海马体功能的改变如何促进精神病的发展?

IF 9.6 1区 医学 Q1 NEUROSCIENCES
Valentina Mancini, Farnaz Delavari, Tae-Yeon Eom, Stanislav S Zakharenko, Eric Schmitt, Stephan Eliez
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引用次数: 0

摘要

本综述探讨了海马功能障碍在精神病病理生理中的关键作用,重点关注22q11.2缺失综合征(22q11DS)的翻译见解。越来越多的证据表明,22q11DS是精神分裂症的最高遗传风险因素之一,其个体与特发性精神病具有共同的神经生物学脆弱性,其特征是认知能力下降和非典型大脑发育,特别是在海马体内。在这里,我们在不同的尺度上探索22q11DS人类和同源小鼠模型中海马功能障碍的翻译证据。在神经元水平上,缺陷包括神经迁移受损,锥体神经元树突棘密度降低,神经发生减少。这些缺陷会导致神经回路水平的改变,如谷氨酸传递改变和长期增强功能受损,从而导致记忆障碍。此外,小白蛋白阳性中间神经元(PVI)的低兴奋性破坏了海马中的伽马带振荡。在网络水平上,在22q11DS小鼠模型和人类中都观察到海马-前额叶同步减少和连通性低下。这些发现支持了一个模型,在这个模型中,神经迁移中的神经发育缺陷导致回路功能障碍,从而影响大规模的神经动力学和认知。至关重要的是,在出现精神病症状的22q11DS携带者中,海马-前额叶连通性低下以及兴奋性和抑制性神经递质之间的不平衡加剧。在22q11DS小鼠模型中,针对树突棘密度和PVI功能的研究显示了逆转神经和认知缺陷的潜力,提出了新的治疗策略。这些治疗的效果随年龄的不同而不同,这突出了确定关键发育窗口期进行干预的必要性。总之,这篇综述强调海马体是理解和治疗精神障碍的一个靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How does altered function of the hippocampus contribute to the development of psychosis?

This review explores the critical role of hippocampal dysfunction in the pathophysiology of psychosis, focusing on translational insights from 22q11.2 deletion syndrome (22q11DS). Converging evidence indicates that individuals with 22q11DS, one of the highest genetic risk factors for schizophrenia, exhibit a shared neurobiological vulnerability with idiopathic psychosis, characterized by cognitive decline and atypical brain development, particularly within the hippocampus. Here we explore translational evidence for hippocampal dysfunction in humans with 22q11DS and the homologous mouse models at different scales. At the neuronal level, deficits include impaired neural migration, reduced dendritic spine density of pyramidal neurons, and decreased neurogenesis. These deficits contribute to circuit-level alterations such as altered glutamatergic transmission and impaired long-term potentiation, leading to memory impairment. Moreover, hypoexcitability of parvalbumin-positive interneurons (PVI) disrupts gamma-band oscillations in the hippocampus. At the network level, reduced hippocampal-prefrontal synchrony and hypoconnectivity are observed in both mouse models and humans with 22q11DS. These findings support a model in which neurodevelopmental deficits in neural migration result in circuit dysfunction, which impacts large-scale neural dynamics and cognition. Crucially, hippocampal-prefrontal hypoconnectivity and imbalances between excitatory and inhibitory neurotransmitters are exacerbated in 22q11DS carriers with psychotic symptoms. Studies targeting dendritic spine density and PVI function in 22q11DS mouse models show potential for reversing neural and cognitive deficits, suggesting new therapeutic strategies. The effectiveness of these treatments varies with age, highlighting the need to identify critical developmental windows for intervention. In conclusion, this review emphasizes the hippocampus as a target for understanding and treating psychotic disorders.

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来源期刊
Biological Psychiatry
Biological Psychiatry 医学-精神病学
CiteScore
18.80
自引率
2.80%
发文量
1398
审稿时长
33 days
期刊介绍: Biological Psychiatry is an official journal of the Society of Biological Psychiatry and was established in 1969. It is the first journal in the Biological Psychiatry family, which also includes Biological Psychiatry: Cognitive Neuroscience and Neuroimaging and Biological Psychiatry: Global Open Science. The Society's main goal is to promote excellence in scientific research and education in the fields related to the nature, causes, mechanisms, and treatments of disorders pertaining to thought, emotion, and behavior. To fulfill this mission, Biological Psychiatry publishes peer-reviewed, rapid-publication articles that present new findings from original basic, translational, and clinical mechanistic research, ultimately advancing our understanding of psychiatric disorders and their treatment. The journal also encourages the submission of reviews and commentaries on current research and topics of interest.
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