König B, Kluge H, Haase K, Brandsch C, Stangl G I, Eder K
Institute of Agricultural and Nutritional Sciences, Martin-Luther-University Halle-Wittenberg, D-06108 Halle (Saale), Germany.
Poult Sci. 2007 Jun;86(6):1187-95. doi: 10.1093/ps/86.6.1187.
Expression of peroxisome proliferator-activated receptor-alpha (PPARalpha) has been shown in liver of chicks, but effects of its activation have not yet been investigated. In this study, laying hens were treated with clofibrate, a synthetic PPARalpha agonist, to investigate the effects of PPARalpha activation on liver lipid metabolism. Hens receiving a diet containing 5 g of clofibrate/kg had a lower food intake and higher liver mRNA concentrations of typical PPARalpha target genes (carnitine palmitoyltransferase 1A, acyl-coenzyme A oxidase, bifunctional enzyme, lipoprotein lipase) involved in hepatic mitochondrial and peroxisomal beta-oxidation and plasma triglyceride clearance than control hens that received the same diet without clofibrate (P<0.05). Hens treated with clofibrate also had lower mRNA concentrations of fatty acid synthase, 3-hydroxy-3-methylglutaryl-coenzyme A reductase, and low-density lipoprotein receptor, proteins involved in fatty acid biosynthesis and cholesterol biosynthesis and uptake, than hens fed the control diet (P<0.05). These changes in clofibrate-treated hens were accompanied by reduced liver triglyceride concentrations, strongly diminished very low density triglyceride and cholesterol concentrations (P<0.05), a disturbed maturation of egg follicles, a complete stop of egg production, and a markedly reduced plasma 17-beta-estradiol concentration (P<0.05). In conclusion, it is shown that clofibrate has complex effects on hepatic lipid metabolism in laying hens that mimic PPARalpha activation in mammals, affect maturation of egg follicles, and lead to a stop of egg production. Because clofibrate treatment strongly reduced food intake in the hens, some of these effects (i.e., egg production) may have been due to a low energy and nutrient intake.
过氧化物酶体增殖物激活受体α(PPARα)已在雏鸡肝脏中被证实有表达,但尚未对其激活作用进行研究。在本研究中,给产蛋母鸡使用合成的PPARα激动剂氯贝丁酯,以研究PPARα激活对肝脏脂质代谢的影响。与接受不含氯贝丁酯的相同日粮的对照母鸡相比,摄入含5 g氯贝丁酯/千克日粮的母鸡采食量较低,参与肝脏线粒体和过氧化物酶体β氧化以及血浆甘油三酯清除的典型PPARα靶基因(肉碱棕榈酰转移酶1A、酰基辅酶A氧化酶、双功能酶、脂蛋白脂肪酶)的肝脏mRNA浓度较高(P<0.05)。用氯贝丁酯处理的母鸡,参与脂肪酸生物合成、胆固醇生物合成及摄取的脂肪酸合酶、3-羟基-3-甲基戊二酰辅酶A还原酶和低密度脂蛋白受体的mRNA浓度也低于饲喂对照日粮的母鸡(P<0.05)。氯贝丁酯处理的母鸡出现的这些变化伴随着肝脏甘油三酯浓度降低、极低密度甘油三酯和胆固醇浓度显著降低(P<0.05)、卵泡成熟受阻、产蛋完全停止以及血浆17-β-雌二醇浓度显著降低(P<0.05)。总之,研究表明氯贝丁酯对产蛋母鸡的肝脏脂质代谢有复杂影响,可模拟哺乳动物中的PPARα激活,影响卵泡成熟并导致产蛋停止。由于氯贝丁酯处理使母鸡采食量大幅降低,其中一些影响(即产蛋)可能是由于能量和营养摄入不足所致。