The effect of aspartate on the energy metabolism in the liver of weanling pigs challenged with lipopolysaccharide
The effect of aspartate on the energy metabolism in the liver of weanling pigs challenged with lipopolysaccharide
复制标题
天门冬氨酸对脂多糖攻击断奶仔猪肝脏能量代谢的影响
DOI:
10.1007/s00394-014-0739-3
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发表时间:
2015-06-01
影响因子:
5
通讯作者:
Yi, Dan
中科院分区:
文献类型:
--
作者:
Kang, Ping;Liu, Yulan;Yi, Dan
AbstractsPurposeThis study was conducted to investigate whether aspartate (Asp) could improve liver energy status in the lipopolysaccharide (LPS)-challenged pigs.MethodsTwenty-four weaned pigs were assigned to four treatments: (1) nonchallenged control (control diet and saline-treated); (2) LPS-challenged control (the same control diet and LPS-challenged); (3) LPS + 0.5 % Asp treatment (0.5 % Asp diet and LPS-challenged); and (4) LPS + 1.0 % Asp treatment (a 1.0 % Asp diet and LPS-challenged). On d 19, the pigs were injected intraperitoneally withEscherichia coliLPS at 100 μg/kg body weight, and the same volume of 0.9 % NaCl solution, respectively. All pigs were slaughtered at 24 h after LPS or saline injection, and the liver was collected for further analysis.ResultsDietary supplementation with Asp improved liver energy status evidenced by the increased ATP concentration and adenylate energy charges, and the decreased AMP concentration and AMP/ATP ratio (p< 0.05). Asp supplementation increased the mRNA expression of key enzymes in hepatic glycolysis and tricarboxylic acid (TCA) cycle, including pyruvate kinase and citrate synthase (p< 0.05), and had a tendency to increase hepatic pyruvate dehydrogenase and isocitrate dehydrogenase β mRNA expression (p< 0.10). In addition, Asp increased the mRNA expressions of hepatic AMP-activated protein kinase (AMPK) α1, AMPKα2, silent information regulator (Sirt1), and proliferator-activated receptor-γ coactivator 1α (PGC1α) (p< 0.05). Moreover, Asp increased AMPKα phosphorylation (p< 0.05).ConclusionsThese results indicated that dietary supplementation of Asp could improve energy status in LPS-injured liver, which might result from motivating the metabolism pathway of TCA cycle and glycolysis and stimulating the AMPK signaling pathway.