Cai Wenke, Zhang Yan, Li Jiguo, Wang Jian
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Department of Cardiovascular Surgery, Kunming General Hospital of Chengdu Military Region of People's Liberation Army, Chengdu 650032, China.
Zhonghua Xin Xue Guan Bing Za Zhi. 2014 Oct;42(10):866-72.
To observe the effects of κ-opioid receptor agonist U50, 488H on myocardial ischemia and reperfusion injury and related mechanism.
Rats were randomly divided into sham operation, myocardial ischemia and reperfusion(I/R, 30 min ischemia followed by 120 min reperfusion), and MI/R+U50, 488H (1.5 mg/kg) and I/R+U50, 488H+ selective κ-opioid receptor antagonist Nor-BNI (2 mg/kg, n = 8 each). The infarction size and the incidence of ventricular arrhythmias were observed.Real-time PCR and DAB staining were used to define the myocardium Toll-like receptor 4(TLR4) expression. Myeloperoxidase level, TNF-α induction and the expression of NF-κB were also examined in rats.
After I/R, the expressions of myocardial TLR4 and NF-κB increased significantly both in ischemia area and area at risk. Compared with I/R, κ-opioid receptor stimulation with U50, 488H significantly attenuated the expressions of TLR4 and NF-κB and reduced myeloperoxidase (MPO) levels, myocardial TNF-α production, myocardial infarct sizes and the incidence of ventricular arrhythmias and arrhythmia score (2.9 ± 0.7 vs. 4.4 ± 0.9, P < 0.05) , above effects of U50, 488H were partly abolished by co-treatment with Nor-BNI.
These data provide evidence for the first time that κ-opioid receptor stimulation could attenuate myocardial I/R injury via downregulating TLR4/NF-κB signaling in rats.
观察κ-阿片受体激动剂U50,488H对心肌缺血再灌注损伤的影响及其相关机制。
将大鼠随机分为假手术组、心肌缺血再灌注组(缺血30分钟后再灌注120分钟)、心肌缺血再灌注+U50,488H组(1.5毫克/千克)和心肌缺血再灌注+U50,488H+选择性κ-阿片受体拮抗剂Nor-BNI组(2毫克/千克,每组n = 8)。观察梗死面积和室性心律失常的发生率。采用实时荧光定量聚合酶链反应和二氨基联苯胺染色法检测心肌Toll样受体4(TLR4)的表达。同时检测大鼠髓过氧化物酶水平、肿瘤坏死因子-α诱导情况及核因子-κB的表达。
缺血再灌注后,缺血区和危险区心肌TLR4和核因子-κB的表达均显著增加。与缺血再灌注组相比,用U50,488H刺激κ-阿片受体会显著减弱TLR4和核因子-κB的表达,降低髓过氧化物酶(MPO)水平、心肌肿瘤坏死因子-α的产生、心肌梗死面积以及室性心律失常的发生率和心律失常评分(2.9±0.7对4.4±0.9,P<0.05),U50,488H的上述作用在与Nor-BNI联合处理后部分被消除。
这些数据首次证明,在大鼠中,κ-阿片受体刺激可通过下调TLR4/核因子-κB信号通路减轻心肌缺血再灌注损伤。