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起始与适应:一种理解精神药物作用的范式

Initiation and adaptation: a paradigm for understanding psychotropic drug action.

作者信息

Hyman S E, Nestler E J

机构信息

Department of Psychiatry, Massachusetts General Hospital, Charlestown 02129, USA.

出版信息

Am J Psychiatry. 1996 Feb;153(2):151-62. doi: 10.1176/ajp.153.2.151.

Abstract

OBJECTIVE

This article describes a paradigm--initiation and adaptation--within which to conceptualize the drug-induced neural plasticity that underlies the long-term actions of psychotropic drugs in the brain.

METHOD

Recent advances in neurobiology are reviewed.

RESULTS

Recent developments in cellular and molecular neurobiology provide new conceptual and experimental tools for understanding the mechanisms by which psychotropic drugs produce long-lived alterations in brain function. Because of the availability of more robust animal models, the mechanisms by which drugs of abuse produce dependence are better understood than the mechanisms by which antidepressants, antipsychotics, and lithium produce their therapeutic effects. Nonetheless, the fundamental types of mechanisms appear to be similar: chronic drug administration drives the production of adaptations in postreceptor signaling pathways, including regulation of neural gene expression. Whether the results are deleterious or therapeutic depends on the precise neural systems targeted by a particular drug.

CONCLUSIONS

Biological investigation in psychiatry has often focused too narrowly on synaptic pharmacology, especially on neurotransmitter turnover and neurotransmitter receptors. This review focuses on molecular and cellular changes in neural function that are produced as adaptations to chronic administration of addictive drugs such as psychostimulants and therapeutic drugs such as antidepressants. To understand normal brain function, psychopathology, and the actions of psychiatric treatments, and to exploit the eventual findings of psychiatric genetics, psychiatric research must now extend its efforts beyond the synapse, to an understanding of cellular and molecular neurobiology (in particular, postreceptor signal transduction) as well as to a better understanding of the architecture and function of neural systems. A paradigm is presented to help understand the long-term effects of psychotropic drugs, including the latency in onset of their therapeutic actions.

摘要

目的

本文描述了一种范式——起始与适应,用于在其中将药物诱导的神经可塑性概念化,这种可塑性是精神药物在大脑中长期作用的基础。

方法

回顾神经生物学的最新进展。

结果

细胞和分子神经生物学的最新发展为理解精神药物在大脑中产生长期功能改变的机制提供了新的概念和实验工具。由于有了更强大的动物模型,滥用药物产生依赖的机制比抗抑郁药、抗精神病药和锂产生治疗作用的机制得到了更好的理解。尽管如此,基本的机制类型似乎是相似的:长期给药会促使受体后信号通路产生适应性变化,包括神经基因表达的调控。结果是有害还是具有治疗作用取决于特定药物所靶向的精确神经系统。

结论

精神病学中的生物学研究常常过于狭隘地聚焦于突触药理学,尤其是神经递质周转和神经递质受体。本综述聚焦于因长期服用成瘾性药物(如精神兴奋剂)和治疗性药物(如抗抑郁药)而产生的神经功能分子和细胞变化。为了理解正常脑功能、精神病理学以及精神科治疗的作用,并利用精神科遗传学的最终研究结果,精神科研究现在必须将其努力从突触扩展到对细胞和分子神经生物学(特别是受体后信号转导)的理解,以及对神经系统结构和功能的更好理解。本文提出了一种范式,以帮助理解精神药物的长期作用,包括其治疗作用起效的潜伏期。

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