Providing a well-balanced supply of essential AA (EAA) can serve as an opportunity to reduce the protein intake for dairy cows by increasing the efficiency of metabolizable protein (or PDIE, its equivalent in the INRA feeding system) utilization for milk protein yield. Our objectives were to compare the effect of supplying an "ideal" EAA profile (EAA+) with an imbalanced AA profile (control) at 2 levels of PDIE/NE(L) (net energy for lactation) supplies to study the interaction between PDIE and AA profiles, and to compare this ideal profile with a simple mixture of the 4 most deficient EAA (4 EAA) in the diets of dairy cows. Six lactating multiparous Holstein cows received 6 treatments with 2 different levels of PDIE supplied by diets and AA infusions in the duodenum according to a changeover design with 3-wk periods. Within each PDIE supply level, the cows received 3 different AA infusions in the duodenum according to a 3×3 Latin square design with 1-wk subperiods, which corresponded to the following treatment groups: control (Glu), 4EAA (Lys, Met, His, Leu), and EAA+ (4 EAA plus Ile, Val, Phe, Trp, and Tyr). In the low and high PDIE treatments, diets and infusions provided 54.7 and 64.0 g/Mcal of PDIE/NE(L), respectively, which corresponded to crude protein levels of 13.6 and 15.2%, respectively. High-PDIE supplies increased the milk protein yield by 163 g/d, the milk protein content by 1.4 g/kg, the milk yield by 4.1 kg/d, and the lactose yield by 178 g/d and decreased the PDIE efficiency of utilization by 12.4%, whereas the N efficiency of utilization remained unaffected. Supplying the 2 EAA profiles (4EAA and EAA+) increased the milk protein yield by 67 g/d, the milk protein content by 1.3g/kg, and the milk yield by 0.9 kg/d, whereas the milk fat and milk lactose contents were decreased by 2.4 and 1.6g/kg, respectively. The responses regarding milk yield and its composition were similar whether the cows received the 4 EAA or the EAA+ treatment. The responses were similar for the milk yield and composition whether the EAA were supplied by low- or high-PDIE supplies. In conclusion, the efficiency of PDIE utilization was improved by 6.6% and the N efficiency was improved by 7.0% by correcting the EAA profiles, independent of the level of PDIE supplied. In addition, the increased efficiency observed, associated with provision of the 4 EAA, was similar to the provision of all EAA (EAA+) in this experiment.
An ideal profile of essential AA (EAA) can improve the efficiency of metabolizable protein (or PDIE, the equivalent in the INRA feeding system) utilization in dairy cows. Compared with other EAA, existing recommendations for the requirements of Arg, Ile, and Val are few and inconsistent. Four multiparous Holstein dairy cows at 22±6 wk of lactation received 4 treatments (duodenal infusions of 445±22.4 g/d of an EAA mixture complementing a low-protein diet in a 4×4 Latin square design with a period length of 1 wk). The control treatment provided a balanced supply (in % of PDIE) of 5.1% Arg, 5.2% Ile, and 5.9% Val, whereas in the 3 subsequent treatments of -Arg, -Ile, and -Val, the concentrations of these 3 EAA were reduced to 3.5, 4.1, and 4.5%, respectively. All treatments were made isonitrogenous and were balanced to provide 7 other EAA (Lys, Met, His, Leu, Phe, Thr, and Trp), according to the recommendations described in the literature. Combined, the diet and the infusions provided 14.3±0.1% crude protein on a dry matter basis, and 66.0±1.2 g of PDIE/Mcal of net energy for lactation. Neither dry matter intake (19.2 kg/d) nor milk yield (30.4±0.4 kg/d) was affected by treatments. The -Arg and -Ile treatments did not modify milk protein synthesis or the efficiency of N utilization. However, the -Val treatment decreased milk protein content by 4.9% and milk crude protein content by 4.3%, and tended to decrease the efficiency of N use for milk protein yield by 3.7% (compared with the control). These effects of Val were related to a decrease in the plasma concentration of Val as well as a trend toward decreasing plasma concentrations of Met, His, and the sum of all EAA and nonessential AA in the -Val treatment, which indicates a different utilization of all AA in response to the Val deficit. The deletion of Ile, compared with the deletion of Val, tended to decrease the milk protein-to-fat ratio by 3.8%. In conclusion, the supply of Arg at 3.5% of PDIE was not limiting for milk protein synthesis. The slight effect on the milk protein-to-fat ratio caused by decreasing the supply of Ile suggests a need to reevaluate the Ile requirement more precisely. A low Val supply could be limiting for milk protein synthesis, provided that the requirements of Lys, Met, and His are met.
The aim of this study was to compare the modifications in mammary gland metabolism by supplying an ideal versus an imbalanced essential AA (EAA) profile at low and high metabolizable protein (or PDIE, its equivalent in the INRA feeding system). Four lactating, multiparous Holstein cows received 4 treatments composed of 2 basal diets containing 2 levels of PDIE (LP or HP) and 2 different infusions of AA mixtures (AA- or AA+) in the duodenum. The AA+ mixture contained Lys, Met, Leu, His, Ile, Val, Phe, Arg, Trp, and Glu, whereas the AA- mixture contained Glu, Pro, and Ser. The infusion mixtures were iso-PDIE. The diet plus infusions provided 13.9 versus 15.8% of crude protein that corresponded to 102 versus 118g/kg of dry matter of PDIE in LP and HP treatments, respectively. The treatments were designed as a 2×2 crossover design of 2 levels of PDIE supply (LP vs. HP) with 28-d periods. Infusions of AA in the duodenum (AA- vs. AA+) were superimposed to diet within each 28-d period according to 2×2 crossover designs with 14-d subperiods. Increasing the PDIE supply tended to increase milk protein yield; however, the efficiency of PDIE utilization decreased and the plasma urea concentration increased, indicating a higher catabolism of AA. The AA+ treatments increased milk protein yield and content similarly at both levels of protein supply. This was explained by an increase in the mammary uptake of all EAA except His and Trp. The mammary uptake of non-EAA (NEAA) was altered to the increase in EAA uptake so that the total AA uptake was almost equal to milk protein output on a nitrogen basis. The ratio between NEAA to total AA uptake decreased from 46% in LPAA- to 40% in LPAA+, HPAA-, and HPAA+ treatments. The PDIE efficiency tended to increase in the AA+ versus the AA- treatments because the NEAA supply and the amount of NEAA not used by the mammary both decreased. Nevertheless, our AA+ treatments seemed not to be the ideal profile: the mammary uptake-to-output ratio for Thr was higher than 1 in LPAA-, but it decreased to 1 in all the other treatments, suggesting that Thr was deficient in these treatments. Conversely, an excess of His was indicated because its uptake was similar in AA+ and AA- treatments. In conclusion, balancing the EAA profile increased milk protein yield and metabolizable protein efficiency at both levels of protein supply by increasing the mammary uptake of EAA and altering the NEAA uptake, leading to less AA available for catabolism.
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