Vignale Karen, Caldas Justina V, England Judy A, Boonsinchai Nirun, Magnuson Andrew, Pollock Erik D, Dridi Sami, Owens Casey M, Coon Craig N
Kemin Agrifoods North America Inc., Des Moines, IA 50301.
Cobb-Vantress, P.O. Box 1030 Siloam Springs, Arkansas, USA.
Poult Sci. 2017 Apr 1;96(4):886-893. doi: 10.3382/ps/pew315.
A study was conducted to evaluate the effect of white striping ( ) of broiler breast muscle ( Pectoralis major ) on protein turnover and gene expression of genes related to protein degradation and fatty acid synthesis. A total of 560 day-old male broiler chicks Cobb 500 were allocated in a total of 16 pens, 35 chicks per pen. A completely randomized design was conducted with a 2 × 3 factorial arrangement (2 scores: severe and normal, and 3 breast meat samples sites). At d 60, 20 birds were randomly selected, euthanized, and scored for white striping. Scoring was either normal ( , no WS) or severe ( ). Also, the same day, 17 birds (16 infused, one control) were randomly selected and infused with a solution of 15 N Phen 40% ( ). Breast muscle tissue was taken for gene expression analysis of the following genes: MuRF1, atrogin-1, IGF-1, insulin receptor ( ), fatty acid synthetase, and acetyl CoA carboxylase ( ). Each bird was humanely euthanized after 10 minutes of infusion and scored for WS (NORM or SEV). Samples of the breast muscle ( Pectoralis major ) were taken at different layers (3 samples per bird: ventral, medial, dorsal), along with a sample of excreta for 3-methylhistidine analysis. Out of the 16 breast samples taken, only 10 were selected for analysis based on the WS score (5 NORM and 5 SEV). No significant differences ( P > 0.05) were found in fractional synthesis rate ( ) between SEV WS, NORM and sample sites for breast meat. However, fractional breakdown rate ( ) was significantly higher in birds with SEV WS compared to NORM (8.2 and 4.28, respectively, P < 0.0001). Birds with SEV WS showed significantly higher ( P < 0.05) relative expression of MuRF1 and slightly higher ( P = 0.07) relative expression of atrogin-1 than the NORM birds. These birds also showed lower ( P < 0.05) relative expression of IGF-1 than NORM birds. Further studies are needed to better understand why birds with severe white striping are degrading more muscular protein and mobilizing more fat.
开展了一项研究,以评估肉鸡胸肌(胸大肌)白色条纹对蛋白质周转以及与蛋白质降解和脂肪酸合成相关基因表达的影响。总共560只1日龄科宝500雄性肉鸡被分配到16个栏中,每个栏35只鸡。采用2×3析因设计(2个评分:严重和正常,以及3个胸肉样本部位)进行完全随机设计。在第60日龄时,随机选择20只鸡,实施安乐死,并对白色条纹进行评分。评分分为正常(,无白色条纹)或严重()。同样在当天,随机选择17只鸡(16只注射,1只对照),并注射15N苯丙氨酸40%的溶液()。采集胸肌组织用于以下基因的表达分析:肌肉萎缩因子1(MuRF1)、肌肉萎缩相关基因1(atrogin-1)、胰岛素样生长因子1(IGF-1)、胰岛素受体()、脂肪酸合成酶和乙酰辅酶A羧化酶()。每只鸡在注射10分钟后实施安乐死,并对白色条纹进行评分(正常或严重)。在不同层次采集胸肌(胸大肌)样本(每只鸡3个样本:腹侧、中间、背侧),同时采集一份排泄物样本用于3-甲基组氨酸分析。在采集的16个胸肌样本中,仅根据白色条纹评分选择10个样本进行分析(5个正常样本和5个严重样本)。严重白色条纹组、正常组和胸肉样本部位之间的蛋白质合成率()未发现显著差异(P>0.05)。然而,严重白色条纹组鸡的蛋白质分解率()显著高于正常组(分别为8.2和4.28,P<0.0001)。严重白色条纹组鸡的MuRF1相对表达显著更高(P<0.05),atrogin-1相对表达略高(P=0.07)。这些鸡的IGF-1相对表达也低于正常组鸡(P<0.05)。需要进一步研究,以更好地理解严重白色条纹的鸡为何会降解更多肌肉蛋白并动员更多脂肪。