Saitoh K, Mori T, Kasai H, Nagayama T, Ohbayashi S
Research Center, Grelan Pharmaceutical Co., Ltd., Tokyo, Japan.
Nihon Yakurigaku Zasshi. 1995 Jul;106(1):51-60. doi: 10.1254/fpj.106.51.
Anti-atheromatous effects of fenofibrate were studied in KHC rabbits with a hereditary deletion in LDL receptors, a defect similar to that in Watanabe heritable hyperlipidemic rabbits. KHC rabbits (10-weeks-old) were given a dietary admixture of fenofibrate (ca. 30 or ca. 100 mg/kg/day) for 20 weeks. Fenofibrate did not change serum total cholesterol, high density lipoprotein and triglyceride levels. Fenofibrate decreased the percent of plaque area formation in the thoracic aorta, but not the degree of foam cell formation, fibrosis and edematous change, and thickness of the intima. Furthermore, fenofibrate markedly inhibited the medial damage with foam cell formation in the aorta at week 20. From these results, we conclude that fenofibrate manifested the anti-atheromatous effect in KHC rabbit and also the previous model of cholesterol-fed rabbits, particularly against the medial damage in KHC rabbits, independent of the hypolipidemic effect.
在低密度脂蛋白受体存在遗传性缺失的KHC兔中研究了非诺贝特的抗动脉粥样硬化作用,该缺陷类似于渡边遗传性高脂血症兔的缺陷。给10周龄的KHC兔喂食含非诺贝特(约30或约100mg/kg/天)的饮食混合物,持续20周。非诺贝特未改变血清总胆固醇、高密度脂蛋白和甘油三酯水平。非诺贝特降低了胸主动脉中斑块面积形成的百分比,但未降低泡沫细胞形成、纤维化和水肿变化的程度以及内膜厚度。此外,非诺贝特在第20周时显著抑制了主动脉中伴有泡沫细胞形成的中膜损伤。从这些结果来看,我们得出结论,非诺贝特在KHC兔以及先前的高胆固醇喂养兔模型中均表现出抗动脉粥样硬化作用,特别是对KHC兔的中膜损伤,且该作用独立于降血脂作用。