Laboratory of Electrophysiology and Cardiovascular Pharmacology, Faculty of Health Sciences, Federal University of Grande Dourados (UFGD), Dourados, MS, Brazil.
Laboratory of Preclinical Research of Natural Products, Paranaense University (UNIPAR), Umuarama, Parana´, Brazil.
J Med Food. 2019 Sep;22(9):919-927. doi: 10.1089/jmf.2019.0017. Epub 2019 Jun 24.
is an important medicinal plant species that is native to South America. Despite extensive popular usage as a hypolipidemic drug, its effects as an atheroprotective agent remain unknown. The aim of this study was to evaluate the effects of an ethanol-soluble fraction that was obtained from (ESEG) leaves against the development of atherosclerosis in rabbits. Male rabbits received a diet that was supplemented with 1% cholesterol (cholesterol-rich diet [CRD]) for 60 days. After 30 days of the CRD, the animals were divided into five groups ( = 6) and treated with ESEG (10, 30, and 100 mg/kg), simvastatin (2.5 mg/kg), or vehicle once daily for 30 days. The negative control group was fed a cholesterol-free diet and treated orally with vehicle. At the end of 60 days, serum lipids, oxidized low-density lipoprotein, thiobarbituric acid reactive substances, nitrotyrosine, and serum interleukin 1 beta (IL-1), IL-6, soluble intercellular adhesion molecule-1 (sICAM-1), and soluble vascular cell adhesion molecule-1 (sVCAM-1) levels were determined. Samples from the aortic arch and thoracic segment were also collected to investigate the tissue antioxidant defense system and perform histopathological analysis. Oral ESEG administration significantly reduced serum lipid levels in CRD-fed rabbits. This treatment also modulated the arterial antioxidant defense system by reducing lipid and protein oxidation. Similarly, serum IL-1, IL-6, sICAM-1, and sVCAM-1 levels significantly decreased, accompanied by a reduction of atherosclerotic lesions in all arterial branches. These findings suggest that ESEG may be a new herbal medicine that can be directly applied for the treatment and prevention of atherosclerotic disease.
是一种原产于南美洲的重要药用植物。尽管它被广泛用作降血脂药物,但作为一种抗动脉粥样硬化药物的作用尚不清楚。本研究旨在评估从 (ESEG)叶子中获得的乙醇可溶部分(ESEG)对兔动脉粥样硬化发展的影响。雄性兔接受补充 1%胆固醇(高胆固醇饮食[CRD])的饮食 60 天。在 CRD 30 天后,将动物分为五组(每组 6 只),并分别用 ESEG(10、30 和 100mg/kg)、辛伐他汀(2.5mg/kg)或载体每日一次处理 30 天。阴性对照组给予无胆固醇饮食,并口服载体处理。60 天后,测定血清脂质、氧化型低密度脂蛋白、硫代巴比妥酸反应物质、硝基酪氨酸和血清白细胞介素 1β(IL-1)、IL-6、可溶性细胞间黏附分子-1(sICAM-1)和可溶性血管细胞黏附分子-1(sVCAM-1)水平。还从主动脉弓和胸段收集样本,以研究组织抗氧化防御系统并进行组织病理学分析。口服 ESEG 给药可显著降低 CRD 喂养兔的血清脂质水平。这种治疗还通过降低脂质和蛋白质氧化来调节动脉抗氧化防御系统。同样,血清 IL-1、IL-6、sICAM-1 和 sVCAM-1 水平显著降低,所有动脉分支的动脉粥样硬化病变减少。这些发现表明,ESEG 可能是一种新的草药,可以直接用于治疗和预防动脉粥样硬化疾病。