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Cardioprotective effect of nicorandil against myocardial injury following cardiac arrest in swine

    作者

    Liang, LN;Zhong, X;Zhou, Y;Hou, ZQ;Hu, HR;Zhu, FF;Chen, JB;Ji, XF;Shang, DY

    作者单位

    [Liang, Li-Ning; Zhong, Xia; Zhou, Yi; Hou, Zhi-Qiang; Hu, Hao-Ran; Zhu, Fang-Fang; Chen, Ji-Bin; Ji, Xian-Fei; Shang, De-Ya] Shandong Univ, Shandong Prov Hosp, Dept Emergency, 324 Jingwu Rd, Jinan 250021, Shandong, Peoples R China.

    摘要

    Introduction: Nicorandil, a vasodilatory drug used to treat angina, was reported to protect against myocardial ischemia- reperfusion injury in various animal models. However, its cardioprotective action following cardiac arrest is unknown. We examined the cardioprotective effects of nicorandil in a porcine model of cardiac arrest and resuscitation.;-;Methods: Ventricular fibrillation was induced electrically for 4 min in anesthetized domestic swine, followed by cardiopulmonary resuscitation. Sixteen successfully resuscitated animals were randomized to saline control (n = 8) or nicorandil (n = 8) groups. Nicorandil (150 mu g/kg) was administered by central intravenous injection at onset of restoration of spontaneous circulation (ROSC), followed by 3 mu g/kg/min infusion until reperfusion end. Sham-operated animals received surgery only (n = 4). Hemodynamic parameters weremonitored continuously. Blood samples were taken at baseline, 5, 30, 180, and 360 min after ROSC. Left ventricular ejection fraction was assessed by echocardiography at baseline and 6 h after ROSC. The animals were euthanized 6 h after ROSC, and the cardiac tissue was removed for analysis.;-;Results: 6 h after ROSC, nicorandil had significantly improved all hemodynamic variables (all P < 0.05) except the maximum rate of left ventricular pressure decline and heart rate (P > 0.05) compared with the control group. Control animals showed elevated cardiac troponin I and lactate levels compared with sham animals, which were significantly decreased following nicorandil treatment (P < 0.05). In the saline control group, the adenosine triphosphate (ATP) content was largely reduced but subsequently rescued by nicorandil (P < 0.05). Histopathologic injurywas reducedwith nicorandil treatment. Nicorandil reduced cardiomyocyte apoptosis as evidenced by reduced terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL)-positive cells, decreased Bax and caspase-3 expression, and increased Bcl-2 expression in the myocardium (all P < 0.05).;-;Conclusion: Nicorandil exhibited cardioprotective effects on myocardial injury following cardiac arrest via improvement in post-resuscitationmyocardial dysfunction and energymetabolism, reduction inmyocardial histopathologic injury, and antiapoptotic effects. (C) 2017 Elsevier Inc. All rights reserved.

    关键词

    K-ATP CHANNELS; CARDIOPULMONARY-RESUSCITATION; VENTRICULAR-FIBRILLATION; ARTERIAL-HYPOTENSION; DYSFUNCTION; HEART
基本信息

  • 所属机构:

    归属医师: 侯志强 周轶 钟霞 季宪飞 商德亚

    PMID:28285861

    UT:000407941000009

    刊名:AMERICAN JOURNAL OF EMERGENCY MEDICINE

    年,卷(期):2017年35卷8期

    页码:1082-1089

    DOI:10.1016/j.ajem.2017.02.051

    附件: pdf

    收录:   SCIE