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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。

Effects of Nicorandil on Inflammation, Apoptosis and Atherosclerotic Plaque Progression.

作者信息

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

机构信息

Department of Internal Medicine II-Division of Cardiology, Medical University of Vienna, 1090 Vienna, Austria.

Ludwig Boltzmann Institute for Cardiovascular Research, 1090 Vienna, Austria.

出版信息

Biomedicines. 2021 Jan 27;9(2):120. doi: 10.3390/biomedicines9020120.

Abstract

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.

摘要

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。

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