• 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

兴奋性毒性神经元损伤后小鼠海马CA3区Nurr1表达的变化。

Change of Nurr1 expression in mouse hippocampal CA3 region following excitotoxic neuronal damage.

作者信息

Lee Choong-Hyun

机构信息

Department of Pharmacy, College of Pharmacy, Dankook University, Cheonan 31116, Republic of Korea.

出版信息

Iran J Basic Med Sci. 2020 Feb;23(2):202-205. doi: 10.22038/IJBMS.2019.38712.9177.

DOI:10.22038/IJBMS.2019.38712.9177
PMID:32405363
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7211359/
Abstract

OBJECTIVES

Nuclear receptor-related protein 1 (Nurr1), one of immediate-early genes, is a member of orphan nuclear receptor family. The aim of this study was to investigate the time-dependent change of Nurr1 protein expression in the mouse hippocampal CA3 region following kainic acid (KA)-induced excitotoxic neuronal damage.

MATERIALS AND METHODS

Male ICR mice were used as experimental animals, and 30 mg/kg KA was administered intraperitoneally. To confirm the KA-induced neuronal damage in the hippocampal CA3 region, Fluoro-Jade B histofluorescence staining was performed. In addition, the time-dependent change of Nurr1 protein expression was also examined using immunohistochemistry and western blot analysis.

RESULTS

Marked neuronal damage was observed in the hippocampal CA3 region at 24 hr after KA injection. In addition, both Nurr1 immunoreactivity and protein level were significantly increased at 6 hr and 12 hr after KA injection, and then decreased at 24 hr after KA injection.

CONCLUSION

This result indicates that KA-induced alteration of Nurr1 protein expression may be associated with the neuronal degeneration in the hippocampal CA3 region after KA injection.

摘要

目的

核受体相关蛋白1(Nurr1)是即刻早期基因之一,属于孤儿核受体家族。本研究旨在探讨海藻酸(KA)诱导的兴奋性毒性神经元损伤后,小鼠海马CA3区Nurr1蛋白表达随时间的变化。

材料与方法

雄性ICR小鼠作为实验动物,腹腔注射30mg/kg KA。为证实KA诱导的海马CA3区神经元损伤,进行了荧光金B组织荧光染色。此外,还采用免疫组织化学和蛋白质印迹分析检测了Nurr1蛋白表达随时间的变化。

结果

KA注射后24小时,海马CA3区观察到明显的神经元损伤。此外,KA注射后6小时和12小时,Nurr1免疫反应性和蛋白水平均显著升高,然后在KA注射后24小时下降。

结论

该结果表明,KA诱导的Nurr1蛋白表达改变可能与KA注射后海马CA3区的神经元变性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa7e/7211359/c90d0b92f6ea/IJBMS-23-202-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa7e/7211359/8a5625044354/IJBMS-23-202-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa7e/7211359/b211b9454483/IJBMS-23-202-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa7e/7211359/c90d0b92f6ea/IJBMS-23-202-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa7e/7211359/8a5625044354/IJBMS-23-202-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa7e/7211359/b211b9454483/IJBMS-23-202-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa7e/7211359/c90d0b92f6ea/IJBMS-23-202-g003.jpg

相似文献

1
Change of Nurr1 expression in mouse hippocampal CA3 region following excitotoxic neuronal damage.兴奋性毒性神经元损伤后小鼠海马CA3区Nurr1表达的变化。
Iran J Basic Med Sci. 2020 Feb;23(2):202-205. doi: 10.22038/IJBMS.2019.38712.9177.
2
Nurr1 mRNA expression in neonatal and adult rat brain following kainic acid-induced seizure activity.海人酸诱导癫痫发作活动后新生和成年大鼠脑中Nurr1 mRNA的表达
Brain Res Mol Brain Res. 1998 Aug 31;59(2):178-88. doi: 10.1016/s0169-328x(98)00143-0.
3
The anti-inflammatory activity of duloxetine, a serotonin/norepinephrine reuptake inhibitor, prevents kainic acid-induced hippocampal neuronal death in mice.度洛西汀(一种5-羟色胺/去甲肾上腺素再摄取抑制剂)的抗炎活性可预防红藻氨酸诱导的小鼠海马神经元死亡。
J Neurol Sci. 2015 Nov 15;358(1-2):390-7. doi: 10.1016/j.jns.2015.10.001. Epub 2015 Oct 3.
4
Effect of Rufinamide on the kainic acid-induced excitotoxic neuronal death in the mouse hippocampus.Rufinamide 对鼠海马区红藻氨酸诱导的兴奋性神经元死亡的影响。
Arch Pharm Res. 2018 Jul;41(7):776-783. doi: 10.1007/s12272-018-1043-1. Epub 2018 Jun 8.
5
Effects of nateglinide and repaglinide administered intracerebroventricularly on the CA3 hippocampal neuronal cell death and hyperglycemia induced by kainic acid in mice.脑室注射那格列奈和瑞格列奈对红藻氨酸诱导的小鼠 CA3 海马神经元细胞死亡和高血糖的影响。
Brain Res Bull. 2014 May;104:36-41. doi: 10.1016/j.brainresbull.2014.02.003. Epub 2014 Apr 2.
6
The time-dependent effect of lipopolysaccharide on kainic acid-induced neuronal death in hippocampal CA3 region: possible involvement of cytokines via glucocorticoid.脂多糖对海人酸诱导的海马 CA3 区神经元死亡的时程效应:细胞因子通过糖皮质激素的可能参与。
Neuroscience. 2010 Feb 17;165(4):1333-44. doi: 10.1016/j.neuroscience.2009.11.060. Epub 2009 Dec 2.
7
Increased hippocampal CA3 vulnerability to low-level kainic acid following lateral fluid percussion injury.侧脑室液体冲击伤后海马CA3区对低剂量海人酸的易损性增加。
J Neurotrauma. 2003 May;20(5):409-20. doi: 10.1089/089771503765355496.
8
Effect of tolbutamide, glyburide and glipizide administered supraspinally on CA3 hippocampal neuronal cell death and hyperglycemia induced by kainic acid in mice.脊髓上给予甲苯磺丁脲、格列本脲和格列吡嗪对小鼠海马CA3区神经元细胞死亡及由 kainic 酸诱导的高血糖的影响。
Brain Res. 2014 May 20;1564:33-40. doi: 10.1016/j.brainres.2014.03.046. Epub 2014 Apr 5.
9
Neuroprotective effect of Arthrospira (Spirulina) platensis against kainic acid-neuronal death.钝顶节旋藻(螺旋藻)对海藻酸诱导的神经元死亡的神经保护作用。
Pharm Biol. 2016 Aug;54(8):1408-12. doi: 10.3109/13880209.2015.1103756. Epub 2016 Jan 22.
10
Effect of pertussis and cholera toxins administered supraspinally on CA3 hippocampal neuronal cell death and the blood glucose level induced by kainic acid in mice.脊髓上给予百日咳毒素和霍乱毒素对红藻氨酸诱导的小鼠海马CA3区神经元细胞死亡及血糖水平的影响。
Neurosci Res. 2014 Dec;89:31-6. doi: 10.1016/j.neures.2014.08.017. Epub 2014 Sep 10.

本文引用的文献

1
Time-Course Changes and New Expressions of MIP-3α and Its Receptor, CCR6, in the Gerbil Hippocampal CA1 Area Following Transient Global Cerebral Ischemia.沙土鼠全脑缺血后海马 CA1 区 MIP-3α 及其受体 CCR6 的时程变化及新表达
Neurochem Res. 2018 Nov;43(11):2102-2110. doi: 10.1007/s11064-018-2632-6. Epub 2018 Sep 10.
2
Effect of Rufinamide on the kainic acid-induced excitotoxic neuronal death in the mouse hippocampus.Rufinamide 对鼠海马区红藻氨酸诱导的兴奋性神经元死亡的影响。
Arch Pharm Res. 2018 Jul;41(7):776-783. doi: 10.1007/s12272-018-1043-1. Epub 2018 Jun 8.
3
Atomoxetine Protects Against NMDA Receptor-mediated Hippocampal Neuronal Death Following Transient Global Cerebral Ischemia.
阿托西汀可预防短暂性全脑缺血后NMDA受体介导的海马神经元死亡。
Curr Neurovasc Res. 2017;14(2):158-168. doi: 10.2174/1567202614666170328094042.
4
Nurr1 overexpression exerts neuroprotective and anti-inflammatory roles via down-regulating CCL2 expression in both in vivo and in vitro Parkinson's disease models.在体内和体外帕金森病模型中,Nurr1过表达通过下调CCL2表达发挥神经保护和抗炎作用。
Biochem Biophys Res Commun. 2017 Jan 22;482(4):1312-1319. doi: 10.1016/j.bbrc.2016.12.034. Epub 2016 Dec 8.
5
The pharmacological stimulation of Nurr1 improves cognitive functions via enhancement of adult hippocampal neurogenesis.对Nurr1的药理学刺激通过增强成体海马神经发生来改善认知功能。
Stem Cell Res. 2016 Nov;17(3):534-543. doi: 10.1016/j.scr.2016.09.027. Epub 2016 Sep 28.
6
BMP2 promotes the differentiation of neural stem cells into dopaminergic neurons via miR-145-mediated upregulation of Nurr1 expression.骨形态发生蛋白2通过miR-145介导的Nurr1表达上调促进神经干细胞向多巴胺能神经元分化。
Am J Transl Res. 2016 Sep 15;8(9):3689-3699. eCollection 2016.
7
Temporal changes in mammalian target of rapamycin (mTOR) and phosphorylated-mTOR expressions in the hippocampal CA1 region of rat with vascular dementia.血管性痴呆大鼠海马CA1区雷帕霉素靶蛋白(mTOR)及磷酸化mTOR表达的时间变化
J Vet Sci. 2017 Mar 30;18(1):11-16. doi: 10.4142/jvs.2017.18.1.11.
8
Active coping of prenatally stressed rats in the forced swimming test: involvement of the Nurr1 gene.产前应激大鼠在强迫游泳试验中的主动应对:Nurr1基因的作用
Stress. 2016 Sep;19(5):506-15. doi: 10.1080/10253890.2016.1193147. Epub 2016 Jun 13.
9
The anti-inflammatory activity of duloxetine, a serotonin/norepinephrine reuptake inhibitor, prevents kainic acid-induced hippocampal neuronal death in mice.度洛西汀(一种5-羟色胺/去甲肾上腺素再摄取抑制剂)的抗炎活性可预防红藻氨酸诱导的小鼠海马神经元死亡。
J Neurol Sci. 2015 Nov 15;358(1-2):390-7. doi: 10.1016/j.jns.2015.10.001. Epub 2015 Oct 3.
10
Effect of pioglitazone on excitotoxic neuronal damage in the mouse hippocampus.吡格列酮对小鼠海马体兴奋性毒性神经元损伤的影响。
Biomol Ther (Seoul). 2015 May;23(3):261-7. doi: 10.4062/biomolther.2014.146. Epub 2015 May 1.