抑郁症的啮齿动物模型:重新检验没有拟人化推理的有效性。

Philip V Holmes
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引用次数: 130

摘要

这篇综述旨在激发人们思考如何在大鼠和小鼠身上建立抑郁模型的新方法。这篇文章的前提是拟人化的推论应该完全从涉及啮齿动物的研究中移除。在过去的30年里,应用动物模型来研究抑郁症在很大程度上是基于非经验的,因此是非科学的关于心理状态的假设,这些假设可能不存在,也肯定无法在啮齿动物身上测量。这样的假设可能导致对一些行为的误解,如运动活动减少或蔗糖消耗减少,作为大鼠抑郁症的症状。以前的研究也过分强调了压力在抑郁症中的因果作用。在回顾了几种常用模型的主要特征之后,本文挑战了关于有效性的传统概念。首先根据研究目标对模型进行评估。筛选潜在的抗抑郁化合物很少或根本不需要考虑模型的有效性。当试图研究抑郁症的神经生物学基础时,效度问题变得更加关键。强调了面部效度的首要重要性,各种行为测量的价值是基于它们与抑郁症患者的离散行为症状的直接相似程度来评估的。描述了一种“神经行为机制”方法。这种方法依赖于制定离散的神经生物学假设来解释个体症状,而不是解释症状的集合或整个疾病。因此,该方法依赖于操作性良好定义的行为变量的实用度量。这篇综述的结论是,理解个体症状的神经生物学基础将最终使我们更好地理解抑郁症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rodent models of depression: reexamining validity without anthropomorphic inference.

This review aims to stimulate new ways of thinking about how to model depression in rats and mice. The article is founded on the premise that anthropomorphic inferences should be removed entirely from research involving rodents. The application of animal models to study depression over the past 30 years has been based largely on nonempirical and hence nonscientific assumptions about psychological states that probably do not exist and certainly cannot be measured in rodents. Such assumptions may have led to the misinterpretation of some behaviors, such as decreased locomotor activity or decreased sucrose consumption, as symptoms of depression in rats. Previous research has also overemphasized the causal role of stress in depression. After reviewing major features of several commonly employed models, this article challenges traditional concepts about validity. Models are first evaluated based on the goals of the research. Screening for potential antidepressant compounds requires little or no consideration of the validity of the model. Issues of validity become more critical when attempting to study the neurobiological basis of depression. The primary importance of face validity is emphasized, and the value of various behavioral measures is assessed based on how directly they resemble discrete behavioral symptoms seen in depressed humans. A "neurobehaviorally mechanistic" approach is described. This approach relies on formulating discrete, neurobiological hypotheses to explain individual symptoms rather than to explain collections of symptoms or the entire disorder. The approach thus relies on pragmatic measures of operationally well-defined behavioral variables. The review concludes with the proposal that understanding the neurobiological basis for individual symptoms will ultimately yield a better understanding of depression.

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