Gonzalez J M, Carter J N, Johnson D D, Ouellette S E, Johnson S E
Department of Animal Sciences, University of Florida, Gainesville 32611, USA.
J Anim Sci. 2007 Aug;85(8):1893-901. doi: 10.2527/jas.2006-624. Epub 2007 Apr 27.
The objective of this study was to evaluate the effects of coadministration of ractopamine-HCl (RAC) and trenbolone acetate plus estradiol (TBA) on LM fiber cross-sectional area (CSA), diameter, fiber-associated myonuclei, and satellite cell number. Culled crossbred beef cows (n = 98; 11 +/- 1.8 yr old; BCS 4.3 +/- 0.03) from a single ranch in south Florida were fed a concentrate diet for 92 d in a 2 x 2, randomized block design. Cows were blocked by BW on arrival into light (initial BW = 369.75 +/- 2.68 kg and end BW = 501.96 +/- 6.90 kg) and heavy (initial BW = 418.31 +/- 2.75 kg and end BW = 522.15 +/- 7.09 kg) groups before assignment to treatment. Factors included dietary treatment (0 or 15 ppm) and implant status (0 or 80 mg of trenbolone acetate + 16 mg of estradiol). Ractopamine was provided in the diet to 2 pens or half the treatments during the final 35 d of feeding. Cows were slaughtered on d 92. Forty-eight hours postmortem, the 6th-rib portions of the LM were obtained from 10 randomly selected carcasses from each treatment group (n = 40). Cryosections (12 mum) were immunostained for dystrophin and myosin heavy chain I or II for the measurement of fiber CSA and type, respectively. Fiber-associated nuclei and satellite cell numbers were measured in serial cryosections. There was a RAC x TBA interaction (P < 0.05). Type I fiber CSA and diameter were increased (P < 0.05) by TBA and RAC. Type I CSA and diameter were larger (P < 0.05) in TBA + RAC than RAC only. Type II fiber CSA and diameter were not affected by TBA (P = 0.48), RAC (P = 0.15), or TBA + RAC (P = 0.60). Satellite cell numbers and fiber-associated nuclei were not affected (P > 0.05) by implant status or ractopamine supplementation. These results indicate that TBA and RAC preferentially increase the size of type I fibers in cull cows.
本研究的目的是评估盐酸莱克多巴胺(RAC)与醋酸群勃龙加雌二醇(TBA)联合使用对腰大肌(LM)纤维横截面积(CSA)、直径、纤维相关肌核及卫星细胞数量的影响。从佛罗里达州南部一个牧场挑选的98头淘汰杂交肉牛(年龄11±1.8岁;体况评分4.3±0.03),按照2×2随机区组设计,饲喂精料92天。牛只在入栏时按体重分为轻体重组(初始体重=369.75±2.68千克,结束体重=501.96±6.90千克)和重体重组(初始体重=418.31±2.75千克,结束体重=522.15±7.09千克),然后再分配到各处理组。处理因素包括日粮处理(0或15 ppm)和埋植状态(0或80毫克醋酸群勃龙+16毫克雌二醇)。在饲喂的最后35天,日粮中向2个栏舍或半数处理组添加莱克多巴胺。牛只在第92天屠宰。宰后48小时,从每个处理组随机选取10头胴体(n=40)获取第6肋处的腰大肌样本。制作12μm厚的冰冻切片,分别进行抗肌萎缩蛋白和肌球蛋白重链I或II免疫染色,以测量纤维CSA和纤维类型。在连续的冰冻切片中测量纤维相关核及卫星细胞数量。存在RAC×TBA互作效应(P<0.05)。TBA和RAC使I型纤维CSA和直径增加(P<0.05)。TBA+RAC组的I型纤维CSA和直径大于仅添加RAC组(P<0.05)。II型纤维CSA和直径不受TBA(P=0.48)、RAC(P=0.15)或TBA+RAC(P=0.60)影响。卫星细胞数量和纤维相关核不受埋植状态或莱克多巴胺添加的影响(P>0.05)。这些结果表明,TBA和RAC优先增加淘汰母牛I型纤维的大小。