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2
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The anticonvulsants lamotrigine, riluzole, and valproate differentially regulate AMPA receptor membrane localization: relationship to clinical effects in mood disorders.抗惊厥药拉莫三嗪、利鲁唑和丙戊酸盐对α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体膜定位有不同调节作用:与情绪障碍临床疗效的关系
Neuropsychopharmacology. 2007 Apr;32(4):793-802. doi: 10.1038/sj.npp.1301178. Epub 2006 Aug 16.
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A randomized trial of an N-methyl-D-aspartate antagonist in treatment-resistant major depression.一项关于N-甲基-D-天冬氨酸拮抗剂治疗难治性重度抑郁症的随机试验。
Arch Gen Psychiatry. 2006 Aug;63(8):856-64. doi: 10.1001/archpsyc.63.8.856.
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Mitoenergetic failure in Alzheimer disease.阿尔茨海默病中的线粒体能量代谢衰竭。
Am J Physiol Cell Physiol. 2007 Jan;292(1):C8-23. doi: 10.1152/ajpcell.00232.2006. Epub 2006 Jun 28.
4
Neural circuitry and neuroplasticity in mood disorders: insights for novel therapeutic targets.情绪障碍中的神经回路与神经可塑性:对新型治疗靶点的见解
NeuroRx. 2006 Jan;3(1):22-41. doi: 10.1016/j.nurx.2005.12.009.
5
Cellular plasticity cascades: targets for the development of novel therapeutics for bipolar disorder.细胞可塑性级联反应:双相情感障碍新型治疗方法开发的靶点
Biol Psychiatry. 2006 Jun 1;59(11):1006-20. doi: 10.1016/j.biopsych.2005.10.021. Epub 2006 Feb 17.
6
A role for AMPA receptors in mood disorders.AMPA受体在情绪障碍中的作用。
Biochem Pharmacol. 2006 Apr 28;71(9):1273-88. doi: 10.1016/j.bcp.2005.12.022. Epub 2006 Jan 24.
7
Glyoxalase 1 and glutathione reductase 1 regulate anxiety in mice.乙二醛酶1和谷胱甘肽还原酶1调节小鼠的焦虑情绪。
Nature. 2005 Dec 1;438(7068):662-6. doi: 10.1038/nature04250. Epub 2005 Oct 23.
8
The neurobiology of depression: inroads to treatment and new drug discovery.抑郁症的神经生物学:治疗途径与新药研发
J Clin Psychiatry. 2005;66 Suppl 7:5-13.
9
Mitochondrial dysfunction in bipolar disorder: evidence from magnetic resonance spectroscopy research.双相情感障碍中的线粒体功能障碍:来自磁共振波谱研究的证据。
Mol Psychiatry. 2005 Oct;10(10):900-19. doi: 10.1038/sj.mp.4001711.
10
Group I metabotropic glutamate receptors reduce excitotoxic injury and may facilitate neurogenesis.I 型代谢型谷氨酸受体可减轻兴奋性毒性损伤,并可能促进神经发生。
Neuropharmacology. 2005;49 Suppl 1:146-56. doi: 10.1016/j.neuropharm.2005.04.029.

针对涉及细胞可塑性级联反应的严重情绪障碍的新型治疗方法

Emerging Novel Treatments for Severe Mood Disorders Involving Cellular Plasticity Cascades.

作者信息

Machado-Vieira Rodrigo, Zarate Carlos A, Manji Husseini K

出版信息

Curr Psychos Ther Rep. 2006 Dec;4(4):181-190. doi: 10.1007/BF02629394.

DOI:10.1007/BF02629394
PMID:25620894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4304661/
Abstract

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.

摘要

情绪障碍是最常见的精神疾病。尽管在理解与情绪调节相关的治疗相关生化途径方面取得了最新进展,但双相情感障碍和重度抑郁症患者的复发率、残留症状和药物难治性仍然很高。越来越多的证据支持这样的观察结果,即情绪障碍伴随着区域性脑容量减少,并伴有细胞萎缩/丧失。在本文中,我们回顾并评论了表明神经营养信号级联可能在情绪障碍的病理生理学和治疗中起作用的数据。这表明有效的治疗需要提供营养和神经化学支持,以增强和维持正常的突触连接,从而使化学信号恢复正常情感功能所需关键回路的最佳功能。对于许多难治性患者,模仿“传统”策略、直接或间接改变单胺能水平的药物可能益处有限。可能对情绪障碍治疗有用的更新的“增强可塑性”策略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。