No abstract

Our objective was to evaluate the effects of supplementing 1mg of 25-OH vitamin D3 (HyD®) and increased vitamin E amount (2000 mg/animal/d) on cattleˈ performance and carcass characteristics when fed a 90-d feedlot finishing diet. A total of 140 Nellore bulls (IBW = 387 ± 28 kg) were distributed in 14 pens (10 animals/pen) in a randomized complete block design (7 pens per treatment). The basal diet was composed by 15% sugarcane bagasse, 72.8% ground corn, 7.6% soybean meal and 4.6 % mineral-vitamin premix (DM basis). The dietary treatments were: 1) Control: No addition of 25-hydroxy-vitamin-D3 (HyD®) and basal Vit. E amount (520 mg/animal per day); 2) HyD+Vit.E: Addition of 1 mg of HyD® plus increased Vit. E amount (2000 mg/animal per day). The animals were fed once daily and had free access to fresh water. Statistical analysis was performed using the MIXED procedure of SAS 9.4. Means comparison was evaluated by tukey test and declared significant at P < 0.05, and tendencies considered when 0.05 < P < 0.10. There was no difference on final body weight (~522.8 kg, P = 0.11), ADG (~1.54 kg/d, P = 0.17), DM intake (~9.9 kg/d, P = 0.41) and G:F (~0.156, P = 0.28) between treatments. Likewise, no differences were observed (P > 0.10) for dressing (~53.5%), REA (~65.5 cm²) and SFT (~4.10 mm). However, feeding HyD+Vit.E tended to increase (P = 0.07) carcass average daily gain (0.993 vs. 0.953 kg/d) and increased (P = 0.04) carcass weight by 4.2 kg compared with control (281.6 vs. 277.4 kg). In conclusion, the combination of HyD and increased vitamin E increases carcass production in feedlot cattle.

The energy content of finishing diets offered to feedlot cattle may vary across countries. We assumed that the lower is the energy content of the finishing diet, the shorter can be the adaptation period to high-concentrate diets without negatively impacting rumen health while still improving feedlot performance. This study was designed to determine the effects of adaptation periods of 6, 9, 14 and 21 days on feedlot performance, feeding behaviour, blood gas profile, carcass characteristics and rumen morphometrics of Nellore cattle. The experiment was designed as a completely randomised block, replicated 6 times, in which 96 20-month-old yearling Nellore bulls (391.1 ± 30.9 kg) were fed in 24 pens (4 animals/pen) according to the adaptation period adopted: 6, 9, 14 or 21 days. The adaptation diets contained 70%, 75% and 80.5% concentrate, and the finishing diet contained 86% concentrate. After adaptation, one animal per pen was slaughtered (n = 24) for rumen morphometric evaluations and the remaining 72 animals were harvested after 88 days on feed. Orthogonal contrasts were used to assess linear, quadratic and cubic relationships between days of adaptation and the dependent variable. Overall, as days of adaptation increased, final BW (P = 0.06), average daily gain (ADG) (P = 0.07), hot carcass weight (P = 0.04) and gain to feed ratio (G : F) (P = 0.07) were affected quadratically, in which yearling bulls adapted by 14 days presented greater final BW, ADG, hot carcass weight and improved G : F. No significant (P > 0.10) days of adaptation effect was observed for any of feeding behaviour variables. As days of adaptation increased, the absorptive surface area of the rumen was affected cubically, where yearling bulls adapted by 14 days presented greater absorptive surface area (P = 0.03). Thus, Nellore yearling bulls should be adapted by 14 days because it led to improved feedlot performance and greater development of rumen epithelium without increasing rumenitis scores.

In the present study, the effects of restricted intake of the final finishing diet as a means of dietary adaptation compared with diets increasing in concentrate content (step-up) over periods of 14 and 21 days on growth performance, carcass characteristics, feeding behaviour and rumen morphometrics of Nellore cattle were evaluated. One hundred and twenty 20 months old Nellore bulls (initial BW = 372.2 kg, s.d. = 21.5 kg) were randomly allocated in 24 pens (n = 5 per pen) and fed for 84 days. The study had a completely randomised design with a 2 × 2 factorial arrangement: adaptation using both 14-day and 21-day step-up and restriction protocols. Each treatment was replicated 6 times. One bull per pen was slaughtered (n = 24) at the end of adaptation period to evaluate rumen morphometrics. The remaining bulls (n = 96) were slaughtered at the end of experimental period. Interactions were observed (P < 0.05) for growth performance, feeding behaviour and rumen morphometrics variables. Overall, no protocol or adaptation length main effect (P > 0.05) was observed for any of the growth rate and carcass traits evaluated, except for hot carcass weight (P = 0.03) and dressing percentage (P = 0.04), where bulls adapted for 14 days had heavier carcasses and increased dressing percentage when compared with cattle adapted for 21 days. Cattle adapted for 21 days had a larger (P = 0.005) rumen wall absorptive surface area at the end of adaptation period than those adapted for 14 days; however, no differences were detected at the end of finishing period. Thus, Nellore yearling bulls could be adapted for 14 days regardless of the protocol.

Diets for feedlot cattle must be a higher energy density, entailing high fermentable carbohydrate content. Feed additives are needed to reduce possible metabolic disorders. This study aimed to analyze the post-rumen effects of different levels of starch (25%, 35%, and 45%) and additives (monensin or a blend of essential oils and exogenous α-amylase) in diets for Nellore feedlot cattle. The cecum tissue proteome was analyzed via two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) and then differentially expressed protein spots were identified with liquid chromatography–tandem mass spectrometry (LC–MS/MS). The use of blends of essential oils associated with α-amylase as a feed additive promoted the upregulation of enzymes such as triosephosphate isomerase, phosphoglycerate mutase, alpha-enolase, beta-enolase, fructose-bisphosphate aldolase, pyruvate kinase, glyceraldehyde-3-phosphate dehydrogenase (GAPDH), l-lactate dehydrogenase B, l-lactate dehydrogenase A chain, l-lactate dehydrogenase, and ATP synthase subunit beta, which promote the degradation of carbohydrates in the glycolysis and gluconeogenesis pathways and oxidative phosphorylation, support pyruvate metabolism through the synthesis of lactate from pyruvate, and participate in the electron transport chain, producing ATP from ADP in the presence of a proton gradient across the membrane. The absence of proteins related to inflammation processes (leukocyte elastase inhibitors) in the cecum tissues of animals fed essential oils and amylase may be because feed enzymes can remain active in the intestine and aid in the digestion of nutrients that escape rumen fermentation; conversely, the effect of monensin is more evident in the rumen and less than 10% results in post-ruminal action, corroborating the hypothesis that ionophore antibiotics have a limited effect on the microbiota and intestinal fermentation of ruminants. However, the increase in starch in these diets promoted a downregulation of enzymes linked to carbohydrate degradation, probably caused by damage to the cecum epithelium due to increased responses linked to inflammatory injuries.