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14 至 91 日龄荷斯坦犊牛开食料中添加包被蛋氨酸或蛋氨酸类似物对血浆代谢物、生长性能和效率的影响。

Effects of rumen-protected methionine or methionine analogs in starter on plasma metabolites, growth, and efficiency of Holstein calves from 14 to 91 d of age.

机构信息

Department of Animal Science, Cornell University, Ithaca, NY 14853.

The National Federation of Dairy Co-operative Associations (Zen-Raku-Ren), Tokyo, Japan 151-00053.

出版信息

J Dairy Sci. 2020 Nov;103(11):10136-10151. doi: 10.3168/jds.2020-18630. Epub 2020 Sep 18.

DOI:10.3168/jds.2020-18630
PMID:32952015
Abstract

During weaning, methionine (Met) supply decreases as liquid feed intake is reduced and ruminal function is developing. During this transition, the calf starter should both promote ruminal development and provide adequate nutrients post-ruminally. In mature ruminants, rumen-protected Met (RPM) and the Met analogs, 2-hydroxy-4-(methylthio)-butanoic acid (HMTBa) and HMTBa isopropyl ester (HMBi), are used to increase Met supply, stimulate ruminal fermentation, or exert both effects, respectively. To evaluate the effects of these forms of Met on calf performance during development of ruminal function, 74 Holstein calves were raised until 91 d of age, in 2 enrollment periods. Calves were individually housed from birth and, at 14 d of age, balanced for sex and randomly assigned to receive a starter with no added Met (CTRL, n = 20) or one supplemented with RPM (Smartamine M, Adisseo USA Inc., Alpharetta, GA; n = 16), HMTBa (RumenSmart, Adisseo; n = 19), or HMBi (MetaSmart, Adisseo; n = 19). Milk replacer [28% crude protein (CP), 15% fat] was offered up to 1.6 kg of dry matter (DM)/d and fed 3 times daily. Weaning was facilitated from d 49 to 63. The 4 starters (25% CP, 2.5 Mcal of metabolizable energy/kg of DM) were offered ad libitum, and supplement inclusion was set to provide an additional 0.16% DM of Met equivalents, and equal amounts of HMTBa within the analogs. Body weight and stature were measured, and blood was collected and analyzed for plasma urea nitrogen, β-hydroxybutyrate, and free AA on a weekly basis. Supplementation of RPM and HMBi increased free plasma Met, but no differences in growth or feed efficiency compared with calves fed the CTRL starter could be attributed to the additional Met supply alone. The addition of HMBi in the starter increased feed intake and body weight during the last weeks of the experiment. On the contrary, HMTBa failed to increase plasma Met and depressed intake and growth after weaning, likely because the level included in the diet was too high and intake was greater than previous studies, exacerbating the level of HMTBa ingested. No differences were observed in stature, feed efficiency, or non-AA plasma measurements among groups. These results demonstrate that RPM and HMBi are effective sources of metabolizable Met; however, Met was apparently not limiting calves fed the basal diet in this study. The increased feed intake observed with the inclusion of HMBi in the starter during the weaning and early postweaning period might be mediated by its metabolism in the rumen, and further research is needed to determine the mechanisms involved.

摘要

在断奶期间,随着液体饲料摄入量的减少和瘤胃功能的发展,蛋氨酸(Met)的供应减少。在这个过渡期间,犊牛料应既能促进瘤胃发育,又能在瘤胃后提供足够的营养。在成熟反刍动物中,瘤胃保护性 Met(RPM)和 Met 类似物,2-羟基-4-(甲硫基)-丁酸(HMTBa)和 HMTBa 异丙酯(HMBi),用于增加 Met 供应、刺激瘤胃发酵或分别发挥这两种作用。为了评估这些 Met 形式对瘤胃功能发育过程中犊牛生长性能的影响,74 头荷斯坦犊牛在 2 个入组期被饲养至 91 日龄。犊牛从出生开始单独饲养,在 14 日龄时,根据性别和体重进行平衡,并随机分配接受不添加 Met 的开食料(CTRL,n = 20)或添加 RPM(Smartamine M,Adisseo USA Inc.,Alpharetta,GA;n = 16)、HMTBa(RumenSmart,Adisseo;n = 19)或 HMBi(MetaSmart,Adisseo;n = 19)的开食料。牛奶代用品[28%粗蛋白(CP),15%脂肪]每天提供高达 1.6 公斤干物质(DM)/天,每天喂食 3 次。从第 49 天到第 63 天促进断奶。4 种开食料(25%CP,2.5 Mcal 可代谢能/kg DM)自由采食,补充物的添加量设定为提供额外 0.16% DM 的 Met 当量,并且在类似物中添加等量的 HMTBa。每周测量体重和体高,并采集血液进行血浆尿素氮、β-羟丁酸和游离氨基酸分析。与喂食 CTRL 开食料的犊牛相比,RPM 和 HMBi 的添加增加了游离血浆 Met,但不能归因于额外的 Met 供应,生长或饲料效率没有差异。开食料中添加 HMBi 增加了试验最后几周的采食量和体重。相反,HMTBa 未能增加血浆 Met,并在断奶后抑制了采食量和生长,可能是因为日粮中包含的水平过高,采食量大于之前的研究,加剧了摄入的 HMTBa 水平。各组之间在体高、饲料效率或非 AA 血浆测量方面没有差异。这些结果表明,RPM 和 HMBi 是可代谢 Met 的有效来源;然而,在这项研究中,基础日粮喂养的犊牛似乎并不缺乏 Met。在断奶和早期断奶期间,开食料中添加 HMBi 观察到的采食量增加可能与其在瘤胃中的代谢有关,需要进一步研究以确定涉及的机制。

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