Riebel Marco, Brunner Lisa-Marie, Nothdurfter Caroline, Wein Simon, Schwarzbach Jens, Liere Philippe, Schumacher Michael, Rupprecht Rainer
Department of Psychiatry and Psychotherapy, University Regensburg, Universitätsstrasse 84, 93053, Regensburg, Germany.
U1195 Inserm and University Paris-Saclay, Le Kremlin-Bicêtre, Paris, 94276, France.
Eur Arch Psychiatry Clin Neurosci. 2024 Jul 8. doi: 10.1007/s00406-024-01843-7.
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 GABA 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 GABA 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.
最近,γ-氨基丁酸(GABA)系统已成为治疗焦虑症、产后抑郁症和重度抑郁症的焦点。内源性3α-还原甾体,如别孕烯醇酮,是GABA受体的强效正变构调节剂,这一情况已为人所知数十年。目前该行业的发展以及美国食品药品监督管理局(FDA)首次批准使用这些甾体的外源性类似物治疗产后抑郁症,代表了该领域的一大进步。与结合突触受体的苯二氮䓬类药物不同,3α-还原甾体靶向突触和突触外GABA受体。FDA批准的首个用于治疗产后抑郁症的3α-还原甾体是布雷沙诺龙,它是别孕烯醇酮的静脉制剂。已证明它能迅速缓解抑郁症状。一种口服可用的3α-还原甾体是祖拉诺龙,它也于2023年获得FDA批准用于治疗产后抑郁症。尽管已经进行了多项研究,但疗效数据不足以使祖拉诺龙在2023年获得FDA对重度抑郁症的批准。这些3α-还原甾体最突出的副作用是嗜睡、头晕和头痛。除了疗效问题外,还应注意目前的数据将这些化合物的使用限制在两周内。外源性3α-还原甾体的一种替代方法可能是使用诱导内源性神经甾体生成的物质,如转位蛋白18 kDa(TSPO)配体依替福辛。除了其他功能,如抗炎和神经再生特性外,TSPO在甾体生成中的作用也得到了广泛研究。目前,依替福辛是法国唯一可用于治疗焦虑症的临床可用TSPO配体。正在进行研究以评估其抗抑郁潜力。有望神经甾体研究将带来速效抗抑郁药的开发。