Kamath Srinivas, Sokolenko Elysia, Collins Kate, Chan Nicole S L, Mills Natalie, Clark Scott R, Marques Francine Z, Joyce Paul
UniSA Clinical & Health Sciences, University of South Australia, Adelaide, South Australia 5000, Australia.
Discipline of Anatomy and Pathology, School of Biomedicine, University of Adelaide, Adelaide, South Australia 5005, Australia.
Pharmacol Res. 2025 Jan;211:107561. doi: 10.1016/j.phrs.2024.107561. Epub 2024 Dec 26.
Gut microbial dysbiosis or altered gut microbial consortium, in schizophrenia suggests a pathogenic role through the gut-brain axis, influencing neuroinflammatory and neurotransmitter pathways critical to psychotic, affective, and cognitive symptoms. Paradoxically, conventional psychotropic interventions may exacerbate this dysbiosis, with antipsychotics, particularly olanzapine, demonstrating profound effects on microbial architecture through disruption of bacterial phyla ratios, diminished taxonomic diversity, and attenuated short-chain fatty acid synthesis. To address these challenges, novel therapeutic strategies targeting the gut microbiome, encompassing probiotic supplementation, prebiotic compounds, faecal microbiota transplantation, and rationalised co-pharmacotherapy, show promise in attenuating antipsychotic-induced metabolic disruptions while enhancing therapeutic efficacy. Harnessing such insights, precision medicine approaches promise to transform antipsychotic prescribing practices by identifying patients at risk of metabolic side effects based on their microbial profiles. This IUPHAR review collates the current literature landscape of the gut-brain axis and its intricate relationship with schizophrenia while advocating for integrating microbiome assessments and therapeutic management. Such a fundamental shift in proposing microbiome-informed psychotropic prescriptions to optimise therapeutic efficacy and reduce adverse metabolic impacts would align antipsychotic treatments with microbiome safety, prioritising 'gut-neutral' or gut-favourable drugs to safeguard long-term patient outcomes in schizophrenia therapy.
精神分裂症患者的肠道微生物失调或肠道微生物群落改变表明,其通过肠-脑轴发挥致病作用,影响对精神病性、情感和认知症状至关重要的神经炎症和神经递质途径。矛盾的是,传统的精神药物干预可能会加剧这种失调,抗精神病药物,尤其是奥氮平,通过破坏细菌门类比例、减少分类多样性和减弱短链脂肪酸合成,对微生物结构产生深远影响。为应对这些挑战,针对肠道微生物群的新型治疗策略,包括补充益生菌、使用益生元化合物、进行粪便微生物群移植和合理联合药物治疗,有望减轻抗精神病药物引起的代谢紊乱,同时提高治疗效果。利用这些见解,精准医学方法有望通过根据患者的微生物特征识别有代谢副作用风险的患者,从而改变抗精神病药物的处方实践。这篇IUPHAR综述整理了肠-脑轴的当前文献概况及其与精神分裂症的复杂关系,同时倡导整合微生物群评估和治疗管理。在提出基于微生物群的精神药物处方以优化治疗效果并减少不良代谢影响方面的这一根本转变,将使抗精神病治疗与微生物群安全性保持一致,优先选择“肠道中性”或有利于肠道的药物,以保障精神分裂症治疗中患者的长期预后。