• 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

将脆性 X 智力迟钝蛋白与脂氧合酶途径联系起来。

Linking the Fragile X mental retardation protein to the lipoxygenase pathway.

机构信息

Travaux publics et Services gouvernementaux Canada, Bureau de la traduction, 70, rue Crémazie, Gatineau (Québec), Canada K1A 0S5.

出版信息

Med Hypotheses. 2013 Mar;80(3):289-91. doi: 10.1016/j.mehy.2012.11.046. Epub 2013 Jan 10.

DOI:10.1016/j.mehy.2012.11.046
PMID:23313071
Abstract

Fragile X mental retardation is caused by the absence of the FMRP (fragile X mental retardation protein) a RNA-binding protein encoded by the Fmr1 gene. Despite the large number of studies about this syndrome, it is still unclear how the absence of FMRP affects the physiology of the nervous system. It has been reported however that the brain of the Fmr1-KO mouse shows altered membrane protein and lipid oxidation. There is also indirect evidence that FMRP may be involved in a negative feedback mechanism with metabotropic glutamate receptors (mGluRs). In this article, we will discuss several lines of evidences which tend to prove that the lipoxygenase pathway might be the missing link between FMRP and mGluRs.

摘要

脆性 X 智力低下是由 FMRP(脆性 X 智力低下蛋白)缺失引起的,FMRP 是由 Fmr1 基因编码的一种 RNA 结合蛋白。尽管有大量关于这种综合征的研究,但 FMRP 的缺失如何影响神经系统的生理学仍不清楚。然而,据报道,Fmr1-KO 小鼠的大脑显示出膜蛋白和脂质氧化的改变。也有间接证据表明,FMRP 可能参与代谢型谷氨酸受体(mGluRs)的负反馈机制。在本文中,我们将讨论几条证据线,这些证据线倾向于证明脂氧合酶途径可能是 FMRP 和 mGluRs 之间缺失的联系。

相似文献

1
Linking the Fragile X mental retardation protein to the lipoxygenase pathway.将脆性 X 智力迟钝蛋白与脂氧合酶途径联系起来。
Med Hypotheses. 2013 Mar;80(3):289-91. doi: 10.1016/j.mehy.2012.11.046. Epub 2013 Jan 10.
2
Enhanced markers of oxidative stress, altered antioxidants and NADPH-oxidase activation in brains from Fragile X mental retardation 1-deficient mice, a pathological model for Fragile X syndrome.脆性X智力低下1基因缺陷小鼠(脆性X综合征的病理模型)大脑中氧化应激增强标志物、抗氧化剂改变及NADPH氧化酶激活情况
Eur J Neurosci. 2007 Dec;26(11):3169-80. doi: 10.1111/j.1460-9568.2007.05939.x. Epub 2007 Nov 14.
3
Protective effects of melatonin against oxidative stress in Fmr1 knockout mice: a therapeutic research model for the fragile X syndrome.褪黑素对脆性X综合征治疗研究模型Fmr1基因敲除小鼠氧化应激的保护作用
J Pineal Res. 2009 Mar;46(2):224-34. doi: 10.1111/j.1600-079X.2008.00653.x. Epub 2008 Dec 23.
4
Fragile X Mental Retardation Protein (FMRP) controls diacylglycerol kinase activity in neurons.脆性X智力低下蛋白(FMRP)调控神经元中的二酰甘油激酶活性。
Proc Natl Acad Sci U S A. 2016 Jun 28;113(26):E3619-28. doi: 10.1073/pnas.1522631113. Epub 2016 May 27.
5
Fragile X syndrome: from molecular genetics to therapy.脆性X综合征:从分子遗传学到治疗
J Med Genet. 2009 Sep;46(9):577-84. doi: 10.1136/jmg.2008.064667.
6
Metabotropic glutamate receptors and fragile x mental retardation protein: partners in translational regulation at the synapse.代谢型谷氨酸受体与脆性X智力低下蛋白:突触处翻译调控的伙伴
Sci Signal. 2008 Feb 5;1(5):pe6. doi: 10.1126/stke.15pe6.
7
Corticosterone response to acute stress in a mouse model of Fragile X syndrome.脆性X综合征小鼠模型中皮质酮对急性应激的反应。
Psychoneuroendocrinology. 2006 Jul;31(6):781-5. doi: 10.1016/j.psyneuen.2006.02.008. Epub 2006 Apr 18.
8
Increased rates of cerebral glucose metabolism in a mouse model of fragile X mental retardation.脆性X智力障碍小鼠模型中脑葡萄糖代谢率增加。
Proc Natl Acad Sci U S A. 2002 Nov 26;99(24):15758-63. doi: 10.1073/pnas.242377399. Epub 2002 Nov 11.
9
Altered synaptic plasticity in a mouse model of fragile X mental retardation.脆性X智力障碍小鼠模型中突触可塑性的改变
Proc Natl Acad Sci U S A. 2002 May 28;99(11):7746-50. doi: 10.1073/pnas.122205699.
10
Fmr1 knockout mice are impaired in a leverpress escape/avoidance task.Fmr1基因敲除小鼠在杠杆按压逃避/回避任务中表现受损。
Genes Brain Behav. 2006 Aug;5(6):467-71. doi: 10.1111/j.1601-183X.2005.00183.x.

引用本文的文献

1
Antipurinergic therapy corrects the autism-like features in the Fragile X (Fmr1 knockout) mouse model.抗嘌呤能疗法可纠正脆性X(Fmr1基因敲除)小鼠模型中的自闭症样特征。
Mol Autism. 2015 Jan 13;6:1. doi: 10.1186/2040-2392-6-1. eCollection 2015.