Smith S B, Chapman A A, Lunt D K, Harris J J, Savell J W
Department of Animal Science, Texas A & M University, College Station 77843-2471, USA.
J Anim Sci. 2007 May;85(5):1136-43. doi: 10.2527/jas.2006-371. Epub 2007 Jan 15.
We tested the hypothesis that fatty acid biosynthesis and adipocyte diameter and volume would be greater in s.c. and i.m. adipose tissues of calf-fed steers than in yearling-fed steers at a constant BW, due to the greater time on feed for the calf-fed steers. Conversely, we predicted that the capacity for s.c. and i.m. preadipocytes to divide, as estimated by 3H-thymidine incorporation into DNA, would be greater in the less mature adipose tissues of calf-fed steers and in yearling-fed steers at 16 mo of age than in yearling-fed steers fed to 18 mo of age. Brangus steers were fed a corn-based finishing diet as calves (calf-fed; n = 9) or yearlings (n = 4) to 16 mo of age (CA yearling-fed); another group of yearlings (n = 5) was fed to a constant-BW end point of 530 kg (CW yearling-fed). Both groups of yearling-fed steers had free access to native pasture until 12 mo of age. At slaughter, the fifth to eighth thoracic rib section of the LM was removed, and fresh s.c. and i.m. adipose tissues were removed for in vitro incubations. There were no differences in the number of s.c. adipocytes/g or mean peak volumes of adipocytes across production groups (P > or = 0.14). However, s.c. adipose tissue of CA yearling-fed steers contained greater proportions of smaller adipocytes (<1,500 pL) than calffed or CW yearling-fed steers, and similar results were observed for i.m. adipose tissue. Acetate incorporation into total lipids was greater (P = 0.02) in s.c. adipose tissue of CA yearling-fed steers than in calf-fed or CW yearling-fed steers, and tended to be different (P = 0.10) across production groups in i.m. adipose tissue. The production system x cell fraction interaction was significant (P = 0.03) for s.c. adipose tissue DNA synthesis, which was greatest in adipocytes from CA yearling-fed steers, whereas there were no differences across production system in stromal vascular (SV) DNA synthesis. For i.m. adipose tissue, DNA synthesis was greatest in adipocytes and SV cells from CA yearling-fed calves, and was greater in SV cells than in adipocytes (both P = 0.01). Therefore, stage of adipose tissue development more strongly influenced fatty acid synthesis, adipocyte volume, and DNA synthesis than age at sampling, final BW, or time on the finishing diet.
由于犊牛育肥阉牛的育肥时间更长,在体重恒定的情况下,其皮下和肌内脂肪组织中的脂肪酸生物合成、脂肪细胞直径和体积会比周岁育肥阉牛更大。相反,我们预测,通过将³H-胸腺嘧啶掺入DNA来估计,犊牛育肥阉牛不太成熟的脂肪组织以及16月龄的周岁育肥阉牛的皮下和肌内前脂肪细胞的分裂能力,会比育肥至18月龄的周岁育肥阉牛更强。将布蓝格斯阉牛作为犊牛(犊牛育肥组;n = 9)或周岁牛(n = 4)饲养至16月龄(CA周岁育肥组),饲喂以玉米为基础的育肥日粮;另一组周岁牛(n = 5)饲喂至体重恒定终点530千克(CW周岁育肥组)。两组周岁育肥阉牛在12月龄前均可自由采食天然牧场的草料。屠宰时,取下背最长肌的第五至第八胸肋部分,分离新鲜的皮下和肌内脂肪组织用于体外培养。各生产组间皮下脂肪细胞数量/克或脂肪细胞平均峰值体积均无差异(P≥0.14)。然而,CA周岁育肥阉牛的皮下脂肪组织中,较小脂肪细胞(<1500皮升)的比例高于犊牛育肥组或CW周岁育肥组,肌内脂肪组织也观察到类似结果。CA周岁育肥阉牛皮下脂肪组织中乙酸掺入总脂质的量高于犊牛育肥组或CW周岁育肥组(P = 0.02),肌内脂肪组织中各生产组间也存在差异趋势(P = 0.10)。皮下脂肪组织DNA合成存在显著的生产系统×细胞组分交互作用(P = 0.03),其中CA周岁育肥阉牛脂肪细胞中的DNA合成最高,而基质血管(SV)DNA合成在各生产系统间无差异。对于肌内脂肪组织,CA周岁育肥牛犊的脂肪细胞和SV细胞中的DNA合成最高,且SV细胞中的DNA合成高于脂肪细胞(P均 = 0.01)。因此,脂肪组织发育阶段对脂肪酸合成、脂肪细胞体积和DNA合成的影响,比采样时的年龄、最终体重或育肥日粮饲喂时间更为显著。