Department of Psychiatry, Zucker Hillside Hospital, Northwell Health, Glen Oaks, NY 10128, USA.
Department of Psychiatry and Molecular Medicine, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY 11549, USA.
Biomolecules. 2024 Jul 25;14(8):906. doi: 10.3390/biom14080906.
Schizophrenia is a frequently debilitating and complex mental disorder affecting approximately 1% of the global population, characterized by symptoms such as hallucinations, delusions, disorganized thoughts and behaviors, cognitive dysfunction, and negative symptoms. Traditional treatment has centered on postsynaptic dopamine antagonists, commonly known as antipsychotic drugs, which aim to alleviate symptoms and improve functioning and the quality of life. Despite the availability of these medications, significant challenges remain in schizophrenia therapeutics, including incomplete symptom relief, treatment resistance, and medication side effects. This opinion article explores advancements in schizophrenia treatment, emphasizing molecular mechanisms, novel drug targets, and innovative delivery methods. One promising approach is novel strategies that target neural networks and circuits rather than single neurotransmitters, acknowledging the complexity of brain region interconnections involved in schizophrenia. Another promising approach is the development of biased agonists, which selectively activate specific signaling pathways downstream of receptors, offering potential for more precise pharmacological interventions with fewer side effects. The concept of molecular polypharmacy, where a single drug targets multiple molecular pathways, is exemplified by KarXT, a novel drug combining xanomeline and trospium to address both psychosis and cognitive dysfunction. This approach represents a comprehensive strategy for schizophrenia treatment, potentially improving outcomes for patients. In conclusion, advancing the molecular understanding of schizophrenia and exploring innovative therapeutic strategies hold promise for addressing the unmet needs in schizophrenia treatment, aiming for more effective and tailored interventions. Future research should focus on these novel approaches to achieve better clinical outcomes and improve the functional level and quality of life for individuals with schizophrenia.
精神分裂症是一种常见的使人虚弱和复杂的精神障碍,影响全球约 1%的人口,其特征是出现幻觉、妄想、思维和行为紊乱、认知功能障碍和阴性症状等症状。传统的治疗方法侧重于突触后多巴胺拮抗剂,通常称为抗精神病药物,旨在缓解症状,改善功能和生活质量。尽管有这些药物可用,但精神分裂症的治疗仍然存在重大挑战,包括症状缓解不完全、治疗抵抗和药物副作用。本文探讨了精神分裂症治疗的进展,强调了分子机制、新的药物靶点和创新的给药方法。一种有前途的方法是针对神经网络和回路的新策略,而不是针对单一的神经递质,这是因为认识到涉及精神分裂症的脑区相互连接的复杂性。另一种有前途的方法是开发偏向激动剂,它选择性地激活受体下游的特定信号通路,为具有更少副作用的更精确的药理学干预提供了潜力。分子多药物疗法的概念是指一种药物针对多种分子途径,KarXT 就是一个很好的例子,它是一种将 xanomeline 和 trospium 结合在一起的新药,用于治疗精神病和认知功能障碍。这种方法代表了精神分裂症治疗的综合策略,有可能改善患者的预后。总之,深入了解精神分裂症的分子机制并探索创新的治疗策略有望满足精神分裂症治疗的未满足需求,旨在实现更有效和有针对性的干预措施。未来的研究应重点关注这些新方法,以实现更好的临床结果,并提高精神分裂症患者的功能水平和生活质量。