Lenz Max, Kaun Christoph, Krychtiuk Konstantin A, Haider Patrick, Brekalo Mira, Maier Nadine, Goederle Laura, Binder Christoph J, Huber Kurt, Hengstenberg Christian, Wojta Johann, Hohensinner Philipp J, Speidl Walter S
Department of Internal Medicine II-Division of Cardiology, Medical University of Vienna, 1090 Vienna, Austria.
Ludwig Boltzmann Institute for Cardiovascular Research, 1090 Vienna, Austria.
Biomedicines. 2021 Jan 27;9(2):120. doi: 10.3390/biomedicines9020120.
Nicorandil, a balanced vasodilator, is used in the second-line therapy of angina pectoris. In this study, we aimed to illuminate the effects of nicorandil on inflammation, apoptosis, and atherosclerotic plaque progression. Twenty-five LDL-R -/- mice were fed a high-fat diet for 14 weeks. After 6 weeks mice were randomly allocated to treatment with nicorandil (10 mg/kg/day) or tap water. Nicorandil treatment led to a more stable plaque phenotype, displaying an increased thickness of the fibrous cap ( = 0.014), a significant reduction in cholesterol clefts ( = 0.045), and enhanced smooth muscle cell content ( = 0.009). In endothelial cells nicorandil did not reduce the induction of adhesion molecules or proinflammatory cytokines. In HO challenged endothelial cells, pretreatment with nicorandil significantly reduced the percentage of late apoptotic/necrotic cells ( = 0.016) and the ratio of apoptotic to living cells ( = 0.036). Atherosclerotic lesions of animals treated with nicorandil exhibited a significantly decreased content of cleaved caspase-3 ( = 0.034), lower numbers of apoptotic nuclei ( = 0.040), and reduced 8-oxogunanine staining ( = 0.039), demonstrating a stabilizing effect of nicorandil in established atherosclerotic lesions. We suggest that nicorandil has a positive effect on atherosclerotic plaque stabilization by reducing apoptosis.
尼可地尔是一种平衡血管扩张剂,用于心绞痛的二线治疗。在本研究中,我们旨在阐明尼可地尔对炎症、细胞凋亡和动脉粥样硬化斑块进展的影响。25只低密度脂蛋白受体基因敲除(LDL-R -/-)小鼠接受了14周的高脂饮食喂养。6周后,将小鼠随机分为两组,分别给予尼可地尔(10毫克/千克/天)或自来水进行处理。尼可地尔治疗导致斑块表型更稳定,表现为纤维帽厚度增加(P = 0.014),胆固醇裂隙显著减少(P = 0.045),平滑肌细胞含量增加(P = 0.009)。在内皮细胞中,尼可地尔并未降低黏附分子或促炎细胞因子的诱导。在过氧化氢(HO)刺激的内皮细胞中,尼可地尔预处理显著降低了晚期凋亡/坏死细胞的百分比(P = 0.016)以及凋亡细胞与活细胞的比例(P = 0.036)。接受尼可地尔治疗的动物的动脉粥样硬化病变显示,裂解的半胱天冬酶-3含量显著降低(P = 0.034),凋亡核数量减少(P = 0.040),8-氧代鸟嘌呤染色减少(P = 0.039),这表明尼可地尔对已形成的动脉粥样硬化病变具有稳定作用。我们认为,尼可地尔通过减少细胞凋亡对动脉粥样硬化斑块稳定具有积极作用。