Karuna Therapeutics, Boston, Massachusetts; Department of Psychiatry and Neurology, Washington University of St. Louis, St. Louis, Missouri.
Karuna Therapeutics, Boston, Massachusetts.
Biol Psychiatry. 2024 Oct 15;96(8):627-637. doi: 10.1016/j.biopsych.2024.03.014. Epub 2024 Mar 25.
Achieving optimal treatment outcomes for individuals living with schizophrenia remains challenging, despite 70 years of drug development efforts. Many chemically distinct antipsychotics have been developed over the past 7 decades with improved safety and tolerability but with only slight variation in efficacy. All antipsychotics currently approved for the treatment of schizophrenia act as antagonists or partial agonists at the dopamine D receptor. With only a few possible exceptions, antipsychotic drugs have similar and modest efficacy for treating positive symptoms and are relatively ineffective in addressing the negative and cognitive symptoms of the disease. The development of novel treatments focused on targeting muscarinic acetylcholine receptors (mAChRs) has been of interest for more than 25 years following reports that treatment with a dual M/M-preferring mAChR agonist resulted in antipsychotic-like effects and procognitive properties in individuals living with Alzheimer's disease and schizophrenia; more recent clinical trials have confirmed these findings. In addition, advances in our understanding of the receptor binding and activation properties of xanomeline at specific mAChRs have the potential to inform future drug design targeting mAChRs.
尽管在过去 70 年里药物研发取得了进展,但要实现精神分裂症患者的最佳治疗效果仍然具有挑战性。在过去的 70 年里,已经开发出了许多化学性质不同的抗精神病药物,它们在安全性和耐受性方面有所改善,但疗效只有轻微的变化。目前批准用于治疗精神分裂症的所有抗精神病药物都是多巴胺 D 受体的拮抗剂或部分激动剂。除了少数可能的例外,抗精神病药物在治疗阳性症状方面具有相似且适度的疗效,而在解决疾病的阴性和认知症状方面相对无效。在报告称双重 M/M 偏好型毒蕈碱乙酰胆碱受体 (mAChR) 激动剂治疗可导致阿尔茨海默病和精神分裂症患者出现抗精神病样效应和认知促进作用后,针对毒蕈碱乙酰胆碱受体 (mAChR) 的新型治疗方法的开发已引起关注超过 25 年;最近的临床试验证实了这些发现。此外,我们对 xanomeline 在特定 mAChR 上的受体结合和激活特性的理解的进步有可能为未来针对 mAChR 的药物设计提供信息。