Luci Sebastian, Giemsa Beatrice, Kluge Holger, Eder Klaus
Institut für Agrar- und Ernährungswissenschaften, Martin-Luther-Universität Halle-Wittenberg, Emil-Abderhalden-Strasse 26, D-06108 Halle/Saale, Germany.
Am J Physiol Regul Integr Comp Physiol. 2007 Jul;293(1):R70-7. doi: 10.1152/ajpregu.00603.2006. Epub 2007 Mar 15.
This study investigated the effect of clofibrate treatment on expression of target genes of peroxisome proliferator-activated receptor (PPAR)-alpha and various genes of the lipid metabolism in liver and adipose tissue of pigs. An experiment with 18 pigs was performed in which pigs were fed either a control diet or the same diet supplemented with 5 g clofibrate/kg for 28 days. Pigs treated with clofibrate had heavier livers, moderately increased mRNA concentrations of various PPAR-alpha target genes in liver and adipose tissue, a higher concentration of 3-hydroxybutyrate, and markedly lower concentrations of triglycerides and cholesterol in plasma and lipoproteins than control pigs (P < 0.05). mRNA concentrations of sterol regulatory element-binding proteins (SREBP)-1 and -2, insulin-induced genes (Insig)-1 and Insig-2, and the SREBP target genes acetyl-CoA carboxylase, 3-methyl-3-hydroxyglutaryl-CoA reductase, and low-density lipoprotein receptor in liver and adipose tissue and mRNA concentrations of apolipoproteins A-I, A-II, and C-III in the liver were not different between both groups of pigs. In conclusion, this study shows that clofibrate treatment activates PPAR-alpha in liver and adipose tissue and has a strong hypotriglyceridemic and hypocholesterolemic effect in pigs. The finding that mRNA concentrations of some proteins responsible for the hypolipidemic action of fibrates in humans were not altered suggests that there were certain differences in the mode of action compared with humans. It is also shown that PPAR-alpha activation by clofibrate does not affect hepatic expression of SREBP target genes involved in synthesis of triglycerides and cholesterol homeostasis in liver and adipose tissue of pigs.
本研究调查了氯贝丁酯处理对猪肝脏和脂肪组织中过氧化物酶体增殖物激活受体(PPAR)-α靶基因及各种脂质代谢基因表达的影响。对18头猪进行了一项实验,将猪分为两组,一组饲喂对照日粮,另一组饲喂添加了5 g氯贝丁酯/千克的相同日粮,持续28天。与对照猪相比,用氯贝丁酯处理的猪肝脏更重,肝脏和脂肪组织中各种PPAR-α靶基因的mRNA浓度适度增加,3-羟基丁酸浓度更高,血浆和脂蛋白中的甘油三酯和胆固醇浓度显著降低(P<0.05)。两组猪肝脏和脂肪组织中固醇调节元件结合蛋白(SREBP)-1和-2、胰岛素诱导基因(Insig)-1和Insig-2以及SREBP靶基因乙酰辅酶A羧化酶、3-甲基-3-羟基戊二酰辅酶A还原酶和低密度脂蛋白受体的mRNA浓度,以及肝脏中载脂蛋白A-I、A-II和C-III的mRNA浓度没有差异。总之,本研究表明,氯贝丁酯处理可激活猪肝脏和脂肪组织中的PPAR-α,并对猪具有强烈的降甘油三酯和降胆固醇作用。在人类中负责贝特类药物降血脂作用的某些蛋白质的mRNA浓度未改变这一发现表明,与人类相比,其作用方式存在一定差异。研究还表明,氯贝丁酯激活PPAR-α不会影响猪肝脏和脂肪组织中参与甘油三酯合成和胆固醇稳态的SREBP靶基因的肝脏表达。