涉及细胞可塑性级联反应的严重情绪障碍的新疗法。

Rodrigo Machado-Vieira, Carlos A Zarate, Husseini K Manji
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引用次数: 0

摘要

情绪障碍是最普遍的精神障碍。尽管最近在了解与情绪调节相关的治疗相关生化途径方面取得了进展,但双相情感障碍和重度抑郁症患者仍存在高复发率、残留症状和药理学难治性。越来越多的证据支持这样的观察:情绪障碍伴随着区域性脑容量减少和细胞萎缩/丧失。在这篇文章中,我们回顾并批判了表明神经营养信号级联可能在情绪障碍的病理生理和治疗中发挥作用的数据。这表明有效的治疗需要同时提供营养和神经化学支持,这有助于增强和维持正常的突触连接,从而允许化学信号恢复正常情感功能所必需的关键回路的最佳功能。对于许多难治性患者,直接或间接改变单胺能水平的模仿“传统”策略的药物可能效果有限。较新的“可塑性增强”策略可能在治疗情绪障碍中有实用价值,包括谷氨酸释放抑制剂、NMDA拮抗剂、AMPA增强剂、cAMP磷酸二酯酶抑制剂和糖皮质激素受体拮抗剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Emerging Novel Treatments for Severe Mood Disorders Involving Cellular Plasticity Cascades.

Mood disorders are the most prevalent psychiatric disorders. Despite recent advances in the understanding of therapeutically relevant biochemical pathways associated with mood regulation, patients with bipolar disorder and major depression present high rates of recurrences, residual symptoms, and pharmacologic refractoriness. Increasing evidence supports the observations that mood disorders are accompanied by regional brain volumetric reductions accompanied by cellular atrophy/loss. In this paper, we review and critique the data suggesting that neurotrophic signaling cascades may play a role in the pathophysiology and treatment of mood disorders. This suggests that effective treatments will need to provide both trophic and neurochemical support, which serves to enhance and maintain normal synaptic connectivity, thereby allowing the chemical signal to reinstate optimal functioning of critical circuits necessary for normal affective functioning. For many refractory patients, drugs mimicking "traditional" strategies, which directly or indirectly alter monoaminergic levels, may be of limited benefit. Newer "plasticity enhancing" strategies that may have utility in the treatment of mood disorders include inhibitors of glutamate release, NMDA antagonists, AMPA potentiators, cAMP phosphodiesterase inhibitors, and glucocorticoid receptor antagonists.

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