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本文引用的文献

1
Liver X receptor activation enhances blood-brain barrier integrity in the ischemic brain and increases the abundance of ATP-binding cassette transporters ABCB1 and ABCC1 on brain capillary cells.肝 X 受体的激活增强了缺血性脑内的血脑屏障完整性,并增加了脑毛细血管细胞上的三磷酸腺苷结合盒转运蛋白 ABCB1 和 ABCC1 的丰度。
Brain Pathol. 2012 Mar;22(2):175-87. doi: 10.1111/j.1750-3639.2011.00517.x. Epub 2011 Sep 16.
2
Molecular Mechanisms Underlying Cell Death in Spinal Networks in Relation to Locomotor Activity After Acute Injury in vitro.急性损伤后体外运动活性相关的脊髓网络细胞死亡的分子机制。
Front Cell Neurosci. 2011 Jun 17;5:9. doi: 10.3389/fncel.2011.00009. eCollection 2011.
3
MK801 attenuates secondary injury in a mouse experimental compression model of spinal cord trauma.MK801 减轻小鼠实验性脊髓创伤压迫模型中的继发性损伤。
BMC Neurosci. 2011 Apr 14;12:31. doi: 10.1186/1471-2202-12-31.
4
Resveratrol improves neuron protection and functional recovery in rat model of spinal cord injury.白藜芦醇可改善脊髓损伤大鼠模型中的神经元保护和功能恢复。
Brain Res. 2011 Feb 16;1374:100-9. doi: 10.1016/j.brainres.2010.11.061. Epub 2010 Nov 25.
5
Effects of axon degeneration on oligodendrocyte lineage cells: dorsal rhizotomy evokes a repair response while axon degeneration rostral to spinal contusion induces both repair and apoptosis.轴突退变对少突胶质细胞谱系细胞的影响:背根切断术引发修复反应,而脊髓挫伤前轴突退变则同时诱导修复和细胞凋亡。
Glia. 2010 Aug 15;58(11):1304-19. doi: 10.1002/glia.21009.
6
Liver X receptor agonist treatment reduced splanchnic ischemia and reperfusion injury.肝 X 受体激动剂治疗可减少内脏缺血再灌注损伤。
J Leukoc Biol. 2010 Feb;87(2):309-21. doi: 10.1189/jlb.0609438. Epub 2009 Dec 22.
7
Liver X receptor agonist treatment regulates inflammatory response after spinal cord trauma.肝 X 受体激动剂治疗调控脊髓创伤后的炎症反应。
J Neurochem. 2010 Feb;112(3):611-24. doi: 10.1111/j.1471-4159.2009.06471.x. Epub 2009 Nov 4.
8
Inflammation in transgenic mouse models of neurodegenerative disorders.神经退行性疾病转基因小鼠模型中的炎症
Biochim Biophys Acta. 2010 Oct;1802(10):889-902. doi: 10.1016/j.bbadis.2009.10.013. Epub 2009 Oct 31.
9
Coordination of inflammation and metabolism by PPAR and LXR nuclear receptors.PPAR和LXR核受体对炎症与代谢的协调作用
Curr Opin Genet Dev. 2008 Oct;18(5):461-7. doi: 10.1016/j.gde.2008.07.016. Epub 2008 Sep 7.
10
RAR/RXR and PPAR/RXR Signaling in Spinal Cord Injury.脊髓损伤中的 RAR/RXR 和 PPAR/RXR 信号转导。
PPAR Res. 2007;2007:29275. doi: 10.1155/2007/29275.

实验性脊髓横断损伤大鼠肝脏X受体α和Bcl-2相关X蛋白的基因表达谱分析

Gene expression profiling of liver X receptor α and Bcl-2-associated X protein in experimental transection spinal cord-injured rats.

作者信息

Mohammadi Esmat, Ghaedi Kamran, Esmailie Abolghasem, Rahgozar Soheila

机构信息

Cell and Molecular Biology Division, Biology Department, School of Sciences, University of Isfahan, Isfahan, Iran.

出版信息

J Spinal Cord Med. 2013 Jan;36(1):66-71. doi: 10.1179/2045772312Y.0000000032.

DOI:10.1179/2045772312Y.0000000032
PMID:23433337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3555109/
Abstract

BACKGROUND

Study of molecular responses to central nervous system injury would be helpful for controlling the harmful pathways post-injury and triggering the useful pathways required for the treatment of injury.

OBJECTIVE

To investigate the expression level of liver X receptor α (LXRα) which has anti-inflammatory effects and pro-apoptotic Bcl-2-associated X protein (Bax) upon spinal cord injury (SCI).

DESIGN

To induce SCI, transection was carried out at T9 level of male Wister rats. Approximately 8 mm of rostral, caudal, and epicenter tissues of injured sites in treated rats were chosen for quantitative real-time polymerase chain reaction at the 6, 24, and 72 hours, and 7 and 10 days post-surgery.

RESULTS

Our results showed a complicated temporal and spatial pattern of alteration in LXRα and Bax mRNA expression levels after SCI. LXRα expression level followed a homologues pattern (additive and subtractive wave) with a difference in time at three areas of studied. Rostral, caudal, and epicenter expression patterns of Bax were dissimilar in these areas. Gradual increase in the expression of Bax without any decrease at the rostral area was observed, presumably indicating the active transcription process of this gene, regardless of its protein situation.

CONCLUSION

A time lapse significant change in Bax expression level was observed only in the epicenter of injury, emphasizing that apoptotic responses are limited to this area. Furthermore, an increase in LXRα transcription level was observed first in rostral area and then extended to epicentral and caudal areas, implying that inflammation responses extended from rostral to caudal areas.

摘要

背景

研究中枢神经系统损伤的分子反应,将有助于控制损伤后的有害途径,并激活损伤治疗所需的有益途径。

目的

研究具有抗炎作用的肝脏X受体α(LXRα)和促凋亡蛋白Bcl-2相关X蛋白(Bax)在脊髓损伤(SCI)后的表达水平。

设计

通过横断雄性Wister大鼠T9节段诱导脊髓损伤。在术后6、24、72小时以及7和10天,选取处理组大鼠损伤部位的约8mm头端、尾端及损伤中心组织进行实时定量聚合酶链反应。

结果

我们的结果显示脊髓损伤后LXRα和Bax mRNA表达水平呈现复杂的时空变化模式。LXRα表达水平呈现同源模式(增减波),在所研究的三个区域存在时间差异。Bax在头端、尾端和损伤中心区域的表达模式不同。在头端区域观察到Bax表达逐渐增加且无下降,这可能表明该基因的转录过程活跃,而不考虑其蛋白质状态。

结论

仅在损伤中心观察到Bax表达水平随时间显著变化,这表明凋亡反应仅限于该区域。此外,首先在头端区域观察到LXRα转录水平升高,然后扩展到损伤中心和尾端区域,这意味着炎症反应从头端扩展到尾端区域。