包头医学院学报
包頭醫學院學報
포두의학원학보
JOURNAL OF BAOTOU MEDICAL COLLEGE
2015年
1期
1-2
,共2页
贾建新%闫旭升%宋嵬%蔡志平%杨占君%张明%崔成立
賈建新%閆旭升%宋嵬%蔡誌平%楊佔君%張明%崔成立
가건신%염욱승%송외%채지평%양점군%장명%최성립
Aβ1-42%Morris水迷宫%认知功能
Aβ1-42%Morris水迷宮%認知功能
Aβ1-42%Morris수미궁%인지공능
Aβ1-42%Morris water maze%Cognitive performance
目的:探讨可溶性Aβ1-42寡聚体双侧海马CA1区注射是否对Wistar大鼠认知功能具有损害作用。方法:雄性 Wistar大鼠40只随机分为空白对照组(Intact group)、假手术组(Sham group)、溶剂对照组(Vehicle group)、Aβ组(Aβgroup)4组,空白对照组不做任何处理,假手术组仅行双侧海马CA1区插管,溶剂对照组对双侧海马CA1区注射与Aβ组等体积的灭菌双蒸水(dd H2O),Aβ组给双侧海马CA1区注射可溶性Aβ1-42寡聚体;注射后两周用Morris水迷宫检测各组行为学表现。结果:Aβ注射可以明显增加大鼠逃避潜伏期与上台前路程( P <0.01),对大鼠平均游泳速度无影响,而Intact、Sham、Vehicle组之间差异无统计学意义( P >0.05);空间探索实验结果显示,Aβ注射可明显减小大鼠目标象限时间百分比( P <0.01)与穿越平台次数( P <0.05)。结论:双侧海马 CA1区注射可溶性Aβ1-42寡聚体对大鼠认知功能有明显损害作用。
目的:探討可溶性Aβ1-42寡聚體雙側海馬CA1區註射是否對Wistar大鼠認知功能具有損害作用。方法:雄性 Wistar大鼠40隻隨機分為空白對照組(Intact group)、假手術組(Sham group)、溶劑對照組(Vehicle group)、Aβ組(Aβgroup)4組,空白對照組不做任何處理,假手術組僅行雙側海馬CA1區插管,溶劑對照組對雙側海馬CA1區註射與Aβ組等體積的滅菌雙蒸水(dd H2O),Aβ組給雙側海馬CA1區註射可溶性Aβ1-42寡聚體;註射後兩週用Morris水迷宮檢測各組行為學錶現。結果:Aβ註射可以明顯增加大鼠逃避潛伏期與上檯前路程( P <0.01),對大鼠平均遊泳速度無影響,而Intact、Sham、Vehicle組之間差異無統計學意義( P >0.05);空間探索實驗結果顯示,Aβ註射可明顯減小大鼠目標象限時間百分比( P <0.01)與穿越平檯次數( P <0.05)。結論:雙側海馬 CA1區註射可溶性Aβ1-42寡聚體對大鼠認知功能有明顯損害作用。
목적:탐토가용성Aβ1-42과취체쌍측해마CA1구주사시부대Wistar대서인지공능구유손해작용。방법:웅성 Wistar대서40지수궤분위공백대조조(Intact group)、가수술조(Sham group)、용제대조조(Vehicle group)、Aβ조(Aβgroup)4조,공백대조조불주임하처리,가수술조부행쌍측해마CA1구삽관,용제대조조대쌍측해마CA1구주사여Aβ조등체적적멸균쌍증수(dd H2O),Aβ조급쌍측해마CA1구주사가용성Aβ1-42과취체;주사후량주용Morris수미궁검측각조행위학표현。결과:Aβ주사가이명현증가대서도피잠복기여상태전로정( P <0.01),대대서평균유영속도무영향,이Intact、Sham、Vehicle조지간차이무통계학의의( P >0.05);공간탐색실험결과현시,Aβ주사가명현감소대서목표상한시간백분비( P <0.01)여천월평태차수( P <0.05)。결론:쌍측해마 CA1구주사가용성Aβ1-42과취체대대서인지공능유명현손해작용。
Objective:To explore whether soluble Aβ1-42 oligomers injection could impair cognitive performance in Wistar rats .Methods:Forty male rats were randomly divided into four groups:Intact group, Sham group, Vehicle group and Aβgroup.Two weeks after the injection of soluble Aβ1-42 oligomers, the Morris water maze (MWM) test was performed to analyze the effect of soluble Aβ1-42 oligomers on cognitive per-formance in rats.Results:The escape latency and path length of rats was significantly prolonged in Aβgroup ( P <0.01), without significant effect on mean swim speed.There was no significant difference among the Intact、Sham and Vehicle group.In the probe trails, soluble Aβ1-42 ol-igomers injection could significantly decrease the time percentage in the target quadrant ( P <0.01)and cut down the times in crossing platform ( P <0.05).Conclusion: Soluble Aβ1-42 oligomers injection can bring about impairment to the cognitive performance in rats.