Kern S A, Pritchard R H, Blair A D, Scramlin S M, Underwood K R
Department of Animal Science, South Dakota State University, Brookings 57007.
Department of Animal Science, South Dakota State University, Brookings 57007
J Anim Sci. 2014 Nov;92(11):5275-84. doi: 10.2527/jas.2014-7891. Epub 2014 Sep 24.
Subcutaneous fat and marbling both increase in beef cattle during the feeding phase but are antagonistic in regard to their contribution to beef carcass value. The objective of this study was to determine whether cellular factors associated with marbling development change with growth stage throughout the feeding period and whether they are correlated to marbling relative to carcass composition. Twenty-four steers of known origin with the cytosine and thymine (CT) leptin genotype were allotted to 3 harvest groups. Six steers per harvest group were harvested at the following predetermined points: 35 d on feed (early feeding period, EF), average live weight of 464 kg (middle feeding period, MF), and 1.17-cm 12th-rib subcutaneous fat thickness (late feeding period, LF). Longissmus muscle samples were collected within 30 min postmortem and snap frozen for real-time PCR and Western blot analysis of lipoprotein lipase, adenosine monophosphate-activated protein kinase α (AMPKα), stearoyl-coenzyme A desaturase (SCD), PPARγ, C/EBP-β, and myostatin. Carcass data were recorded, and LM samples were collected and aged 2, 7, 14, and 21 d postmortem for Warner-Bratzler shear force determination. Carcass composition was estimated by dissection of the 9-10-11 rib section and subsequent proximate analysis of the soft tissue. Intramuscular fat content of the LM increased linearly throughout the feeding period, giving additional support to marbling as an early developing tissue. Expression of AMPKα was found to be downregulated, whereas SCD expression was upregulated in the LF group relative to the first 2 harvest groups. Additionally, SCD and PPARγ were downregulated in the EF group relative to the latter 2 harvest groups. These changes in gene expression resulted in a linear increase in only PPARγ protein abundance, whereas myostatin tended to increase quadratically. A correlation was found between intramuscular fat and PPARγ abundance. This gives further evidence of the importance of adipocyte hyperplasia in increasing marbling. Targeting and increasing PPARγ expression may serve as a mechanism to increase marbling deposition. Last, LF steaks were more tender than MF or EF steaks, indicating improved tenderness with increased days on feed.
在育肥阶段,肉牛的皮下脂肪和大理石花纹都有所增加,但它们对牛肉胴体价值的贡献却是相反的。本研究的目的是确定与大理石花纹发育相关的细胞因子是否会在整个育肥期随生长阶段而变化,以及它们与相对于胴体组成的大理石花纹是否相关。将24头已知来源、具有胞嘧啶和胸腺嘧啶(CT)瘦素基因型的公牛分配到3个屠宰组。每个屠宰组的6头公牛在以下预定时间点屠宰:采食35天(育肥前期,EF)、平均活重464千克(育肥中期,MF)以及第12肋皮下脂肪厚度达1.17厘米(育肥后期,LF)。在屠宰后30分钟内采集背最长肌样本,并速冻以用于脂蛋白脂肪酶、腺苷单磷酸激活蛋白激酶α(AMPKα)、硬脂酰辅酶A去饱和酶(SCD)、过氧化物酶体增殖物激活受体γ(PPARγ)、CCAAT增强子结合蛋白β(C/EBP-β)和肌肉生长抑制素的实时PCR和蛋白质印迹分析。记录胴体数据,并采集背最长肌样本,在屠宰后2、7、14和21天进行沃纳-布拉茨勒剪切力测定。通过解剖第9 - 10 - 11肋部分并随后对软组织进行近似分析来估计胴体组成。整个育肥期内,背最长肌的肌内脂肪含量呈线性增加,这进一步支持了大理石花纹是一种早期发育组织的观点。相对于前两个屠宰组,在LF组中发现AMPKα的表达下调,而SCD的表达上调。此外,相对于后两个屠宰组,EF组中的SCD和PPARγ表达下调。这些基因表达的变化仅导致PPARγ蛋白丰度呈线性增加,而肌肉生长抑制素则呈二次趋势增加。发现肌内脂肪与PPARγ丰度之间存在相关性。这进一步证明了脂肪细胞增生在增加大理石花纹方面的重要性。靶向并增加PPARγ表达可能是增加大理石花纹沉积的一种机制。最后,LF组的牛排比MF组或EF组的牛排更嫩,表明随着采食天数增加,嫩度有所改善。