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黄金兰,陆璐,黄丹,钟振国.三七总皂苷对快速老化模型小鼠大脑β-分泌酶活性及含量的影响[J].,2013,33(07):0944-9047
三七总皂苷对快速老化模型小鼠大脑β-分泌酶活性及含量的影响
Effect of PNS on the Activity and Content of BACE1 in the Brain of SAMP8 Mice with Alzheimer′s Disease
  
DOI:10.7661/CJIM.2013.07.0944
中文关键词:  三七总皂苷  快速老化SAMP8 小鼠  β-分泌酶
英文关键词:Panax notoginseng saponin  senescence accelerated mouse-prone 8  BACE1
基金项目:国家自然科学基金资助项目(No30960489,No. 81160512);广西自然科学基金项目(No2010GXNSFD013050)
Author NameAffiliationE-mail
黄金兰,陆璐,黄丹   
钟振国 广西医科大学药学院(南宁530021) zhongzg@gxtcmu.edu.cn 
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中文摘要:
      目的研究三七总皂苷(Panax notoginseng saponin, PNS)对快速老化小鼠亚系8(senescence accelerated mouse-prone 8,SAMP8) 小鼠大脑β-分泌酶(Beta-site amyloid precursor protein cleavage enzyme,BACE,主要是BACE1)活性及含量的影响。方法选择SAMP8 32只,随机分为对照组、PNS高剂量组(200 mg/kg)、PNS低剂量组(100 mg/kg)和石杉碱甲组(0.3 mg/kg), 每组8只,对照组给予等容积双蒸水灌胃。每天灌胃1次,连续给药2个月。分别采用直接荧光法和Western blot法检测SAMP8大脑BACE1的活性和BACE1蛋白含量。结果PNS高低剂量组(高剂量组:2.008±0.031;低剂量组:2.221±0.029)和石杉碱甲组(2.267±0.076)相对荧光单位(RFU/μg)值均比对照组(2.403±0.058)低(P<0.01)。PNS高低剂量组(高剂量组:0.900±0.028;低剂量组:1.000±0.032)和石杉碱甲组(0.837±0.080)BACE1蛋白表达均比对照组低(2.210±0.074,P<0.01)。结论高于100 mg/kg的PNS可以降低SAMP8脑内BACE1活性,下调BACE1蛋白表达。
英文摘要:
      ObjectiveTo explore the effect of Panax notoginseng saponin (PNS) on the activity and content of β-secretase in the brain of senescence accelerated mouse-prone 8 (SAMP8) mice with Alzheimer′s disease. MethodsTotally 32 SAMP8 mice were randomly divided into the normal control group, the high dose PNS group (200 mg/kg), the low dose group (100 mg/kg), and the huperzine A group (0.3 mg/kg), 8 in each group. Equal volume of double distilled water was given to those in the normal control group. All medication was given by gastrogavage, once daily for two successive months. The activity of BACE1 was assayed by direct immunofluorescent method (DIF). The content of BACE1 protein was detected by Western blot. ResultsThe relative fluorescence units (RFU/μg) was 2.008±0.031 in the high dose PNS group, 2.221±0.029 in the low dose PNS group, and 2.267±0.076 in the huperzine A group, all lower than that in the normal control group (2.403±0.058; all P<0.01). The content of BACE1 protein was 0.900±0.028 in the high dose PNS group, 1.000±0.032 in the low dose PNS group, and 0.837±0.080 in the huperzine A group, all lower than that in the normal control group (2.210±0.074, all P<0.01). ConclusionPNS higher than 100 mg/kg could decrease the activity of BACE1 and down-regulate the content of BACE1 protein in the brain of SAMP8 mice.
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