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JoVE Journal
Neuroscience
约束以诱导小鼠和大鼠的压力
约束以诱导小鼠和大鼠的压力
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
Restraint to Induce Stress in Mice and Rats

约束以诱导小鼠和大鼠的压力

Full Text
3,195 Views
03:48 min
December 6, 2024

DOI: 10.3791/67387-v

Karl T. Schmidt1

1Department of Psychological and Brain Sciences,Fairfield University

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This article discusses methods for inducing stress responses in rodent models, specifically using physical restraint stress in mice and rats. The research examines how stress impacts neurobiological mechanisms, particularly concerning substance use disorders, and evaluates the effects on noradrenergic systems following stress exposure.

Key Study Components

Area of Science

  • Neuroscience
  • Psychobiology
  • Animal models of stress

Background

  • Stress can significantly influence behavioral responses and neurobiological processes.
  • The link between stress and substance use disorders is an area of active research.
  • Restraint stress is a commonly used method due to its ease of use and adaptability.
  • Noradrenergic signaling alterations have been associated with heightened arousal and PTSD.

Purpose of Study

  • To investigate the behavioral effects of stress and its relation to substance use disorders.
  • To assess the physiological changes in noradrenergic systems resulting from stress exposure.
  • To provide a detailed methodology for implementing physical restraint stress in rodent models.

Methods Used

  • Rodent models, specifically mice and rats, were utilized for the stress exposure studies.
  • Physical restraint was applied using modified conical tubes to ensure ventilation.
  • The selected groups included home cage control, acute restraint stress, and chronic restraint stress.
  • Stress exposure duration was defined based on group assignments, with monitoring every 20 minutes during restraint.
  • Post-stress, animals were returned to their home cages, and physiological changes were assessed.

Main Results

  • Plasma corticosterone levels increased significantly after single stress exposure.
  • Repeated stress resulted in a reduction of corticosterone levels compared to naive controls.
  • Altered norepinephrine release was noted across various stimulation parameters following stress exposure.
  • These findings highlight the lasting impact of stress on neurochemical systems.

Conclusions

  • The study validates the use of restraint stress as a model for investigating the neurobiological impacts of stress.
  • The insights into noradrenergic alterations can inform approaches to substance use disorder interventions.
  • Overall, this research enhances understanding of the mechanistic pathways linking stress and behavioral disorders.

Frequently Asked Questions

What are the advantages of using restraint stress in research?
Restraint stress is cost-effective and easy to perform, allowing researchers to model aspects of various human disorders.
How is the restraint stress method implemented?
Mice or rats are placed in modified conical tubes with ventilation, and their physical behavior is monitored during and after the stress exposure.
What biological responses are observed following stress exposure?
Notable changes include increased corticosterone levels and altered norepinephrine release, both relevant to stress-related disorders.
How can this method be adapted for different studies?
The parameters of stress exposure—such as duration and frequency—can be modified to investigate various neurobiological outcomes.
What key limitations should be considered when using this model?
Consideration must be given to the individual variability in stress response and potential welfare issues associated with physical restraint.
What are some future research directions following this study?
Future studies may focus on the specific mechanisms underlying altered drug-induced behaviors resulting from stress exposure.

本文介绍了在小鼠和大鼠中使用物理约束应力诱导应激反应的程序。讨论了在啮齿动物模型中选择和使用约束应力时应注意的其他注意事项。

我的研究重点是影响压力影响的神经生物学机制、滥用药物的行为影响以及两者之间的交集。简而言之,我的实验室试图回答压力经历如何导致物质使用障碍,以及我们如何制定干预措施来解决这种关系。我的研究表明,压力暴露会以一种超越压力体验的方式改变去甲肾上腺素能系统。

去甲肾上腺素能信号的这些增加可能强调了 PTSD 和其他疾病特征性觉醒反应的增加。与其他压力诱发方法相比,约束成本低廉、易于执行,可用于模拟人类疾病的各个方面,包括焦虑、抑郁、物质使用障碍和创伤后应激障碍,并且可以适应广泛的参数。未来,我的实验室将专注于压力或暴露导致药物诱导行为变化的潜在机制。

首先,将小鼠随机分配到家笼对照组、急性约束压力组或慢性约束压力组。根据分配的组确定压力暴露的持续时间。接下来,修改 50 毫升锥形管,使用带有 1/8 英寸钻头的电钻打通风孔。

均匀地隔开孔,让空气流通穿过管子,确保鼠标无论位置如何都可以呼吸。在与动物住房和行为测试区域分开的测试室中,将分配的鼠标放入修改后的锥形管中。牢固地系上盖子,将动物限制在指定的约束期内。

然后,将约束管水平放置在平坦的表面上。如有必要,用实验室胶带或移液器盆固定试管,以防止其滚动。每 20 分钟监测一次被束缚的动物是否有异常行为。

暴露压力后,将鼠标放回家笼。将大鼠随机分配到家笼对照组、急性约束压力组或慢性约束压力组。对于市售的约束管,将大鼠插入设备中,调整塞子以紧贴受试者的体型,然后将其锁定到位。

确保老鼠得到适当的限制,以防止头对尾转动,同时允许正常呼吸。在与动物住房和行为测试分开的测试室中,将分配的大鼠放入指定的约束长度的约束管中。将每根管子水平放置在平坦的表面上。

应激后,将大鼠放回笼子里,自由获取食物和水。单次应激暴露后血浆皮质酮浓度显著高于初始对照组,但在反复应激小鼠中这种升高降低。反复应激暴露在各种光遗传学刺激参数中显着增加了去甲肾上腺素的释放。

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神经科学 第 214 期 生理变化 遗传学 神经生物学 免疫学 转基因小鼠 血浆皮质酮 去甲肾上腺素释放 急性应激 慢性应激 动物受试者 应变 性别 年龄

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