期刊文献+

谷胱甘肽S-转移酶π、DNA拓扑异构酶Ⅱ及P-糖蛋白在难治性癫癎患者脑内的表达 被引量:3

Glutathione S-transferase π, DNA topoisomeraseⅡ, and P-glycoprotein expression in brain of patients with refractory epilepsy
原文传递
导出
摘要 目的探讨谷胱甘肽S-转移酶π(GST-π)、DNA拓扑异构酶Ⅱ(TopoⅡ)及P-糖蛋白(P-gp)在难治性癫癎(RE)患者脑内的表达及意义。方法32例RE患者手术切除标本,采用免疫组化方法检测GST-π、TopoⅡ及P-gp表达。8例脑血管畸形患者作为对照。结果对照组正常脑组织内星形胶质细胞及血管内皮细胞中有少量GST-π表达(2·2),癫癎组GST-π表达明显增强(10·9,P<0·05)。TopoⅡ在对照组中无表达,癫癎组2例标本有少量表达(0·4,P>0·05)。对照组中P-gp只在脑内血管内皮细胞中少量表达,癫癎组P-gp则在星形胶质细胞及血管内皮细胞中大量表达(12·9,P<0·01)。结论GST-π、P-gp在RE患者脑内表达可能与患者对抗癫癎药耐药有关。 Objective To investigate the effects and expression of glutathione S-transferase (GST-π), DNA topoisomerase Ⅱ (Topo Ⅱ ) and P-glycoprotein (P-gp) in brain of patients with refractory epilepsy.Motheds The specimens were obtained from 32 patients with refractory epilepsy and 8 patients with arteriovenous malformations as controls, and immunohistochemistry for GST-π, Topo Ⅱ and P-gp was used. Results GST-π immunoreactivity in several capillary endothelial cells and astrocytes was found in normal brain samples (2. 2 ± 2. 6), it was significantly increased in samples from epileptic patients ( 10. 9 ± 9. 8, P 〈 0. 05). Topo Ⅱ immunoreactivity was not identified in normal samples, but found in 2 samples of epileptic patients (0. 4 ± 1.6, P 〉0. 05). P-gp immunoreactivity was only found in capillary endothelial in normal samples, but it was identified in several astrocytes and increased in capillary endothelial cells in samples from epileptic patients (12.9 ±9.7, P〈0,01). Conclusion Overexpression of GST-π, P-gp in patients with refractory epilepsy might play a role in pharmacoresistance to antiepileptic drugs,
出处 《中华神经科杂志》 CAS CSCD 北大核心 2005年第9期540-542,共3页 Chinese Journal of Neurology
  • 相关文献

参考文献7

  • 1Tishler DM, Weinberg KT, Hinton DR, et al. MDR1 gene expression in brain of patients with medically intractable eplipsy. Epilepsia, 1995, 36: 1-6.
  • 2Sisodiya SM, Lin WR, Harding BN, et al. Drug resistance in epilepsy: expression of drug resistance proteins in common causes of refractory epilepsy. Brain, 2002, 125 (Pt 1): 22-31.
  • 3Baranczyk-Kuzma A, Kuzma M, Gutowicz M, et al. Glutathione S-transferase pi as a target for tricyclic antidepressants in human brain. Acta Biochim Pol, 2004, 51: 207-212.
  • 4Wang JF, Shao L, Sun X, et al. Glutathione S-transferase is a novel target for mood stabilizing drugs in primary cultured neurons. J Neurochem, 2004, 88: 1477-1484.
  • 5Pinkus R, Bergelson S, Daniel V. Phenobarbital induction of AP-1 binding activity mediates activation of glutathione S-transferase and quinone reductase gene expression. Biochem J, 1993, 290 (Pt 3):637-640.
  • 6Tang W, Borel AG, Abbott FS. Conjugation of glutathione with a toxic metabolite of valproic acid, (E)-2-propyl-2,4-pentadienoic acid, catalyzed by rat hepatic glutathione-S-transferases. Duag Metab Dispos, 1996, 24: 436-446.
  • 7Dieckhaus CM, Roller SG, Santos WL, et al. Role of glutathione S-transferases A1-1, M1-1, and P1-1 in the detoxification of 2-phenylpropenal, a reactive felbamate metabolite. Chem Res Toxicol,2001, 14: 511-516.

同被引文献47

引证文献3

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部