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银杏叶提取物GBE50对兔心肌组织bcl-2、bcl-xL基因表达的影响 被引量:12

Effect of gene expression of bcl-2 and bcl-xL in rabbit myocardium by Ginko biloba extract GBE50
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摘要 目的探讨新型银杏叶提取物GBE50对兔心肌细胞抗凋亡基因bcl2、bclxL表达的影响。方法成年雄性新西兰大白兔随机分为GBE50组和对照组,GBE50组每日按体重100mg·kg-1口饲给予新型银杏叶提取物GBE50,对照组仅给予赋形剂2羧甲基纤维素钠,饲养4周后,处死动物,取左室心肌组织,采用RTPCR技术在凝胶电泳成像基础上半定量检测bcl2、bclxL基因的表达水平。结果GBE50组bcl2、bclxL基因的表达显著高于对照组(P<0.05)。结论新型银杏叶提取物GBE50可促进兔心肌细胞抗凋亡基因bcl2、bclxL的表达。 AIM: To investigate affection of the novel Ginko biloba extract GBE50 on bcl-2、bcl-xL gene expression in rabbit myocardium. METHODS: Adult male New Zealand rabbits were randomly divided into 2 groups. GBE50 group were orally administrated with 100 mg/kg GBE50 daily. Control group were only administrated vehicle 2% CMC-Na. After being raised for 4 weeks, the animals were killed and the ventricular tissue were excised. We performed reverse transcriptase polymerase (RT-PCR) to measure gene expression of bcl-2、bcl-xL. Semiquantitative analysis method based on gel electrophoresis image was adopted to compare gene expression among groups. RESULTS : The gene expression of bcl-2、bcl-xL significantly increased in GBE50 group compared with control group. CONCLUSION: The novel Ginko biloba extract GBE50 can promote expression of the antiapoptotic gene bcl-2、bcl-xL in rabbit myocardium.
出处 《中成药》 CAS CSCD 北大核心 2005年第1期60-62,共3页 Chinese Traditional Patent Medicine
关键词 银杏叶提取物 BCL-2 BCL-XL 基因表达 Ginko biloba extract bcl-2 bcl-xL gene expression
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参考文献7

  • 1沈剑刚,张德良,忻文娟,赵保路,丘幸生,姜泊,冯戬云.一氧化氮和氧自由基诱导缺氧再给氧心肌细胞凋亡的bcl-2和p53信号通路研究[J].中国科学(C辑),2002,32(5):436-446. 被引量:5
  • 2Thiagarajan G, Chandani S, Harinarayana Rao S. et al. Molecular and cellular assessment of ginkgo biloba extract as a possible ophthalmic drug. Exp Eye Res, 2002,75(4) :421-30.
  • 3Baudouin, C, Ettaiche, M, Fredj-Reygrobellet, D. et al. Effects of Ginkgo biloba extracts in a model of tractional retinal detachment. Lens and Eye Toxicity Research, 1992, 9(2): 513-519.
  • 4Kajstura J, Cheng W, Reiss K, et al. Apoptotic and necrotic myocyte cell deaths are independent contributing variables of infarct size in rats. Lab Invest, 1996, 74:86-107.
  • 5Misao J, Hayakawa Y, Ohno M, et al. Expression of bcl-2 protein, an inhibitor of apoptOsis, and Bax, an accelerator of apoptosis, in ventricular myocytes of human hearts with myocardial infarction. Circulation, 1996, 94(7): 1506-12.
  • 6Adams J M, Cory S. The Bcl-2 protein family: Arbiters of cell survival. Science, 1998, 281 (5381) :1322-1326.
  • 7Minn A J, Velez P, Schendel SL, et al. Bcl-x (L) forms an ion channel in synthetic lipid membranes. Nature, 1997, 385(6614) :353-7.

二级参考文献29

  • 1Mastrangelo A J, Betenbaugh M. Overcoming apoptosis: new methods for improvingprotein-expression systems. TIBTECH, 1998, 16: 88~95
  • 2Tanaka M, Ito H, Adachi S, et al. Hypoxia induces apoptosis with enhanced expression of Fas antigen messenger RNA in cultured neonatal rat cardiocardiac myocytes. Circ Res, 1994, 75(3): 426~433
  • 3Gottlieb R A, Burleson K O, Kloner R A, et al. Reperfusion injury induces apoptosis in rabbit cardiocardiac myocytes. J Clin Invest, 1994, 94: 1621~1628
  • 4Kajstura J, Cheng W, Reiss K, et al. Apoptotic and necrotic myocyte cell deaths are independent contributing variables of infarct size in rats. Lab Invest, 1996, 74(1): 86~107
  • 5Me?mer U K, Ankarcrona M, Nicotera P, et al. p53 expression in nitric oxide-induced apoptosis. FEBS Lett, 1994, 355: 23~26
  • 6Me?mer U K, Reimer D M, Reed J C, et al. Nitric oxide induced ploy(ADP-ribose)polymerase cleavage in RAW 264.7 macrophage apoptosis is blocked by bcl-2. FEBSLett, 1996, 384(2): 162~166
  • 7Dimmeler S, Zeiher A M. Nitric oxide and apoptosis: another paradigm for the double-dged role of nitric oxide. Nitric Oxide, 1997, 1(4): 275~281
  • 8Moncada S, Palmer R M J, Higgs E A. Nitric oxide: physiology, pathology and pharmacology. Pharmaco Rev, 1991, 43: 109~142
  • 9Me?mer U K, Brune B. Nitric oxide (NO) in apototic versus Necroic RAW 264.7 macrophage cell death: the role of NO-donor exposure, NAD+ content, and p53 accumulation. Arch Biochem Biophys, 1996, 327(1): 1~10
  • 10Brune G, Me?mer U K, Sandau K. The role of nitric oxide incell injury. Toxic Lett, 1995, 82/83: 233-237

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