Effects of methionine hydroxy copper supplementation on lactation performance, nutrient digestibility, and blood biochemical parameters in lactating cows

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Abstract

The objective of this study was to investigate the effects of methionine hydroxy Cu [(HMTBA)2-Cu] supplementation on lactation performance, nutrient digestibility, and blood biochemical parameters in lactating cows. Thirty lactating Holstein cows were assigned to 1 of 3 treatments in a randomized block design: (1) Cu sulfate only (S): 12mg of Cu provided by CuSO4 per kilogram of concentrate; (2) Cu sulfate and (HMTBA)2-Cu (SM): 6mg of Cu provided by CuSO4 and 6mg of Cu provided by (HMTBA)2-Cu per kilogram of concentrate; or (3) (HMTBA)2-Cu only (M): 12mg of Cu provided by (HMTBA)2-Cu per kilogram of concentrate. The level of dietary Cu was determined according to the NRC (2001) requirement. This experiment lasted for 120 d, with the first 20 d for adaptation and with sample and data collection beginning on d 21. The milk yield and 4% fat-corrected milk yield of cows in the SM treatment tended to increase compared with those in the S and M treatments. Cows fed SM also tended to have higher NDF and ADF apparent digestibility values than did cows fed S or M. Plasma Cu concentration significantly increased for the SM treatment compared with the S and M treatments. Cows fed S had higher plasma K concentration than did cows in the other 2 treatments. In conclusion, replacing one-half of the dietary Cu sulfate with (HMTBA)2-Cu increased plasma Cu concentration and tended to improve the neutral and acid detergent fiber apparent digestibility values and the lactation performance of lactating dairy cattle. © 2012 American Dairy Science Association.

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Wang, F., Li, S. L., Xin, J., Wang, Y. J., Cao, Z. J., Guo, F. C., & Wang, Y. M. (2012). Effects of methionine hydroxy copper supplementation on lactation performance, nutrient digestibility, and blood biochemical parameters in lactating cows. Journal of Dairy Science, 95(10), 5813–5820. https://doi.org/10.3168/jds.2011-4182

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