Effects of Amount and Profile of Amino Acids Supply on Lactation Performance, Mammary Gland Metabolism, and Nitrogen Efficiency in Holstein Dairy Cows

Simple Summary Efficiency of nitrogen utilization (ENU) for productive purposes is low (20–30%), partially due to post-absorptive amino acid (AA) catabolism. Catabolism can be reduced by increasing mammary AA removal from the blood, allowing less AA to reach non-mammary tissues. Reducing the AA supply did not decrease milk protein yield and increased ENU, while altering AA profile did not affect ENU. Infusing AA into a low protein diet increased energy corrected milk due to changes in mammary metabolism. Such response seemed to be not only due to substrate effect but also to the regulatory role of the infused AA. Abstract To evaluate the effects of amount and profile of amino acid (AA) on milk protein yield (MPY), mammary metabolism, and efficiency of nitrogen use (ENU), ten cows were used in 5 × 5 replicated Latin squares and fed a positive control (16.1% crude protein-CP) or two lower CP diets (14.6 and 13.2%) with or without essential AA (EAA) infusion. The EAA solutions provided predicted limiting EAA in each treatment and were continuously infused into the abomasum of the cows. Milk production and MPY were not affected by treatment (mean 35.4 kg/d and 1.03 kg/d, respectively). Efficiency of nitrogen utilization was increased as dietary CP decreased but was not affected by EAA infusion (p < 0.01). Energy-corrected milk production was increased by EAA infusion into 13.2% CP, but not into 14.6% CP diet (p = 0.09), reaching the positive control value. Infusions increased mammary affinity for non-infused EAA (Ile, Phe, Thr, and Trp), allowing the same MPY despite lower arterial concentrations of these AA. Higher arterial concentrations of infused EAA did not increase their mammary uptake and MPY (p = 0.40; p = 0.85). Mammary metabolism did not fully explain changes in N efficiency, suggesting that it might be driven by less extramammary catabolism as AA supply was reduced.

[1]  M. Wattiaux,et al.  Plasma essential amino acid concentration and profile are associated with performance of lactating dairy cows as revealed through meta-analysis and hierarchical clustering. , 2022, Journal of dairy science.

[2]  S. A. Arriola Apelo,et al.  Insulin potentiates essential amino acids effects on mechanistic target of rapamycin complex 1 signaling in MAC-T cells. , 2020, Journal of dairy science.

[3]  S. A. Arriola Apelo,et al.  Post-ruminal supplies of glucose and casein, but not acetate, stimulate milk protein synthesis in dairy cows through differential effects on mammary metabolism. , 2020, Journal of dairy science.

[4]  Shengguo Zhao,et al.  Effect of Heat Stress on Bacterial Composition and Metabolism in the Rumen of Lactating Dairy Cows , 2019, Animals : an open access journal from MDPI.

[5]  X. Y. Lin,et al.  Effects of rumen-protected methionine and other essential amino acid supplementation on milk and milk component yields in lactating Holstein cows. , 2019, Journal of dairy science.

[6]  J. Dijkstra,et al.  Mammary gland metabolite utilization in response to exogenous glucose or long-chain fatty acids at low and high metabolizable protein levels. , 2019, Journal of dairy science.

[7]  J. Cant,et al.  Maintenance of plasma branched-chain amino acid concentrations during glucose infusion directs essential amino acids to extra-mammary tissues in lactating dairy cows. , 2018, Journal of dairy science.

[8]  D. Sabatini Twenty-five years of mTOR: Uncovering the link from nutrients to growth , 2017, Proceedings of the National Academy of Sciences.

[9]  Jianxin Liu,et al.  Essential amino acid ratios and mTOR affect lipogenic gene networks and miRNA expression in bovine mammary epithelial cells , 2016, Journal of Animal Science and Biotechnology.

[10]  Board on Agriculture Nutrient Requirements of Dairy Cattle , 2016 .

[11]  D. Sabatini,et al.  Structural basis for leucine sensing by the Sestrin2-mTORC1 pathway , 2016, Science.

[12]  G. Cantalapiedra-Hijar,et al.  Diets rich in starch improve the efficiency of amino acids use by the mammary gland in lactating Jersey cows. , 2015, Journal of dairy science.

[13]  C. Parys,et al.  Relationships between circulating plasma concentrations and duodenal flows of essential amino acids in lactating dairy cows. , 2015, Journal of dairy science.

[14]  S. Lemosquet,et al.  Changes in mammary metabolism in response to the provision of an ideal amino acid profile at 2 levels of metabolizable protein supply in dairy cows: Consequences on efficiency. , 2015, Journal of dairy science.

[15]  A. Gehman,et al.  Effects of slow-release urea and rumen-protected methionine and histidine on performance of dairy cows. , 2015, Journal of dairy science.

[16]  C. Parys,et al.  Effect of dietary protein level and rumen-protected amino acid supplementation on amino acid utilization for milk protein in lactating dairy cows. , 2015, Journal of dairy science.

[17]  S. A. Arriola Apelo,et al.  Effects of reduced dietary protein and supplemental rumen-protected essential amino acids on the nitrogen efficiency of dairy cows. , 2014, Journal of dairy science.

[18]  S. A. Arriola Apelo,et al.  Invited review: Current representation and future trends of predicting amino acid utilization in the lactating dairy cow. , 2014, Journal of dairy science.

[19]  N. St-Pierre,et al.  Isoleucine, leucine, methionine, and threonine effects on mammalian target of rapamycin signaling in mammary tissue. , 2014, Journal of dairy science.

[20]  J. Loor,et al.  Supplemental Smartamine M or MetaSmart during the transition period benefits postpartal cow performance and blood neutrophil function. , 2013, Journal of dairy science.

[21]  P. Faverdin,et al.  Milk protein synthesis in response to the provision of an "ideal" amino acid profile at 2 levels of metabolizable protein supply in dairy cows. , 2012, Journal of dairy science.

[22]  C. Parys,et al.  Rumen-protected lysine, methionine, and histidine increase milk protein yield in dairy cows fed a metabolizable protein-deficient diet. , 2012, Journal of dairy science.

[23]  G. Lobley,et al.  Triennial Lactation Symposium: Mammary metabolism of amino acids in dairy cows. , 2012, Journal of animal science.

[24]  M. Hanigan,et al.  Isoleucine and leucine independently regulate mTOR signaling and protein synthesis in MAC-T cells and bovine mammary tissue slices. , 2012, The Journal of nutrition.

[25]  B. Larget,et al.  Effect of dietary crude protein on ammonia-N emission measured by herd nitrogen mass balance in a freestall dairy barn managed under farm-like conditions. , 2010, Animal : an international journal of animal bioscience.

[26]  Yuehua Wu,et al.  Effects of dietary supplementation of methionine and lysine on milk production and nitrogen utilization in dairy cows. , 2010, Journal of dairy science.

[27]  H. Lapierre,et al.  Changes in production and mammary metabolism of dairy cows in response to essential and nonessential amino acid infusions. , 2010, Journal of dairy science.

[28]  A. Hristov,et al.  A meta-analysis of the effects of dietary protein concentration and degradability on milk protein yield and milk N efficiency in dairy cows. , 2009, Journal of dairy science.

[29]  N. Kristensen,et al.  Nitrogen recycling through the gut and the nitrogen economy of ruminants: an asynchronous symbiosis. , 2008, Journal of animal science.

[30]  G. Lobley,et al.  Effect of casein and propionate supply on mammary protein metabolism in lactating dairy cows. , 2006, Journal of dairy science.

[31]  L. Armentano,et al.  Technical note: development of a tool to insert abomasal infusion lines into dairy cows. , 2006, Journal of dairy science.

[32]  G. Broderick,et al.  Effect of dietary crude protein concentration on milk production and nitrogen utilization in lactating dairy cows. , 2006, Journal of dairy science.

[33]  M. Hanigan,et al.  A model of net amino acid absorption and utilization by the portal-drained viscera of the lactating dairy cow. , 2004, Journal of dairy science.

[34]  J France,et al.  An integrative model of amino acid metabolism in the liver of the lactating dairy cow. , 2004, Journal of theoretical biology.

[35]  M. Hanigan,et al.  Milk protein synthesis as a function of amino acid supply. , 2004, Journal of dairy science.

[36]  K. Beauchemin,et al.  Effects of increasing levels of refined cornstarch in the diet of lactating dairy cows on performance and ruminal pH. , 2003, Journal of dairy science.

[37]  K. H. Nahm,et al.  Efficient Feed Nutrient Utilization to Reduce Pollutants in Poultry and Swine Manure , 2002 .

[38]  Bill Hunter,et al.  European Commission , 1992, The International Encyclopedia of Higher Education Systems and Institutions.

[39]  G. Lobley,et al.  Amino acid exchange by the mammary gland of lactating goats when histidine limits milk production. , 2000, Journal of dairy science.

[40]  Ermias Kebreab,et al.  A review of efficiency of nitrogen utilisation in lactating dairy cows and its relationship with environmental pollution , 2000 .

[41]  G. Broderick,et al.  Effect of replacing alfalfa silage with high moisture corn on ruminal protein synthesis estimated from excretion of total purine derivatives. , 1999, Journal of dairy science.

[42]  G. Lobley,et al.  Quantitation of blood and plasma amino acids using isotope dilution electron impact gas chromatography/mass spectrometry with U-(13)C amino acids as internal standards. , 1999, Rapid communications in mass spectrometry : RCM.

[43]  G. Lobley,et al.  Alternative models for analyses of liver and mammary transorgan metabolite extraction data , 1998, British Journal of Nutrition.

[44]  G. Broderick,et al.  A statistical evaluation of animal and nutritional factors influencing concentrations of milk urea nitrogen. , 1997, Journal of dairy science.

[45]  G. Broderick,et al.  Excretion of purine derivatives by Holstein cows abomasally infused with incremental amounts of purines. , 1997, Journal of dairy science.

[46]  Giuseppe Licitra,et al.  Standardization of procedures for nitrogen fractionation of ruminant feeds , 1996 .

[47]  J. Cant,et al.  Mammary amino acid utilization in dairy cows fed fat and its relationship to milk protein depression. , 1993, Journal of dairy science.

[48]  P. V. Soest,et al.  Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. , 1991, Journal of dairy science.

[49]  G. Broderick,et al.  Use of Plasma Amino Acid Concentration to Identify Limiting Amino Acids for Milk Production , 1974 .

[50]  R. S. Emery,et al.  Correlation of Milk Fat with Dietary and Metabolic Factors in Cows Fed Restricted-Roughage Rations Supplemented with Magnesium Oxide or Sodium Bicarbonate , 1965 .

[51]  H. Tyrrell,et al.  Prediction of the energy value of cow's milk. , 1965, Journal of dairy science.

[52]  A. L. Chaney,et al.  Modified reagents for determination of urea and ammonia. , 1962, Clinical chemistry.

[53]  J. Dijkstra,et al.  Challenges in ruminant nutrition: towards minimal nitrogen losses in cattle , 2013 .

[54]  M. Hanigan,et al.  Evaluation of a representation of the limiting amino acid theory for milk protein synthesis. , 2000 .

[55]  D. Mertens,et al.  Effects of sodium sulfite on recovery and composition of detergent fiber and lignin. , 1996, Journal of AOAC International.

[56]  X. B. Chen,et al.  ESTIMATION OF MICROBIAL PROTEIN SUPPLY TO SHEEP AND CATTLE BASED ON URINARY EXCRETION OF PURINE DERIVATIVES - AN OVERVIEW OF THE TECHNICAL DETAILS , 1995 .

[57]  N. Benevenga,et al.  Toxicities of methionine and other amino acids. , 1974, Journal of agricultural and food chemistry.

[58]  G. Vogels,et al.  Differential analyses of glyoxylate derivatives. , 1970, Analytical biochemistry.

[59]  F. Challenger Biological methylation. , 1951, Advances in enzymology and related subjects of biochemistry.