Suppr超能文献

在遗传性疾病小鼠模型的行为内表型分析中考虑记忆的所有属性的重要性。

The importance of considering all attributes of memory in behavioral endophenotyping of mouse models of genetic disease.

作者信息

Hunsaker Michael R

机构信息

Department of Neurological Surgery, University of California, Davis, CA 95616, USA.

出版信息

Behav Neurosci. 2012 Jun;126(3):371-80. doi: 10.1037/a0028453.

Abstract

In order to overcome difficulties in evaluating cognitive function in mouse models of genetic disorders, it is critical to take into account the background strain of the mouse and reported phenotypes in the clinical population being studied. Recent studies have evaluated cognitive function across a number of background strains and found that spatial memory assayed by the water maze and contextual fear conditioning often does not provide optimal results. The logical extension to these results is to emphasize not only spatial, but all attributes or domains of memory function in behavioral phenotyping experiments. A careful evaluation of spatial, temporal, sensory/perceptual, affective, response, executive, proto-linguistic, and social behaviors designed to specifically evaluate the cognitive function each mouse model can be performed in a rapid, relatively high throughput manner. Such results would not only provide a more comprehensive snapshot of brain function in mouse disease models than the more common approach that approaches nonspecific spatial memory tasks to evaluate cognition, but also would better model the disorders being studied.

摘要

为了克服在遗传性疾病小鼠模型中评估认知功能的困难,考虑小鼠的背景品系以及所研究临床群体中报告的表型至关重要。最近的研究评估了多个背景品系的认知功能,发现通过水迷宫和情境恐惧条件反射测定的空间记忆通常无法提供最佳结果。这些结果的合理延伸是,在行为表型实验中不仅要强调空间记忆,还要强调记忆功能的所有属性或领域。可以以快速、相对高通量的方式对空间、时间、感觉/知觉、情感、反应、执行、原语言和社交行为进行仔细评估,以专门评估每个小鼠模型的认知功能。这样的结果不仅能比采用非特异性空间记忆任务来评估认知的更常见方法提供小鼠疾病模型中脑功能更全面的概况,还能更好地模拟所研究的疾病。

相似文献

5
Water and T-maze protocols are equally efficient methods to assess spatial memory in 3xTg Alzheimer's disease mice.
Behav Brain Res. 2017 Jul 28;331:54-66. doi: 10.1016/j.bbr.2017.05.005. Epub 2017 May 13.
6
Impaired spatial working and reference memory in segmental trisomy (Ts65Dn) mice.
Behav Brain Res. 1998 Feb;90(2):199-201. doi: 10.1016/s0166-4328(97)00116-2.
7
Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders.
Prog Neurobiol. 2012 Feb;96(2):220-41. doi: 10.1016/j.pneurobio.2011.12.001. Epub 2012 Jan 13.
8
Behavioral phenotyping of Nestin-Cre mice: implications for genetic mouse models of psychiatric disorders.
J Psychiatr Res. 2014 Aug;55:87-95. doi: 10.1016/j.jpsychires.2014.04.002. Epub 2014 Apr 12.
9
Minocycline restores spatial but not fear memory in olfactory bulbectomized rats.
Eur J Pharmacol. 2012 Dec 15;697(1-3):59-64. doi: 10.1016/j.ejphar.2012.09.005. Epub 2012 Oct 7.
10
Systems genetics identifies Hp1bp3 as a novel modulator of cognitive aging.
Neurobiol Aging. 2016 Oct;46:58-67. doi: 10.1016/j.neurobiolaging.2016.06.008. Epub 2016 Jun 17.

引用本文的文献

1
MeCP2 gene therapy ameliorates disease phenotype in mouse model for Pitt Hopkins syndrome.
Neurotherapeutics. 2024 Sep;21(5):e00376. doi: 10.1016/j.neurot.2024.e00376. Epub 2024 Jun 14.
2
Adaptation of the Arizona Cognitive Task Battery for use with the Ts65Dn mouse model (Mus musculus) of Down syndrome.
J Comp Psychol. 2017 Aug;131(3):189-206. doi: 10.1037/com0000069. Epub 2017 Mar 23.
3
mNos2 deletion and human NOS2 replacement in Alzheimer disease models.
J Neuropathol Exp Neurol. 2014 Aug;73(8):752-69. doi: 10.1097/NEN.0000000000000094.

本文引用的文献

1
Choice-specific sequences in parietal cortex during a virtual-navigation decision task.
Nature. 2012 Mar 14;484(7392):62-8. doi: 10.1038/nature10918.
2
Investigation of the neuroanatomical substrates of reward seeking following protracted abstinence in mice.
J Physiol. 2012 May 15;590(10):2427-42. doi: 10.1113/jphysiol.2011.225219. Epub 2012 Mar 5.
4
Striatal direct pathway modulates response time in execution of visual discrimination.
Eur J Neurosci. 2012 Mar;35(5):784-97. doi: 10.1111/j.1460-9568.2012.08005.x. Epub 2012 Feb 22.
6
Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders.
Prog Neurobiol. 2012 Feb;96(2):220-41. doi: 10.1016/j.pneurobio.2011.12.001. Epub 2012 Jan 13.
7
Capturing the fragile X premutation phenotypes: a collaborative effort across multiple cohorts.
Neuropsychology. 2012 Mar;26(2):156-64. doi: 10.1037/a0026799. Epub 2012 Jan 16.
8
Low sociability in BTBR T+tf/J mice is independent of partner strain.
Physiol Behav. 2012 Dec 5;107(5):649-62. doi: 10.1016/j.physbeh.2011.12.025. Epub 2012 Jan 8.
9
Female CGG knock-in mice modeling the fragile X premutation are impaired on a skilled forelimb reaching task.
Neurobiol Learn Mem. 2012 Feb;97(2):229-34. doi: 10.1016/j.nlm.2011.12.006. Epub 2011 Dec 21.
10
Neurocognitive endophenotypes of impulsivity and compulsivity: towards dimensional psychiatry.
Trends Cogn Sci. 2012 Jan;16(1):81-91. doi: 10.1016/j.tics.2011.11.009. Epub 2011 Dec 10.

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