Moneimsin Effects on Digestibility, Ruminal Protein Escape and Microbial Protein Synthesis on High-Fiber Diets
- 1 September 1985
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Animal Science
- Vol. 61 (3) , 654-660
- https://doi.org/10.2527/jas1985.613654x
Abstract
The influence of monensin level (0, 6.1, 12.2, 18.3 and 36.6 ppm) on diet fiber digestibility, mocrobial protein synthesis and ruminal escape of dietary protein was evaluated in two steer metabolism trials. A growth trial was conducted to study possible interactions of forage quality and monensin level. In metabolism trial 1, four ruminal-cannulated steers were assigned to four monensin levels in a 4 × 4 Latin square design to measure fiber digestibility, rate of passage and protein metabolism. In metabolism trial 2, five duodenal-cannulated steers were assigned to five monensin levels in a 5 × 5 Latin square design to measure fiber digestibility, bacterial N flow and plant N flow. In the two metabolism trials, the level of monensin influenced organic matter (OM) digestibility, neutral detergent fiber (NDF) digestibility and ruminal NDF digestibility quadratically, with the intermediate levels of monensin being superior either to the high level of monensin or no monensin. A quadratic increase in particulate disappearance rate (P=.09) and no effect (P=.95) on liquid disappearance were also observed in trial 1. In trial 1, monensin level quadratically decreased (P=.10) the bacterial protein concentration and increased (P=.02) the ratio of total N:diaminopimilic acid in whole rumen contents. In trial 2, no overall difference in duodenal N flow (P=.64) or flow of individual amino acids (P=.46) was observed. In the growth trial, no interaction of cornstalk quality and monensin was observed (P<.38). Monensin linearly decreased feed intake (P=.09) and quadratically affected daily gain (P=.03) and feed/gain (P=.07). The 100-mg level, which corresponds to the 18.3-ppm level in the metabolism trials, was superior to either the 0- or 200-mg level in this trial (P=.07). Copyright © 1985. American Society of Animal Science. . Copyright 1985 by American Society of Animal ScienceKeywords
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