中华行为医学与脑科学杂志
中華行為醫學與腦科學雜誌
중화행위의학여뇌과학잡지
CHINESE JOURNAL OF BEHAVIORAL MEDICINE AND BRAIN SCIENCE
2013年
7期
587-590
,共4页
夏春波%蒋常文%刘源劼%刘漫君%陈清莲%罗玉琨%蒙丽恒%刘璟%唐金良
夏春波%蔣常文%劉源劼%劉漫君%陳清蓮%囉玉琨%矇麗恆%劉璟%唐金良
하춘파%장상문%류원할%류만군%진청련%라옥곤%몽려항%류경%당금량
学习记忆障碍%X-连锁凋亡抑制蛋白%海马%神经元凋亡%转录反式激活因子
學習記憶障礙%X-連鎖凋亡抑製蛋白%海馬%神經元凋亡%轉錄反式激活因子
학습기억장애%X-련쇄조망억제단백%해마%신경원조망%전록반식격활인자
Learning and memory impairment%X-linked inhibitor of apoptosis protein%Hippocampus%Neuron apoptosis%Trans-activator of transcription
目的 探讨TAT-XIAP融合蛋白对学习记忆障碍大鼠的影响及其与大脑海马神经元凋亡的关系,为学习记忆的深入研究提供实验依据.方法 利用基因工程技术制备具有生物学活性的TAT-XIAP融合蛋白,通过D-半乳糖(D-Gal)腹腔注射和Aβ1-42海马注射建立学习记忆障碍大鼠模型,将大鼠随机分为TAT-XIAP组(左侧脑室注射TAT-XIAP融合蛋白,每天80 mg/kg,共3d)和模型组(侧脑室注射等体积PBS)各30只,采用水迷宫评价大鼠的学习记忆能力,TUNEL法检测大鼠海马神经元凋亡.结果 1TAT-XIAP组大鼠在各象限入水至爬上平台的时间均明显缩短,平均值为(48.31±9.44)s,明显低于模型组的(87.80±10.32)s(P<0.05);TAT-XIAP组大鼠穿越平台的次数、在原平台象限游程百分比、在原平台象限时间百分比均明显增加,分别为(4.78±0.93)次、(47.39±5.84)%、(48.43±5.75)%,与模型组比较,差异有统计学意义(P<0.05).2 TAT-XIAP组大鼠海马凋亡神经元明显减少,凋亡神经元计数为(16.37±3.15)个/mm2,模型组为(54.66±7.20)个/mm2,两者差异有统计学意义(P<0.05).结论 TAT-XIAP融合蛋白可明显改善学习记忆障碍大鼠学习记忆功能,其机制可能与大鼠海马神经元凋亡减少有关.
目的 探討TAT-XIAP融閤蛋白對學習記憶障礙大鼠的影響及其與大腦海馬神經元凋亡的關繫,為學習記憶的深入研究提供實驗依據.方法 利用基因工程技術製備具有生物學活性的TAT-XIAP融閤蛋白,通過D-半乳糖(D-Gal)腹腔註射和Aβ1-42海馬註射建立學習記憶障礙大鼠模型,將大鼠隨機分為TAT-XIAP組(左側腦室註射TAT-XIAP融閤蛋白,每天80 mg/kg,共3d)和模型組(側腦室註射等體積PBS)各30隻,採用水迷宮評價大鼠的學習記憶能力,TUNEL法檢測大鼠海馬神經元凋亡.結果 1TAT-XIAP組大鼠在各象限入水至爬上平檯的時間均明顯縮短,平均值為(48.31±9.44)s,明顯低于模型組的(87.80±10.32)s(P<0.05);TAT-XIAP組大鼠穿越平檯的次數、在原平檯象限遊程百分比、在原平檯象限時間百分比均明顯增加,分彆為(4.78±0.93)次、(47.39±5.84)%、(48.43±5.75)%,與模型組比較,差異有統計學意義(P<0.05).2 TAT-XIAP組大鼠海馬凋亡神經元明顯減少,凋亡神經元計數為(16.37±3.15)箇/mm2,模型組為(54.66±7.20)箇/mm2,兩者差異有統計學意義(P<0.05).結論 TAT-XIAP融閤蛋白可明顯改善學習記憶障礙大鼠學習記憶功能,其機製可能與大鼠海馬神經元凋亡減少有關.
목적 탐토TAT-XIAP융합단백대학습기억장애대서적영향급기여대뇌해마신경원조망적관계,위학습기억적심입연구제공실험의거.방법 이용기인공정기술제비구유생물학활성적TAT-XIAP융합단백,통과D-반유당(D-Gal)복강주사화Aβ1-42해마주사건립학습기억장애대서모형,장대서수궤분위TAT-XIAP조(좌측뇌실주사TAT-XIAP융합단백,매천80 mg/kg,공3d)화모형조(측뇌실주사등체적PBS)각30지,채용수미궁평개대서적학습기억능력,TUNEL법검측대서해마신경원조망.결과 1TAT-XIAP조대서재각상한입수지파상평태적시간균명현축단,평균치위(48.31±9.44)s,명현저우모형조적(87.80±10.32)s(P<0.05);TAT-XIAP조대서천월평태적차수、재원평태상한유정백분비、재원평태상한시간백분비균명현증가,분별위(4.78±0.93)차、(47.39±5.84)%、(48.43±5.75)%,여모형조비교,차이유통계학의의(P<0.05).2 TAT-XIAP조대서해마조망신경원명현감소,조망신경원계수위(16.37±3.15)개/mm2,모형조위(54.66±7.20)개/mm2,량자차이유통계학의의(P<0.05).결론 TAT-XIAP융합단백가명현개선학습기억장애대서학습기억공능,기궤제가능여대서해마신경원조망감소유관.
Objective To investigate the TAT-XIAP fusion protein on learning and memory impairment in rats and its relationship with the brain hippocampus neuron apoptosis,and to provide experimental evidence for the in-depth study of learning and memory.Methods Using genetic engineering technology to prepare biologically active fusion protein TAT-XIAP,D-galactose (D-Gal) by intraperitoneal injection and Aβ1-42 by hippocampal injection,rat model was established by injection of learning and memory impairment.The rats were randomly divided into TAT-XIAP groups (left lateral cerebral ventricle injection of TAT-XIAP fusion protein,80 mg/kg per day,3 days) and model group (lateral cerebral ventricle injection of an equal volume of PBS),each group 30 rats.Learning and memory of rats were measured by water maze,and rat hippocampal neuronal apoptosis were measured by TUNEL assay.Results The time was significantly shorter into the water to climb up platform in each quadrant of TAT-XIAP rats,with an average of (48.31 ± 9.44)s,and it was significantly lower than the model group((87.80± 10.32) s,P < 0.05).The number through the platform,target quadrant swim away a percentage and time in the target quadrant percentage were significantly increased in TAT-XIAP group rats(respectively,4.78 ±0.93,(47.39± 5.84) %,(48.43 ± 5.75) %).It was significant difference with the model group comparison (P < 0.05).Apoptosis of neuron reduced significantly in hippocampus of TAT-XIAP group rats,apoptosis of neuron count was 16.37±3.15 pieces per square millimeter,and model group was 54.66 ± 7.20 pieces per square millimeter.It was significant difference compared by statistical analysis(P <0.05).Conclusion TAT-XIAP fusion protein can significantly improve learning and memory function of learning and memory impairment in rats,which may be related to decreasing neurons apoptosis in hippocampus.