首页> 美国卫生研究院文献>Journal of Animal Science >Feedlot performance and biological responses to coated and non-coated steroidal implants containing trenbolone acetate and estradiol benzoate in finishing beef steers
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Feedlot performance and biological responses to coated and non-coated steroidal implants containing trenbolone acetate and estradiol benzoate in finishing beef steers

机译:饲料表现和生物反应对含有醋酸甲酮醋酸甲酸酯和雌二醇苯甲酸酯的涂层和非涂层甾体植入物

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摘要

Predominately Angus steers (n = 24; initial BW = 435 ± 28.3 kg) were used to evaluate non-coated (NC) and coated implants (CI) containing equal amounts of trenbolone acetate (TBA; 200 mg) and estradiol benzoate (EB; 28 mg) in finishing steers on sera metabolite responses, gene expression, and immunohistochemical analyses of the Longissimus muscle (LM). Performance data were analyzed as a randomized complete block design, and all other data were analyzed as repeated measures for a completely randomized design. Treatments were no implant (NI), NC (Synovex-PLUS; Zoetis, Parsippany, NJ), and CI (Synovex-One Feedlot) implant. There were 2 pen replicates per treatment (n = 4 steers/pen). LM biopsies, blood, and BW were collected before feeding on days 0, 14, 28, 56, 84, 112, and 133, with final BW being captured on day 140. Genes of interest were determined by RT-qPCR using two housekeeping genes. Sera was analyzed for estradiol-17β (E2),17β-trenbolone (TbOH), insulin-like growth factor 1 (IGF-I), NEFA, and urea-N (SUN). An α of 0.10 determined significance for performance and sera data; α of 0.05 was used for gene and histology data. No performance differences (P ≥ 0.10) were detected. An implant × day interaction (P ≤ 0.10) for E2, IGF-I, and SUN was detected; implants elevated (P ≤ 0.10) E2, 17β-TbOH, and IGF-I; and decreased SUN across day of the study, meaning sera metabolites are not altered with time on feed. An implant × day interaction was detected for myogenic factor 5 (MYF-5) positive cells and proportions of MHCIIX. In LM, CI had greater (P < 0.10) IGF-I in LM over NI. CI increased (P < 0.05) G protein-coupled estrogen receptor 1 (GPER1) expression, as well as, GPER1 semi-quantitative scores over NI and NC. An implant × day interaction (P ≤ 0.05) for estrogen and androgen receptor-positive nuclei was detected; implants had increased (P ≤ 0.05) estrogen and androgen receptor-positive nuclei compared to NI. CIs increase genes associated with muscle tissue growth.
机译:主要是Angus Steers(n = 24;初始BW = 435±28.3kg)用于评估含有相等数量的醋酸醋酸醋酸醋酸醋酸醋酸醋酸酯(TBA; 200mg)和雌二醇苯甲酸酯(EB; eB;)的非涂覆(NC)和涂覆的植入物(CI)(EB; 28毫克)在血清代谢物反应,基因表达和Longissimus肌肉(LM)的免疫组织化学分析上的精加工。分析性能数据作为随机完整的块设计,并分析所有其他数据作为完全随机设计的重复措施。治疗没有植入物(Ni),NC(Synovex-Plus; Zoetis,Parsippany,NJ)和CI(Synovex-One Feedlot)植入物。每次治疗有2个笔复制(n = 4个Steers / PEN)。在喂食时收集LM活组织检查,血液和BW,在第0,14,28,56,84,112和133天,最终BW在第140天捕获。利用两个家务基因的RT-QPCR确定感兴趣的基因。分析血清的雌二醇-17β(E2),17β - 螺旋酮(TBOH),胰岛素样生长因子1(IGF-1),NeFA和尿素-N(太阳)。 0.10的α确定性能和血清数据的意义; α为0.05用于基因和组织学数据。没有检测到性能差异(p≥0.10)。检测到植入物×天相互作用(P≤0.10),用于E2,IGF-I和SUN;植入物升高(p≤0.10)E2,17β-TBOH和IGF-I;在研究日横跨研究时,阳光下降,意味着血清代谢物没有随着饲料的时间而改变。检测植入×日相互作用,用于肌原源性因子5(MYF-5)阳性细胞和MHCIIX的比例。在LM中,CI在LM上具有更大的(P <0.10)IGF-1。 CI增加(P <0.05)G蛋白偶联雌激素受体1(GPER1)表达,以及GPER1在Ni和NC上进行半定量分数。检测雌激素和雄激素受体阳性核的植入物×天相互作用(p≤0.05);与Ni相比,植入物增加(p≤0.05)雌激素和雄激素受体阳性核。 CIS增加与肌肉组织生长相关的基因。

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