南方医科大学学报
南方醫科大學學報
남방의과대학학보
JOURNAL OF SOUTHERN MEDICAL UNIVERSITY
2013年
10期
1442-1447
,共6页
散发性老年性痴呆%洗心汤%SAD模型%O-GlcNAc糖基转移酶%O-GlcNAc糖苷酶
散髮性老年性癡呆%洗心湯%SAD模型%O-GlcNAc糖基轉移酶%O-GlcNAc糖苷酶
산발성노년성치태%세심탕%SAD모형%O-GlcNAc당기전이매%O-GlcNAc당감매
sporadic Alzheimer's disease%Xixin decoction%O-GlcNAc transferase%O-GlcNAc glycosidase
目的建立SAD动物模型,研究名方洗心汤对SAD模型大鼠脑组织tau蛋白O-GlcNAc糖基化修饰中蛋白质O位N-乙酰葡萄糖胺糖基转移酶(OGT)、和糖苷酶(O-GlcNAcase)的影响,探讨名方洗心汤防治SAD的可能作用机制。方法将SPF级健康雄性SD大鼠随机分为假手术组、模型组、多奈哌齐对照组、名方洗心汤小、中、大剂量组。治疗结束及行为学测试之后,以免疫组化及蛋白印迹方法检测大鼠脑组织tau蛋白O-GlcNAc糖基化修饰过程中OGT、O-GlcNAcase酶表达的变化。结果名方洗心汤能显著提高SAD大鼠海马OGT的表达,降低O-GlcNAcase的表达,组间差异有统计学意义(P<0.05,P<0.01)。多奈哌齐对照组与SAD模型组相比无显著性差异(P>0.05)。结论名方洗心汤能够调节O-GlcNAc糖基转移酶和糖苷酶的表达,从而提高SAD大鼠海马组织tau蛋白O-GlcNAc糖基化修饰水平。
目的建立SAD動物模型,研究名方洗心湯對SAD模型大鼠腦組織tau蛋白O-GlcNAc糖基化脩飾中蛋白質O位N-乙酰葡萄糖胺糖基轉移酶(OGT)、和糖苷酶(O-GlcNAcase)的影響,探討名方洗心湯防治SAD的可能作用機製。方法將SPF級健康雄性SD大鼠隨機分為假手術組、模型組、多奈哌齊對照組、名方洗心湯小、中、大劑量組。治療結束及行為學測試之後,以免疫組化及蛋白印跡方法檢測大鼠腦組織tau蛋白O-GlcNAc糖基化脩飾過程中OGT、O-GlcNAcase酶錶達的變化。結果名方洗心湯能顯著提高SAD大鼠海馬OGT的錶達,降低O-GlcNAcase的錶達,組間差異有統計學意義(P<0.05,P<0.01)。多奈哌齊對照組與SAD模型組相比無顯著性差異(P>0.05)。結論名方洗心湯能夠調節O-GlcNAc糖基轉移酶和糖苷酶的錶達,從而提高SAD大鼠海馬組織tau蛋白O-GlcNAc糖基化脩飾水平。
목적건립SAD동물모형,연구명방세심탕대SAD모형대서뇌조직tau단백O-GlcNAc당기화수식중단백질O위N-을선포도당알당기전이매(OGT)、화당감매(O-GlcNAcase)적영향,탐토명방세심탕방치SAD적가능작용궤제。방법장SPF급건강웅성SD대서수궤분위가수술조、모형조、다내고제대조조、명방세심탕소、중、대제량조。치료결속급행위학측시지후,이면역조화급단백인적방법검측대서뇌조직tau단백O-GlcNAc당기화수식과정중OGT、O-GlcNAcase매표체적변화。결과명방세심탕능현저제고SAD대서해마OGT적표체,강저O-GlcNAcase적표체,조간차이유통계학의의(P<0.05,P<0.01)。다내고제대조조여SAD모형조상비무현저성차이(P>0.05)。결론명방세심탕능구조절O-GlcNAc당기전이매화당감매적표체,종이제고SAD대서해마조직tau단백O-GlcNAc당기화수식수평。
Objective:To study the effects of Xixin decoction (XXD) on O-GlcNAc transferase (OGT) and O-GlcNAc glycosidase in O-GlcNAc glycosylation of tau proteins in the brain of rats with sporadic Alzheimer's disease (SAD) and explore the possible mechanism. Methods Male SD rats were randomly divided into sham-operated group, model group, donepezil group, and low-, moderate-, and high-dose XXD groups. After treatment and behavioral test, the rats were sacrificed for detecting the expressions of OGT and O-GlcNAc glycosidase in the brain using immunohistochemistry and Western blotting. Results XXD significantly enhanced the expressions of OGT in the hippocampus of SAD rats and lowered the expression of O-GlcNAc glycosidase (P<0.05 or 0.01). OGT and O-GlcNAc glycosidase expressions showed no significant differences between the model group and donepezil group (P>0.05). Conclusion XXD can regulate the expression of OGT and O-GlcNAc glycosidase to enhance O-GlcNAc glycosylation of tau proteins in the hippocampus of SAD rats.