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本文引用的文献

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Regional expression of multidrug resistance genes in genetically epilepsy-prone rat brain after a single audiogenic seizure.单次听源性癫痫发作后遗传性癫痫易感大鼠脑中多药耐药基因的区域表达
Epilepsia. 2002 Nov;43(11):1318-23. doi: 10.1046/j.1528-1157.2002.156702.x.
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MDR1 up-regulated by apoptotic stimuli suppresses apoptotic signaling.
Pharm Res. 2002 Sep;19(9):1323-9. doi: 10.1023/a:1020302825511.
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Transient increase of P-glycoprotein expression in endothelium and parenchyma of limbic brain regions in the kainate model of temporal lobe epilepsy.颞叶癫痫红藻氨酸模型中边缘脑区内皮和实质中P-糖蛋白表达的短暂增加。
Epilepsy Res. 2002 Oct;51(3):257-68. doi: 10.1016/s0920-1211(02)00156-0.
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Activation of hypoxia-inducible factor-1 in the rat cerebral cortex after transient global ischemia: potential role of insulin-like growth factor-1.短暂性全脑缺血后大鼠大脑皮质中缺氧诱导因子-1的激活:胰岛素样生长因子-1的潜在作用
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Expression of multidrug resistance genes MVP, MDR1, and MRP1 determined sequentially before, during, and after hyperthermic isolated limb perfusion of soft tissue sarcoma and melanoma patients.
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P-Glycoprotein-mediated efflux of phenobarbital, lamotrigine, and felbamate at the blood-brain barrier: evidence from microdialysis experiments in rats.P-糖蛋白介导的苯巴比妥、拉莫三嗪和非氨酯在血脑屏障处的外排:来自大鼠微透析实验的证据。
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Differential regulation of P-glycoprotein genes in primary rat hepatocytes by collagen sandwich and drugs.胶原蛋白夹心培养法和药物对原代大鼠肝细胞中P-糖蛋白基因的差异调节
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Expression of the multidrug transporter P-glycoprotein in brain capillary endothelial cells and brain parenchyma of amygdala-kindled rats.多药转运蛋白P-糖蛋白在杏仁核点燃大鼠脑毛细血管内皮细胞和脑实质中的表达。
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The impact of multiple drug resistance (MDR) proteins on chemotherapy and drug discovery.
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Hypoxia-inducible factor-1-dependent regulation of the multidrug resistance (MDR1) gene.缺氧诱导因子-1对多药耐药(MDR1)基因的依赖性调控。
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多药耐药蛋白1/ P-糖蛋白在部分皮质缺血模型中的瞬时表达

Transient expression of MDR-1/P-glycoprotein in a model of partial cortical devascularization.

作者信息

Ramos Alberto Javier, Lazarowski Alberto, Villar Marcelo J, Brusco Alicia

机构信息

Facultad de Ciencias Biomédicas, Universidad Austral, Pilar, Buenos Aires, Argentina.

出版信息

Cell Mol Neurobiol. 2004 Feb;24(1):101-7. doi: 10.1023/b:cemn.0000012728.19117.73.

DOI:10.1023/b:cemn.0000012728.19117.73
PMID:15049514
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11529942/
Abstract
  1. MDR-1 gene product confer to expressing cells the multidrug resistance phenotype to a broad range of drugs and xenobiotics. 2. It is known that different stress signals are able to induce MDR-1 expression through different promoters. 3. In a rat model of ischemia by partial cortical devascularization we studied the expression profile and the cellular localization of MDR-1 after 1, 3, 7, 14 and 28 days post lesion (DPL). 4. Using two different antibody clones we found that MDR-1 is expressed in cortical and striatal neurons ipsilateral to the devascularizing lesion, starting at 1DPL, showing a maximum at 7DPL to be thereafter reduced until undetectable levels by 28DPL. 5. MDR-1 expression may be defining a neuronal subset with a particular pharmacological profile.
摘要
  1. MDR - 1基因产物赋予表达细胞对多种药物和外源性物质的多药耐药表型。2. 已知不同的应激信号能够通过不同的启动子诱导MDR - 1表达。3. 在部分皮质去血管化诱导的大鼠缺血模型中,我们研究了损伤后1、3、7、14和28天(DPL)MDR - 1的表达谱和细胞定位。4. 使用两种不同的抗体克隆,我们发现MDR - 1在去血管化损伤同侧的皮质和纹状体神经元中表达,从损伤后1天开始,在7天达到峰值,此后逐渐降低,到28天时降至不可检测水平。5. MDR - 1表达可能定义了一个具有特定药理学特征的神经元亚群。