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AMP-activated protein kinase and carbohydrate response element binding protein: A study of two potential regulatory factors in the hepatic lipogenic program of broiler chickens

机译:AMP激活的蛋白激酶和碳水化合物反应元件结合蛋白:肉鸡肝脏脂肪生成程序中两个潜在调节因子的研究

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This study investigated the effects of fasting and refeeding on AMP-activated protein kinase (AMPK) and carbohydrate response element binding protein (ChREBP) mRNA, protein and activity levels; as well as the expression of lipogenic genes involved in regulating lipid synthesis in broiler chicken (Gallus gallus) liver. Fasting for 24 or 48 h produced significant declines in plasma glucose (at 24 h), insulin and thyroid hormone (T_3) levels that were accompanied by changes in mRNA expression levels of hepatic lipogenic genes. The mRNA levels of malic enzyme (ME), ATP-citrate lyase (ACL), acetyl-CoA carboxylase α (ACCα), fatty acid synthase (FAS), stearoyl-CoA desaturase-1 (SCD-1) and thyroid hormone responsive Spot 14 (Spot 14) declined in response to fasting. Refeeding for 24 h increased mRNA levels for each of these genes, characterized by a significant increase (‘overshoot’) above fed control values. No change in mRNA expression of the two AMPK alpha subunit genes was observed in response to fasting or refeeding. In contrast, ChREBP and sterol regulatory element binding protein-1 (SREBP-1) mRNA levels decreased during fasting and increased with refeeding. Phosphorylation of AMPK alpha subunits increased modestly after a 48 h fast. However, there was no corresponding change in the phosphorylation of ACC, a major downstream target of AMPK. Protein level and DNA-binding activity of ChREBP increased during fasting and declined upon refeeding as measured in whole liver tissue extracts. In general, evidence was found for coordinate transcriptional regulation of lipogenic program genes in broiler chicken liver, but specific regulatory roles for AMPK and ChREBP in that process remain to be further characterized.
机译:这项研究调查了禁食和再喂食对AMP激活的蛋白激酶(AMPK)和碳水化合物反应元件结合蛋白(ChREBP)mRNA,蛋白和活性水平的影响;以及调节肉鸡鸡肝脏中脂质合成的脂肪生成基因的表达。空腹24或48小时会导致血浆葡萄糖(24小时),胰岛素和甲状腺激素(T_3)水平显着下降,并伴随着肝脂肪基因基因mRNA表达水平的变化。苹果酸酶(ME),ATP柠檬酸裂合酶(ACL),乙酰辅酶A羧化酶α(ACCα),脂肪酸合酶(FAS),硬脂酰辅酶A去饱和酶1(SCD-1)和甲状腺激素反应性斑点的mRNA水平14(地点14)因禁食而下降。再次饲喂24小时,这些基因中的每个基因的mRNA水平都会升高,其特征是饲喂的控制值显着增加(“超调”)。没有观察到响应禁食或重新喂养两个AMPK alpha亚基基因的mRNA表达的变化。相反,ChREBP和固醇调节元件结合蛋白1(SREBP-1)mRNA的水平在禁食期间降低,并随着再喂养而增加。禁食48小时后,AMPKα亚基的磷酸化适度增加。但是,AMPK的主要下游靶点ACC的磷酸化没有相应的变化。如在全肝组织提取物中测得的,ChREBP的蛋白质水平和DNA结合活性在禁食期间增加,而在再次进食后下降。总的来说,已经发现了在肉鸡鸡肝中调节脂肪生成程序基因的转录调控的证据,但是AMPK和ChREBP在该过程中的特定调控作用仍有待进一步表征。

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