Neurosteroids and translocator protein 18 kDa (TSPO) ligands as novel treatment options in depression.

IF 3.5 3区 医学 Q1 CLINICAL NEUROLOGY European Archives of Psychiatry and Clinical Neuroscience Pub Date : 2024-07-08 DOI:10.1007/s00406-024-01843-7
Marco Riebel, Lisa-Marie Brunner, Caroline Nothdurfter, Simon Wein, Jens Schwarzbach, Philippe Liere, Michael Schumacher, Rainer Rupprecht
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Abstract

Recently, the gamma-aminobutyric acid (GABA) system has come into focus for the treatment of anxiety, postpartum depression, and major depressive disorder. Endogenous 3α-reduced steroids such as allopregnanolone are potent positive allosteric modulators of GABAA receptors and have been known for decades. Current industry developments and first approvals by the U.S. food and drug administration (FDA) for the treatment of postpartum depression with exogenous analogues of these steroids represent a major step forward in the field. 3α-reduced steroids target both synaptic and extrasynaptic GABAA receptors, unlike benzodiazepines, which bind to synaptic receptors. The first FDA-approved 3α-reduced steroid for postpartum depression is brexanolone, an intravenous formulation of allopregnanolone. It has been shown to provide rapid relief of depressive symptoms. An orally available 3α-reduced steroid is zuranolone, which also received FDA approval in 2023 for the treatment of postpartum depression. Although a number of studies have been conducted, the efficacy data were not sufficient to achieve approval of zuranolone in major depressive disorder by the FDA in 2023. The most prominent side effects of these 3α-reduced steroids are somnolence, dizziness and headache. In addition to the issue of efficacy, it should be noted that current data limit the use of these compounds to two weeks. An alternative to exogenous 3α-reduced steroids may be the use of substances that induce endogenous neurosteroidogenesis, such as the translocator protein 18 kDa (TSPO) ligand etifoxine. TSPO has been extensively studied for its role in steroidogenesis, in addition to other functions such as anti-inflammatory and neuroregenerative properties. Currently, etifoxine is the only clinically available TSPO ligand in France for the treatment of anxiety disorders. Studies are underway to evaluate its antidepressant potential. Hopefully, neurosteroid research will lead to the development of fast-acting antidepressants.

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神经类固醇和转运蛋白 18 kDa (TSPO) 配体作为抑郁症的新型治疗方案。
最近,γ-氨基丁酸(GABA)系统成为治疗焦虑症、产后抑郁症和重度抑郁症的焦点。内源性 3α 还原型类固醇(如异孕烷酮)是 GABAA 受体的强效正性异位调节剂,几十年前就已为人所知。目前的行业发展以及美国食品药品管理局(FDA)首次批准使用这些类固醇的外源性类似物治疗产后抑郁症,标志着该领域向前迈出了一大步。3α 还原型类固醇同时针对突触和突触外的 GABAA 受体,而不像苯二氮卓类药物只与突触受体结合。美国食品和药物管理局批准的第一种治疗产后抑郁症的 3α 还原型类固醇是异丙孕酮的静脉注射制剂 brexanolone。事实证明,它能迅速缓解抑郁症状。口服 3α 还原型类固醇是唑拉诺龙,它也于 2023 年获得美国食品及药物管理局批准用于治疗产后抑郁症。虽然进行了多项研究,但疗效数据并不足以让美国食品及药物管理局在 2023 年批准唑拉诺龙用于治疗重度抑郁症。这些 3α 还原型类固醇最突出的副作用是嗜睡、头晕和头痛。除了疗效问题外,还应注意的是,目前的数据显示,这些化合物的使用期限为两周。除外源性 3α 还原型类固醇外,还可以使用诱导内源性神经类固醇生成的物质,如转运体蛋白 18 kDa(TSPO)配体 etifoxine。除了抗炎和神经再生等其他功能外,TSPO 在类固醇生成过程中的作用也得到了广泛的研究。目前,依替福辛是法国临床上唯一可用于治疗焦虑症的 TSPO 配体。评估其抗抑郁潜力的研究正在进行中。希望神经类固醇研究能够开发出速效抗抑郁药。
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来源期刊
CiteScore
8.80
自引率
4.30%
发文量
154
审稿时长
6-12 weeks
期刊介绍: The original papers published in the European Archives of Psychiatry and Clinical Neuroscience deal with all aspects of psychiatry and related clinical neuroscience. Clinical psychiatry, psychopathology, epidemiology as well as brain imaging, neuropathological, neurophysiological, neurochemical and moleculargenetic studies of psychiatric disorders are among the topics covered. Thus both the clinician and the neuroscientist are provided with a handy source of information on important scientific developments.
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