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贝特类药物治疗后大鼠脂蛋白对铜诱导氧化的敏感性降低:脂肪酸组成的影响。

Decreased susceptibility to copper-induced oxidation of rat-lipoproteins after fibrate treatment: influence of fatty acid composition.

作者信息

Vázquez M, Merlos M, Adzet T, Laguna J C

机构信息

Dept. Farmacología y Quimica Terapéutica, Universitario de Pedralbes, Barcelona, Spain.

出版信息

Br J Pharmacol. 1996 Mar;117(6):1155-62. doi: 10.1111/j.1476-5381.1996.tb16710.x.

Abstract
  1. The effect of clofibrate (CFB), bezafibrate (BFB), and gemfibrozil (GFB) on plasma lipoprotein (VLDL and LDL) concentration, composition and resistance to copper-induced oxidation has been studied in male Sprague-Dawley rats after a 15 day treatment. 2. Plasma triglyceride levels were reduced by CFB (41%) and BFB (39%). This effect was related to a significant reduction (67% for CFB and 56% for BFB) in the amount of circulating VLDL-protein. 3. Plasma total cholesterol was reduced by 28% and 45% in CFB- and BFB-treated animals, respectively, mainly by modification of the cholesteryl ester fraction. In contrast, GFB significantly increased total cholesterol (27%). No modification in the LDL protein or lipid content was introduced by fibrates, although GFB decreased the proportion of LDL-triglycerides, at the expense of an increase in total cholesterol. 4. The fatty acid species carried by VLDL and LDL were affected after fibrate treatment. In general, both particles showed an increase in monounsaturated fatty acids (MUFA) (18:1) and a decrease in polyunsaturated fatty acids (PUFA) species (18:2 n-6, 20:4 n-6, 18:3 n-3, 20:5 n-3). As a consequence, the ratio of PUFA/(SFA+MUFA) for the whole lipoproteins was markedly reduced. 5. The degree of copper-induced VLDL- and LDL-oxidation was assessed by means of the analysis of lysine content, thiobarbituric acid reactive substances (TBARS) production and conjugated dienes formation. Lipoproteins obtained from fibrate-treated rats were more resistant to the oxidative challenge. For each lipoprotein, BFB was the most effective drug, followed by CFB and GFB. 6. The observed antioxidant effect can be ascribed to two independent phenomena produced by fibrates: the reduction of the amount of substrate for the oxidation process due to their hypolipidemic activity, and the alteration in the type of fatty acids transported by the lipoproteins towards an enrichment in species resistant to the oxidation process. 7. As similar lipoprotein fatty acid changes have been reported after fibrate treatment in human subjects, an antioxidant effect of fibrates in human therapy, independent of their well known hypolipidaemic activity, should be expected.
摘要
  1. 研究了氯贝丁酯(CFB)、苯扎贝特(BFB)和吉非贝齐(GFB)对雄性斯普拉格-道利大鼠进行15天治疗后血浆脂蛋白(极低密度脂蛋白和低密度脂蛋白)浓度、组成及对铜诱导氧化的抗性的影响。2. CFB(41%)和BFB(39%)降低了血浆甘油三酯水平。这种作用与循环中极低密度脂蛋白蛋白量的显著减少有关(CFB为67%,BFB为56%)。3. CFB和BFB治疗的动物血浆总胆固醇分别降低了28%和45%,主要是通过改变胆固醇酯部分。相比之下,GFB显著增加了总胆固醇(27%)。贝特类药物未改变低密度脂蛋白的蛋白质或脂质含量,尽管GFB降低了低密度脂蛋白甘油三酯的比例,但以总胆固醇增加为代价。4. 贝特类药物治疗后,极低密度脂蛋白和低密度脂蛋白携带的脂肪酸种类受到影响。一般来说,两种颗粒的单不饱和脂肪酸(MUFA)(18:1)均增加,多不饱和脂肪酸(PUFA)种类(1十八碳二烯酸、二十碳四烯酸、十八碳三烯酸、二十碳五烯酸)均减少。因此,整个脂蛋白的PUFA/(饱和脂肪酸+单不饱和脂肪酸)比值显著降低。5. 通过分析赖氨酸含量、硫代巴比妥酸反应性物质(TBARS)生成和共轭二烯形成来评估铜诱导的极低密度脂蛋白和低密度脂蛋白氧化程度。从贝特类药物治疗的大鼠获得的脂蛋白对氧化应激更具抗性。对于每种脂蛋白,BFB是最有效的药物,其次是CFB和GFB。6. 观察到的抗氧化作用可归因于贝特类药物产生的两个独立现象:由于其降血脂活性,氧化过程底物量减少;脂蛋白转运的脂肪酸类型发生改变,向抗氧化过程的种类富集。7. 由于在人类受试者中进行贝特类药物治疗后也报道了类似的脂蛋白脂肪酸变化,因此预计贝特类药物在人类治疗中具有抗氧化作用,这与其众所周知的降血脂活性无关。

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