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不同抗氧化剂的药理剂量对高脂血症家兔氧化参数及动脉粥样硬化形成的影响。

The effect of pharmacological doses of different antioxidants on oxidation parameters and atherogenesis in hyperlipidaemic rabbits.

作者信息

Djahansouzi S, Braesen J H, Koenig K, Beisiegel U, Kontush A

机构信息

Biochemisches Labor, Pav. 39, Medizinische Kern- und Poliklinik, Universitätskrankenhaus Eppendorf, Martinistrasse 52, 20246, Hamburg, Germany.

出版信息

Atherosclerosis. 2001 Feb 1;154(2):387-98. doi: 10.1016/s0021-9150(00)00510-4.

Abstract

The oxidation hypothesis of atherosclerosis implies that antioxidants are able to inhibit lipoprotein oxidation in the arterial wall and thereby retard atherogenesis. Since most of the animal studies performed have used very high doses of antioxidants, it is to date unknown whether antioxidants are effective antiatherosclerotic agents when given in pharmacological doses. Here we addressed this question using homozygous Watanabe heritable hyperlipidaemic (WHHL) rabbits as an animal model of atherosclerosis. The rabbits were divided into four groups, each consisting of ten animals. They received either a standard diet or a diet containing 4.3 mg ubiquinone-10, or 4.3 mg vitamin E or 15 mg probucol/kg body weight daily. After 12 months, the extent of aortic atherosclerosis was assessed as the intima thickness, media thickness and intima-to-media ratio in 14 cross sections equally distributed over the whole aorta. To evaluate the antioxidant effects of the diet, lipophilic and hydrophilic antioxidants, lipids, fatty acids and plasma oxidizability were measured after 0, 3 and 6 months of feeding. We found that supplementation with probucol significantly decreased aortic intima-to-media ratio compared to controls. The antiatherosclerotic action of probucol was accompanied by its beneficial action on plasma oxidizability and some plasma antioxidants. No decrease in aortic atherosclerosis was measured in ubiquinone-10- and vitamin E-supplemented rabbits, despite the fact that both antioxidants decreased plasma oxidizability and ubiquinone-10 increased the plasma levels of antioxidants. Taken together, these data suggest that pharmacological doses of probucol retard atherogenesis in WHHL rabbits by an antioxidant mechanism, while ubiquinone-10 and vitamin E at these dosages are ineffective in this highly hyperlipidaemic model. The measurement of some oxidation-related parameters in plasma, such as lipophilic antioxidants, polyunsaturated fatty acids and lipoprotein oxidizability, may be useful in assessing the risk of atherogenesis in humans.

摘要

动脉粥样硬化的氧化假说表明,抗氧化剂能够抑制动脉壁中的脂蛋白氧化,从而延缓动脉粥样硬化的发生。由于大多数已进行的动物研究使用的是非常高剂量的抗氧化剂,因此至今尚不清楚以药理剂量给予抗氧化剂时,它们是否为有效的抗动脉粥样硬化药物。在此,我们使用纯合子渡边遗传性高脂血症(WHHL)兔作为动脉粥样硬化的动物模型来解决这个问题。将兔子分为四组,每组十只动物。它们分别接受标准饮食或每天每千克体重含有4.3毫克泛醌-10、或4.3毫克维生素E、或15毫克普罗布考的饮食。12个月后,在整个主动脉均匀分布的14个横截面中,将主动脉粥样硬化的程度评估为内膜厚度、中膜厚度和内膜与中膜之比。为了评估饮食的抗氧化作用,在喂食0、3和6个月后测量亲脂性和亲水性抗氧化剂、脂质、脂肪酸和血浆氧化能力。我们发现,与对照组相比,补充普罗布考可显著降低主动脉内膜与中膜之比。普罗布考的抗动脉粥样硬化作用伴随着其对血浆氧化能力和一些血浆抗氧化剂的有益作用。在补充泛醌-10和维生素E的兔子中,未检测到主动脉粥样硬化的减轻,尽管这两种抗氧化剂都降低了血浆氧化能力,并且泛醌-10提高了血浆抗氧化剂水平。综上所述,这些数据表明,药理剂量的普罗布考通过抗氧化机制延缓了WHHL兔的动脉粥样硬化发生,而在这个高度高脂血症模型中,这些剂量的泛醌-10和维生素E无效。测量血浆中的一些氧化相关参数,如亲脂性抗氧化剂、多不饱和脂肪酸和脂蛋白氧化能力,可能有助于评估人类动脉粥样硬化的风险。

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