Yang Li-Hong, Du Yuan-Hao, Li Jing
Section of Acu-moxibustion, First Affiliated Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China.
Zhen Ci Yan Jiu. 2017 Feb 25;42(1):9-13.
To observe the regulation of APJ and its ligand Apelin on the angiogenesis pathway after cerebral infarction and the intervention effect of acupuncture.
Wistar rats were randomly divided into model group(=90), electroacupuncture(EA) group(=90), sham operation group(=90) and control group(=10). The first three groups were further divided into 1,3,6,9,12,24 h and 3,7, 12 d subgroups(=10 in each subgroup). The cerebral infarction model was established by middle cerebral artery occlusion (MCAO). EA(15 Hz, 2 mA) was applied to "Shuigou" (GV 26) for 20 min in the EA group. The 1, 3, 6, 9, 12, 24 h subgroups were treated immediately after modeling, the 3, 7, 9 d subgroups were treated once daily for 3, 7 or 9 days. Real-time fluorescent quantitative (RT-PCR) and Western blot were applied to detect the changes of Apelin and APJ in cerebrovascular endothelial cells, respectively.
Compared with the control group, the expression of Apelin-APJ mRNA was decreased in the model group(12 h, 12 d, <0.05, <0.01); After EA, the Apelin mRNA expression was increased in the 12 h and 7 d subgroups (<0.01), while the APJ mRNA expression was increased in the 6, 9, 12 h subgroups(<0.05, <0.01). Compared with the control group, the Apelin(1, 3, 6, 24 h and 3, 7, 12 d) and APJ(1, 3, 6, 9 h and 3 d) protein expressions were decreased in the model group(<0.01, <0.05); After EA, the Apelin protein expression was increased in the 6, 24 h and 3, 7, 12 d subgroups (<0.05, <0.01), while the APJ protein expression was increased in the 1, 9, 12, 24 h and 3, 7, 12 d subgroups (<0.05, <0.01).
EA can up-regulate the expression of Apelin-APJ mRNA and protein of cerebral vascular endothelial cell in MCAO rats which has an important role in the establishment of blood vessel regeneration and collateral circulation.
观察APJ及其配体Apelin对脑梗死血管生成途径的调控作用以及针刺的干预效果。
将Wistar大鼠随机分为模型组(n = 90)、电针组(n = 90)、假手术组(n = 90)和对照组(n = 10)。前三组再进一步分为1、3、6、9、12、24 h及3、7、12 d亚组(每组n = 10)。采用大脑中动脉闭塞(MCAO)法建立脑梗死模型。电针组于“水沟”(GV 26)穴施加电针(15 Hz,2 mA),留针20 min。1、3、6、9、12、24 h亚组于造模后立即治疗,3、7、9 d亚组每日治疗1次,连续治疗3、7或9 d。分别采用实时荧光定量(RT-PCR)和蛋白质免疫印迹法检测脑血管内皮细胞中Apelin和APJ的变化。
与对照组比较,模型组Apelin-APJ mRNA表达在12 h、12 d降低(P < 0.05,P < 0.01);电针后,12 h和7 d亚组Apelin mRNA表达升高(P < 0.01),6、9、12 h亚组APJ mRNA表达升高(P < 0.05,P < 0.01)。与对照组比较,模型组Apelin(1、3、6、24 h及3、7、12 d)和APJ(1、3、6、9 h及3 d)蛋白表达降低(P < 0.01,P < 0.05);电针后,6、24 h及3、7、12 d亚组Apelin蛋白表达升高(P < 0.05,P < 0.01),1、9、12、24 h及3、7、12 d亚组APJ蛋白表达升高(P < 0.05,P < 0.01)。
电针可上调MCAO大鼠脑血管内皮细胞Apelin-APJ mRNA和蛋白表达,对血管再生及侧支循环建立具有重要作用。