Crofton Elizabeth J, Zhang Yafang, Green Thomas A
Center for Addiction Research, Mitchell Center for Neurodegenerative Diseases, Department of Pharmacology and Toxicology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Center for Addiction Research, Mitchell Center for Neurodegenerative Diseases, Department of Pharmacology and Toxicology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555, United States.
Neurosci Biobehav Rev. 2015 Feb;49:19-31. doi: 10.1016/j.neubiorev.2014.11.017. Epub 2014 Nov 29.
One hallmark of psychiatric conditions is the vast continuum of individual differences in susceptibility vs. resilience resulting from the interaction of genetic and environmental factors. The environmental enrichment paradigm is an animal model that is useful for studying a range of psychiatric conditions, including protective phenotypes in addiction and depression models. The major question is how environmental enrichment, a non-drug and non-surgical manipulation, can produce such robust individual differences in such a wide range of behaviors. This paper draws from a variety of published sources to outline a coherent hypothesis of inoculation stress as a factor producing the protective enrichment phenotypes. The basic tenet suggests that chronic mild stress from living in a complex environment and interacting non-aggressively with conspecifics can inoculate enriched rats against subsequent stressors and/or drugs of abuse. This paper reviews the enrichment phenotypes, mulls the fundamental nature of environmental enrichment vs. isolation, discusses the most appropriate control for environmental enrichment, and challenges the idea that cortisol/corticosterone equals stress. The intent of the inoculation stress hypothesis of environmental enrichment is to provide a scaffold with which to build testable hypotheses for the elucidation of the molecular mechanisms underlying these protective phenotypes and thus provide new therapeutic targets to treat psychiatric/neurological conditions.
精神疾病的一个显著特征是,由于遗传和环境因素的相互作用,个体在易感性与恢复力方面存在巨大的连续差异。环境丰富化范式是一种动物模型,有助于研究一系列精神疾病,包括成瘾和抑郁模型中的保护性表型。主要问题在于,环境丰富化这种非药物、非手术的操作,如何能在如此广泛的行为中产生如此显著的个体差异。本文综合各种已发表的资料,概述了接种应激作为产生保护性丰富化表型的一个因素的连贯假说。其基本原理表明,生活在复杂环境中并与同种个体进行非攻击性互动所产生的慢性轻度应激,可以使处于丰富环境中的大鼠对随后的应激源和/或滥用药物产生抵抗力。本文回顾了丰富化表型,思考了环境丰富化与隔离的本质,讨论了环境丰富化最合适的对照,并对皮质醇/皮质酮等同于应激这一观点提出了质疑。环境丰富化的接种应激假说的目的是提供一个框架,用以构建可检验的假说,以阐明这些保护性表型背后的分子机制,从而为治疗精神/神经疾病提供新的治疗靶点。