Institute of Nutritional Physiology 'Oskar Kellner', Leibniz Institute for Farm Animal Biology (FBN), Dummerstorf, Germany.
PLoS One. 2013 Nov 19;8(11):e76705. doi: 10.1371/journal.pone.0076705. eCollection 2013.
Epidemiological and experimental data indicate that caloric restriction in early postnatal life may improve liver lipid metabolism in low birth weight individuals. The present study investigated transcriptional and metabolic responses to low (U) and normal (N) birth weight (d 75, T1) and postnatal feed restriction (R, 60% of controls, d 98, T2) followed by subsequent refeeding until d 131 of age (T3). Liver tissue studies were performed with a total of 42 female pigs which were born by multiparous German landrace sows. Overall, 194 genes were differentially expressed in the liver of U vs. N (T1) animals with roles in lipid metabolism. The total mean area and number of lipid droplets (LD) was about 4.6- and 3.7 times higher in U compared to N. In U, the mean LD size (µm(2)) was 24.9% higher. 3-week feed restriction reduced total mean area of LDs by 58.3 and 72.7% in U and N, respectively. A functional role of the affected genes in amino acid metabolism was additionally indicated. This was reflected by a 17.0% higher arginine concentration in the liver of UR animals (vs. NR). To evaluate persistency of effects, analyses were also done after refeeding period at T3. Overall, 4 and 22 genes show persistent regulation in U and N animals after 5 weeks of refeeding, respectively. These genes are involved in e.g. processes of lipid and protein metabolism and glucose homeostasis. Moreover, the recovery of total mean LD area in U and N animals back to the previous T1 level was observed. However, when compared to controls, the mean LD size was still reduced by 23.3% in UR, whereas it was increased in NR (+24.7%). The present results suggest that short-term postnatal feed restriction period programmed juvenile U animals for an increased rate of hepatic lipolysis in later life.
流行病学和实验数据表明,在生命早期限制热量摄入可能会改善低出生体重个体的肝脏脂质代谢。本研究调查了低(U)和正常(N)出生体重(第 75 天,T1)以及随后的出生后喂养限制(R,对照组的 60%,第 98 天,T2)对转录和代谢的反应,随后在第 131 天恢复喂养(T3)。这项研究共对 42 头由德国长白母猪多胎产的雌性猪进行了肝脏组织研究。总的来说,194 个基因在 U 与 N(T1)动物的肝脏中差异表达,这些基因在脂质代谢中起作用。U 组肝脏中总平均脂滴(LD)面积和数量分别比 N 组高 4.6-和 3.7 倍。U 组的平均 LD 大小(µm(2))高 24.9%。3 周的喂养限制使 U 和 N 中总平均 LD 面积分别减少了 58.3%和 72.7%。受影响基因在氨基酸代谢中的功能作用也得到了进一步的证实。这反映在 UR 动物肝脏中的精氨酸浓度高出 17.0%(vs. NR)。为了评估这些影响的持久性,在 T3 时的恢复喂养期也进行了分析。总的来说,在恢复喂养 5 周后,U 和 N 动物中分别有 4 个和 22 个基因表现出持久的调控。这些基因涉及脂质和蛋白质代谢以及葡萄糖稳态等过程。此外,U 和 N 动物的总平均 LD 面积恢复到之前的 T1 水平。然而,与对照组相比,UR 动物的平均 LD 大小仍然降低了 23.3%,而 NR 动物则增加了 24.7%。本研究结果表明,短期的出生后喂养限制期使幼年期 U 动物编程为以后生活中肝内脂肪分解率增加。