IUPHAR review – Novel therapeutic targets for schizophrenia treatment: A translational perspective

IF 10.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmacological research Pub Date : 2025-04-01 Epub Date: 2025-03-10 DOI:10.1016/j.phrs.2025.107690
Veronica Begni , Alessia Marchesin , Marco Andrea Riva
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Abstract

Schizophrenia is a severe and debilitating psychiatric disorder that profoundly impacts cognitive, emotional, and social functioning. Despite its devastating personal and societal toll, current treatments often provide only partial relief, underscoring the urgent need for innovative therapeutic strategies. This review explores emerging approaches that target the complex neurobiological underpinnings of schizophrenia, moving beyond traditional dopamine-centric models. Among these, some novel drugs still employ multimodal mechanisms, simultaneously targeting dopaminergic and serotonergic systems to enhance efficacy and tolerability. Given the well-documented excitatory/inhibitory imbalance in schizophrenia, significant efforts have been directed toward addressing NMDA receptor hypofunctionality. However, strategies targeting this pathway have yet to demonstrate consistent clinical efficacy. In contrast, therapies targeting the cholinergic system have shown greater promise. For instance, the xanomeline-trospium combination, which modulates muscarinic receptors, has recently gained approval, and other molecules with similar mechanisms are currently under development. Beyond these approaches, novel strategies are being explored to target innovative pathways, including neuroplasticity, neuroinflammation, and mitochondrial dysfunction. These efforts are often designed as part of a combinatorial strategy to enhance the efficacy of currently available antipsychotic drugs. Despite significant progress, challenges remain in translating experimental discoveries into effective clinical applications. Future research should prioritize biomarker-driven approaches and precision medicine to optimize individualized treatment outcomes. By integrating these emerging therapeutic targets, schizophrenia treatment may evolve toward a more comprehensive and personalized approach, addressing the disorder’s full spectrum of symptoms and improving patient quality of life.
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IUPHAR综述:精神分裂症治疗的新靶点:翻译的视角
精神分裂症是一种严重的精神疾病,严重影响认知、情感和社会功能。尽管它对个人和社会造成了毁灭性的损失,但目前的治疗方法往往只能提供部分缓解,因此迫切需要创新的治疗策略。这篇综述探讨了针对精神分裂症复杂神经生物学基础的新兴方法,超越了传统的以多巴胺为中心的模型。其中,一些新药仍采用多模式机制,同时靶向多巴胺能和血清素能系统,以提高疗效和耐受性。鉴于精神分裂症中充分记录的兴奋性/抑制性失衡,已针对解决NMDA受体功能低下作出了重大努力。然而,针对这一途径的策略尚未显示出一致的临床疗效。相比之下,针对胆碱能系统的治疗显示出更大的希望。例如,调节毒蕈碱受体的xanomeline-trospium组合最近获得了批准,其他具有类似机制的分子目前正在开发中。除了这些方法,新的策略正在探索针对创新途径,包括神经可塑性,神经炎症和线粒体功能障碍。这些努力通常被设计为组合策略的一部分,以提高目前可用的抗精神病药物的疗效。尽管取得了重大进展,但在将实验发现转化为有效的临床应用方面仍然存在挑战。未来的研究应优先考虑生物标志物驱动的方法和精准医学,以优化个体化治疗结果。通过整合这些新兴的治疗靶点,精神分裂症的治疗可能会朝着更全面和个性化的方向发展,解决这种疾病的所有症状,提高患者的生活质量。
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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来源期刊
Pharmacological research
Pharmacological research 医学-药学
CiteScore
18.70
自引率
3.20%
发文量
491
审稿时长
8 days
期刊介绍: Pharmacological Research publishes cutting-edge articles in biomedical sciences to cover a broad range of topics that move the pharmacological field forward. Pharmacological research publishes articles on molecular, biochemical, translational, and clinical research (including clinical trials); it is proud of its rapid publication of accepted papers that comprises a dedicated, fast acceptance and publication track for high profile articles.
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