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皮质酮复合丙泊酚对大鼠pCREB表达的影响

Effect of cortucisterone and propofol on pCREB expression among Wistar rats
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摘要 目的探讨皮质酮复合丙泊酚对大鼠pCREB表达的影响。方法将24只21 d龄的Wistar大鼠随机分为4组(=6):对照组(Ⅰ组)、丙泊酚组(Ⅱ组)、皮质酮组(Ⅲ组)及丙泊酚+皮质酮组(Ⅳ组),分别以0.9%氯化钠注射液10 ml/kg、丙泊酚100 mg/kg、皮质酮10 mg/kg、丙泊酚100 mg/kg+皮质酮10 mg/kg腹腔注射,连续用药7d后,以免疫组织化学法检测前额叶皮质pCREB的表达。结果与Ⅰ组比较,Ⅱ组、Ⅲ组及Ⅳ组pCREB表达下调(均<0.05);与Ⅱ组、Ⅲ组比较,Ⅳ组pCREB表达减少(均<0.05)。结论 100 mg/kg丙泊酚或10 mg/kg皮质酮多次重复应用,大鼠pCREB的表达减少,两药复合应用时抑制作用增强。 Objective To investigate the effect of cortucisterone and propofol on pCREB expression among Wistar rats.Methods Thirty-two aged 21 days Wistar ats were randomly divided into four groups,with eight rats in each group.The control group(group Ⅰ) was injected with 0.9% sodium chloride injection,with the dose of 10 ml / kg;the propofol group(group Ⅱ) was injected with propofol,with dose of 100mg/kg;the cortucisterone group(group Ⅲ) was injected with cortucisterone,with the dose of 10mg/kg;the propofol and cortucisterone group(group Ⅳ).Were injected with propofol(100 mg/kg) and cortucisterone(10 mg/kg).Seven days later,pCREB expression was detected by immunohistochemical way.Results Compared to group I,expressions decreased in group Ⅱ,group Ⅲ and group Ⅳ(P0.05).Compared to group Ⅱand group Ⅲ,expressions decreased in group Ⅳ(P0.05).Conclusions Inhibition effects are strengthen by propofol combined with cortucisterone,with decrease of pCREB expressions.
出处 《现代实用医学》 2011年第11期1224-1225,1228,F0002,共4页 Modern Practical Medicine
关键词 皮质酮 丙泊酚 PCREB Cortucisterone pCREB Learning Memory
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  • 1Ohl F, Scheich H. Learning-induced plasticity in animal and human auditory cortex [J]. Curr Opin Neurobiol, 2005,15(4) : 470-477.
  • 2Talmi M, Carlier E, Soumireu-Mourat B. Similar effects of aging and corticosterone treatment on mouse hippoeampus function[J]. Neurobioi Aging, 1993, 14 (3) :239-244.
  • 3Barr G, Anderson RE, Owall A, et al. Being awake intermittently during propofolinduced hypnosis: a study ofBIS, explicit and im- plicit memory[J]. Acta anaesthesiol Scand, 2001, 45(4): 834-838.
  • 4Wei H, Xiong W, Yang s, et al. Propoful facilitates the development of long-term depression and impair the maintence of long-term potentiation in the CA1 region of the hippocampus of anesthetized rats[J], neurosci lett, 2002, 32(4): 181-184.
  • 5Warburton EC, Glover CP, Massey PV, et al. cAMP responsive ele- men-binding protein phosphorylation is necessary for Peirrhinall long-term potentiation and recognition memory[J].Neuorsci, 2005,25(27):6296-6303.
  • 6Perazzona B, Isabel G, Preat T, et al. The role of cAMP response element- binding protein in drosophilal long-term memory[J]. Neurosci, 2004, 24(40):8823-8828.
  • 7Moncada D, Viola H. Phosphorylation state of CREB in the rat - hippcampus: a molecular switch between spatial novelty and spa- tial familiarity[J]. J Neurobiol Learn Mem, 2006, 86(1): 9-18.
  • 8Patel NV, Finch CE. The glucocorticoid paradox of caloric re- striction in slowing brain aging[J]. Neurobio Aging, 2002, 23 (2): 707-717.
  • 9Choes ES, Parelkar NK, Kim JY, et al. The protein phosphatase 1/2A inhibitor okadaic acid increase CREB and ELK-1 phospho- rylation and c-foc expression in the rat striatum in vivo[J]. Neuroc- hem, 2004,89(4):383-390.

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