中华神经科杂志
中華神經科雜誌
중화신경과잡지
Chinese Journal of Neurology
2011年
7期
500-503
,共4页
湛彦强%吴军%许杰%尹波%马铭%杜桂焕%刘祖黎%徐威%雷浩%张苏明
湛彥彊%吳軍%許傑%尹波%馬銘%杜桂煥%劉祖黎%徐威%雷浩%張囌明
담언강%오군%허걸%윤파%마명%두계환%류조려%서위%뢰호%장소명
阿尔茨海默病%衰老斑%纳米粒子%四氧化三铁%造影剂%磁共振成像
阿爾茨海默病%衰老斑%納米粒子%四氧化三鐵%造影劑%磁共振成像
아이자해묵병%쇠로반%납미입자%사양화삼철%조영제%자공진성상
Alzheimer's disease%Senile plaques%Nanoparticles%Ferrosoferric oxide%Contrast media%Magnetic resonance imaging
目的 开发具有高度特异性的靶向磁共振对比剂,验证其特异性显示阿尔茨海默病(AD)脑内老年斑的可能性及有效性.方法 利用热分解法获得水相的磁性纳米四氧化三铁颗粒(MNPs),经过表面官能化学修饰,完成MNPs与β淀粉样蛋白肽段1-40(Aβ40)及蛋白质转导结合域(protein transduction domain,Tat-PTD)的连接后,制备出特异性与老年斑相结合的靶向纳米铁造影剂Aβ40-MNPs-Tat PTD,通过尾静脉注射人20只AD鼠和20只阴性对照C57小鼠(4、6、9、12月龄各5只)体内,不同的时间点采用7.0 T动物磁共振检测获得磁共振图像,观察靶向纳米造影剂对脑实质内老年斑信号的强化效果,继之处死小鼠后灌流取脑做连续冰冻切片,进行铁染色和Thioflavine S染色组织学验证.结果 所获得的靶向纳米颗粒Aβ40-MNPs-Tat PTD能够在体外进入细胞内进而改变细胞磁共振T2信号强度.尾静脉注射入AD鼠体内后能特异性负性强化AD鼠脑内老年斑病变,经组织学验证,能够与老年斑染色及铁染色相对应.结论 特异靶向性的磁性纳米铁造影剂Aβ40-MNPs-Tat PTD能特异性地针对小鼠脑内的老年斑病变进行负性强化和标记.
目的 開髮具有高度特異性的靶嚮磁共振對比劑,驗證其特異性顯示阿爾茨海默病(AD)腦內老年斑的可能性及有效性.方法 利用熱分解法穫得水相的磁性納米四氧化三鐵顆粒(MNPs),經過錶麵官能化學脩飾,完成MNPs與β澱粉樣蛋白肽段1-40(Aβ40)及蛋白質轉導結閤域(protein transduction domain,Tat-PTD)的連接後,製備齣特異性與老年斑相結閤的靶嚮納米鐵造影劑Aβ40-MNPs-Tat PTD,通過尾靜脈註射人20隻AD鼠和20隻陰性對照C57小鼠(4、6、9、12月齡各5隻)體內,不同的時間點採用7.0 T動物磁共振檢測穫得磁共振圖像,觀察靶嚮納米造影劑對腦實質內老年斑信號的彊化效果,繼之處死小鼠後灌流取腦做連續冰凍切片,進行鐵染色和Thioflavine S染色組織學驗證.結果 所穫得的靶嚮納米顆粒Aβ40-MNPs-Tat PTD能夠在體外進入細胞內進而改變細胞磁共振T2信號彊度.尾靜脈註射入AD鼠體內後能特異性負性彊化AD鼠腦內老年斑病變,經組織學驗證,能夠與老年斑染色及鐵染色相對應.結論 特異靶嚮性的磁性納米鐵造影劑Aβ40-MNPs-Tat PTD能特異性地針對小鼠腦內的老年斑病變進行負性彊化和標記.
목적 개발구유고도특이성적파향자공진대비제,험증기특이성현시아이자해묵병(AD)뇌내노년반적가능성급유효성.방법 이용열분해법획득수상적자성납미사양화삼철과립(MNPs),경과표면관능화학수식,완성MNPs여β정분양단백태단1-40(Aβ40)급단백질전도결합역(protein transduction domain,Tat-PTD)적련접후,제비출특이성여노년반상결합적파향납미철조영제Aβ40-MNPs-Tat PTD,통과미정맥주사인20지AD서화20지음성대조C57소서(4、6、9、12월령각5지)체내,불동적시간점채용7.0 T동물자공진검측획득자공진도상,관찰파향납미조영제대뇌실질내노년반신호적강화효과,계지처사소서후관류취뇌주련속빙동절편,진행철염색화Thioflavine S염색조직학험증.결과 소획득적파향납미과립Aβ40-MNPs-Tat PTD능구재체외진입세포내진이개변세포자공진T2신호강도.미정맥주사입AD서체내후능특이성부성강화AD서뇌내노년반병변,경조직학험증,능구여노년반염색급철염색상대응.결론 특이파향성적자성납미철조영제Aβ40-MNPs-Tat PTD능특이성지침대소서뇌내적노년반병변진행부성강화화표기.
Objective To develop specific targeted magnetic biomarkers which can selectively mark the senile plaques in Alzheimer' s disease (AD) and verify its feasibility and validity.Methods Aβ1-40 peptide and Tat-PTD ( Tat-protein transduction domain) was binded with dextran-coated ultrasmall superparamagnetic iron oxide ( USPIO) particles.Visualization of plaques in vivo in Alzheimer transgenic mice was investigated at 7.0 Tesla using T2 sequences after intravenous administration of the targeted nanoiron contrast agent and verified by histological staining.Results The targeted nano-iron contrast agent could enter the cultured neural stem cells,and was able to accelerate T2 relaxation rates of water protons in the cells and negatively reinforce the T2 signal intensity in the labeled cells.Plaques were specifically detected in vivo by magnetic resonance imaging ( MRI) and correlated well with histological staining after injection of nano-iron contrast agent into the APP/PS1 mice.Conclusion The targeted nano-iron contrast agent has the ability of selectively labeling the senile plaques in AD brain tissues in vivo,which might enable the early detection of plaques by MRI and can be further applied in the studies of early diagnosis of AD.