Jorge Paulo Afonso Ribeiro, Almeida Eros Antonio de, Ozaki Michiko R, Jorge Mariana, Carneiro Adriano
Faculdade de Ciências Médicas, Unicamp, Campinas, SP.
Arq Bras Cardiol. 2005 Apr;84(4):314-9. doi: 10.1590/s0066-782x2005000400008. Epub 2005 May 2.
To compare the effects of atorvastatin, fluvastatin, pravastatin, and simvastatin on endothelial function, aortic atherosclerosis, and the content of malondialdehyde (MDA) in native and oxidized LDL and in the arterial wall of hypercholesterolemic rabbits after adjusting the dosages of those statins to reduce total serum cholesterol levels to similar values.
Male rabbits were divided into the following 6 groups of 10 animals (n=10): 1) GH (control)--hypercholesterolemic animals; 2) GA--atorvastatin; 3) GF--fluvastatin; 4) GP--pravastatin; 5) GS--simvastatin; and 6) GN--normal. The animals were fed a standard food preparation enriched with 0.5% cholesterol and 2% coconut oil for 45 days. Fifteen days after beginning the experiment, atorvastatin, fluvastatin, pravastatin and simvastatin were administered for 15 days through gavage, and the dosages were adjusted to obtain similar cholesterol values in each group. At the end of the experiment, a blood sample was withdrawn for determining total cholesterol and separating the lipoproteins, and a segment of the thoracic aorta was removed to be used for studying endothelial function and lipid peroxidation, and for measuring aortic atherosclerosis in histological sections.
The statins significantly reduced total serum cholesterol levels, LDL-cholesterol levels, and aortic atherosclerosis. The MDA content was also significantly reduced in native and oxidized LDL, as well as in the arterial wall. Endothelium-dependent relaxation was significantly greater in the treated group compared with that in the hypercholesterolemic group.
The statins, at dosages adjusted, had a significant and similar effect in reducing lipid peroxidation in native and oxidized LDL-C and in arterial walls, in decreasing aortic atherosclerosis, and in reverting endothelial dysfunction.
在调整阿托伐他汀、氟伐他汀、普伐他汀和辛伐他汀剂量以使高胆固醇血症兔的血清总胆固醇水平降至相似值后,比较这几种他汀类药物对内皮功能、主动脉动脉粥样硬化以及天然和氧化低密度脂蛋白(LDL)及动脉壁中丙二醛(MDA)含量的影响。
将雄性兔分为6组,每组10只动物(n = 10):1)GH(对照组)——高胆固醇血症动物;2)GA——阿托伐他汀组;3)GF——氟伐他汀组;4)GP——普伐他汀组;5)GS——辛伐他汀组;6)GN——正常组。给动物喂食富含0.5%胆固醇和2%椰子油的标准食物制剂,持续45天。实验开始15天后,通过灌胃给予阿托伐他汀、氟伐他汀、普伐他汀和辛伐他汀15天,并调整剂量以使每组的胆固醇值相似。实验结束时,采集血样测定总胆固醇并分离脂蛋白,取一段胸主动脉用于研究内皮功能和脂质过氧化,并在组织切片中测量主动脉动脉粥样硬化情况。
他汀类药物显著降低了血清总胆固醇水平、低密度脂蛋白胆固醇水平和主动脉动脉粥样硬化程度。天然和氧化LDL以及动脉壁中的MDA含量也显著降低。与高胆固醇血症组相比,治疗组的内皮依赖性舒张功能明显增强。
调整剂量后的他汀类药物在降低天然和氧化LDL-C以及动脉壁中的脂质过氧化、减轻主动脉动脉粥样硬化和逆转内皮功能障碍方面具有显著且相似的作用。