Table 4.
Plasma metabolites and hormones in feedlot steers receiving diets containing (2 × 2 factorial arrangement): 1) monensin + tylosin (360 mg/steer daily from Rumensin 90 and 90 mg/steer daily from Tylan 40; Elanco Animal Health, Greenfield, IN) and 2) Y. schidigera extract (4 g/steer daily, as-fed basis; Micro-Aid Feed Grade Concentrate; DPI Global, Porterville, CA)1,2
Item | Monensin + tylosin (A) | Y. schidigera extract (B) | P-values | ||||||
---|---|---|---|---|---|---|---|---|---|
Yes | No | SEM | Yes | No | SEM | A | B | A × B | |
Glucose, mg/dL | 99.8 | 101 | 1 | 100 | 101 | 1 | 0.35 | 0.77 | 0.70 |
Insulin, ng/mL | 18.6 | 17.7 | 0.9 | 17.6 | 18.8 | 0.9 | 0.47 | 0.35 | 0.23 |
Insulin-like growth factor I, ng/mL | 168 | 172 | 5 | 170 | 171 | 5 | 0.55 | 0.83 | 0.55 |
Urea-N, mg/dL | 14.5 | 14.0 | 0.3 | 14.0 | 14.3 | 0.3 | 0.16 | 0.40 | 0.74 |
1Steers were housed in four drylot pens equipped with electronic feed bunks (GrowSafe Systems Ltd, Airdrie, AB, Canada) that measured individual feed intake from day −14 to slaughter. Steers were slaughtered (STX Beef; Corpus Christi, TX) in three groups that contained an equivalent number of steers/treatment combination (36 steers on day 114, 36 steers on day 142, and 48 steers on day 170). Treatments were offered to cattle from day 0 to slaughter. Pens housed cattle from the same treatment combination, and cattle rotated across drylot pens every 14 d to account for any potential pen effect.
2Blood samples were collected from all steers prior to feeding on days 0, 28, 56, and 84. A final blood sample was also collected when steer body weight was recorded the day before shipping to slaughter (days 112, 140, and 169). Results from day 0 were included as independent covariate in each respective analysis. No interactions of factor with day were detected (P ≥ 0.23).