期刊文献+

姜黄素对沙土鼠脑缺血/再灌注损伤的海马CA1区细胞凋亡和即早基因c-fos、c-jun、NF-κB表达变化的关系 被引量:24

THE RELATIONSHIP BETWEEN THE EFFECTS OF CURCUMIN ON CEREBRAL ISCHEMIA/REPERFUSION INJURY AND IMMEDIATELY GENIC EXPRESSIONS OF Fos, Jun and NF-κB IN HIPPOCAMPAL CA1 AREA AND ITS SIGNIFICANCE IN GERBILS
下载PDF
导出
摘要 目的探讨姜黄素对沙土鼠海马CA1区缺血/再灌注损伤的影响及与即早基因c-fos、c-jun、NF-κB在海马CA1区表达的关系及意义。方法采用沙土鼠双侧颈总动脉阻断缺血/再灌注损伤模型。动物随机分为假手术组(SH)、脑缺血/再灌注组(I/R)、姜黄素组(CU)、溶剂对照组(SC);每组据再灌注时间点的不同又分多个亚组,每组6只动物。在预定时间点行开阔法行为学检查、TUNEL法海马CA1区凋亡细胞检测,免疫组织化学ABC法测定c-fos、c-jun、NF-κB蛋白在海马CA1区的动态变化。结果姜黄素可显著减少沙土鼠探索活动及海马CA1区凋亡锥体细胞数量(P<0.01)、诱导Fos蛋白及抑制Jun和NF-KB蛋白的表达(P<0.01)。结论姜黄素具有脑保护作用,调控即早基因c-fos、c-jun和NF-κB的表达可能是作用机制之一。 To explore the relationship between the effects of curcumin on cerebral ischemic/reperfusion injury and immediately genic expressions of Fos, Jun and NF-κB in hippocampal CA1 area. Methods: Gerbils were randomly divided into sham group (SH), is-chemia/reperfusion group(I/R), curcumin group (CU) and .solvent control group(SC). Forebrain ischemia was induced by occlusion of bilateral common carotid arteries. Observations were carried out in each group 15 min, 1h,2h,6h, 1d, 3d, 5d and 7d after is-chemia: open field test was used to examine the behavioral change, the apoptosis neurons in hippocampal CA1 region was counted, the expression of Fos, Jun and NF-κB in hippocampal CA1 was detected by SABC immunocytochemical technique. Results: The behav-ioral mark and the number of apoptosis neurons in hippocampal CA1 region was much less in CU group than in I/R group( P〈 0.01 ) The expression of Fos was more and the expression of Jun and NF-κB was less in CA1 area in CU group than in I/R group(P〈 0.01 ). Conclusion: Curcumin can significantly protect neurons against cerebral ischemia, increasing the expression Fos and decreas-ing the expression of Jun and NF-κB may be the protective mechanisms.
出处 《中国应用生理学杂志》 CAS CSCD 北大核心 2007年第2期184-188,共5页 Chinese Journal of Applied Physiology
基金 江苏省教育厅基金资助课题(03KJB320142) 浙江省自然科学基金资助课题(Y205200)
关键词 姜黄素 c-fos C-JUN NF-ΚB 沙土鼠 海马 脑缺血 curcumin c-fos c-jun NF-κB gerbil hippocampal brain ischemia
  • 相关文献

参考文献8

  • 1Hsuuw Y D,Chang C K,Chan W H,et al.Curcumin prevents methylglyoxal-induced oxidative stress and apoptosis in mouse embryonia stem cells and blastocysts[J].J Cell Physiol,2005,205(3):379-386.
  • 2Kitagawa K,Matsumoto M,Tagaya M,et al.Ischemic tolerance phenomenon found in the brain[J].Brain Res,1990,528(1):21-24.
  • 3Akin P T,Liu P K,Hsu C Y.Immediate early gene expression in response to cerebral ischemia:friend or foe[J]? Stroke,1996,27:1682-1687.
  • 4Dragunow M,Beilharz E,Sirimanne E,et al.Immediate-early gene protein expression in neurons undergoing delayed death,but not necrosis,following hypoxic-ischemic injury to the young rat brain[J].Brain Res Mol Brain Res,1994,25:19-33.
  • 5方慧,张军.c-jun原癌基因及其表达产物的研究进展[J].国外医学(分子生物学分册),2002,24(5):263-266. 被引量:17
  • 6王磊,王鲁宁,叶玲.早期即刻基因与老年性痴呆[J].国外医学(神经病学.神经外科学分册),2002,29(3):277-279. 被引量:7
  • 7吴丽娟,蒋建新,朱佩芳,康格非.NF-κB信号转导途径研究进展[J].国外医学(临床生物化学与检验学分册),2002,23(5):260-262. 被引量:20
  • 8Shen F,Fan X,Liu B,et al.Overexpression of cyclin D1-CDK4 in silica-induced transformed cells is due to activation of ERKs,JNKs-AP-1 pathway[J].Toxicol Lett,2006,160(3):185-189.

二级参考文献19

  • 1Rudi B, Karen H, Sofie VH, et al. A20 and A20-binding protein as cellular inhibitors of nuclear factor-κB-dependent gene expression and apoptosis[J]. Biochem Pharmacol,2000,60(8): 1143-1151.
  • 2Roberts ML, Cowsert LM. Interleukin-1 beta and reactive oxygen species mediate activation of c-jun NH2-terminal kinas, in human epithelial cells, by two independent pathways[J]. Biochem Biophys Res Commun,1998,251:166-172.
  • 3Jianping Y, Min D, Xiaoying I, et al. On the role of hydroxyl radical and the effect of tetrandrine on nuclear factor-κB activation by phorbol 12-myristate 13-acetate [J].Annals of Clinical and Laboratory Science, 2000,30(1) : 65-71.
  • 4Andrew B, Luke AJ. Oxidative stress and nuclear factor-κB activation[J]. Biol Pharmacology, 2000,59:12-23.
  • 5Sergey AT, Kevin NP, Alicia AS, et al. Protein kinase C and calcineurin synergize to activate IκB kinase and NF-κB in T lymphocytes[J]. J Biol Chem, 1997,274 (33): 22923-22931.
  • 6Marco K, Sofie VH, Karen H, et al. Functional redundancy of the zinc fingers of A20 for inhibition of NF-κB activation and protein-protein interactions[J]. FEBS Lett,2001,498:93-97.
  • 7Lee EG, Boone DL, Chai S, et al. Failure to regulate TNF-α induced NF-κB and death responses in A20 deficient mice[J]. Science, 2000,289: 2350-2354.
  • 8Arch RH, Gedrich RW, Thompson CB. Tumor necrosis factor receptor-asociated factors (TRAFs)-α family of adapter proteins that regulates life and death[J]. Gene Dev,1998,12: 2821-2830.
  • 9Van HS, Delaei F, Heyninck K,et al. Identification of a novel A20-binding inhibitor of nuclear factor-kappa B activation termed ABIN-2[J]. J Biol Chem,2001,10 ;276(32):30216-30223.
  • 10Zhang SQ, Kovalenko A, Cantarella G, et al. Recritment of the IKK signalosome to the p55 TNF receptor: RIP and A20 bind to NEMO(IKK γ)upon receptor stimulation[J].Immunity, 2001,12: 301-311.

共引文献41

同被引文献452

引证文献24

二级引证文献117

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