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1. 湖北中医学院针灸骨伤系
2. 华中科技大学同济医学院
3. 武汉市第七医院,武汉,430061
纸质出版日期:2008
移动端阅览
孟培燕, 孙国杰, 刘胜洪, 等. 电针预处理对血管性痴呆大鼠神经细胞谷氨酸-NMDA受体信号转导通路的影响[J]. 针刺研究, 2008,(2):103-106.
MENG Pei-yan, SUN Guo-jie, LIU Sheng-hong1, et al. Effect of Electroacupuncture Pretreatment on Glutamate-NMDAR Signal Pathway in Hippocampal Neurons of Vascular Dementia Rats[J]. Acupuncture research, 2008, (2): 103-106.
孟培燕, 孙国杰, 刘胜洪, 等. 电针预处理对血管性痴呆大鼠神经细胞谷氨酸-NMDA受体信号转导通路的影响[J]. 针刺研究, 2008,(2):103-106. DOI:
MENG Pei-yan, SUN Guo-jie, LIU Sheng-hong1, et al. Effect of Electroacupuncture Pretreatment on Glutamate-NMDAR Signal Pathway in Hippocampal Neurons of Vascular Dementia Rats[J]. Acupuncture research, 2008, (2): 103-106. DOI:
目的:观察电针预处理对血管性痴呆(vascular dementia
VD)大鼠防治作用的可能机制。方法:将SD大鼠随机分为正常组、假手术组、模型组、电针预处理组。采用改良线栓法制备VD模型。电针预处理"百会""肾俞""后三里"穴
连续波
频率为100次/min
强度1 mA
每日1次
连续进行10 d。用比色法测定各组大鼠海马谷氨酸(Glu)含量的变化
原位杂交法测定海马N-甲基-D-天冬氨酸受体1(NMDAR 1)mRNA表达的变化。结果:模型组海马Glu含量、NMDAR 1 mRNA表达明显高于假手术组(P<0.01)
电针预处理组海马Glu含量、NMDAR 1 mRNA表达明显低于模型组(P<0.05)。结论:电针预处理可降低VD鼠海马组织Glu含量
下调海马NMDAR 1的表达
因而有可能通过减轻Glu-NMDAR信号路径诱导的细胞凋亡发生
保护脑细胞。
Objective To observe the effect of electroacupuncture(EA) pretreatment on hippocampal glutamate(Glu) content and N-methyl-D-aspartate receptor(NMDAR)1 mRNA expression in rats with vascular dementia(VD) so as to explore its underlying mechanism in improving VD.Methods A total of 72 SD rats were randomized into control(n=16)
sham-operation(n=16)
model(n=20) and EA pretreatment(n=20) groups.VD model was established by modified middle cerebral artery occlusion.EA(1 mA
1.7 Hz) was applied to "Baihui"(GV 20)
"Shenshu"(BL 23) and "Zusanli"(ST 36)
once daily for 10 days.Glu content of right hippocampus tissue was detected with chromatometry.NMDAR1mRNA expression of hippocampus was detected by in situ hybridization histochemistry.Results In comparison with sham operation group
Glu content and NMDAR1 mRNA expression of hippocampus in model group increased significantly(P<0.01).Compared with model group
Glu content and NMDAR1mRNA expression of hippocampus in EA pretreatment group decreased significantly(P<0.01
0.05).Conclusion EA pretreatment can suppress the increase of Glu content
down-regulate NMDAR1mRNA expression in VD rats
which may contribute to its effect in relieving VD via reducing apoptosis and protecting cerebral neurons.
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