is essential for developing more effective treatments for MDD.
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