[电针预处理对心肌缺血再灌注损伤大鼠顶核GABAA受体及交感神经活动的影响]。

Shuai-Ya Wang, Qi Shu, Pian-Pian Chen, Fan Zhang, Xiang Zhou, Qian-Yi Wang, Jie Zhou, Xia Wei, Ling Hu, Qing Yu, Rong-Lin Cai
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引用次数: 0

摘要

目的:观察电针(EA)预处理对心肌缺血再灌注损伤(MIRI)大鼠心功能、交感神经活动、心肌损伤指标及冠状核GABAA受体的影响,探讨电针预处理改善MIRI的神经调节机制。方法:将60只雄性SD大鼠随机分为假手术组、模型组、EA组、激动剂组和激动剂+EA组,每组12只。结扎左冠状动脉前降支建立MIRI模型。EA组和激动剂+EA组分别在双侧“神门”(ht7)和“通里”(ht5)处进行EA,连续波,频率2 Hz,强度1 mA,每次30 min,每天1次,连续7天。干预后,建立MIRI模型。激动剂组在造模前连续7天在顶核内注射muscone (GABAA受体激动剂,1 g/L),每次150 μL,每天1次。激动剂+EA组于EA介入前30 min将muscone注射于顶核。采用PowerLab标准Ⅱ导联采集心电图数据,分析ST段位移和心率变异性(HRV);ELISA法检测血清去甲肾上腺素(NE)、肌酸激酶同工酶MB (CK-MB)、心肌肌钙蛋白I (cTnI)水平;TTC染色测定心肌梗死面积;HE染色观察心肌组织形态;采用免疫组织化学和实时荧光定量PCR检测顶核GABAA受体的阳性表达和mRNA表达。结果:与假手术组比较,模型组大鼠ST段位移和HRV低频高频比(LF/HF)增加(镰状核PPPA受体增加)(镰状核PPPPA受体减少)(镰状核PPPPA受体增加)(p)。EA预处理可改善MIRI大鼠心肌损伤,其机制可能与抑制顶核GABAA受体表达,从而下调交感神经兴奋性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effects of electroacupuncture pretreatment on GABAA receptor of fastigial nucleus and sympathetic nerve activity in rats with myocardial ischemia reperfusion injury].

Objective: To observe the effects of electroacupuncture (EA) pretreatment on cardiac function, sympathetic nerve activity, indexes of myocardial injury and GABAA receptor in fastigial nucleus in rats with myocardial ischemia reperfusion injury (MIRI), and to explore the neuroregulatory mechanism of EA pretreatment in improving MIRI.

Methods: A total of 60 male SD rats were randomly divided into a sham operation group, a model group, an EA group, an agonist group and an agonist+EA group, 12 rats in each group. The MIRI model was established by ligation of the left anterior descending coronary artery. EA was applied at bilateral "Shenmen" (HT 7) and "Tongli" (HT 5) in the EA group and the agonist+EA group, with continuous wave, in frequency of 2 Hz and intensity of 1 mA, 30 min each time, once a day for 7 consecutive days. After intervention, the MIRI model was established. In the agonist group, the muscone (agonist of GABAA receptor, 1 g/L) was injected in fastigial nucleus for 7 consecutive days before modeling, 150 μL each time, once a day. In the agonist+EA group, the muscone was injected in fastigial nucleus 30 min before EA intervention. The data of electrocardiogram was collected by PowerLab standard Ⅱ lead, and ST segment displacement and heart rate variability (HRV) were analyzed; the serum levels of norepinephrine (NE), creatine kinase isoenzyme MB (CK-MB) and cardiac troponin I (cTnI) were detected by ELISA; the myocardial infarction area was measured by TTC staining; the morphology of myocardial tissue was observed by HE staining; the positive expression and mRNA expression of GABAA receptor in fastigial nucleus were detected by immunohistochemistry and real-time PCR.

Results: Compared with the sham operation group, in the model group, ST segment displacement and ratio of low frequency to high frequency (LF/HF) of HRV were increased (P<0.01), HRV frequency domain analysis showed enhanced sympathetic nerve excitability, the serum levels of NE, CK-MB and cTnI were increased (P<0.01), the percentage of myocardial infarction area was increased (P<0.01), myocardial fiber was broken and interstitial edema was serious, the positive expression and mRNA expression of GABAA receptor in fastigial nucleus were increased (P<0.01). Compared with the model group, in the EA group, ST segment displacement and LF/HF ratio were decreased (P<0.01), HRV frequency domain analysis showed reduced sympathetic nerve excitability, the serum levels of NE, CK-MB and cTnI were decreased (P<0.01), the percentage of myocardial infarction area was decreased (P<0.01), myocardial fiber breakage and interstitial edema were lightened, the positive expression and mRNA expression of GABAA receptor in fastigial nucleus were decreased (P<0.01). Compared with the EA group, in the agonist group and the agonist+EA group, ST segment displacement and LF/HF ratio were increased (P<0.01), HRV frequency domain analysis showed enhanced sympathetic nerve excitability, the serum levels of NE, CK-MB and cTnI were increased (P<0.01), the percentage of myocardial infarction area was increased (P<0.01), myocardial fiber breakage and interstitial edema were aggravated, the positive expression and mRNA expression of GABAA receptor in fastigial nucleus were increased (P<0.01).

Conclusion: EA pretreatment can improve the myocardial injury in MIRI rats, and its mechanism may be related to the inhibition of GABAA receptor expression in fastigial nucleus, thereby down-regulating the excitability of sympathetic nerve.

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