• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Lsamp 缺陷型小鼠的焦虑降低和攻击行为减少。

Lower anxiety and a decrease in agonistic behaviour in Lsamp-deficient mice.

机构信息

Department of Physiology, University of Tartu, Tartu, Estonia.

出版信息

Behav Brain Res. 2011 Feb 2;217(1):21-31. doi: 10.1016/j.bbr.2010.09.019. Epub 2010 Oct 1.

DOI:10.1016/j.bbr.2010.09.019
PMID:20888367
Abstract

In rodents, the Lsamp gene has been implicated in trait anxiety, fear reaction and fear conditioning. Human data link the LSAMP gene to several psychiatric disorders. In this study, we presented a general phenotypic characterization of Lsamp gene-deficient mouse line, created by deleting exon 1b. These mice displayed no gross sensory-motor deficiencies, no overt abnormalities and performed normally in memory and learning tests. However, they responded with increased activity to new environments. Moreover, they displayed reduced anxiety and notable deviations in social behaviour, such as lack of whisker trimming, reduced aggressiveness and reduced dominance. One possible explanation for the anxiolytic-like effect of the deletion of the Lsamp gene is a shift in balance in the Gabra1 and Gabra2 genes in the temporal lobe in favor of the Gabra2 transcript, encoding α2 subunit of GABA(A) receptors that mediate the stimulating effect of GABA agonists. The overall phenotype of Lsamp-deficient mice, characterized by decreased anxiety and several alterations in social behaviour, makes them a good model for studying the molecular mechanisms behind inadequate social behaviours observed in several psychiatric disorders.

摘要

在啮齿动物中,Lsamp 基因与特质焦虑、恐惧反应和恐惧条件作用有关。人类数据将 LSAMP 基因与几种精神疾病联系起来。在这项研究中,我们展示了一种由删除外显子 1b 而创建的 Lsamp 基因缺失小鼠系的一般表型特征。这些小鼠没有明显的感觉运动缺陷,没有明显的异常,并且在记忆和学习测试中表现正常。然而,它们对新环境的反应活动增加。此外,它们表现出焦虑减轻和明显的社交行为偏差,例如缺乏胡须修剪、攻击性降低和支配地位降低。Lsamp 基因缺失的抗焦虑样效应的一个可能解释是,颞叶中 Gabra1 和 Gabra2 基因的平衡向 Gabra2 转录本转移,该转录本编码 GABA(A)受体的 α2 亚基,GABA 激动剂的刺激作用通过该受体介导。Lsamp 缺陷小鼠的整体表型,表现为焦虑减轻和几种社交行为改变,使它们成为研究几种精神疾病中观察到的社交行为不足的分子机制的良好模型。

相似文献

1
Lower anxiety and a decrease in agonistic behaviour in Lsamp-deficient mice.Lsamp 缺陷型小鼠的焦虑降低和攻击行为减少。
Behav Brain Res. 2011 Feb 2;217(1):21-31. doi: 10.1016/j.bbr.2010.09.019. Epub 2010 Oct 1.
2
Deletion of the Lsamp gene lowers sensitivity to stressful environmental manipulations in mice.Lsamp 基因缺失降低了小鼠对应激性环境处理的敏感性。
Behav Brain Res. 2012 Mar 1;228(1):74-81. doi: 10.1016/j.bbr.2011.11.033. Epub 2011 Dec 2.
3
Relation between increased anxiety and reduced expression of alpha1 and alpha2 subunits of GABA(A) receptors in Wfs1-deficient mice.Wfs1基因缺陷小鼠中焦虑增加与GABA(A)受体α1和α2亚基表达降低之间的关系。
Neurosci Lett. 2009 Aug 28;460(2):138-42. doi: 10.1016/j.neulet.2009.05.054. Epub 2009 May 27.
4
Lsamp⁻/⁻ mice display lower sensitivity to amphetamine and have elevated 5-HT turnover.Lsamp⁻/⁻ 小鼠对安非他命的敏感性较低,5-HT 周转率升高。
Biochem Biophys Res Commun. 2013 Jan 4;430(1):413-8. doi: 10.1016/j.bbrc.2012.11.077. Epub 2012 Dec 1.
5
Increased sensitivity to psychostimulants and GABAergic drugs in Lsamp-deficient mice.Lsamp 缺陷型小鼠对精神兴奋剂和 GABA 能药物的敏感性增加。
Pharmacol Biochem Behav. 2019 Aug;183:87-97. doi: 10.1016/j.pbb.2019.05.010. Epub 2019 Jun 1.
6
Prodynorphin gene deletion increased anxiety-like behaviours, impaired the anxiolytic effect of bromazepam and altered GABAA receptor subunits gene expression in the amygdala.促肾上腺皮质激素原基因缺失可增加焦虑样行为,削弱溴替唑仑的抗焦虑作用,并改变杏仁核中 GABAA 受体亚基基因的表达。
J Psychopharmacol. 2011 Jan;25(1):87-96. doi: 10.1177/0269881110367724. Epub 2010 Jun 8.
7
Deficit in emotional learning in neurotrimin knockout mice.神经调节素基因敲除小鼠的情绪学习缺陷。
Behav Brain Res. 2017 Jan 15;317:311-318. doi: 10.1016/j.bbr.2016.09.064. Epub 2016 Sep 28.
8
Enhanced anxiety, depressive-like behaviour and impaired recognition memory in mice with reduced expression of the vesicular glutamate transporter 1 (VGLUT1).囊泡谷氨酸转运体1(VGLUT1)表达降低的小鼠出现焦虑增强、类抑郁行为及识别记忆受损。
Eur J Neurosci. 2007 Jan;25(1):281-90. doi: 10.1111/j.1460-9568.2006.05259.x.
9
Wfs1-deficient mice display impaired behavioural adaptation in stressful environment.Wfs1基因缺陷小鼠在应激环境中表现出行为适应受损。
Behav Brain Res. 2009 Mar 17;198(2):334-45. doi: 10.1016/j.bbr.2008.11.007. Epub 2008 Nov 11.
10
GABAergic dysfunction in mGlu7 receptor-deficient mice as reflected by decreased levels of glutamic acid decarboxylase 65 and 67kDa and increased reelin proteins in the hippocampus.代谢型谷氨酸受体7(mGlu7)缺陷小鼠中的γ-氨基丁酸(GABA)能功能障碍,表现为海马中谷氨酸脱羧酶65和67kDa水平降低以及Reelin蛋白增加。
Brain Res. 2010 Jun 2;1334:12-24. doi: 10.1016/j.brainres.2010.03.078. Epub 2010 Mar 29.

引用本文的文献

1
The IgLON family of cell adhesion molecules expressed in developing neural circuits ensure the proper functioning of the sensory system in mice.在发育中的神经回路中表达的 IgLON 细胞粘附分子家族确保了小鼠感觉系统的正常功能。
Sci Rep. 2024 Sep 30;14(1):22593. doi: 10.1038/s41598-024-73358-z.
2
Phenotypic Insights Into Anti-IgLON5 Disease in IgLON5-Deficient Mice.IgLON5基因缺陷小鼠抗IgLON5病的表型研究
Neurol Neuroimmunol Neuroinflamm. 2024 May;11(3):e200234. doi: 10.1212/NXI.0000000000200234. Epub 2024 Apr 24.
3
The Role of IgLON Cell Adhesion Molecules in Neurodegenerative Diseases.
IgLON 细胞黏附分子在神经退行性疾病中的作用。
Genes (Basel). 2023 Sep 28;14(10):1886. doi: 10.3390/genes14101886.
4
Depression-Associated Gene-Deficiency Induces Alterations in the Monoaminergic Neurotransmission Enhancing Time-Dependent Sensitization to Amphetamine in Male Mice.抑郁症相关基因缺陷导致单胺能神经传递改变,增强雄性小鼠对苯丙胺的时间依赖性敏感。
Brain Sci. 2022 Dec 10;12(12):1696. doi: 10.3390/brainsci12121696.
5
Behavioral Phenotyping of Bbs6 and Bbs8 Knockout Mice Reveals Major Alterations in Communication and Anxiety.Bbs6 和 Bbs8 基因敲除小鼠的行为表型分析揭示了其在交流和焦虑方面的主要改变。
Int J Mol Sci. 2022 Nov 22;23(23):14506. doi: 10.3390/ijms232314506.
6
Spatiotemporal expression of IgLON family members in the developing mouse nervous system.IgLON 家族成员在发育中鼠神经系统中的时空表达。
Sci Rep. 2021 Oct 1;11(1):19536. doi: 10.1038/s41598-021-97768-5.
7
Alternative Promoter Use Governs the Expression of IgLON Cell Adhesion Molecules in Histogenetic Fields of the Embryonic Mouse Brain.替代启动子控制着 IgLON 细胞黏附分子在胚胎鼠脑组织发生场中的表达。
Int J Mol Sci. 2021 Jun 28;22(13):6955. doi: 10.3390/ijms22136955.
8
Depression-Associated Gene Pathway Is Altered by Antidepressant Treatment.抗抑郁治疗改变与抑郁相关的基因通路。
Cells. 2020 Jul 31;9(8):1818. doi: 10.3390/cells9081818.
9
Concurrent and Delayed Behavioral and Monoamine Alterations by Excessive Sucrose Intake in Juvenile Mice.幼年小鼠过量摄入蔗糖后行为和单胺的同时及延迟改变
Front Neurosci. 2020 May 19;14:504. doi: 10.3389/fnins.2020.00504. eCollection 2020.
10
Neural cell adhesion molecule Negr1 deficiency in mouse results in structural brain endophenotypes and behavioral deviations related to psychiatric disorders.小鼠神经细胞黏附分子 Negr1 缺失导致与精神障碍相关的结构性大脑表型和行为偏差。
Sci Rep. 2019 Apr 1;9(1):5457. doi: 10.1038/s41598-019-41991-8.