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[电针预处理不同电流强度对急性心肌缺血小鼠心功能及巨噬细胞极化的影响]

[Effect of different electrical current intensities of electroacupuncture preconditioning on cardiac function and macrophage polarization in mice with acute myocardial ischemia].

作者信息

Yang Wen-Xiu, Chen Li-Yao, Yang Jia-Li, Shi Jun-Jing, Ma Nai-Qi, Peng Yong-Jun, Lu Sheng-Feng

机构信息

Key Laboratory of Acupuncture and Medicine Combination of Ministry of Education, Nanjing University of Chinese Medicine, Nanjing 210023, China; Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing 210029.

Key Laboratory of Acupuncture and Medicine Combination of Ministry of Education, Nanjing University of Chinese Medicine, Nanjing 210023, China.

出版信息

Zhen Ci Yan Jiu. 2022 Nov 25;47(11):955-61. doi: 10.13702/j.1000-0607.20211011.

DOI:10.13702/j.1000-0607.20211011
PMID:36453671
Abstract

OBJECTIVE

To observe the effect of different intensities of electroacupuncture (EA) preconditioning on car-diac function and polarization state of macrophages in mice with acute myocardial ischemia (AMI), so as to explore its possible mechanism underlying improvement of AMI.

METHODS

A total of 50 male C57BL/6J mice were randomly divided into sham ope-ration, AMI model, and EA pretreatment groups (0.5 mA, 1 mA, 3 mA subgroups), with 10 mice in each group/subgroup. The mice in the EA pretreatment groups were subjected to EA stimulation of bilateral "Neiguan"(PC6) with 0.5, 1.0 and 3 mA respectively and frequency of 2 Hz/15 Hz for 20 min, once a day, for 3 days. The acute myocardial ischemia model was established by ligating the anterior descending branch (ADB) of the left coronary artery, while the sham operation only had a surgical suture trans-passed below the ADB but without ligation. The myocardial infarction area was measured after TTC staining, and the cardiac function [left ventricular ejection fraction (EF), short-axis contraction rate (FS)] was detected by using echocardiography. The M1 macrophages were labeled with CD11b+F480+CD206, M2 macrophages were labeled with CD11b+F480+CD206 and detected by using flow cytometry, and the expression levels of myocardial interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), Toll-like receptor-4 (TLR4) proteins were detected by using Western blot.

RESULTS

Compared with the sham operation group, the model group had a significant increase in the infarction area (<0.000 1), number of cardiac macrophages and percentage of M1 type macrophages (<0.000 1), and the expression levels of myocardial IL-1β, TNF-α, TLR4 proteins (<0.001, <0.01), and a remarkable decrease in the levels of EF, FS and the percentage of M2 type macrophages (<0.000 1). In contrast to those of the model group, the area of myocardial infarction (<0.000 1, <0.01), expression levels of myocardial IL-1β, TNF-α, TLR4 proteins (<0.01, <0.05, <0.001) in the 0.5 mA, 1 mA and 3 mA groups, number of macrophages and percentage of M1 macrophages (<0.05) in the 1 mA group were significantly decreased, while the levels of EF and FS (<0.000 1, <0.05, <0.001) in the 3 EA groups, and percentage of M2 macrophage (<0.05) in the 1 mA group were significantly increased. Comparison among the 3 EA groups displayed that the effects of 1 mA group were significantly superior to those of 0.5 and 3 mA groups in up-regulating EF and FS (<0.01, <0.001), and in down-regulating the area of infarct myocardium (<0.01, <0.000 1), and the expression of TLR4 protein (<0.01), and 0.5 mA group in the expression of IL-1β and TNF-α proteins (<0.05).

CONCLUSION

EA preconditioning with electrical current intensities of 0.5 mA, 1 mA and 3 mA can effectively reduce myocardial infarction size, improve cardiac function in mice with AMI, which may be related with its effects in reducing the number of cardiac macrophages and down-regulating the expression of myocardial IL-1β, TNF-α and TLR4 proteins. The therapeutic effect of 1 mA is better than that of 0.5 and 3 mA.

摘要

目的

观察不同强度电针预处理对急性心肌缺血(AMI)小鼠心功能及巨噬细胞极化状态的影响,探讨其改善AMI的可能机制。

方法

将50只雄性C57BL/6J小鼠随机分为假手术组、AMI模型组和电针预处理组(0.5 mA、1 mA、3 mA亚组),每组/亚组10只。电针预处理组小鼠分别采用0.5、1.0和3 mA强度电针刺激双侧“内关”(PC6),频率为2 Hz/15 Hz,每次20 min,每日1次,共3天。通过结扎左冠状动脉前降支建立急性心肌缺血模型,假手术组仅在左冠状动脉前降支下穿线但不结扎。TTC染色后测量心肌梗死面积,采用超声心动图检测心功能[左心室射血分数(EF)、短轴缩短率(FS)]。用CD11b+F480+CD206标记M1巨噬细胞,用CD11b+F480+CD206标记M2巨噬细胞,采用流式细胞术检测,用Western blot检测心肌白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)、Toll样受体4(TLR4)蛋白表达水平。

结果

与假手术组比较,模型组梗死面积(<0.000 1)、心肌巨噬细胞数量及M1型巨噬细胞百分比(<0.000 1)、心肌IL-1β、TNF-α、TLR4蛋白表达水平(<0.001,<0.01)显著增加,EF、FS水平及M2型巨噬细胞百分比(<0.000 1)显著降低。与模型组比较,0.5 mA、1 mA和3 mA组心肌梗死面积(<0.000 1,<0.01)、心肌IL-1β、TNF-α、TLR4蛋白表达水平(<0.01,<0.05,<0.001)、巨噬细胞数量及1 mA组M1巨噬细胞百分比(<

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