电针对Alzheimer病大鼠额叶与海马区免疫炎性反应的影响
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
目的观察阿尔茨海默病(AD)模型大鼠额叶与海马区的免疫炎性反应、P_(38)MAPK的磷酸化及其超微病理的变化等,以及电针治疗对其的影响,探讨电针防治AD的可能机制,为针刺临床提供新的理论依据。
     方法110只24月龄SD大鼠,采用Y型水迷路法粗筛,获正常老年大鼠103只,再从103只SD大鼠中随机选出30只,分别归入正常组和假手术组,每组15只。双侧Meynert核注射微量凝聚态Aβ_(1-40)制备AD动物模型,造模完成后第31天,对大鼠再次进行Y型水迷路法筛选,凡15次测试中正确次数较造模前下降1/3者为造模成功。将造模成功的大鼠随机归入模型组16只,电针组17只。选取“百会”、“太溪”、“足三里”进行电针治疗,每天1次,6天为1疗程,疗程间隔1天,共治疗2疗程。Morris水迷宫行为学实验检测其学习记忆能力,免疫组化SABC法观察大鼠额叶与海马区IL-1β、TNF-α的变化,rt-PCR检测IL-1βmRNA和TNF-αmRNA的表达,Western-blot法观察p-P_(38)MAPK的量,透射电镜观察AD大鼠额叶与海马区神经元超微结构。全部数据输入计算机,用SPSS13.0统计软件包进行处理,实验结果以((?)±s)表示。
     结果(1)Morris水迷宫检测发现:在定位航行实验中,第1天,模型组、电针组逃避潜伏期较正常组、假手术组明显延长(P<0.01);模型组与电针组之间、正常组与假手术组之间无差异(P>0.05);第2、3、4、5天,各组大鼠均随着训练次数增加,潜伏期越来越短,但潜伏期长短明显不一,正常组和假手术组约在25s内找到平台,模型组约需60s,但电针组在40s内可找到平台,其逃避潜伏期较模型组明显缩短(P<0.01)。在空间探索实验中,模型组与正常组、假手术组相比,原平台象限游泳时间比和原平台象限跨越次数比均显著减小(P<0.01),10%百分比和30%百分比明显增加(P<0.01);电针组与模型组比较,原平台象限游泳时间比和原平台象限跨越次数比明显增加(P<0.01),10%百分比和30%百分比明显减少(P<0.01)。(2)模型组GFAP与CD68阳性细胞、IL-1β与TNF-α表达增加,染色增强,与正常组、假手术组相比有非常显著性意义(P<0.01);经电针治疗后表达显著减少,与模型组比较,差异有非常显著性(P<0.01)。(3)rt-PCR检测表明:模型组额叶与海马区IL-1βmRNA、TNF-αmRNA的表达较正常组、假手术组增强(P<0.05-0.01),电针组IL-1βmRNA、TNF-αmRNA表达显著减少,与模型组比较,P<0.05-0.01。(4)Western-blot显示:各组大鼠额叶与海马区均有p-P_(38)MAPK的表达,模型组表达最高,与正常组、假手术组相比具有非常显著性意义(P<0.01);经电针治疗后额叶与海马区p-P_(38)MAPK表达减少,与模型组相比,差异具有非常显著性意义(P<0.01)。(5)透射电镜下模型组额叶与海马区可见一些神经细胞变性,其内细胞器可见内质网扩张,线粒体肿胀和空泡样变;电针组神经元细胞核基本正常,少数神经细胞可见线粒体轻度肿胀,正常组和假手术组神经细胞则无上述变化,神经细胞胞膜完整,胞浆基质电子密度均匀,生物膜完整,结构清楚,未见明显病变。
     结论本实验的结果表明:Meynert核注射微量凝聚态Aβ_(1-40)可诱发CNS的免疫炎性反应。电针百会、太溪、足三里可减少额叶与海马区小胶质细胞和星形胶质细胞的活化,下调IL-1β与TNF-α、IL-1βmRNA与TNF-αmRNA的表达及P_(38)MAPK的磷酸化,从而阻抑额叶与海马区炎性反应,拮抗Aβ_(1-40)对CNS的毒性作用,抑制神经元变性、坏死。
Objective To observe the immunological inflammatory reaction, phosphorylation of P_(38)MAPK,and neuronic ultrastructural change in frontal lobe and hippocampus of Alzheimer's disease(AD) rats,and the effect of electroacupuncture on them.And to explore the possible mechanism of treating AD by electroacupuncture.
     Methods 103 normal SD rats were selected out from 110 rats with 24 months by the method of Y type water maze.Then from the 103 rats,30 rats were randomly selected into normal group and sham-operation group,with 15 rats in each group.The model of Alzheimer disease was established by stereotaxis injection agglutinated Aβ_(1-40) into rat's bilateral Meynert basal nuclei.On the thirty-first day after model preparation,the rats were screened again with the method of Y type water maze.In 15 tests,if the correct times lower 1/3 than that before,the model was the successful model.The model rats were randomly selected into model group and(EA) group,with 16 rats in model group and 17rats in EA group.The points of "Baihui"、"Taixi" and "Zusanli" were selected to treat the rats in EA group by electroacupuncture. The treatment was once a day and 6 days was a course of treatment.The next time of therapy continued after one day's rest,and the total treatment time was 2 courses.The learning and memory ability was tested in the ethology experiment by Morris water maze,the expression change of microglia、astrocytes,IL-1βand TNF-αof frontal lobe and hippocampus in rats were observed by immunohistochemical method of S ABC,the expression of IL-1βmRNA and TNF-αmRNA were observed by RT-PCR,the phosphorylation of P_(38)MAPK were observed by Western-blot,the neuronic ultrastructural change of frontal lobe and hippocampus in rats were observed by transmission electron microscope.All data were put into the computer and analyzed by SPSS13.0 statistical package.The experiment results were expressed as mean±standard deviation((?) x±s).
     Results(1) To indicate by the results in the ethology experiment by Morris water maze:In the location see trial,on the first day,the escape latent period in model group and EA group was remarkably longer than that in normal group and sham-operation group(P<0.01);there was no significant difference between model group and EA group,normal group and sham-operation group(P>0.05);on the second day、third day、fourth day and fifth day,the escape latent period in EA group was obviously shorter than model group(P<0.01).And the escape latent period shortened gradually in each group as the swimming days increased,but there were obviously difference between them.In space search test,time percentage and frequency percentage of spanning the platform quadrant remarkably decreased,10% percentage and 30%percentage remarkably increased in the rats of model group,there were significant differences compared with normal group and sham-operation group(P<0.01);time percentage and frequency percentage in EA group remarkably increased,10%percentage and 30%percentage in EA group evidently decreased,there were significant differences compared with model group(P<0.01).(2) The number of positive cells of GFAP and CD68, and the expression of IL-1βand TNF-αin model group obviously increased, their dyeing was deepened,there were significant differences in comparison with normal group and sham-operation group(P<0.01);After the treatment of electroacupuncture,they remarkably decreased,there were significant differences in comparison with model group,P<0.01.(3) To sign in the experiment of RT-PCR:the expression of IL-1βmRNA and TNF-αmRNA in frontal lobe and hippocampus of model group evidently enhanced,there were significant differences in comparison with normal group and sham-operation group(P<0.05-0.01);the expression of IL-βmRNA and TNF-αmRNA in EA group obviously reduced,compareing with model group,P< 0.05-0.01.(4) To show in the experiment of Western-blot:There were expression of p-P_(38)MAPK in frontal lobe and hippocampus of each group,but the expression in model group was maximum,there were significant differences in comparison with normal group and sham-operation group(P< 0.01);After the treatment of electroacupuncture,the expression remarkably decreased,there were significant differences in comparison with model group(P<0.01).(5) in frontal lobe and hippocampus of the rats in model group, we observed some nerve cells degenerated by transmission electron microscope,endoplasmic reticulum of inter organelle expanded and mitochondriom swelled.However,in frontal lobe and hippocampus of rats in EA group,cell nucleus was almost normal and mitochondrion in organelle swelled a little.There weren't above-mentioned changes in the nerve cells of frontal lobe and hippocampus of the rats in normal group and sham-operation group.The cell membrane was integral,electron density in ground substance of cytoplasm was well-distributed,biomembrane was integral and the structure was clear.There weren't obvious pathological changes in the nerve cells of the rats in these two groups.
     Conclusion The results in present research indicated that agglutinated Aβ_(1-40) injected into rat's bilateral Meynert basal nuclei could cause the immunological inflammatory reaction in central nervous system. Electroacupuncture can decrease the number of microglial cells vivid and astrocytes vivid,reduce the expression of IL-1βand TNF-α、IL-1βmRNA and TNF-αmRNA、p-P_(38)MAPK,thereby restrain inflammatory reaction in frontal lobe and hippocampus of AD rats,antagonize toxic action in central nervous system caused by ABBBBBBB_(1-40),inhibitory nerve cells to degenerate and necrosis.
引文
[1]王维治.神经病学[M],第五版.北京:人民卫生出版社,2004,7.
    [2]秋民,乔晋,韩建峰,等.陕西省西安地区中老年人痴呆及其主要亚型发病率调查[J].中华流行病学杂志,2005,26(7):529-532.
    [3]洪震,周玢,黄茂盛,等.上海城乡老年期痴呆患者死亡率和生存预示因素研究[J].中华流行病学杂志,2005,26(6):404-407.
    [4]陈可冀.老年性痴呆基础和临床研究进展思考[J].中国中西医结合杂志.1998,18(6):323.
    [5]李谷才,尹端沚,夏姣云,等.阿尔茨海默病发病机理研究进展[J].脑与神经疾病杂志,2005,13(4):311-312.
    [6]陈新平,陈彪.阿尔茨海默病病因学及发病机制研究进展[J].中国现代神经疾病杂志,2005,5(3):152-155.
    [7]Casal C,Serratosa J,Tusell JM.Efects of beta AP-peptides on activation of the transcription factor NF-kappa B and in cell proliferation in glial cell cultures[J].Neurosci Res,2004,48(3):315-323.
    [8]刘江红.老年性痴呆的免疫机制研究进展[J].中国神经免疫学和神经病学杂志,2004,11(2):111-114.
    [9]王德生,张守信.老年性痴呆[M].北京:人民卫生出版社,2001.10
    [10]王琳,韩杰,张昱.Alzheimer病病人血清与脑脊液白细胞介素-1及肿瘤坏死因子水平检测的研究[J].中华神经科杂志,2002,35(6):339-341.
    [11]Paresce DM,Chung H,Maxfield FR.Slow degradation of aggregates of the Alzheimer's disease amyloid beta-protein by microglial cells[J].J Biol Chem 1997,272(46):29390-7.
    [12]Aliyama H,Barger S,Barnum S,et al.Inflammation and Alzheimer's disease[J].Neurobiol Aging,2000,21(3):383-241.
    [13]欧阳颀,李忠仁,穆艳云,等.针刺治疗阿耳茨海默病临床疗效对照研究[J].中国针灸,1999,19(7):399.
    [14]欧阳颀,李忠仁,穆艳云,等.针刺对16例阿耳茨海默病患者智能障碍影响的对照观察[J].安徽中医临床杂志,1999,11(3):158.
    [15]杨增瑞,来丽萍,李平,等.针刺对快速老化痴呆模型小白鼠脑内Ach含量及AchE活性影响的实验研究[J].天津中医,1999,16(3):20.
    [16]石学敏,韩景献,李平,等.针刺对老化痴呆鼠脑兴奋性氨基酸水平影响的实验研究[J]冲国针灸,1998,18(11):689.
    [17]吕家祥.针药并施治疗老年痴呆症30例[J].陕西中医,1993,14(2):80.
    [18]王少锦,康锁彬,李爱英.针刺拟痴呆大鼠对脑内自由基系统与胆碱能系统功能影响相关性的分析[J].针刺研究,2004,29(6):102-106.
    [19]沈政,林庶芝.生理心理学[M],第1版.北京:北京大学出版社,1993,11-12.
    [20]Labeshima T.Trial to produce animal model of Alzheimer's disease by continuou infusion of beta-amyloid protein to the rat cerebralventricle Nihon Shinkei Seishin Yakurigaku Zasshi,1995,15(5):441.
    [21]包新民,舒斯云.大鼠脑立体定位图谱[M].北京:人民卫生出版社,1991,21.
    [22]徐淑云.药理实验方法学[M].北京:人民卫生出版社,1991,661-662.
    [23]Morris R.Development of a water maze procedure for studying spatial learning in the rat[J].Neurosci Meth,1984,11(1):47-60.
    [24]盛树力.老年性痴呆:从分子生物学到临床诊治[M].北京:科学技术文献出版社,1999:1-22.
    [25]Morris RGM,Garrud P,Rawlins JNP,etal.Place navigation impaired in rats with hippocampal lesions[J].Nature,1982,297:681.
    [26]Frick KM,Baxter MG,Markowaska AL,et al.Age-related spatial reference and working memory deficits assessed in the water maze[J].Neurobiology of Aging,1995,16(2):149.
    [27]柯尊记,姚志彬,陈以慈.老年学习记忆减退大鼠空间参考记忆和工作记忆能力的改变[J].中国行为医学科学,1999,8(4):245-248.
    [28]Lue LF,Walker DG,Rogers J.Modeling microglial activation in Alzheimer's disease with human postmortem microglial eultures[J].Neurobiol Aging,2001,22:945-956.
    [29]Golde TE.Inflammation takes on Alzheimer disease[J].NatureMed,2002,8(9):936-938.
    [30]Caginn A,Brooks DJ,Kennedy AM et al.In viro measurement of activated microglia in dementia[J].Lancet,2001;358:461-467.
    [31]StreitW J.Microglia and Alzheimer's disease pathogenesis[J].J NeurosciRes,2004,77(1):1-8.
    [32]Rogers J,Lue L F.Microglial chemotaxis,activation,and phagocytosis of amyloid beta peptide as linked phenomena inAlzheimer's disease[J].Neurochem Int,2001,39(5-6):333-340.
    [33]Bamberger ME,Harris ME,McDonald DR,et al.A cell surface receptor complex for fibrillar beta-amyloidmediatesmicroglial activation[J].J Neurosci,2003,23(7):2665-2674.
    [34]Orr C F,Rowe D B,Halliday G M.An inflammatory review of Parkinson's disease[J].Prog Neurobio,l 2002,68(5):325-340.
    [35]Vehamas A,Kawas C,Stewart W,et al.Immune reactive cells in seniplaques and cognitive in Alzheimer's disease[J].Neurobiol Aging,2003,24(2):321-331.
    [36]Kozlov A S,Angulo M C,Audinat E,et al.Target cell-specific modulation of neuronalactivity by astrocytes[J].Neuroscience,2006,103(26):10058-10063.
    [37]骆明军,程玲,刘胜洪,等.电针对缺血再灌注大鼠脑内小胶质细胞活化的影响[J].中国针灸,2004,24(5):351-353.
    [38]Delacourte A,David JP,Sergeant N,et al.The biochemical pathway of neurofi brillary degeneration in aging and Alzheimer's disease [J].Neurology,1999,52(6):1158.
    [39]Landreth GE,Heneka MT.Anti-inflammatory actions of peroxisome proliferator-actived receptor gamma agonists in Alzheimer's disease[J].Neurobiol Aging,2001,22:937-944
    [40]廖文辉,王文杰.阿尔采末病中的炎症反应[J].生理科学进展,2004,35(2):181.
    [41]Griffin WS.Inflammation and neurodegenerative disease[J].Am J Clin Nutr,2006,83:470-474.
    [42]Weisman D,Hakimian E,Ho GJ,etal.Interleukins,Inflammation,and Mechanisms of Alzheimer's Disease[J].Vitam Horm,2006,74:505-530.
    [43]Yucesoy B,Peila R,White LR,et al.Association of interleukin-1 gene polymorphisms with dementia in a community-based sample:The Honolulu-Asia Aging Study[J].Neurobiol Aging,2006,27:211-217.
    [44]James AR,Nicoll MD,Robert E,et al.Association of interleukin-1 Gene Polymorophisms with Alzheime disease[J].Ann Neurol,2000,47:365-368.
    [45]Licastro F,Veglia F,Chiappelli M,et al.A polymorphism of the interleukin-1 beta gene at position +3953 influences progression and neuro-pathologica hallmarks of Alzheimer's disease[J].Neurobio Aging,2004,25:1017-1022.
    [46]Shepherd CE,Thiel E,McCann H,etal.Cortical inflammation in Alzherimer disease but not dementia with Lewy bodies[J].Arch Neurol,2000,57:817.
    [47]Lio D,Annoni G,Licastro F,et al.Tumor necrosis factor-a_308A/G polymorphism is associated with age at onset of Alzheimer's disease[J].Mech Ageing Dev,2006,127:567-571.
    [48]Mrak RE,Griffin WS.Potential inflammatory biomarkers in Alzheimer's disease[J].J Alzheimers Dis,2005,8:369-75.
    [49]Lindberg C,Chromek M,Ahrengart L,et al.Soluble interleukin-1 receptor type Ⅱ,IL-18 and caspase-1 in mild cognitive impairment and severe Alzheimer's disease[J].Neurochem Int,2005,46:551-7.
    [50]Griffin WS.Inflammation and neurodegenerative disease[J].Am J Clin Nutr,2006,83:470S-4.
    [51]Sheng JG,Zhu SG,Jones RA,et al.Interleukin-1 promotes expression and phosphorylation of neurofilament and tau proteins in vivo[J].Exp Neurol,2000,163(2):388.
    [52]Sheng JG,Jones RA,Zhou XQ,et al.Interleukin-1 promotion of MAPK-p38 overexpression in experimental animals and in Alzheimer's disease potential significance for tau protein phosphorylation[J].Neurochem Int,2001,39(5-6):341.
    [53]Suk K,Lee J,Hur J,et al.Activation induced cell death of ratastrocytes[J].Brain Res,2001,900(2):342-347.
    [54]Rossi D,Brambilla L,Valori CF,et al.Defective tumor necrosis factor-alpha dependent control of astrocyte glutamate release in a transgenic mouse model of Alzheimer's disease[J].J Biol Chem,2005,280:42088-96.
    [55]Huang Y,Erdmann N,Peng H,et al.The role of TNF related apoptosis-inducing ligand in neurodegenerative disease[J].Cell Mol Immunol,2005,2:113-22.
    [56]Suk K,Lee J,Hur J,et al.Activation induced cell death of rat astrocytes[J].BrainRes,2003,900(2):342-347.
    [57]Rohn TT,Rissan RA,Davis MC,et al.Caspase-9 activation and caspase cleavage of tau in the Alzheimer's disease brain[J].Nerobiol Dis,2002,11(2):341-354.
    [58]Culpan D,MacGowan SH,Ford JM,et al.Tumour necrosis factor-a gene polymorphisms and Alzheimer's disease[J].Neurosci Lett,2003,350:61-65.
    [59]张春兵,李忠仁,沈梅红.针药结合改善痴呆模型大鼠学习记忆能力的机理初探[J].江苏中医药,2003;24(2):51.
    [60]王少锦,康锁彬,李爱英.针刺拟痴呆大鼠对脑内自由基系统与胆碱能系统功能影响相关性的分析[J].针刺研究,2004,29(2):102.
    [61]穆艳云,李忠仁,沈梅红,等.针药结合治疗学习记忆障碍机制[J].上海针灸杂志,2003,22(3):3-5.
    [62]Yu J,Yu T,Han J.Aging-related changes in the transcriptionalprofile of cerebrum in senescence-acceleratedmouse(SAMP 10) is remarkably retarded by acupuncture[J].AcupunctElectrotherRes,2005,30(l-2):27-42
    [63]马骋,闫丽萍,沈梅红.电针对大鼠海马兴奋性突触后电位长时程增强的作用[J].南京中医药大学学报,2003,19(3):169-171.
    [64]Widmann C,Gibson S,Jarpe MB,et al.Mitogen-activated protein kinasexonservation of a three-kinase module from yeast to human[J].Physiol Rev,1999,79(1):143-180.
    [65]Mielke K,Herdegen T.JNK and p38 stresskinases-degenerative effectors of signal-transduction-cascades in the nervous system[J].Prog Neurobiol,2000,61(1):45-60.
    [66]Schechter R,Beju D,Miller KE.The elect of insulin deficiency on tau and neurofilament in the insulin knockout mouse[J].Biochem Biophys ResCommun,2005,34(4):979-986.
    [67]Zhu X,Rottkamp C A,Boux H,et al.Activation of p38 kinase links tau phosphorylation,oxidativestress,and cellcycle-related events in Alzheimer disease[J]J Neuropathol Exp Neurol,2000,59(10):880-888.
    [68]Pei J J,Braak E,Braak H,et al.Localization of active forms of C-jun kinase(JNK)and p38 kinase in Alzeimer's disease brains at different stages of neurofibrillary degeneration[J].J Alzeimers Dis,2001,3(1):41-48.
    [69]Akiyama H,Barger S,Barnum S,et al.Inflammation and Alzheimer's disease[J].NeurobiolAging,2000,21(3):383-421.
    [70]Chen B,Chen Y,Lin W.Involvement of p38 mitogenactivated protein kinase in lipopolysaccharide-induced iNOS and COX-2 expression in J774macrophages[J].Immunology,1999,97(1):124-129.
    [71]Pasinetti G M,Aisen P S.Cyclooxy-genase-2 expression is increased in frontal cortex of Alzheimer's disease brain[J].Neuroscience,1998,87(2):319-324.
    [72]Yoshida H,Hastie CJ,McLauchlan H,et al.Phosphorylation of microtubule-associated protein tau by isoforms of c-Jun N-terminal kinase(JNK)[J].J Neurochem,2004,90(2):352-358.
    [73]万顺伦,孙锦平,李召峰.应激后大鼠下丘脑磷酸化p38MAPK的变化及电针足三里穴的调节作用[J].中华物理医学与康复杂志,2005,27(4):202-204.
    [74]李秀珍,张宝成,韩恩吉.淀粉样蛋白与Alzheimer病[J].现代康复,2000,4(5):727.
    [75]罗焕敏,肖飞.D-半乳糖和三氯化铝诱导小鼠产生类阿尔茨海默病变[J].中国药理学与毒理学杂志,2004,18:22-26.
    [76]罗焕敏,陈子晟.一种新的老年痴呆动物模型[J].中国老年学杂志,2003,23:179-182.
    [77]Donald LP and Sangram SS.Cellular and molecular biology of Alzheimer's disease and animal models[J].Ann.Rev.Med.l994,45:435-436.
    [78]Kuo H,Ingram DK,Walker LC,et al.Similarities in the age-related hippocampal deposition of periodic acidschiff-positive granules in the senescence-accelerated mouse P8 and C57BL/6 mouse strains[J]. Neuroscience,1996,74:733-40.
    [79]Lewis J,Maurizi CP,Jones GH,et al.Neurofibrillary tangles,amyotrophy and progressive motor disturbance in mice expressing mutant(P301L) tau protein[J].Nature Genet,2000,25:402-405.
    [80]马宜明,李俊,金涌.中医药关于老年性痴呆的发病机制及治疗进展[J].安徽医药,2002,64:3-5.
    [81]郭新春.抗老年痴呆胶囊治疗老年期痴呆临床观察[J].中国中医药信息杂志,2001,8(3):68-69.
    [82]张桂娟,马民,马义.脑康冲剂治疗阿尔茨海默病的临床与实验研究[J].中国老年学杂志,2006,5(26):619-620.
    [83]周志昆,曾红兵,黄兆胜,等.补肾活血方对阿尔茨海默病模型大鼠脑内胶质细胞的影响[J].中国中医基础学,2005,11(6):425-427.
    [84]王彩霞,李德新,姜哲浩,等.理脾阴正方提高Alzheimer痴呆模型动物学习记忆能力的机理探讨[J].辽宁中医杂志,2002,29(4):242-243.
    [85]陈家旭,杨维益.神经-内分泌-免疫网络研究概况及其与中医肝脏关系的探讨[J].北京中医大学学报,1995,18(4):7.
    [86]何朝,吴正治,李耀芳,等.补肝养髓方对自发老年性痴呆小鼠相关神经肽影响的实验研究[J]冲国中医药科技,2003,10(3):160-162.
    [87]周大兴,李昌煜,林乾良.石菖蒲对小鼠学习记忆的促进作用[J].中草药,1992,23(8):417-419.
    [88]Torreilles F,Touchon J.Pathogenic theories and intrathecal analysis of the sporadic form ofAlzhemi er's disease[J].ProgNeurobio,l 2002,66:191-203.
    [89]Corder E H,Saunders A M,StrittmatterW J,et al.Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families[J].Science,1993,261(5123):921-923.
    [90]CitronM,Westaway D,XiaW,et al.Mutant presenilins of Alzheimer's disease increase production of42-residue amyloid beta-protein in both transfected cells and transgenic mice[J].NatMed,1997,3(1):67-72.
    [91]王瑛,张海音,陈生弟.阿尔茨海默病的发病机制研究进展[J].中国神经免疫学和神经病学杂志,2002,9(1):42.
    [92]Mayeux R,Lee J H,Romas S N,et al.Chromosome-12 mapping of late-onsetAlzheimer disease among Caribbean Hispanics[J].Am JHum Genet,2002,70(1):237-243.
    [93]Barghorn S,Zheng-Fischh(o|¨)fer Q,Ackmann M,etal.Structure,microtubule interactions,and paired helical filament aggregation by tau mutants of frontotemporal dementias [J].Biochemistry,2000,39(38):11714-11721.
    [94]Alvarez V,Alvarez R,Lahoz C H,et al.Association between an alpha(2)macroglobulin DNA polymorphism and late-onsetAlzheimer's disease[J].Biochem Biophys Res Commun,1999,264(1):48-50.
    [95]蔡建光,印大中.阿尔茨海默病主要相关基因及其功能蛋白研究进展[J].中国神经免疫学和神经病学杂志,2006,13(2):120-123.
    [96]Kawahara M,Kato M,Kuroda Y.Effects of aluminum on the neurotoxicity of primary cultured neurons and on the aggregation of beta-amyloid protein[J].Brain research bulletin,2001,55(2):221-217.
    [97]马春,王爱民.脑的老化与痴呆[M].北京:北京医科大学与中国协和医科大学联合出版社,1995.76.
    [98]Matison MP,Wang H,Michaelis EK.Developmental expression,compartmentalization,and possible role in excitoxicity of aputative NMDA receptor in cultured hippocampal neurons[J].Brain Res 1991;565(1):94-108.
    [99]McLellan ME,Kajdasz ST,Hyman BT,et al.In vivo imaging of reactive oxygen species specifically associated with thioflavine S-positiv amyloid plaques by multiphoton microscopy[J].JNeurosci,2003 Ma15,23(6):2212.
    [100]Townsend KP,Obregon D,Quadros A,et al.Proinflammatory and vasoactive effects of Abeta in the cerebrovasculature[J].Ann N YAcad Sci,2002 Nov,977:65.
    [101]Torreilles F,Touchon J.Pathogenic theories and intrathecal analysis of the sporadic from ofAlzheimers' disease[J].Progress in Neurobiology,2002,66:191-203.
    [102]LambertMP,Barlow AK,Chromy BA,et a.Diffusible,nonfibrillar ligands derived from Abeta1-42 are potent central nervous system neurotoxins[J].Proc.Nat.l Acad.Sci USA,1998,95:6448-6453.
    [103]王琳,韩杰,张昱.Alzheimer病病人血清与脑脊液白细胞介素-1及肿瘤坏死因子水平检测的研究[J].中华神经科杂志,2002,35(6):339-341.
    [104]Akiyama H,Barger S,Barnum S,et al.Inflammation andAlzheimer's disease[J].NeurobiolAging,2000,21(3):383-421.
    [105]HüllM,Lieb K,Fiebich B L.Pathways of inflammatoryactivation in Alzheimer's disease:potential targets fordisease modifying drugs[J].CurrMed Chem,2002,9(1):83-88.
    [106]Vina J,Lloret A,Orti R,et al.Molecular bases of the treatment of Alzheimer's disease with antioxidants:prevention of oxidative stress[J].Mol Aspects Med,2004,25:117-123.
    [107]Boyd-KimballD,Mohmmad AbdulH,Reed T,et al.Role of phenylalanine 20 in Alzheimer's amyloid beta-peptide(1-42)-induced oxidative stress and neurotoxicity[J].Chem ResToxico,2004,17(12):1743-1749.
    [108]洪震,周玢,黄茂盛,等.阿尔茨海默病的保护因索-运动和户外活动[J].中国临床康复,2003,7(1):24-5,43.
    [109]李求兵,梅荣.老年痴呆症的中西医诊断与治疗[M].北京:中国医药科技出版社,1999:167.
    [110]Hardy J.Molecular genetics of Alzheimer's disease.Acta Neurol Scand (Suppl),1996,165:13-17
    [111]Trojanowski J Q,et al.Phosphrylation of neuronal cytoskeletal proteins in Alzheimer's disease.Ann NY Acad Sci,1994,747:92-109.
    [112]Migliorea L,Fontanaa I,Colognatoa R,et al.Searching for the role and the most suitable biomarkers of oxidative stress in Alzheimer s disease and in other neurodegenerative diseases.Neurobiology of Aging,2005,26:587-595.
    [113]Tortosa A,Lopez E.Ferrer,Bcl-2 and Bax protein expression in Alzheimer s disease.Acta Neuropathol Bcrl,1998,95:407-412.
    [114]高曲文,陈俊抛,田时雨,等.β淀粉样蛋白诱导脑内神经元凋亡及褪黑素的保护作用.中华神经科杂志,2000,33(1):7-9.
    [115]王米渠,曾祥国,马向东,等.恐伤肾造模对子代鼠脑超微结构的观察[J].成都中医药大学学报,1996,19(4):34-35.
    [116]胡汉波,王米渠,余曙光,等.恐吓孕鼠对子鼠成年期和成年后行为学影响的跳台实验研究[J].中国行为医学杂志,1998,7(2):83-84.
    [117]田金洲,杨承芝,盛彤,等.可疑痴呆人群中阿尔茨海默氏病临床前的认知损害及其与中医证候的关系[J].湖北中医杂志,1999,11(4):49-51.
    [118]杨柏灿,刘仁人.Alzheimer型痴呆的中医证型研究[J].上海中医药杂志,2000,34(4):12-14.
    [119]郭新春.抗老年痴呆胶囊治疗老年期痴呆临床观察[J].中国中医药信息杂志,2001,8(3):68-69.
    [120]郭苏云,张映梅.补肾益脑为主治疗老年性痴呆[J].云南中医学院学报,2003,26(1):40.
    [121]王彩霞,李德新,姜哲浩,等.理脾阴正方提高Alzheimer痴呆模型动物学习记忆能力的机理探讨[J].辽宁中医杂志,2002,29(4):242-243.
    [122]杨柏灿,刘仁人,薛人华,等.Alzheimer型痴呆的中医证型研究[J].上海中医药杂志,2000,(4):12-14.
    [123]欧阳颀,李忠仁,穆艳云,等.针刺治疗阿尔茨海默病临床疗效对照研究[J].中国针灸,1999,19(7):399.
    [124]张卫.针灸对老年痴呆模型小鼠防治作用的实验研究[J].山西中医,2001,17(10):633.
    [125]朱崇霞,张雯,程为平,等.针刺百会、大椎对拟血管性痴呆大鼠 GSH-PX、CAT的影响[J].上海针灸杂志,2004,23(3):40.
    [126]王中林.艾灸、电针、穴位注射对小鼠衰老模型空间分辨学习能力的影响[J].南京中医药大学学报,1999,15(5):304.
    [1]韩景献.痴呆的“三焦气化失司论”与针刺治疗老年期痴呆的研究[C]//天津市中西医结合学会.天津市中西医结合学会2006年学术年会论文集.天津:天津市中西医结合学会,2006:1.
    [2]许萍.针刺治疗老年性痴呆93例[J].中国民间疗法.2004,12(11):14-15.
    [3]许建阳,王发强,单保慈,等.针刺治疗老年性痴呆的认知能力及其脑功能成像的研究[J].中国中西医结合影像学杂志.2004,2(2):85-87.
    [4]姜国华,徐强,张洋.针刺对老年性痴呆神经行为学影响的临床研究[J].针灸临床杂志.2004,20(4):1-3.
    [5]唐勇,余曙光,蓝群.针刺对老年痴呆认知功能及自由基的影响[J].安徽中医临床杂志,2000,12(6):508-509.
    [6]唐勇,余曙光,陈瑾.针刺对老年性痴呆认知功能及AchE的影响[J].上海针灸杂志,2001,20(3):6-7.
    [7]董洪涛,金渊光,白英.针刺治疗老年性痴呆11例[J].上海中医药大学学报,2002,16(3):26-28.
    [8]董洪涛,白英.针刺疗法对老年性痴呆患者MMSE量表得分的影响[J].中医外治杂志,2002,11(3):6.
    [9]欧阳颀,李忠仁,穆艳云,等.针刺治疗阿尔茨海默病临床疗效对照研究[J].中国针灸,1999,19(7):399.
    [10]贺丹,李瑞利,李风鸾.脑复活因子穴位注射疗法治疗阿尔茨海默病疗效观察[J].脑与神经疾病杂志,2000,8(2):109-111.
    [11]梅静,刘春光,孙利.针灸治疗老年性痴呆76例[J].中国民间疗法.2003,11(12):13-14.
    [12]吴迪.针灸治疗早老性痴呆36例[J].四川中医,2003,22(3):93-94.
    [13]马梅青.安神醒脑汤配合针灸治疗老年性痴呆56例[J].陕西中医,2003,23(8):701-702.
    [14]李忠仁,穆艳云,欧阳颀.针刺加当归芍药散治疗阿尔茨海默病对照性研究[J].中国临床康复,2002,6(19):2848.
    [15]穆艳云,李忠仁.针药结合治疗阿尔茨海默病临床研究[J].上海针灸杂志,2001,20(3):3-5.
    [16]刘刚,袁立霞.针刺配合音乐疗法治疗阿尔茨海狱病的临床观察[J].中国针灸.2005,25(6):390-392
    [17]候安乐,卜渊.针刺药氧治疗老年期痴呆32例临床研究[J].中国针灸,2000,20(7):397
    [18]周友龙,贾建平.穴位埋线治疗阿尔茨海默病临床观察.中国针灸,2008,28(1):37-40.
    [19]王中林,陶勇,徐恒泽,等.艾灸、电针、穴位注射对小鼠衰老模型空间分辨学习能力的影响[J].京中医药大学学报,1999,15(5):30.
    [20]罗玳红,唐纯志,赖新生.电针对老年性痴呆模型大鼠学习记忆影响的实验研究[J].新中医,2003,35(11):77-78.
    [21]沈卫东,李鼎,方军.针灸对拟痴呆大鼠记忆功能的影响.上海针灸杂志,2000;19(4):36
    [22]褚芹,于建春,韩景献.针刺对快速老化痴呆模型小白鼠SAMP8认知功能的改善作用[J].中国行为医学科学,2005,11:964.
    [23]肖川.针刺不同间隔时间对SAMP10小鼠神经行为学影响[D]//硕士学位论文.天津:天津中医药大学,2005.
    [24]刘雨星,梁繁荣,余曙光,等.电针对穹隆-海马伞损伤老年痴呆大鼠学习记忆行为影响的实验研究.中国康复医学杂志,2004;19(3):188
    [25]欧阳颀,李忠仁,穆艳云,等.针刺对大鼠学习记忆的促进作用与其抗氧化作用的关系[J].南京中医药大学学报(自然科学版),2002,18(2):110-112.
    [26]张春兵,李忠仁,沈梅红.针药结合改善痴呆模型大鼠学习记忆能力的机理初探[J].江苏中医药,2003;24(2):51.
    [27]余曙光,周奇志,张新如,等.针刺对老年痴呆模型大小鼠AchE活性影响的实验研究[J].针灸临床杂志,2002,18(9):43.
    [28]王少锦,李爱英,张雪静.针刺督脉穴对拟AD大鼠海马区AchE、ChAT 活性的影响[J].南京中医药大学学报,2004,20(5):289.
    [29]张卫,刘来虎,殷克敬.针灸对老年痴呆模型小鼠防治作用的实验研究[J].陕西中医,2001;22(10):633.
    [30]杨增瑞,来丽萍,李平,等.针刺对快速老化痴呆模型小白鼠脑内Ach含量及AchE活性影响的实验研究[J].天津中医,1999,16(3):20.
    [31]董洪涛,白英.针刺对多因素AD模型海马ChE活性影响的实验研究[J].实用老年医学,2002,16(2):85-87.
    [32]包永欣,吕冠华.针刺对痴呆小鼠记忆障碍和单胺神经递质的影响.上海针灸杂志,2003;22(7):23
    [33]王旭慧,董承超,韩景献.针灸对快速老化痴呆小白鼠脑组织CA神经递质的影响[J].上海针灸杂志,2003,22(1):21.
    [34]王少锦,康锁彬,李爱英.针刺拟痴呆大鼠对脑内自由基系统与胆碱能系统功能影响相关性的分析[J].针刺研究,2004,29(2):102.
    [35]刘一凡,石学敏,韩景献,等.针刺对快速老化脑萎缩模型小鼠抗氧化酶活性的影响[J].中国针灸,2002,22(5):327.
    [36]刘庆忠,刘一凡,郑灏泳,等.针刺对SAM-P/10小鼠脑组织CAT、GSH-Px活性的影响[J].针灸临床杂志,2001,17(4):51-53.
    [37]徐强,韩玉生,姜国华,等.针刺对多因素AD大鼠乙酰胆碱酯酶的超氧化物歧化酶的影响[J].针灸临床杂志,2004,20(9):45-46.
    [38]唐纯志,赖新生,杨君军,等.电针对老年性痴呆大鼠脑内SOD、MDA、GSH-Px影响的实验研究[J].陕西中医,2005,26(2):180-181.
    [39]朱书秀,周丽莎,孙国杰.电针对阿尔茨海默病模型大鼠行为学及海马区IL-1β、TNF-α的影响.陕西中医学院学报,2008,31(4):55-57.
    [40]朱梅,高洪泉,刘瑞丰,等.针刺“足三里”、“关元”穴对老年大鼠肝脏内噬细胞功能影响的实验研究[J].针灸临床杂志,2003,19(6):52-53.
    [41]高洪泉,朱梅,王英.针刺老年大鼠“足三里”、“关元”穴对免疫影响的实验研究[J].针灸临床杂志,2002,18(5):53-55.
    [42]Yu J,Yu T,Han J.Aging-related changes in the transcriptionalprofile of cerebrum in senescence-acceleratedmouse(SAMP 10) is remarkably retarded by acupuncture[J].AcupunctElectrotherRes,2005,30(1-2):27-42
    [43]陆明霞,于建春,于涛.针刺对快速老化模型鼠脑中衰老相关基因表达的调整作用[J]冲国针灸,2003,23(1):48-51.
    [44]温延益,韩景献,李平,等.针刺对快速老化鼠脑、肝细胞核活性基因的影响[J].中医杂志,2002,43(1):28-29.
    [45]付于.针刺对快速老化痴呆小鼠SAMP10行为学及前脑、皮层、海马衰老相关基因表达影响的实验研究[D].天津:天津中医药大学,2005.
    [46]罗玳红,赖新生,唐纯志.电针治疗对老年性痴呆大鼠血清β淀粉样蛋白及生长因子水平的影响[J].中国中医药信息杂志,2003,10(10):22-23.
    [47]石学敏,韩景献,赵俊宏,等.针刺对脑萎缩模型小白鼠细胞核蛋白及染色质非组蛋白的影响[J].中国针灸,1999,(1):43.
    [48]刘涛.SAMP10海马、皮层衰老相关蛋白的增龄变化即针刺对其表达影响的实验研究[D].天津:天津中医药大学,2005.
    [49]褚芹.SAMP8行为学、海马比较蛋白质组学的增龄变化及针刺干预作用的研究[D].天津:天津中医药大学,2006.
    [50]张月峰,于建春,李谈,等.“益气调血,扶本培元”针法对快速老化小鼠SAMP8海马和颞叶皮质神经元数量及形态的影响[J].上海针灸杂志,2005,124(9):40-44.
    [51]张月峰.针刺对SAMP8大脑神经元丢失干预作用的实验研究[D].天津:天津中医药大学,2005.
    [52]梁跃.针刺对SAMP10海马、皮层神经元可塑性干预作用的实验研究[D].天津:天津中医药大学,2006.
    [53]马骋,闫丽萍,沈梅红.电针对大鼠海马兴奋性突触后电位长时程增强的作用[J].南京中医药大学学报,2003,19(3):169-171.
    [54]余曙光,王宗勤,周奇志,等.针刺对老年痴呆大鼠海马、皮层电图的影响[J].中国中医基础医学杂志,2002;8(12):48
    [55]张志雄,原淑娟,吴宝宗.电针对半乳糖所致大鼠空间学习记忆障碍及海马齿状回LTP诱导的干预作用[J].针刺研究,2001,26(4):247-252.
    [56]董洪涛,白英.针刺对含apoEε4基因AD患者P认知电位影响[J].上海针灸杂志,2001,20(6):9-11.
    [57]王少锦,孙宴辉,赵志国,等.“提督醒脑”针法对早老性痴呆大鼠中枢胆碱能系统的影响[J].针刺研究,2000,25(3):175-178.
    [1]Rogers J,Webster S,Lue LF,et al.Inflammation and Alzheimer's disease pathogenesis[J].Neurobiol Aging,1996,17(5):681.
    [2]王德生,张守信.老年性痴呆[M].北京:人民卫生出版社,2001.10
    [3]杜泽英,李晓玉.阿尔采末病与免疫炎症反应的相关性[J].生理科学进展,1998,29(3):253.
    [4]Cagnin A,Brooks DJ,Kennedy AM,et al.Invivomeasurement of activated microglia in demetia[J].Lancet,2001,358(9280):461-467.
    [5]王琳,韩杰,张昱.Alzheimer病病人血清与脑脊液白细胞介素-1及肿瘤坏死因子水平检测的研究[J].中华神经科杂志,2002,35(6):339-341.
    [6]McGeerPL.神经退行性变的免疫学机制[J].国外医学·药学分册,1997,24(2):94-97.
    [7]Breitner JC.NSAIDs and Alzheimer's disease:how far to generalize from trials[J].Lancet Neurol,2003,2(9):527.
    [8]VilhardtF.Microglia phagocyte and glia cell[J].Int J Biochem Cell Biol,2005,37(1):17-21.
    [9]HanischU K.Microglia as a source and target of cytokines[J].Glia,2002,40(2):140-155.
    [10]Morgan D.Modulation of microglial activation state following passive immunization in amyloid depositing transgenic mice[J]Neurochem Int,2006,49(2):190.
    [11]Xiang Z,Haroutunian V,Ho L,et al.Microglia activation in the brain as inflammatory biomarker of Alzheimer's disease neuropathology and clinical dementia[J].Dis Markers,2006,22(1-2):95.
    [12]Wang T,Zhang W,Pei Z,et al.Reactive microgliosis participates in MPP+-induced dopaminergic neurodegeneration:role of 67 kDa laminin receptor[J].FASEBJ,2006,20(7):906.
    [13]Nelson PT,Soma LA,Lavi E.Microglia in diseases of the central nervous system.Ann Med,2002,34:491-500.
    [14]LiuB,Hong JS.Role of microglia ini nflammation-mediated neurodegenerative diseases:mechanisms and strategies for therapeutic intervention.JPharmacolExpTher,2003,304:l-7.
    [15]Tilleux S,Hermans E.Neuroinflammation and regulation of glial glutamate uptake in neurological disorders[J]J Neurosci Res,2007,85(10):2059.
    [16]Qian L,Hong JS,Flood PM.Role of microglia in inflammation mediated degeneration of dopaminergic neurons meuroprotective effect of interleukin 10[J]J Neural Transm Suppl,2006,70:367.
    [17]Parachikova A,Agadjanyan MG,Cribbs DH,et al.Inflammatory changes parallel the early stages of Alzheimer disease[J].Neurobiol Aging,2006,28(12):1821.
    [18]Butovsky O,Koronyo-Hamaoui M,Kunis G,et al.Glatiramer acetate fights against Alzheimer's disease by inducing dendritic-like microglia expressing insulin-like growth factor l[J].Proc Natl Acad Sci USA,2006,103(31):11784.
    [19]Bamberger ME,Harris ME,McDonald DR,et al.A cell surface receptor complex for fibrillar beta-amyloidmediatesmicroglial activation[J].J Neurosci,2003,23(7):2665-2674.
    [20]Li L,Liu L,Barger SW.Interleukin-1 mediates pathological effects of microglia on tau phosphorylation and on synaptophysin synthesis in cortical neurons through a p38-MAPK pathway[J].J Neurosci,2003,23(5):1605-1611.
    [21]Wilcock DM,DiCarlo G,Henderson D.Intracranially administered antiAβ antibodies reduce β-amyloid deposition by mechanisms both in dependent of associated with microglial activation[J].J Neurosci,2003,23(9):3745.
    [22]Vehamas A,Kawas C,Stewart W,et al.Immune reactive cells in senileplaques and cognitive in Alzheimer's disease[J].Neurobiol Aging,2003,24(2):321-331.
    [23]Eeinstra E,Wilzak N.Astroctyes in chronic active multiple sclerosis plaques express MHC classs II molecules.Neureport 2000;11:89-91
    [24]Ralay R H,Craft J M,Hu W,et al.Gliaas a therapeutic target:selective suppression of human amyloid-beta-induced upregulation of brain proinflammatory cytokine production attenuates neurodegeneration[J].J Neurosci,2006,26(2):662-670.
    [25]DeWitt DA,Perry GA strocytes regulate microglial phagocytosis of senile plaque cores of Alzheimer's disease[J].Exp Neurol,2004,149(2):329-340.
    [26]周慧芳,薛冰,王晓民.免疫应答异常与中枢神经系统退变性疾病.基础医学与临床,2002,22(3):200-205.
    [27]Griffin WS.Inflammation and neurodegenerative disease[J].Am J Clin Nutr,2006,83:470-474.
    [28]Weisman D,Hakimian E,Ho GJ,etal.Interleukins,Inflammation,and Mechanisms of Alzheimer's Disease[J].Vitam Horm,2006,74:505-530.
    [29]Sheng JG,Jones RA,Zhou XQ,et al.Interleukin-1 promotion of MAPK-p38 overexpression in experimental animals and in Alzheimer's disease:potential significance for tau protein phosphorylation[J].Neurochem Int,2001,39(5-6):341.
    [30]Sheng JG,Zhu SG,Jones RA,et al.Interleukin-1 promotes expression and phosphorylation of neurofilament and tau proteins in vivo[J].Exp Neurol,2000,163(2):388.
    [31]Zhu SG,Sheng JG,Jones RA,et al.Increased interleukin-lb converting enzyme expression and activity in Alzheimer disease[J]J Neuropatho Exp Neurol,2004,58(6):582-587.
    [32]Shepherd CE,Thiel E,McCann H,et al.Cortical inflammation in Alzherimer disease but not dementia with Lewy bodies[J].Arch Neurol,2000,57:817.
    [33]Lio D,Annoni G,Licastro F,et al.Tumor necrosisfactor-a_308A/G polymorphism is associated with age at onset of Alzheimer's disease[J].Mech Ageing Dev,2006,127:567-571.
    [34]Stalder AK,Carson MJ,Pagenstecher A,at el.Late-onset chronic inflammatory encephalopathy in immune competent and severe combined immune deficient(SCID)mice with astrocyte targeted expression of tumor necrosis factor[J].Am J Pathol,1998,153(3):767-783.
    [35]Su JH,Anderson AJ,Cribbs DH,et al.Fas and Fas ligand are associated with neuritic degeneration in the AD brain and participate in Beta-amyloid-induced neuronal death[J].Neurobiol Dis,2003,12(3):182-193.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700