使用血浆游离氨基酸剂量反应技术评估血液采样时间点,以确定反刍保护蛋氨酸补充剂的相对生物利用率

Nancy L. Whitehouse , Devan L. Chirgwin , Charles G. Schwab , Daniel Luchini , Nelson Lobos , André F. Brito
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引用次数: 0

摘要

目前,使用血浆游离AA剂量反应技术计算瘤胃保护AA补充剂的相对生物利用率(RBV)时,需要在奶牛每8小时(5:00、13:00和21:00)喂食一次的拉丁方形实验中,在每个阶段的最后3天,分别在5:00喂食后的2、4、6和8小时采集血液样本。本研究的目的是确定当前的血液采样方案是否能捕捉到一天 24 小时内血浆中金属元素浓度可能发生的变化,从而充分确定 Smartamine M(SM)中金属元素的 RBV。五头多胎泌乳荷斯坦奶牛采用 5 × 5 拉丁正方形设计,每 7 天为一个周期。处理方法为:(1) 对照组(腹腔灌注自来水);(2) 12 克/天腹腔灌注 dl-Met;(3) 24 克/天腹腔灌注 dl-Met;(4) 15 克/天饲喂 Met(20 克/天饲喂 SM);(5) 30 克/天饲喂 Met(40 克/天饲喂 SM)。从每个阶段的第 5 天开始至第 7 天结束,每隔 2 小时通过颈静脉导管收集喂食后的血液样本。血浆金属元素分析是在氯甲酸酯衍生化后使用气相色谱法进行的。血浆中金属元素的浓度是5:00喂食后2-8小时、13:00喂食后2-8小时、21:00喂食后2-8小时和5:00喂食后2-24小时各天的平均值。此外,血浆中的 Met 浓度在输注 0、12 和 24 克 dl-Met,以及喂食 0、15 和 30 克 Met 时均有所下降。在 2 至 8 小时、10 至 16 小时、18 至 24 小时和 2 至 24 小时采样期间,从 SM 计算出的 Met RBV 平均值分别为 83.8%、83.6%、87.4% 和 83.0%。2 至 8 小时和 2 至 24 小时采样期的 RBV 估计值相似,这表明我们最初的血液采样方案在确定反刍保护 Met 产品的 RBV 方面似乎是可靠的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of blood sampling time points to determine the relative bioavailability of ruminally protected methionine supplements using the plasma free amino acid dose-response technique
The calculation of the relative bioavailability (RBV) of rumen-protected AA supplements using the plasma free AA dose-response technique currently relies on blood samples obtained 2, 4, 6, and 8 h after the 0500 h feeding during the last 3 d of each period in Latin square experiments with cows fed every 8 h (0500, 1300, and 2100 h). The objective of this study was to determine if this current blood sampling protocol captures the changes that may occur in plasma Met concentrations within a 24-h day to adequately determine the RBV of Met from Smartamine M (SM). Five multiparous lactating Holstein cows were used in a 5 × 5 Latin square design with 7-d periods. Treatments were (1) control (abomasal infusion of tap water), (2) 12 g/d of abomasally infused dl-Met, (3) 24 g/d of abomasally infused dl-Met, (4) 15 g/d of fed Met (20 g/d of SM), and (5) 30 g/d of fed Met (40 g/d of SM). Blood samples were collected via jugular catheters every 2 h after the 0500 h feeding starting on d 5 and ending on d 7 of each period. Plasma Met analysis was conducted using gas chromatography after chloroformate derivatization. Plasma Met concentration was averaged across days for 2–8 h after the 0500 h feeding, 2–8 h after the 1300 h feeding, 2–8 h after the 2100 h feeding, and 2–24 h after the 0500 h feeding. In addition, plasma Met concentration was regressed on 0, 12, and 24 g of infused dl-Met and 0, 15, and 30 g of fed Met. The calculated RBV of Met from SM averaged 83.8%, 83.6%, 87.4%, and 83.0% for the 2–8 h, 10–16 h, 18–24 h, and 2–24 h sampling periods, respectively. The similarity in the estimations of RBV for the 2–8 h and 2–24 h sampling periods indicates that our original blood sampling protocol seems reliable for determining the RBV of ruminally protected Met products.
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JDS communications
JDS communications Animal Science and Zoology
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