Department of Animal Science, Texas A & M University, College Station, TX 77843, USA.
J Anim Sci. 2013 May;91(5):2091-8. doi: 10.2527/jas.2012-5801. Epub 2013 Mar 5.
We hypothesized that supplementing finishing diets with palm oil would promote adipocyte differentiation in subcutaneous adipose tissue of feedlot steers, and that soybean oil supplementation would depress adipocyte differentiation. Twenty-eight Angus steers were assigned randomly to 3 groups of 9 or 10 steers and fed a basal diet without additional fat (control), with 3% palm oil (rich in palmitic acid), or with 3% soybean oil (rich in polyunsaturated fatty acids), for 10 wk, top-dressed daily. Palm oil had no effect (P > 0.05) on ADG, food intake, or G:F, whereas soybean oil depressed ADG (P = 0.02), food intake (P = 0.04), and G:F (P = 0.05). Marbling scores tended (P = 0.09) to be greater in palm oil-fed steers (Modest(09)) than in soybean oil-fed steers (Small(55)). Subcutaneous adipocyte mean volume was greater in palm oil-fed steers (515.9 pL) than in soybean-supplemented cattle (395.6 pL; P = 0.01). Similarly, glucose and acetate incorporation into total lipids in vitro was greater in subcutaneous adipose tissue of palm oil-fed steers (119.9 and 242.8 nmol·3h(-1)·10(5) cells, respectively) than adipose tissue of soybean oil-fed steers in (48.9 and 95.8 nmol·3h(-1)·10(5) cells, respectively). Glucose-6-phosphate dehydrogenase and NADP-malate dehydrogenase activities were greater (P ≤ 0.05) in subcutaneous adipose tissue of palm oil-fed steers than in adipose tissue of control steers. Palm oil did not increase palmitic acid or decrease oleic acid in subcutaneous adipose tissue or LM, but decreased (P ≤ 0.05) myristoleic, palmitoleic, and cis-vaccenic acid in adipose tissue, indicating a depression in stearoyl-coenzyme A desaturase activity. Soybean oil increased the proportion of α-linolenic acid in adipose tissue and muscle and increased linoleic acid and 18:1trans-10 in muscle. We conclude that palm oil supplementation promoted lipid synthesis in adipose tissue without depressing feed efficiency or increasing the palmitic acid content of beef.
我们假设在育肥牛的皮下脂肪组织中添加棕榈油补充剂会促进脂肪细胞分化,而添加大豆油补充剂会抑制脂肪细胞分化。28 头安格斯牛被随机分为 3 组,每组 9 或 10 头牛,分别饲喂不含额外脂肪的基础日粮(对照组)、3%棕榈油(富含棕榈酸)或 3%大豆油(富含多不饱和脂肪酸),为期 10 周,每日顶部撒布。棕榈油对 ADG、采食量或 G:F 没有影响(P>0.05),而大豆油降低了 ADG(P=0.02)、采食量(P=0.04)和 G:F(P=0.05)。大理石花纹评分在棕榈油组(中等(09))中趋于(P=0.09)高于大豆油组(小(55))。棕榈油组牛的皮下脂肪细胞平均体积大于大豆油组(515.9 pL)(395.6 pL;P=0.01)。同样,棕榈油组牛的体外葡萄糖和乙酸盐掺入总脂质的量也大于大豆油组(分别为 119.9 和 242.8 nmol·3h(-1)·10(5) 细胞)(分别为 48.9 和 95.8 nmol·3h(-1)·10(5) 细胞)。葡萄糖-6-磷酸脱氢酶和 NADP-苹果酸脱氢酶活性在棕榈油组牛的皮下脂肪组织中高于对照组牛(P≤0.05)。棕榈油并没有增加皮下脂肪组织或 LM 中的棕榈酸或减少油酸,但降低了脂肪组织中的豆蔻酸、棕榈油酸和顺式 vaccenic 酸(P≤0.05),表明硬脂酰辅酶 A 去饱和酶活性降低。大豆油增加了脂肪组织和肌肉中的 α-亚麻酸比例,并增加了肌肉中的亚油酸和 18:1trans-10。我们得出的结论是,棕榈油补充剂促进了脂肪组织的脂质合成,而不会降低饲料效率或增加牛肉中的棕榈酸含量。