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与精神分裂症前驱期相关的动物模型

Animal Models of Relevance to the Schizophrenia Prodrome.

作者信息

Petty Alice, Howes Oliver, Eyles Darryl

机构信息

Neuroscience Research Australia, Sydney, New South Wales, Australia.

Queensland Brain Institute, University of Queensland, Brisbane, Queensland, Australia.

出版信息

Biol Psychiatry Glob Open Sci. 2021 Dec 9;3(1):22-32. doi: 10.1016/j.bpsgos.2021.12.001. eCollection 2023 Jan.

Abstract

Patients with schizophrenia often undergo a prodromal phase prior to diagnosis. Given the absence of significant therapeutic improvements, attention has recently shifted to the possibility of intervention during this early stage to delay or diminish symptom severity or even prevent onset. Unfortunately, the 20 or so trials of intervention to date have not been successful in either preventing onset or improving long-term outcomes in subjects who are at risk of developing schizophrenia. One reason may be that the biological pathways an effective intervention must target are not static. The prodromal phase typically occurs during late adolescence, a period during which a number of brain circuits and structures are still maturing. We propose that developing a deeper understanding of which circuits/processes and brain structures are still maturing at this time and which processes drive the transition to schizophrenia will take us a step closer to developing better prophylactic interventions. Fortunately, such knowledge is now emerging from clinical studies, complemented by work in animal models. Our task here is to describe what would constitute an appropriate animal model to study and to potentially intervene in such processes. Such a model would allow invasive analysis of the cellular and molecular substrates of the progressive neurobiology that defines the schizophrenia prodrome and hopefully offer valuable insights into potential prophylactic targets.

摘要

精神分裂症患者在确诊前通常会经历前驱期。鉴于目前尚无显著的治疗进展,最近人们的注意力已转向在此早期阶段进行干预的可能性,以期延缓或减轻症状严重程度,甚至预防疾病发作。不幸的是,迄今为止约20项干预试验在预防处于精神分裂症发病风险的受试者发病或改善其长期预后方面均未取得成功。一个原因可能是有效干预必须针对的生物学途径并非一成不变。前驱期通常发生在青春期后期,在此期间许多脑回路和脑结构仍在发育成熟。我们认为,更深入地了解此时哪些回路/过程和脑结构仍在发育成熟,以及哪些过程驱动向精神分裂症的转变,将使我们在开发更好的预防性干预措施方面更进一步。幸运的是,此类知识目前正从临床研究中涌现,并得到动物模型研究的补充。我们在此的任务是描述什么样的动物模型适合用于研究并可能干预此类过程。这样的模型将允许对定义精神分裂症前驱期的进行性神经生物学的细胞和分子基础进行侵入性分析,并有望为潜在的预防靶点提供有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9a6/9874082/928b972d7aae/gr1.jpg

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