Department of Animal Sciences and Division of Nutritional Sciences, University of Illinois, Urbana 61801; College of Veterinary Medicine, Nanjing Agricultural University, 210095 Nanjing, PR China.
Department of Animal Sciences and Division of Nutritional Sciences, University of Illinois, Urbana 61801.
J Dairy Sci. 2018 Sep;101(9):8476-8491. doi: 10.3168/jds.2018-14378. Epub 2018 Jun 13.
The study investigated whether methionine supply during late pregnancy is associated with liver mammalian target of rapamycin (MTOR) pathway phosphorylation, plasma biomarkers, and growth in heifer calves born to cows fed a control diet (CON) or the control diet plus ethylcellulose rumen-protected methionine (MET; 0.09% of dry matter intake) for the last 28 d prepartum. Calves were fed and managed similarly during the first 56 d of age. Plasma was harvested at birth and 2, 7, 21, 42, and 50 d of age and was used for biomarker profiling. Liver biopsies were harvested at 4, 14, 28, and 50 d of age and used for protein expression. Body weight, hip height, hip width, wither height, body length, rectal temperature, fecal score, and respiratory score were measured weekly. Starter intake was measured daily, and average daily gain was calculated during the first 8 wk of age. During the first 7 wk of age, compared with calves in the CON group, calves in the MET group had greater body weight, hip height, wither height, and average daily gain despite similar daily starter intake. Concentration of methionine in plasma was lower at birth but increased markedly at 2 and 7 d of age in MET calves. Plasma insulin, glucose, free fatty acids, and hydroxybutyrate did not differ. A greater ratio of phosphorylated α-serine/threonine kinase (AKT):total AKT protein expression was detected in MET calves, namely due to differences at 4 d of age. The phosphorylated MTOR:total MTOR ratio also was greater in MET calves due to differences at 28 and 50 d (8 d postweaning). The decrease in phosphorylated MTOR:total MTOR between 14 and 28 d in CON calves agreed with the increase in phosphorylated eukaryotic translation initiation factor 4E binding protein 1 (EIF4EBP1):total EIF4EBP1 ratio during the same time frame. The overall expression of phosphorylated ribosomal protein S6 kinase B1 (RPS6KB1):total RPS6KB1 and phosphorylated eukaryotic translation elongation factor 2 (EEF2):total EEF2 was lower in MET calves. Regardless of methionine supply prepartum, there was an 11-fold temporal decrease from 4 to 50 d in phosphorylated AKT:total AKT. Similarly, regardless of methionine supply, there were overall decreases in phosphorylation ratios of AKT, MTOR, RPS6KB1, and eukaryotic translation initiation factor 2A (EIF2A) over time. Data provide evidence of a positive effect of methionine supply during the last month of pregnancy on rates of growth during the first 7 wk of age. Phosphorylation status of some components of the MTOR pathway in neonatal calf liver also was associated with greater maternal supply of methionine. Thus, the data suggest that molecular mechanisms in the liver might be programmed by supply of methionine during late pregnancy. The exact mechanisms coordinating the observed responses remain to be determined.
本研究旨在探究妊娠后期甲硫氨酸的供应是否与牛肝脏哺乳动物雷帕霉素靶蛋白(MTOR)途径磷酸化、血浆生物标志物以及接受对照饮食(CON)或对照饮食加乙基纤维素包被甲硫氨酸(MET;干物质摄入量的 0.09%)预产前 28 天的母牛所生小母牛的生长有关。小牛在出生后的前 56 天内以类似的方式进行饲养和管理。在出生时和 2、7、21、42 和 50 天时采集血浆,用于生物标志物分析。在 4、14、28 和 50 天时采集肝脏活检组织,用于蛋白质表达分析。每周测量体重、臀部高度、臀部宽度、肩高、体长、直肠温度、粪便评分和呼吸评分。每天测量小牛的开食料摄入量,并在 0-8 周龄期间计算平均日增重。在出生后的前 7 周,与 CON 组的小牛相比,MET 组的小牛尽管开食料摄入量相似,但体重、臀部高度、肩高和平均日增重更大。MET 组小牛的血浆甲硫氨酸浓度在出生时较低,但在 2 天和 7 天龄时显著增加。血浆胰岛素、葡萄糖、游离脂肪酸和羟丁酸没有差异。在 MET 组小牛中,α-丝氨酸/苏氨酸激酶(AKT)磷酸化与总 AKT 蛋白表达的比值更高,这主要是由于在 4 天龄时存在差异。由于在 28 天和 50 天(断奶后 8 天)时存在差异,MTOR 磷酸化与总 MTOR 的比值也更大。CON 组小牛在 14-28 天之间磷酸化 MTOR:总 MTOR 的减少与同一时间框架内磷酸化真核翻译起始因子 4E 结合蛋白 1(EIF4EBP1):总 EIF4EBP1 比值的增加一致。MET 组小牛核糖体蛋白 S6 激酶 B1(RPS6KB1)磷酸化与总 RPS6KB1 和磷酸化真核翻译延伸因子 2(EEF2):总 EEF2 的整体表达较低。无论产前甲硫氨酸供应如何,从 4 天到 50 天,磷酸化 AKT:总 AKT 的比例都会有 11 倍的时间下降。同样,无论甲硫氨酸供应如何,随着时间的推移,AKT、MTOR、RPS6KB1 和真核翻译起始因子 2A(EIF2A)的磷酸化比值都会总体下降。这些数据为妊娠最后一个月甲硫氨酸供应对小牛出生后前 7 周的生长速度的积极影响提供了证据。新生小牛肝脏中 MTOR 途径某些成分的磷酸化状态也与母体甲硫氨酸供应增加有关。因此,数据表明,肝脏中的分子机制可能是通过妊娠后期甲硫氨酸的供应来编程的。协调观察到的反应的确切机制仍有待确定。