• 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

雄性和雌性基因敲除小鼠的行为、神经递质和转录组分析。

Behavioral, neurotransmitter and transcriptomic analyses in male and female KO mice.

作者信息

McCarthy Deirdre M, Vied Cynthia, Trupiano Mia X, Canekeratne Angeli J, Wang Yuan, Schatschneider Christopher, Bhide Pradeep G

机构信息

Department of Biomedical Sciences, Florida State University College of Medicine, Tallahassee, FL, United States.

Center for Brain Repair, Florida State University College of Medicine, Tallahassee, FL, United States.

出版信息

Front Behav Neurosci. 2024 Sep 6;18:1458502. doi: 10.3389/fnbeh.2024.1458502. eCollection 2024.

DOI:10.3389/fnbeh.2024.1458502
PMID:39308631
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11412825/
Abstract

INTRODUCTION

Fragile X syndrome is an inherited X-linked disorder associated with intellectual disabilities that begin in childhood and last a lifetime. The symptoms overlap with autism spectrum disorder, and the syndrome predominantly affects males. Consequently, FXS research tends to favor analysis of social behaviors in males, leaving a gap in our understanding of other behavioral traits, especially in females.

METHODS

We used a mouse model of FXS to analyze developmental, behavioral, neurochemical, and transcriptomic profiles in males and females.

RESULTS

Our behavioral assays demonstrated locomotor hyperactivity, motor impulsivity, increased "approach" behavior in an approach-avoidance assay, and deficits in nest building behavior. Analysis of brain neurotransmitter content revealed deficits in striatal GABA, glutamate, and serotonin content. RNA sequencing of the ventral striatum unveiled expression changes associated with neurotransmission as well as motivation and substance use pathways. Sex differences were identified in nest building behavior, striatal neurotransmitter content, and ventral striatal gene expression.

DISCUSSION

In summary, our study identified sex differences in specific behavioral, neurotransmitter, and gene expression phenotypes and gene set enrichment analysis identified significant enrichment of pathways associated with motivation and drug reward.

摘要

引言

脆性X综合征是一种遗传性X连锁疾病,与始于儿童期并持续终生的智力残疾有关。其症状与自闭症谱系障碍重叠,且该综合征主要影响男性。因此,脆性X综合征的研究倾向于对男性的社会行为进行分析,这使得我们对其他行为特征的理解存在空白,尤其是在女性方面。

方法

我们使用脆性X综合征的小鼠模型来分析雄性和雌性小鼠的发育、行为、神经化学和转录组特征。

结果

我们的行为分析表明,小鼠存在运动活动亢进、运动冲动性、在趋避试验中“趋近”行为增加以及筑巢行为缺陷。对脑神经递质含量的分析显示,纹状体中γ-氨基丁酸、谷氨酸和血清素含量存在缺陷。腹侧纹状体的RNA测序揭示了与神经传递以及动机和物质使用途径相关的表达变化。在筑巢行为、纹状体神经递质含量和腹侧纹状体基因表达方面发现了性别差异。

讨论

总之,我们的研究确定了特定行为、神经递质和基因表达表型中的性别差异,并且基因集富集分析确定了与动机和药物奖赏相关途径的显著富集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/3ad786a5d0db/fnbeh-18-1458502-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/e38af021850f/fnbeh-18-1458502-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/3bd86212ad00/fnbeh-18-1458502-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/bdb0fe349205/fnbeh-18-1458502-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/3ad786a5d0db/fnbeh-18-1458502-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/e38af021850f/fnbeh-18-1458502-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/3bd86212ad00/fnbeh-18-1458502-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/bdb0fe349205/fnbeh-18-1458502-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901a/11412825/3ad786a5d0db/fnbeh-18-1458502-g004.jpg

相似文献

1
Behavioral, neurotransmitter and transcriptomic analyses in male and female KO mice.雄性和雌性基因敲除小鼠的行为、神经递质和转录组分析。
Front Behav Neurosci. 2024 Sep 6;18:1458502. doi: 10.3389/fnbeh.2024.1458502. eCollection 2024.
2
Sex-specific modulation of early life vocalization and cognition by Fmr1 gene dosage in a mouse model of Fragile X Syndrome.脆性 X 综合征小鼠模型中 Fmr1 基因剂量对早期发声和认知的性别特异性调节。
Biol Sex Differ. 2024 Feb 21;15(1):18. doi: 10.1186/s13293-024-00594-3.
3
Parallel learning and cognitive flexibility impairments between knockout mice and individuals with fragile X syndrome.基因敲除小鼠与脆性X综合征患者之间的平行学习和认知灵活性损伤。
Front Behav Neurosci. 2023 Jan 5;16:1074682. doi: 10.3389/fnbeh.2022.1074682. eCollection 2022.
4
Tau reduction attenuates autism-like features in Fmr1 knockout mice.Tau 蛋白减少可减轻 Fmr1 敲除小鼠的自闭症样特征。
Mol Autism. 2023 Nov 7;14(1):42. doi: 10.1186/s13229-023-00574-1.
5
The GABA(A) receptor agonist THIP ameliorates specific behavioral deficits in the mouse model of fragile X syndrome.GABA(A) 受体激动剂 THIP 可改善脆性 X 综合征小鼠模型的特定行为缺陷。
Dev Neurosci. 2011;33(5):395-403. doi: 10.1159/000332884. Epub 2011 Nov 8.
6
Modeling fragile X syndrome in the Fmr1 knockout mouse.在Fmr1基因敲除小鼠中模拟脆性X综合征。
Intractable Rare Dis Res. 2014 Nov;3(4):118-33. doi: 10.5582/irdr.2014.01024.
7
Age-specific autistic-like behaviors in heterozygous Fmr1-KO female mice.杂合子Fmr1基因敲除雌性小鼠的年龄特异性自闭症样行为
Autism Res. 2017 Jun;10(6):1067-1078. doi: 10.1002/aur.1743. Epub 2017 Mar 16.
8
Effects of Fmr1 Gene Mutations on Sex Differences in Autism-Like Behavior and Dendritic Spine Development in Mice and Transcriptomic Studies.脆性 X 智力低下 1 基因(Fmr1)突变对自闭症样行为和树突棘发育的性别差异的影响及转录组学研究。
Neuroscience. 2023 Dec 1;534:16-28. doi: 10.1016/j.neuroscience.2023.10.001. Epub 2023 Oct 16.
9
Negative Effects of Chronic Rapamycin Treatment on Behavior in a Mouse Model of Fragile X Syndrome.慢性雷帕霉素治疗对脆性X综合征小鼠模型行为的负面影响。
Front Mol Neurosci. 2018 Jan 12;10:452. doi: 10.3389/fnmol.2017.00452. eCollection 2017.
10
Paradoxical effect of baclofen on social behavior in the fragile X syndrome mouse model.巴氯芬对脆性 X 综合征小鼠模型社会行为的矛盾影响。
Brain Behav. 2018 Jun;8(6):e00991. doi: 10.1002/brb3.991. Epub 2018 Apr 26.

引用本文的文献

1
Therapeutic Effects of Pharmacological Modulation of Serotonin Brain System in Human Patients and Animal Models of Fragile X Syndrome.血清素脑系统的药理学调节对脆性X综合征人类患者及动物模型的治疗作用
Int J Mol Sci. 2025 Mar 11;26(6):2495. doi: 10.3390/ijms26062495.
2
Molecular Pathways, Neural Circuits and Emerging Therapies for Self-Injurious Behaviour.自我伤害行为的分子通路、神经回路及新兴疗法
Int J Mol Sci. 2025 Feb 24;26(5):1938. doi: 10.3390/ijms26051938.

本文引用的文献

1
Cell-type-specific disruption of cortico-striatal circuitry drives repetitive patterns of behavior in fragile X syndrome model mice.细胞类型特异性破坏皮质纹状体回路导致脆性 X 综合征模型小鼠出现重复行为模式。
Cell Rep. 2023 Aug 29;42(8):112901. doi: 10.1016/j.celrep.2023.112901. Epub 2023 Jul 27.
2
Parallel learning and cognitive flexibility impairments between knockout mice and individuals with fragile X syndrome.基因敲除小鼠与脆性X综合征患者之间的平行学习和认知灵活性损伤。
Front Behav Neurosci. 2023 Jan 5;16:1074682. doi: 10.3389/fnbeh.2022.1074682. eCollection 2022.
3
Pirenperone relieves the symptoms of fragile X syndrome in Fmr1 knockout mice.
哌仑西平可缓解 Fmr1 敲除小鼠脆性 X 综合征的症状。
Sci Rep. 2022 Dec 5;12(1):20966. doi: 10.1038/s41598-022-25582-8.
4
Transgenerational transmission of aspartame-induced anxiety and changes in glutamate-GABA signaling and gene expression in the amygdala.阿斯巴甜诱导的焦虑的跨代传递以及杏仁核中谷氨酸-γ-氨基丁酸信号和基因表达的变化。
Proc Natl Acad Sci U S A. 2022 Dec 6;119(49):e2213120119. doi: 10.1073/pnas.2213120119. Epub 2022 Dec 2.
5
Acute and Repeated Administration of NLX-101, a Selective Serotonin-1A Receptor Biased Agonist, Reduces Audiogenic Seizures in Developing Fmr1 Knockout Mice.选择性5-羟色胺-1A受体偏向性激动剂NLX-101的急性和重复给药可减少发育中的Fmr1基因敲除小鼠的听源性惊厥。
Neuroscience. 2023 Jan 15;509:113-124. doi: 10.1016/j.neuroscience.2022.11.014. Epub 2022 Nov 21.
6
Gene therapy using human FMRP isoforms driven by the human promoter rescues fragile X syndrome mouse deficits.使用由人类启动子驱动的人类FMRP亚型进行基因治疗可挽救脆性X综合征小鼠的缺陷。
Mol Ther Methods Clin Dev. 2022 Oct 7;27:246-258. doi: 10.1016/j.omtm.2022.10.002. eCollection 2022 Dec 8.
7
Translational validity and methodological underreporting in animal research: A systematic review and meta-analysis of the Fragile X syndrome (Fmr1 KO) rodent model.翻译后文本:动物研究中的转化有效性和方法学报告不足:脆性 X 综合征(Fmr1 KO)啮齿动物模型的系统评价和荟萃分析。
Neurosci Biobehav Rev. 2022 Aug;139:104722. doi: 10.1016/j.neubiorev.2022.104722. Epub 2022 Jun 8.
8
Fragile X Syndrome in a Female With Homozygous Full-Mutation Alleles of the FMR1 Gene.一名携带FMR1基因纯合完全突变等位基因的女性的脆性X综合征
Cureus. 2021 Jul 12;13(7):e16340. doi: 10.7759/cureus.16340. eCollection 2021 Jul.
9
The fragile X mental retardation protein promotes adjustments in cocaine self-administration that preserve reinforcement level.脆性 X 智力低下蛋白促进可卡因自我给药的调整,以维持强化水平。
Eur J Neurosci. 2021 Aug;54(3):4920-4933. doi: 10.1111/ejn.15356. Epub 2021 Jun 28.
10
An "Omic" Overview of Fragile X Syndrome.脆性X综合征的“组学”概述
Biology (Basel). 2021 May 13;10(5):433. doi: 10.3390/biology10050433.