Departments of *Anatomy, Histology and Embryology; and †Pharmacology, University of Split School of Medicine, Split, Croatia.
J Cardiovasc Pharmacol. 2017 Nov;70(5):293-299. doi: 10.1097/FJC.0000000000000519.
Effects of white wine (WW) consumption on the expression of inflammatory markers/mediators (MMP-2, MMP-9, NF-ĸB p65 and TGF-β1) in myocardial tissue after experimentally induced permanent myocardial ischemia was investigated. Male Sprague-Dawley rats were given either a combination of WW and water or only water, for 28 days. After coronary ligation, animals were left to survive for 24 hours. Three representative areas: infarct/ischemic, peri-infarct/border zone, and control/non-ischemic zones were analyzed for expression of immunoreactivity by measuring the threshold area % of signal density. For MMP-9, significantly smaller expression was found in all 3 zones of wine drinking animals (P < 0.001). There was no difference in MMP-2 immunoreactivity between the 2 groups, except in peri-infarct zones, where the signal was significantly decreased (P < 0.001). The same pattern of expression was found for the NF-κB p65 signal, although no differences between experimental groups were observed for TGF-β1. White wine consumption decreases the expression of the 3 investigated inflammatory markers/mediators in the peri-infarct zone, suggesting its significant modulatory effect. For MMP-9 and MMP-2, expression was similar to the effect of postischemic reperfusion. No effect on TGF-β1 was observed, highlighting its role in being the master-switch, changing from the inflammatory to the proliferative stage of infarct healing.
研究了白葡萄酒(WW)摄入对实验性永久性心肌缺血后心肌组织中炎症标志物/介质(MMP-2、MMP-9、NF-κB p65 和 TGF-β1)表达的影响。雄性 Sprague-Dawley 大鼠给予 WW 和水的混合物或仅水,共 28 天。结扎冠状动脉后,动物存活 24 小时。通过测量信号密度的阈值面积 %,分析梗死/缺血、梗死周边/边界区和对照/非缺血区 3 个代表性区域的免疫反应性表达。对于 MMP-9,饮酒动物的所有 3 个区域的表达均显著降低(P < 0.001)。两组之间 MMP-2 免疫反应性无差异,但在梗死周边区信号明显降低(P < 0.001)。NF-κB p65 信号的表达模式相同,但 TGF-β1 两组之间无差异。白葡萄酒摄入可降低梗死周边区 3 种研究炎症标志物/介质的表达,表明其具有显著的调节作用。对于 MMP-9 和 MMP-2,其表达与缺血后再灌注的作用相似。未观察到 TGF-β1 的作用,突出了其作为主开关的作用,从炎症阶段转变为梗死愈合的增殖阶段。