Influence of monensin on Holstein steers fed high-concentrate diets containing soybean meal or urea

J Anim Sci. 1997 Oct;75(10):2571-9. doi: 10.2527/1997.75102571x.

Abstract

We conducted two growth trials to evaluate the effects of monensin on amino acid sparing. When Holstein steers were fed a 90% concentrate diet supplemented with soybean meal (13.5% CP), the DMI, ADG, and efficiencies of feed and nitrogen utilization were greater than with urea (P < .10). Monensin improved ADG with both nitrogen supplements (P < .01), but the positive effects of monensin on efficiencies of feed (P = .12) and nitrogen (P = .26) utilization were greater for soybean meal than for urea. Increasing amounts of monensin (0, 11, or 22 mg/kg of DM) caused a linear increase in DMI with urea. Diets with soybean had greater intakes than diets with urea (P < .01); the greatest intake was of a soybean diet with monensin at 11 mg/kg of DM. Holstein steers fed soybean meal at 13.5% CP had lower DMI and greater efficiencies of feed and nitrogen utilization than steers fed 16.7% CP (P < .10). Crude protein level had no effect on ADG (P > .10). Monensin always increased the efficiencies of feed and nitrogen utilization (P < .05), but these trends were greater for diets with 16.7 than for those with 13.5% CP. Overall, monensin decreased DMI (P < .01), but this effect was greater for 16.7% than for 13.5% CP. Because the positive effects of monensin on diet NEg (P = .16) and efficiency of nitrogen utilization (P = .26) were greater for soybean meal than for urea, it seemed that monensin was sparing amino acids.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle / growth & development*
  • Cattle / metabolism
  • Cattle / physiology
  • Coccidiostats / pharmacology*
  • Diet / veterinary*
  • Dietary Supplements
  • Dose-Response Relationship, Drug
  • Eating / drug effects
  • Eating / physiology
  • Glycine max / standards*
  • Male
  • Monensin / pharmacology*
  • Nitrogen / metabolism
  • Random Allocation
  • Urea / pharmacology*
  • Weight Gain / drug effects
  • Weight Gain / physiology

Substances

  • Coccidiostats
  • Urea
  • Monensin
  • Nitrogen