Stern R A, Ashwell C M, Dasarathy S, Mozdziak P E
1Prestage Department of Poultry Science,North Carolina State University,Raleigh,NC 27695,USA.
2Department of Pathobiology,Lerner Research Institute,Cleveland Clinic,Cleveland,OH 44195,USA.
Animal. 2015 Jun;9(6):992-9. doi: 10.1017/S1751731115000117. Epub 2015 Feb 18.
Myogenesis is facilitated by four myogenic regulatory factors and is significantly inhibited by myostatin. The objective of the current study was to examine embryonic gene regulation of myostatin/myogenic regulatory factors, and subsequent manipulations of protein synthesis, in broiler embryos under induced hyperammonemia. Broiler eggs were injected with ammonium acetate solution four times over 48 h beginning on either embryonic day (ED) 15 or 17. Serum ammonia concentration was significantly higher (P<0.05) in ammonium acetate injected embryos for both ED17 and ED19 collected samples when compared with sham-injected controls. Expression of mRNA, extracted from pectoralis major of experimental and control embryos, was measured using real-time quantitative PCR for myostatin, myogenic regulatory factors myogenic factor 5, myogenic determination factor 1, myogenin, myogenic regulatory factor 4 and paired box 7. A significantly lower (P<0.01) myostatin expression was accompanied by a higher serum ammonia concentration in both ED17 and ED19 collected samples. Myogenic factor 5 expression was higher (P<0.05) in ED17 collected samples administered ammonium acetate. In both ED17 and ED19 collected samples, myogenic regulatory factor 4 was lower (P⩽0.05) in ammonium acetate injected embryos. No significant difference was seen in myogenic determination factor 1, myogenin or paired box 7 expression between treatment groups for either age of sample collection. In addition, there was no significant difference in BrdU staining of histological samples taken from treated and control embryos. Myostatin protein levels were evaluated by Western blot analysis, and also showed lower myostatin expression (P<0.05). Overall, it appears possible to inhibit myostatin expression through hyperammonemia, which is expected to have a positive effect on embryonic myogenesis and postnatal muscle growth.
成肌作用由四种生肌调节因子促进,并受到肌肉生长抑制素的显著抑制。本研究的目的是检测诱导高氨血症状态下肉鸡胚胎中肌肉生长抑制素/生肌调节因子的胚胎基因调控以及随后的蛋白质合成调控。从胚胎第(ED)15天或17天开始,在48小时内给肉鸡胚蛋注射四次醋酸铵溶液。与假注射对照组相比,在ED17和ED19采集样本时,注射醋酸铵的胚胎血清氨浓度显著更高(P<0.05)。使用实时定量PCR检测从实验胚胎和对照胚胎胸大肌中提取的mRNA,检测肌肉生长抑制素、生肌调节因子生肌因子5、生肌决定因子1、肌细胞生成素、生肌调节因子4和配对盒7的表达。在ED17和ED19采集的样本中,血清氨浓度较高时,肌肉生长抑制素表达显著较低(P<0.01)。在ED17采集的注射醋酸铵的样本中,生肌因子5表达较高(P<0.05)。在ED17和ED19采集的样本中,注射醋酸铵的胚胎中生肌调节因子4较低(P≤0.05)。在不同采集年龄的样本处理组之间,生肌决定因子1、肌细胞生成素或配对盒7的表达没有显著差异。此外,从处理胚胎和对照胚胎采集的组织学样本的BrdU染色没有显著差异。通过蛋白质印迹分析评估肌肉生长抑制素蛋白水平,结果也显示肌肉生长抑制素表达较低(P<0.05)。总体而言,似乎可以通过高氨血症抑制肌肉生长抑制素的表达,这有望对胚胎成肌作用和出生后肌肉生长产生积极影响。