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精神障碍中的可塑性失衡:精神病学的神经科学,对诊断和研究的启示

Plasticity imbalance in mental disorders the neuroscience of psychiatry: implications for diagnosis and research.

作者信息

Peled Avi

机构信息

Sha'ar Menashe Mental Health Center, Mobile Post Hefer 38814, Hadera, Israel.

出版信息

Med Hypotheses. 2005;65(5):947-52. doi: 10.1016/j.mehy.2005.05.007.

Abstract

In 1895 Freud tried to explain mental disorders using the neurophysiological knowledge of his time. He soon abandoned this attempt realizing it was immature considering the neuroscientific knowledge available to him. For the rest of his career he limited himself to psychological formulations. Along the same lines, lacking etiology for mental disorders, the diagnostic system of psychiatry is exclusively descriptive. The need for a brain related diagnosis of mental disorders is important for developing better treatments and more reliable diagnosis. Today with the development of neuroscience it is time to go back to Freud's initial attempts and explain mental disorders as altered neuronal organizations in the brain. The neural network level is chosen as the relevant description level for mental functions. Plasticity is chosen as a general concept for neuronal dynamics explaining neuropathology of psychiatric disorders. Plasticity is divided according to timescales into "fast plasticity," "slow plasticity" and "stable plasticity". It is proposed that normal mental functions require optimal balance among all the plasticity timescales. Mental disorders arise when such balance is disturbed, thus mental disorders could be reformulated as deficiencies of the different plasticity processes. Changes in coherence synchrony and phase-locking membrane potentials in cortically spread neuronal ensembles are all expressions of fast plasticity. Synaptogenic and neurogenic processes, such as brain derived neurotrophic factor-dependent processes, are defined as slow plasticity. Finally those synaptic and neuronal pathways that consolidated into long lasting circuits are referred to as stable plasticity. With the aid of a neural network model simulating the plasticity imbalance, a mathematical formulation could be realized for mental disorders. Once achieved this mathematical formulation could form a guiding framework for interpreting brain-imaging data collected from psychiatric patients. Such a model is realized using interconnected "modules" each simulating the relevant plasticity dynamics relevant for the model. Diagnosing plasticity imbalance has some advantages over current descriptive psychiatric diagnosis. It is brain-related thus less stigmatising in the sense that mental disorders are brain disorders and not "person" disorders. The diagnostic system is much more flexible allowing for a high degree of variations and combinations in the description of the disorders thus naturally accounting for comorbidities. Most importantly, this diagnostic model is brain-related offering research targets for intervention and a theoretical framework guiding such interventions.

摘要

1895年,弗洛伊德试图运用当时的神经生理学知识来解释精神障碍。但他很快就放弃了这一尝试,因为考虑到他所掌握的神经科学知识,他意识到这个尝试还不成熟。在他余下的职业生涯中,他将自己局限于心理学方面的阐述。同样,由于缺乏精神障碍的病因学,精神病学的诊断系统完全是描述性的。对精神障碍进行与大脑相关的诊断,对于开发更好的治疗方法和更可靠的诊断至关重要。如今,随着神经科学的发展,是时候回到弗洛伊德最初的尝试,将精神障碍解释为大脑中神经元组织的改变了。神经网络层面被选为精神功能的相关描述层面。可塑性被选为神经元动力学的一个通用概念,用于解释精神疾病的神经病理学。可塑性根据时间尺度分为“快速可塑性”“缓慢可塑性”和“稳定可塑性”。有人提出,正常的精神功能需要所有可塑性时间尺度之间达到最佳平衡。当这种平衡受到干扰时,精神障碍就会出现,因此精神障碍可以重新定义为不同可塑性过程的缺陷。皮层扩散神经元集合中相干同步和锁相膜电位的变化都是快速可塑性的表现。诸如脑源性神经营养因子依赖性过程等突触生成和神经生成过程被定义为缓慢可塑性。最后,那些巩固为持久回路的突触和神经元通路被称为稳定可塑性。借助一个模拟可塑性失衡的神经网络模型,可以实现对精神障碍的数学表述。一旦实现,这个数学表述可以形成一个指导框架,用于解释从精神病患者身上收集到的脑成像数据。这样一个模型是通过相互连接的“模块”实现的,每个模块都模拟与模型相关的可塑性动力学。诊断可塑性失衡比当前的描述性精神病诊断有一些优势。它与大脑相关,因此在某种意义上减少了污名化,即精神障碍是大脑疾病而非“个人”疾病。诊断系统更加灵活,在对疾病的描述中允许高度的变化和组合,从而自然地解释了共病现象。最重要的是,这个诊断模型与大脑相关,为干预提供了研究靶点,并提供了指导此类干预的理论框架。

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