Suppr超能文献

基于活动的厌食症用于模拟小鼠的易感性和恢复力。

Activity-based Anorexia for Modeling Vulnerability and Resilience in Mice.

作者信息

Beeler Jeff A, Burghardt Nesha S

机构信息

Department of Psychology, Queens College, CUNY, Flushing, NY, USA.

Psychology Program, The Graduate Center, CUNY, New York, NY, USA.

出版信息

Bio Protoc. 2021 May 5;11(9):e4009. doi: 10.21769/BioProtoc.4009.

Abstract

Activity-based anorexia (ABA) is a widely used rodent model of anorexia nervosa. It involves combining limited access to food with unlimited access to a running wheel, leading to a paradoxical decrease in food intake, hyperactivity, and life-threatening weight loss. Although initially characterized in rats, ABA has been tested in mice with results that vary based on strain, sex, age, the amount of time food is available, and the number of days of food restriction. Here, we present our ABA protocol for modeling both vulnerability and resilience to diet and exercise in C57BL/6 female mice. While vulnerable mice exhibit the expected increase in running, reduction in food intake, and excessive weight loss, resilient mice exhibit an adaptive increase in food intake, decrease in total wheel running, and weight stabilization. In contrast to previous ABA studies in which resilience is defined by the relative rate of weight loss, our protocol leads to a resilient phenotype that more closely resembles the maintenance of a stable bodyweight exhibited by most humans who diet and exercise without developing anorexia nervosa. This protocol will be useful for future studies aimed at identifying the physiological and neural adaptations underlying both resilience and vulnerability to this eating disorder.

摘要

基于活动的厌食症(ABA)是一种广泛使用的神经性厌食症啮齿动物模型。它包括将有限的食物获取与无限的跑步轮使用相结合,导致食物摄入量出现反常减少、多动以及危及生命的体重减轻。尽管ABA最初是在大鼠中得到描述,但它已在小鼠中进行了测试,结果因品系、性别、年龄、食物供应时间以及食物限制天数的不同而有所差异。在此,我们展示我们用于模拟C57BL/6雌性小鼠对饮食和运动的易感性及恢复力的ABA方案。易感性小鼠表现出预期的跑步增加、食物摄入量减少以及过度体重减轻,而恢复力小鼠则表现出食物摄入量的适应性增加、总跑步轮使用量减少以及体重稳定。与以往将恢复力定义为体重减轻相对速率的ABA研究不同,我们的方案产生的恢复力表型更类似于大多数节食和运动但未患神经性厌食症的人所表现出的稳定体重维持情况。该方案将有助于未来旨在确定这种饮食失调的恢复力和易感性背后的生理和神经适应性的研究。

相似文献

1
Activity-based Anorexia for Modeling Vulnerability and Resilience in Mice.
Bio Protoc. 2021 May 5;11(9):e4009. doi: 10.21769/BioProtoc.4009.
3
Vulnerable and Resilient Phenotypes in a Mouse Model of Anorexia Nervosa.
Biol Psychiatry. 2021 Dec 15;90(12):829-842. doi: 10.1016/j.biopsych.2020.06.030. Epub 2020 Jul 16.
7
Adolescent female C57BL/6 mice with vulnerability to activity-based anorexia exhibit weak inhibitory input onto hippocampal CA1 pyramidal cells.
Neuroscience. 2013 Jun 25;241:250-67. doi: 10.1016/j.neuroscience.2013.03.020. Epub 2013 Mar 21.
9
Sex differences in response to activity-based anorexia model in C57Bl/6 mice.
Physiol Behav. 2017 Mar 1;170:1-5. doi: 10.1016/j.physbeh.2016.12.014. Epub 2016 Dec 12.

引用本文的文献

3
Development of activity-based anorexia requires PKC-δ neurons in two central extended amygdala nuclei.
Cell Rep. 2024 Mar 26;43(3):113933. doi: 10.1016/j.celrep.2024.113933. Epub 2024 Mar 8.
4
Establishment of a Murine Chronic Anorexia Nervosa Model.
Cells. 2023 Jun 24;12(13):1710. doi: 10.3390/cells12131710.
6
Pathway-specific GABAergic inhibition contributes to the gain of resilience against anorexia-like behavior of adolescent female mice.
Front Behav Neurosci. 2022 Oct 13;16:990354. doi: 10.3389/fnbeh.2022.990354. eCollection 2022.
7
Development of an Open Face Home Cage Running Wheel for Testing Activity-Based Anorexia and Other Applications.
eNeuro. 2022 Oct 28;9(5). doi: 10.1523/ENEURO.0246-22.2022. Print 2022 Sep-Oct.
8
A Novel Microcontroller-Based System for the Wheel-Running Activity in Mice.
eNeuro. 2021 Nov 22;8(6). doi: 10.1523/ENEURO.0260-21.2021. Print 2021 Nov-Dec.

本文引用的文献

1
Vulnerable and Resilient Phenotypes in a Mouse Model of Anorexia Nervosa.
Biol Psychiatry. 2021 Dec 15;90(12):829-842. doi: 10.1016/j.biopsych.2020.06.030. Epub 2020 Jul 16.
2
Identifying novel phenotypes of vulnerability and resistance to activity-based anorexia in adolescent female rats.
Int J Eat Disord. 2013 Nov;46(7):737-46. doi: 10.1002/eat.22149. Epub 2013 Jul 13.
3
Adolescent female C57BL/6 mice with vulnerability to activity-based anorexia exhibit weak inhibitory input onto hippocampal CA1 pyramidal cells.
Neuroscience. 2013 Jun 25;241:250-67. doi: 10.1016/j.neuroscience.2013.03.020. Epub 2013 Mar 21.
4
Olanzapine, but not fluoxetine, treatment increases survival in activity-based anorexia in mice.
Neuropsychopharmacology. 2012 Jun;37(7):1620-31. doi: 10.1038/npp.2012.7. Epub 2012 Mar 7.
5
The activity-based anorexia mouse model.
Methods Mol Biol. 2012;829:377-93. doi: 10.1007/978-1-61779-458-2_25.
6
7
Difference in susceptibility to activity-based anorexia in two inbred strains of mice.
Eur Neuropsychopharmacol. 2007 Feb;17(3):199-205. doi: 10.1016/j.euroneuro.2006.04.007. Epub 2006 Jun 2.
8
Development of, and recovery from, activity-based anorexia in female rats.
Physiol Behav. 2003 Nov;80(2-3):273-9. doi: 10.1016/j.physbeh.2003.08.008.
9
Activity as a function of a restricted feeding schedule.
J Comp Physiol Psychol. 1954 Oct;47(5):362-3. doi: 10.1037/h0060276.
10
Elevation of activity level in the rat following transition from ad libitum to restricted feeding.
J Comp Physiol Psychol. 1953 Dec;46(6):429-33. doi: 10.1037/h0062565.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验