Department of Neuroscience, Tufts University School of Medicine, 136 Harrison Ave, Boston, MA, 02111, USA.
Department of Psychiatry and Taylor Family Institute for Innovative Psychiatric Research, Washington University in St. Louis School of Medicine, 660 S. Euclid Ave., St. Louis, MO, 63110, USA.
Neuropsychopharmacology. 2024 Jan;49(1):73-82. doi: 10.1038/s41386-023-01626-z. Epub 2023 Jun 27.
Like other classes of treatments described in this issue's section, neuroactive steroids have been studied for decades but have risen as a new class of rapid-acting, durable antidepressants with a distinct mechanism of action from previous antidepressant treatments and from other compounds covered in this issue. Neuroactive steroids are natural derivatives of progesterone but are proving effective as exogenous treatments. The best understood mechanism is that of positive allosteric modulation of GABA receptors, where subunit selectivity may promote their profile of action. Mechanistically, there is some reason to think that neuroactive steroids may separate themselves from liabilities of other GABA modulators, although research is ongoing. It is also possible that intracellular targets, including inflammatory pathways, may be relevant to beneficial actions. Strengths and opportunities for further development include exploiting non-GABAergic targets, structural analogs, enzymatic production of natural steroids, precursor loading, and novel formulations. The molecular mechanisms of behavioral effects are not fully understood, but study of brain network states involved in emotional processing demonstrate a robust influence on affective states not evident with at least some other GABAergic drugs including benzodiazepines. Ongoing studies with neuroactive steroids will further elucidate the brain and behavioral effects of these compounds as well as likely underpinnings of disease.
与本期“治疗方法”章节中描述的其他治疗类别一样,神经活性甾体类物质已被研究了数十年,它们作为一种新型快速作用、持久的抗抑郁药而受到关注,其作用机制与以前的抗抑郁治疗方法以及本期涵盖的其他化合物不同。神经活性甾体类物质是孕酮的天然衍生物,但作为外源性治疗方法已被证明有效。最被理解的机制是 GABA 受体的正变构调节,其中亚基选择性可能促进其作用模式。从机制上讲,有一些理由认为神经活性甾体类物质可能与其他 GABA 调节剂的副作用分离,尽管研究仍在进行中。细胞内靶点,包括炎症途径,也可能与有益作用有关。进一步开发的优势和机会包括利用非 GABA 能靶点、结构类似物、天然甾体的酶促生产、前体加载和新型制剂。行为效应的分子机制尚未完全了解,但对涉及情绪处理的大脑网络状态的研究表明,这些化合物对情感状态有很强的影响,而至少一些其他 GABA 能药物(包括苯二氮䓬类药物)则没有明显的影响。正在进行的神经活性甾体类物质研究将进一步阐明这些化合物对大脑和行为的影响,以及可能对疾病的基础。