[Effect of Electroacupuncture on ATP-sensitive Potassium Channel and Protein Kinase mRNA Ex- pression in Myocardial Ischemia Model Rats].

中国中西医结合杂志 Pub Date : 2017-04-01
Wei Wang, Ji-Quan Li, Xiang-Yu Meng, Yi-Guo Chen, Qin Jing
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Abstract

Objective To observe the effect of electroacupuncture (EA) at different acupoints on mRNA expressions of ATP-sensitive potassium channel (Kir6. 1, Kir6. 2) and conjugated protein (SUR2A, SUR2B) and protein kinases (PKA, PKG and PKC132) in myocardial ischemia model rats. Methods Myocardial ischemia model was established in healthy male SD rats via subcutaneously injec- ting ISO (85 mg/kg) multipointedly (medial root of limbs and the back). Then they were randomly divided into 4 groups, i.e., the model group, Neiguan (PC6) group, Lieque (LU7) group, non-acupoint group, 10 in each group. Besides, another 10 healthy rats were recruited as the control group. Corresponding EA was performed at respective acupoints to rats in Neiguan (PC6) group, Lieque (LU7) group, non-acu- point group, with dense-sparse wave, 2 -3 mA, 2 -20 Hz, needle retaining time of 20 min, once per day for 7 successive days. mRNA expression levels of Kir6. 1 and Kir6. 2, SUR2A, SUR2B, PKA, PKG, and PKCβ₂ in left ventricular myocardium were analyzed by Real-time PCR. Results Compared with the con- trol group, mRNA expressions of each index increased in the model group (P <0. 01). Compared with the model group, mRNA expressions of each index significantly decreased in Neiguan (PC6) group and Lieque (LU7) group (P<0. 01). Compared with Neiguan (PC6) group, mRNA expressions of each index significantly increased in Lieque (LU7) group and non-acupoint group (P <0. 01). Compared with Lieque (LU7) group, mRNA expressions of each index significantly increased in non-acupoint group (P <0. 05). Conclusion EA at Neiguan (PC6) could reverse mRNA expression changes of ATP-sensitive potassium channel (Kir6. 1 and Kir6. 2)and conjugated proteins (SUR2A and SUR2B) and protein kinases (PKA, PKG, and PKCβ₂).

电针对心肌缺血模型大鼠atp敏感钾通道及蛋白激酶mRNA表达的影响。
目的观察电针(EA)不同穴位对atp敏感钾通道(Kir6) mRNA表达的影响。1, Kir6。2)和偶联蛋白(SUR2A、SUR2B)和蛋白激酶(PKA、PKG、PKC132)在心肌缺血模型大鼠中的表达。方法健康雄性SD大鼠多点皮下注射ISO (85 mg/kg)(四肢内侧根和背部),建立心肌缺血模型。然后随机分为模型组、内关(PC6)组、利克(LU7)组、无穴组4组,每组10只。另取健康大鼠10只作为对照组。内关(PC6)组、利克(LU7)组、非穴位组大鼠分别在相应穴位行电针,波密稀疏,2 -3 mA, 2 -20 Hz,持针时间20 min,每天1次,连续7 d。Kir6的mRNA表达水平。1和Kir6。Real-time PCR检测左心室心肌2、SUR2A、SUR2B、PKA、PKG、PKCβ 2。结果与对照组比较,模型组大鼠各指标mRNA表达均升高(P
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