摘要
[目的]探讨电针对血管性痴呆(VD)大鼠学习记忆障碍的治疗效应及其作用的分子机制。[方法]SD雄性大鼠60 只,除假手术组10只外,其他大鼠均采用4-血管阻断法复制VD模型,存活大鼠随机分为电针组14只,尼莫通组13只, 模型组13只;电针组针刺“百会”和“大椎”两穴,尼莫通组以12 mg/kg灌胃给药,假手术组与模型组未予任何治疗。采用Morris水迷宫观察治疗20 d后各组大鼠在学习记忆方面的变化,并检测血红素氧化酶(HO)的蛋白表达和信使核糖核酸(mRNA)表达。[结果]与假手术组比较,模型组逃避潜伏期、HO-1蛋白表达、HO-1 mRNA表达增高(P<0.01);与模型组比较,电针组、尼莫通组逃避潜伏期、HO-1蛋白表达均显著减少(P<0.01),HO-1 mRNA表达水平均降低(P<0.05); 电针组与尼莫通组比较,各指标均无显著性差异(P>0.05)。[结论]电针治疗改善VD模型大鼠学习记忆能力与尼莫通治疗相仿,两法均可能与减少海马和皮质神经元细胞HO-1蛋白表达及HO-1 mRNA表达有关。
[Objective] To observe the effect of electroacupuncture (EA) on the disorder of learning and memory in rats with vascular dementia (VD) and to explore its molecular mechanism. [Methods] Among 60 male SD rats, 10 rats were in sham-operation group and the other 50 rats were used to establish models of global ischemia and reperfusion by fourvessel occlusion (4-VO) method. Then the survival model rats were randomized into EA group (n = 14), model group (n = 15) and nimotop group (n = 15). EA group was treated with EA at points of Baihui (GV20) and Dazhui (GV14), nimotop group with nimotop 12 mg/kg, and sham-operation group and model group did not receive any treatment. After a 20-day treatment, the changes of learning and memory behavior in rats were detected by Morris water maze, as well as the protein expression and mRNA expression of heme oxygenase (HO). [ Results ] The escape latent period, HO-1 protein expression and HO-1 mRNA-expression were increased obviously in model rats (P 〈 0.01 compared with the sham-operation group), and decreased obviously in EA and nimotop groups ( P 〈 0.01 or P 〈 0.05 compared with the model group). The differences of the above three parameters were insignificant between EA group and nimotop group (P 〉 0.05). [Conclusion] EA can improve the learning and memory behavior in rats with VD and this may be related to the decrease of HO-1 protein expression and HO-1 mRNA-expression in cortex and hippocampal
出处
《广州中医药大学学报》
CAS
2005年第6期445-449,共5页
Journal of Guangzhou University of Traditional Chinese Medicine
关键词
痴呆
血管性/针灸疗法
穴
百会
穴
大椎
疾病模型
动物
大鼠
DEMENTIA, VASCULAR/acup-mox therapy
POINT GV20 (BAIHUI)
POINT GV14 (DAZHUI)
DISEASE MODELS, ANIMAL
RATS