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窜动行为:一种为区分和可重复性而设计的小鼠运动行为定量模式。

Darting behavior: a quantitative movement pattern designed for discrimination and replicability in mouse locomotor behavior.

作者信息

Kafkafi Neri, Pagis Michal, Lipkind Dina, Mayo Cheryl L, Bemjamini Yoav, Golani Ilan, Elmer Gregory I

机构信息

National Institute on Drug Abuse, National Institutes of Health, 5500 Nathan Shock Drive, The Johns Hopkins Bayview Medical Center, Bldg. C, Baltimore, MD 21224, USA.

出版信息

Behav Brain Res. 2003 Jun 16;142(1-2):193-205. doi: 10.1016/s0166-4328(03)00003-2.

Abstract

In the open-field behavior of rodents, Software for Exploring Exploration (SEE) can be used for an explicit design of behavioral endpoints with high genotype discrimination and replicability across laboratories. This ability is demonstrated here in the development of a measure for darting behavior. The behavior of two common mouse inbred strains, C57BL/6J (B6) and DBA/2J (D2), was analyzed across three different laboratories, and under the effect of cocaine or amphetamine. "Darting" was defined as having higher acceleration during progression segments while moving less during stops. D2 mice darted significantly more than B6 mice in each laboratory, despite being significantly less active. These differences were maintained following cocaine administration (up to 20mg/kg) and only slightly altered by amphetamine (up to 5mg/kg) despite a several fold increase in activity. The replicability of darting behavior was confirmed in additional experiments distinct from those used for its design. The strategy leading to the darting measure may be used to develop additional discriminative and replicable endpoints of open-field behavior.

摘要

在啮齿动物的旷场行为中,探索性探索软件(SEE)可用于明确设计行为终点,具有高基因型辨别能力且能在不同实验室间重复。本文通过开发一种衡量窜动行为的方法来展示这种能力。对两种常见的近交系小鼠C57BL/6J(B6)和DBA/2J(D2)在三个不同实验室中、在可卡因或苯丙胺作用下的行为进行了分析。“窜动”被定义为在前进阶段具有更高的加速度,而在停顿期间移动较少。在每个实验室中,D2小鼠的窜动都明显多于B6小鼠,尽管其活动明显较少。给予可卡因(高达20mg/kg)后,这些差异依然存在,并且尽管活动增加了几倍,但在给予苯丙胺(高达5mg/kg)后差异仅略有改变。窜动行为的可重复性在与其设计所使用的实验不同的其他实验中得到了证实。导致窜动测量的策略可用于开发旷场行为的其他具有辨别力和可重复性的终点。

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