Leibniz Institute for Farm Animal Biology (FBN), 18196 Dummerstorf, Germany.
J Dairy Sci. 2010 Dec;93(12):5867-76. doi: 10.3168/jds.2010-3342.
Feeding rumen-protected fat (RPF) can improve energy supply for dairy cows but it affects glucose metabolism. Glucose availability is a precondition for high milk production in dairy cows. Therefore, this study investigated endocrine regulation of glucose homeostasis and hepatic gene expression related to glucose production because of RPF feeding in lactating cows. Eighteen Holstein dairy cows during second lactation were fed either a diet containing RPF (mainly C16:0 and C18:1; FD; n = 9) or a control diet based on corn starch (SD; n = 9) for 4 wk starting at 98 d in milk (DIM). Feed intake and milk yield were measured daily and milk composition once a week. Blood samples were taken weekly for analyses of plasma triglyceride, nonesterified fatty acids (NEFA), β-hydroxybutyrate, bilirubin, urea, lactate, glucose, insulin, and glucagon. At 124 DIM, an intravenous glucose tolerance test (GTT; 1g/kg of BW(0.75)) was performed after a 12-h period without food. Blood samples were taken before and 7, 14, 21, and 28 min after glucose administration, and plasma concentrations of glucose, insulin, and glucagon were measured. Glucose half-life as well as areas under the concentration curve for glucose, insulin, and glucagon were calculated. After slaughter at d 28 of treatment, liver samples were taken to measure mRNA abundance of pyruvate carboxylase, cytosolic phosphoenolpyruvate carboxykinase, glucose 6-phosphatase (G6Pase), and facilitative glucose transporter 2. Dry matter intake, but not energy and protein intake, was lower in FD than in SD. Milk yield during lactation decreased more in SD than in FD, and milk protein was lower in FD than in SD. Plasma concentrations of triglycerides and NEFA were higher in FD than in SD. Plasma insulin concentrations were lower and the glucagon:insulin ratios were higher in FD than in SD. Fasting glucose concentration before GTT was lower, and fasting glucagon concentrations tended to be higher in FD than in SD. In liver, fat content tended to be higher and G6Pase mRNA abundance was lower in FD than in SD. Lower hepatic G6Pase mRNA abundance was associated with reduced fasting plasma glucose concentrations, but the glucose-induced insulin response was not affected by RPF feeding. Hepatic G6Pase gene expression might be affected by DMI and might be involved in the regulation of glucose homeostasis in dairy cows, resulting in a lower hepatic glucose output after RPF feeding.
给反刍保护脂肪(RPF)可以改善奶牛的能量供应,但会影响葡萄糖代谢。葡萄糖的可用性是奶牛高产奶的前提。因此,本研究旨在调查泌乳奶牛 RPF 喂养对葡萄糖稳态的内分泌调节以及与葡萄糖生成相关的肝基因表达。18 头处于第二次泌乳期的荷斯坦奶牛从 98 天泌乳(DIM)开始,分别饲喂含有 RPF(主要为 C16:0 和 C18:1;FD;n=9)的日粮或基于玉米淀粉的对照日粮(SD;n=9),持续 4 周。每天测量饲料摄入量和产奶量,每周测量一次乳成分。每周采集一次血样,用于分析血浆甘油三酯、非酯化脂肪酸(NEFA)、β-羟丁酸、胆红素、尿素、乳酸、葡萄糖、胰岛素和胰高血糖素。在 124 DIM 时,在禁食 12 小时后进行静脉葡萄糖耐量试验(GTT;1g/kg BW(0.75))。在给予葡萄糖前以及 7、14、21 和 28 分钟后采集血样,并测量血浆葡萄糖、胰岛素和胰高血糖素浓度。计算葡萄糖半衰期以及葡萄糖、胰岛素和胰高血糖素浓度曲线下面积。在处理的第 28 天屠宰后,取肝样测量丙酮酸羧化酶、细胞质磷酸烯醇丙酮酸羧激酶、葡萄糖 6-磷酸酶(G6Pase)和易化葡萄糖转运蛋白 2 的 mRNA 丰度。FD 的干物质摄入量低于 SD,但能量和蛋白质摄入量无差异。SD 的泌乳期产奶量下降大于 FD,而 FD 的乳蛋白产量低于 SD。FD 的血浆甘油三酯和 NEFA 浓度高于 SD。FD 的血浆胰岛素浓度较低,胰高血糖素:胰岛素比值较高。GTT 前的空腹血糖浓度较低,FD 的空腹胰高血糖素浓度较高。FD 的肝脂肪含量较高,G6Pase mRNA 丰度较低。肝 G6Pase mRNA 丰度较低与空腹血浆葡萄糖浓度降低有关,但 RPF 喂养并未影响葡萄糖诱导的胰岛素反应。肝 G6Pase 基因表达可能受 DMI 影响,并可能参与奶牛葡萄糖稳态的调节,导致 RPF 喂养后肝葡萄糖输出减少。