Emerging trends in antipsychotic and antidepressant drug development: Targeting nonmonoamine receptors and innovative mechanisms

Hitoshi Osaka, Tetsufumi Kanazawa
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Abstract

The domain of psychiatric drug development is currently witnessing a notable transformation, with a paramount emphasis on targeting nonmonoamine receptors and exploring inventive mechanisms of action. This paper presents an overview of the ongoing advancements in antipsychotic and antidepressant drug development. Historically, antipsychotics predominantly targeted dopamine receptors, but there is now an escalating interest in drugs that act on alternative receptors, exemplified by the TAAR1 receptor. One noteworthy candidate is Ulotaront (SEP‐363856), an agent acting as a TAAR1 agonist with 5‐HT1A agonist activity, demonstrating promising outcomes in the treatment of schizophrenia, devoid of extrapyramidal symptoms or metabolic side‐effects. Similarly, MIN‐101 (Roluperidone) and KarXT are currently in development, with its focus on addressing the symptoms in schizophrenia. In the domain of antidepressants, novel therapeutic approaches have surfaced, such as Auvelity, a Food and Drug Administration (FDA)‐approved NMDA receptor antagonist synergistically combined with Bupropion to enhance its effects. Another notable candidate is Zuranolone, operating as a GABA A receptor‐positive allosteric modulator, showcasing efficacy in treating major depressive disorder (MDD) and postpartum depression. Additionally, TAK‐653 (NBI‐1065845) and MJI821 (Onfasprodil) have emerged as potential antidepressants targeting AMPA receptors and NMDA receptor 2B (NR2B) negative allosteric modulation, respectively. This paper underscores the transformative potential of these novel drug candidates in psychiatric treatment and their ability to address cases that were previously treatment‐resistant. By focusing on nonmonoamine receptors and introducing innovative mechanisms, these drugs offer a promising prospect of improved outcomes for individuals suffering from schizophrenia and MDD. Thus, sustained attention and dedication to the development of such drugs are essential to augmenting the therapeutic options available for psychiatric patients.
抗精神病和抗抑郁药物开发的新趋势:瞄准非单胺受体和创新机制
精神科药物研发领域目前正经历着一场引人注目的变革,重点是以非单胺受体为靶点和探索创造性的作用机制。本文概述了抗精神病药物和抗抑郁药物研发领域正在取得的进展。一直以来,抗精神病药物主要以多巴胺受体为靶点,但现在人们对作用于替代受体(如 TAAR1 受体)的药物越来越感兴趣。Ulotaront (SEP-363856)就是一个值得关注的候选药物,它是一种具有 5-HT1A 激动剂活性的 TAAR1 激动剂,在治疗精神分裂症方面取得了良好的疗效,而且没有锥体外系症状或代谢副作用。同样,MIN-101(Roluperidone)和 KarXT 目前也在开发之中,主要用于治疗精神分裂症的症状。在抗抑郁药领域,新的治疗方法也已浮出水面,如 Auvelity,这是一种经美国食品药品管理局(FDA)批准的 NMDA 受体拮抗剂,与安非他酮协同作用可增强疗效。另一个值得关注的候选药物是Zuranolone,它是一种GABA A受体阳性异位调节剂,在治疗重度抑郁障碍(MDD)和产后抑郁症方面具有显著疗效。此外,TAK-653(NBI-1065845)和MJI821(Onfasprodil)也已成为潜在的抗抑郁药物,它们分别以AMPA受体和NMDA受体2B(NR2B)负异位调节为靶点。本文强调了这些候选新药在精神病治疗中的变革潜力,以及它们解决以往治疗耐药病例的能力。通过关注非单胺受体并引入创新机制,这些药物有望改善精神分裂症和多发性硬化症患者的治疗效果。因此,持续关注并致力于这类药物的开发对于增加精神病患者的治疗选择至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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