Zarei Leila, Bahrami Mehran, Farhad Negin, Froushani Seyyed Meysam Abtahi, Abbasi Ata
Solid Tumor Research Center, Urmia University of Medical Sciences, Iran.
Student Research Committee, Urmia University of Medical Sciences, Iran.
Adv Clin Exp Med. 2018 Dec;27(12):1631-1636. doi: 10.17219/acem/74552.
Atherosclerosis (AS) is one of the most prevalent causes of death around the world. Since there are different types of risk factors, different types of medications focus on preventing atheromas and plaques from establishing or on preventing established plaques from growing.
The aim of this study was to evaluate the effect of all-trans retinoic acid (atRA) on AS in a rabbit model of fat-induced AS.
Atherosclerosis was induced by a high-fat diet (HFD) for 75 days. Thirty rabbits were randomly divided into 5 groups. Group 1 was the negative control group and received a normal diet. The animals in the other groups were fed a HFD. Group 2 (the AS positive control group) received no drugs, Group 3 received atorvastatin orally (20 mg/kg/day), Group 4 received atRA (5 mg/kg/day, orally), and Group 5 received both drugs. All medications were started on day 45 and continued until the end of the study. Fasting blood samples were obtained for lipid profile evaluation. The aorta sections were evaluated for maximum wall and intima thickness.
Oral administration of atRA, atorvastatin or their combination significantly improved serum lipid profile (p < 0.001). Atorvastatin and atRA significantly decreased serum total cholesterol and LDL-cholesterol levels in HFD (p < 0.001). No difference was found in serum HDL-cholesterol levels among the studied groups. The HFD group (Group 2 - positive control) showed significant intima irregularities with fat deposition and foamy macrophage accumulation (atheroma). Administration of atRA and atorvastatin significantly decreased the size of atherosclerotic plaques (intima thickness). The maximum vessel wall and intima thickness were significantly decreased after atRA and atorvastatin administration (p < 0.001). No difference was found between atRA and atorvastatin effectiveness, but combination therapy significantly decreased AS size in comparison to using either of the drugs alone (p < 0.001).
In reducing AS plaque size, atRA is as effective as atorvastatin. Additionally, the combination therapy of atRA and atorvastatin decreased AS size much more effectively, showing their synergistic effect. atRA can also improve the serum lipid profile.
动脉粥样硬化(AS)是全球最常见的死亡原因之一。由于存在不同类型的风险因素,不同类型的药物专注于预防动脉粥样瘤和斑块的形成,或预防已形成的斑块生长。
本研究旨在评估全反式维甲酸(atRA)对脂肪诱导的AS兔模型中AS的影响。
通过高脂饮食(HFD)诱导动脉粥样硬化75天。30只兔子随机分为5组。第1组为阴性对照组,给予正常饮食。其他组动物给予高脂饮食。第2组(AS阳性对照组)不给予药物,第3组口服阿托伐他汀(20mg/kg/天),第4组口服atRA(5mg/kg/天),第5组给予两种药物。所有药物均在第45天开始使用,并持续至研究结束。采集空腹血样进行血脂谱评估。评估主动脉切片的最大管壁和内膜厚度。
口服atRA、阿托伐他汀或它们的组合显著改善了血脂谱(p<0.001)。阿托伐他汀和atRA显著降低了高脂饮食组的血清总胆固醇和低密度脂蛋白胆固醇水平(p<0.001)。研究组之间的血清高密度脂蛋白胆固醇水平没有差异。高脂饮食组(第2组 - 阳性对照组)显示内膜明显不规则,有脂肪沉积和泡沫巨噬细胞聚集(动脉粥样瘤)。给予atRA和阿托伐他汀显著减小了动脉粥样硬化斑块的大小(内膜厚度)。给予atRA和阿托伐他汀后,最大血管壁和内膜厚度显著降低(p<0.001)。atRA和阿托伐他汀的有效性没有差异,但联合治疗与单独使用任何一种药物相比,显著减小了AS的大小(p<0.001)。
在减小AS斑块大小方面,atRA与阿托伐他汀一样有效。此外,atRA和阿托伐他汀的联合治疗更有效地减小了AS的大小,显示出它们的协同作用。atRA还可以改善血脂谱。