Dietary copper effects on lipid metabolism, performance, and ruminal fermentation in finishing steers

Sixty Angus steers (391.1+/-6.1 kg) were used to determine the effects of dietary Cu concentration on lipid metabolism and ruminal fermentation. Steers were stratified by weight and randomly assigned to treatments. Treatments consisted of 0 (control), 10, or 20 mg of supplemental Cu (as CuSO4)/kg diet DM. Steers were housed in pens equipped with individual electronic Calan gate feeders. On d 86 and 92, ruminal fluid was collected from two steers/treatment for IVDMD determination. Equal numbers of steers per treatment were slaughtered after receiving the finishing diets for 96 or 112 d. Gain, feed intake, feed efficiency, IVDMD, and ruminal VFA molar proportions were not affected by Cu supplementation. Copper supplementation increased (P < .05) liver Cu concentrations, and steers supplemented with 20 mg Cu/kg DM had higher (P < .05) liver Cu concentrations than steers supplemented with 10 mg Cu/kg DM. Serum total cholesterol concentrations were reduced by d 56 and at subsequent sampling dates in steers receiving supplemental Cu. Longissimus muscle cholesterol concentrations were lower (P < .10) in steers supplemented with Cu. Backfat depth was less (P < .05) in steers receiving supplemental Cu, but marbling scores were similar across treatments. Unsaturated fatty acid composition of longissimus muscle was increased (P < .05) and saturated fatty acid composition tended (P < .12) to be reduced in Cu-supplemented steers. Polyunsaturated fatty acid concentrations were higher (P < .05) in steers receiving Cu. These results indicate that addition of 10 or 20 mg Cu/kg to a high-concentrate diet containing 4.9 mg Cu/kg DM alters lipid and cholesterol metabolism in steers but does not affect ruminal fermentation.     

Effects of dietary copper source and concentration on carcass characteristics and lipid and cholesterol metabolism in growing and finishing steers

We conducted an experiment to determine the effects of dietary copper (Cu) source and level on carcass characteristics, longissimus muscle fatty acid composition, and serum and muscle cholesterol concentrations in steers. Sixty Angus and Angus x Hereford steers were stratified by weight and initial liver Cu concentration within a breed and randomly assigned to treatments. Treatments consisted of: 1) control (no supplemental Cu); 2) 20 mg Cu/kg DM from Cu sulfate (CuSO4); 3) 40 mg Cu/kg DM from CuSO4; 4) 20 mg Cu/kg DM from Cu citrate; 5) 20 mg Cu/kg DM from Cu proteinate; and 6) 20 mg Cu/kg DM from tribasic Cu chloride. A corn silage-soybean meal-based diet was fed for 56 d. Steers were then switched to a high-concentrate diet. Equal numbers (n = 5) of steers per treatment were slaughtered after receiving the finishing diets for either 101 or 121 d. Serum cholesterol was not affected by treatment during the growing phase but was decreased (P < .05) in steers supplemented with Cu by d 84 of the finishing period and remained lower (P < . 05) at subsequent sampling periods. Longissimus muscle cholesterol concentration tended to be reduced (P < .11) by Cu supplementation. Hot carcass weight and backfat were lower (P < .05) in animals receiving supplemental Cu. However, Cu-supplemented and control steers had similar marbling scores. Longissimus muscle polyunsaturated fatty acid concentrations (18:2 and 18:3) were increased (P < .07) and saturated fatty acid concentrations tended (P < . 11) to be reduced by Cu supplementation. These results indicate that as little as 20 mg of supplemental Cu/kg diet can reduce backfat and serum cholesterol and increase muscle polyunsaturated fatty acids in steers fed high-concentrate diets.     

Dietary copper effects on lipid metabolism and circulating catecholamine concentrations in finishing steers

Forty-eight Angus and Hereford x Angus steers were used to determine the effects of copper (Cu) on lipid and catecholamine metabolism. Steers were stratified by weight within breed and randomly assigned to treatments. Treatments consisted of 0 (control, no supplemental Cu), 10, or 40 mg of supplemental Cu (from Cu2(OH)3Cl)/kg DM. Steers were fed a corn silage-soybean meal-based growing diet for 42 d. Animals were then switched to a high-concentrate finishing diet and remained on the same dietary treatments. On d 70, indwelling jugular catheters were nonsurgically inserted into five steers per treatment. Blood samples were obtained from steers after a 24-h period of feed withdrawal, 1 h after feeding, and after i.v. administration of norepinephrine and were subsequently analyzed for nonesterified fatty acid (NEFA) and catecholamine concentrations. Average daily gain over the finishing period was higher (P < 0.06) in steers receiving supplemental Cu. Serum total cholesterol concentrations were reduced (P < 0.05) on d 84 and 112 in steers supplemented with Cu. Serum norepinephrine (P < 0.14) and NEFA concentrations following feed withdrawal tended (P < 0.12) to be higher in Cu-supplemented steers. Postfeeding norepinephrine concentrations tended to be higher (P < 0.14) in Cu-supplemented steers. Nonesterifled fatty acid concentrations were lower (P < 0.10) in Cu-supplemented steers after norepinephrine administration. Backfat depth was decreased (P < 0.10) and longissimus muscle polyunsaturated fatty acid percentages were increased (P < 0.10) in steers receiving supplemental Cu. These results indicate that Cu addition to a finishing diet containing 5 mg Cu/kg DM alters lipid metabolism. The reduction in backfat depth may be due to copper altering catecholamine metabolism in steers.     

Effects of dietary copper concentration and source on performance and copper status of growing and finishing steers

Performance and Cu status were measured in growing and finishing steers supplemented with different copper (Cu) concentrations and sources. Sixty Angus (n = 36) and Angus x Hereford (n = 24) steers were stratified by weight and initial liver Cu concentration within a breed and randomly assigned to treatments. Treatments consisted of 1) control (no supplemental Cu); 2) 20 mg Cu/kg DM from Cu sulfate (CuSO4); 3) 40 mg Cu/kg DM from CuSO4; 4) 20 mg Cu/ kg DM from Cu citrate (C6H4Cu2O7); 5) 20 mg Cu/kg DM from Cu proteinate; and 6) 20 mg Cu/kg DM from tribasic Cu chloride (Cu2(OH)3Cl). A corn silage-soybean meal-based diet that was analyzed to contain 10.2 mg of Cu/kg DM was fed for 56 d. Steers were then switched to a high-concentrate diet that was analyzed to contain 4.9 mg of Cu/kg DM. Equal numbers of steers per treatment were slaughtered after receiving the finishing diets for either 101 or 121 d. Performance was not affected by Cu level or source during the growing phase. Gain, feed intake, and feed efficiency were reduced (P < .05) by Cu supplementation during the finishing phase. Plasma and liver Cu concentrations were higher in steers receiving supplemental Cu at the end of both the growing and finishing phases. Steers supplemented with 40 mg Cu/kg DM from CuSO4 had higher (P < .05) liver Cu concentrations than those supplemented with 20 mg Cu/kg DM from CuSO4. Liver Cu concentrations did not increase over the finishing phase relative to liver Cu concentrations at the end of the growing phase. These results indicate that as little as 20 mg/kg of supplemental Cu can reduce performance in finishing steers.     

Lasalocid and dietary sodium and potassium effects on mineral metabolism, ruminal volatile fatty acids and performance of finishing steers

Thirty Angus steers averaging 357 kg were used to: 1) determine the effect of feeding lasalocid (33 mg/kg diet) on mineral metabolism and 2) determine the effects of varying dietary sodium (Na) and potassium (K) on finishing steers fed lasalocid. Treatments consisted of: 1) control (.25% Na, .5% K); 2) lasalocid (.05% Na, .5% K); 3) lasalocid (.25% Na, .5% K); 4) lasalocid (.05% Na, 1.4% K) and 5) lasalocid (.25% Na, 1.4% K). Ruminal fluid and blood samples were collected on d 28 and 90 of the 102-d study. Gain and feed conversion tended to be higher for steers fed lasalocid with the exception of the .05% Na, 1.4% K treatment. Control steers had lower (P less than .05) erythrocyte K concentrations, reduced (P less than .05) soluble concentrations of magnesium and copper in ruminal fluid and decreased plasma concentrations of zinc (P less than .05) and phosphorus (P less than .10) at 90 d compared with steers fed lasalocid and similar concentrations of Na (.25%) and K (.5%). Increasing dietary Na from .05 to .25% in the presence of lasalocid increased (P less than (P less than .05) molar proportion of ruminal acetate at 28 and 90 d reduced (P less than .05) propionate at 90 d. Increasing K from .5 to 1.4% decreased (P less than .01) soluble Na and increased (P less than .01) soluble K concentrations in ruminal fluid. Steers fed lasalocid (.25% Na, .5% K) had lower concentrations of K (P less than .10) and zinc (P less than .10) in liver than control steers. Sodium and K level also affected tissue concentrations of certain minerals. Results suggest that dietary Na and K influence mineral metabolism and that dietary Na affects ruminal molar proportion of acetate in cattle fed lasalocid.     

Influence of dietary manganese on performance, lipid metabolism, and carcass composition of growing and finishing steers

A study was conducted to determine the effect of dietary Mn on performance of growing and finishing steers, and to evaluate the effect of pharmacological concentrations of Mn on lipid metabolism and subsequent carcass quality in steers. One hundred twenty Angus cross steers were blocked by BW and origin and assigned randomly to one of six treatments (four replicate pens per treatment) providing 0 (control), 10, 20, 30, 120, or 240 mg of supplemental Mn/kg of DM from MnSO4. Steers were fed a corn silage-based growing diet for 84 d, and then switched to a corn-based finishing diet for an average of 112 d. The control growing diet analyzed 29 mg of Mn/kg of DM, whereas the control finishing diet analyzed 8 mg of Mn/kg of DM. Jugular blood samples were obtained on d 56 of the growing and finishing phase for plasma Mn and glucose analysis. Final BW, DMI, ADG, and G:F did not differ (P = 0.38 to P = 0.98) across treatments during growing and finishing phases. Plasma Mn concentrations were not affected by treatment; however, liver and LM Mn at slaughter increased linearly (P = 0.02 and 0.002, respectively) with increasing dietary Mn. Plasma glucose concentrations did not differ (P = 0.90) among treatments. Serum nonesterified fatty acid concentrations tended (P = 0.10) to decrease linearly with increasing dietary Mn on d 56 of the finishing phase. Longissimus muscle lipid concentration was affected quadratically (P = 0.08) by dietary Mn. Muscle lipid seemed to increase slightly when steers were fed 30 or 120 mg of Mn/kg of DM, but decreased with the addition of 240 mg of Mn/kg of DM. Carcass characteristics were not affected by dietary Mn. Manganese concentrations of 29 and 8 mg/kg of DM in the growing and finishing diets, respectively, were adequate for maximizing performance of growing and finishing steers in this experiment. Supplementing physiological or pharmacological concentrations of Mn affected lipid metabolism; however, this did not result in altered carcass characteristics.     

Effects of dietary energy level and protein source on nutrient digestion and ruminal nitrogen metabolism in steers.

Four Simmental steers with ruminal, duodenal, and ileal cannulas were used to examine effects of dietary forage: concentrate ratio and supply of ruminally degradable true protein on site of nutrient digestion and net ruminal microbial protein synthesis. Steers (345 kg) were fed ammoniated corn cob (high forage; HF)- or corn cob/ground corn/cornstarch (low forage; LF)-based diets supplemented with soybean meal (SBM) or a combination of corn gluten meal and blood meal (CB). Diets were fed at 2-h intervals with average DM intake equal to 2.2% of BW. Feeding LF vs HF increased (P less than .05) OM digestion (percentage of intake) in the stomach, small intestine, and total tract. Efficiency of microbial CP synthesis (EMCP; g of N/kg of OM truly fermented) decreased (P less than .05) for LF vs HF (24.1 vs 26.8), but microbial N and total N flows to the small intestine were similar (P greater than .05) between energy levels (average 112 and 209 g/d, respectively). Total N flows to the small intestine were 13.1% greater (P less than .05) for CB than for SBM because of increased (P less than .05) passage of nonmicrobial N. Feeding SBM vs CB increased (P less than .05) EMCP (27.3 vs 23.3) and microbial N flow to the small intestine (127.5 vs 112.5 g/d), but these increases were not likely due to increased ruminal concentrations of ammonia N (NH3 N). Decreased (P less than .05) incorporation of NH3 N into bacterial N and slower turnover rates of ruminal NH3 N for SBM vs CB suggest that direct incorporation of preformed diet components into cell mass increased when SBM was fed. Results of this study suggest that the inclusion of ruminally degradable protein in the diet may increase the supply of products from proteolysis and that this can increase EMCP and microbial protein flow to the small intestine.     

Performance, carcass characteristics, and lipid metabolism in growing and finishing Simmental steers fed varying concentrations of copper.

An experiment was conducted to determine the effects of dietary copper (Cu) on performance, carcass characteristics, and lipid metabolism in Simmental steers. Thirty-six Simmental steers (329.3 +/-11.4 kg) were stratified by weight and randomly assigned to treatments. Treatments consisted of the following: control (no supplemental Cu) and 10 or 40 mg Cu/kg DM from Cu sulfate. Each treatment consisted of six replicate pens, with each pen containing two steers. A corn silage-soybean meal-based diet was fed for 56 d. Steers were then switched to a high concentrate diet. Performance was not affected by treatment during the growing or finishing phases. Plasma Cu concentrations were higher (P < 0.05) in steers receiving supplemental Cu by d 56 of the growing phase and remained higher (P < 0.05) at all 28-d sampling periods during the finishing phase. Liver Cu concentrations were higher (P < 0.001) in steers receiving supplemental Cu at the end of the growing phase and on d 84 and at the end of the finishing phase. Steers supplemented with 40 mg Cu had higher (P < 0.001) liver Cu concentrations than those supplemented with 10 mg Cu/kg DM. Serum and longissimus muscle cholesterol concentrations were similar between treatments. Longissimus muscle and backfat fatty acid composition was similar between treatments. These results indicate that Cu supplementation given to Simmental steers increased Cu status but had no effect on performance, carcass characteristics, or lipid or cholesterol metabolism.     

Effects of buffers on ruminal rate of passage and degradation of soybean meal in steers

Eight rumen-fistulated steers were randomly assigned to medium- and high-concentrate diets supplemented with 0, .75, 2.5 and 5% of either sodium bicarbonate or an artificial saliva salts mixture. Each animal was fed for 21 d at 75 g dry matter/kg body weight . 75. Rates of soybean meal (SBM) degradation were predicted by adjusting digestion rates in nylon bags with respective passage rates of chromium-mordanted SBM particles. Measures of rumen fermentation were made during the incubation period. Liquid dilution rate was determined with 51Cr-EDTA. The high-concentrate diet produced higher (P less than .05) liquid dilution rates than the medium-concentrate diet, but there were no differences in response to the two buffers (P greater than .05). The liquid dilution rates averaged across diets for 0, .75, 2.5 and 5% levels of buffer were 6.2, 6.3, 8.5 and 8.7%/h (SE = .03) and passage rates for SBM were 5.2, 5.2, 6.5 and 6.7%/h (SE = .025). The 2.5 and 5% levels of buffer increased the rate of disappearance of SBM from the nylon bags and buffers fed at these levels also increased rumen pH and NH3-N concentration. Rumen pH was correlated with N disappearance from the nylon bag (r = .903, P less than .05). Buffer levels did not affect degradation rates of SBM.     

Effects of dietary clenbuterol on metabolism of the hindquarters in steers

The objective of this study was to measure acute (d 1) and chronic (d 9) effects of dietary clenbuterol on heart rate, blood flow, oxygen uptake, and net uptake/release of metabolites in the hindquarters of growing steers. The design was a single reversal with two 9-d periods of control or 8 mg clenbuterol/d with 5 d between periods. Within 2 h of initial consumption of 2 mg clenbuterol (d 1), heart rate and blood flow doubled and arterial plasma concentrations of glucose, L-lactate and nonesterified fatty acid (NEFA) increased, whereas alpha-NH2 N and NH3 concentrations decreased, demonstrating an acute response. Uptake of oxygen increased and net uptake of alpha-NH2 N decreased. Net release of both L-lactate and NEFA increased. On d 9, there were no acute responses to clenbuterol consumption; however, heart rate, blood flow, and NEFA concentration remained chronically elevated, and plasma concentrations of acetate and propionate decreased compared with control feeding. Net uptake of alpha-NH2 N, oxygen and release of L-lactate by the hindquarters chronically increased on d 9 of clenbuterol feeding. Changes in both blood flow and arteriovenous (AV) concentration difference contributed to changes in uptake/release. The chronic metabolic changes and oxygen uptake were consistent with increased N retention in the hindquarters through increased protein synthesis, decreased use of acetate and increased reliance on NEFA for cellular energy. In conclusion, the data show that the perturbation of homeostatic regulation by dietary clenbuterol on d 1 evolved to establishment of homeorhetic regulation by d 9 that is consistent with increased skeletal protein accretion in growing steers.     

Effects of forage and sunflower oil levels on ruminal biohydrogenation of fatty acids and conjugated linoleic acid formation in beef steers fed finishing diets

Six Hereford steers (295 kg) cannulated in the proximal duodenum were used to evaluate the effects of forage and sunflower oil level on ruminal biohydrogenation (BH) and conjugated linoleic acid (CLA) outflow. Steers were fed one of six treatment diets in a 3 x 2 factorial arrangement of treatments (grass hay level: 12, 24, or 36% of DM; and sunflower oil level: 2 or 4% of DM) in a 6 x 6 Latin square design. The remainder of the diet was made up of steam rolled corn and protein/mineral supplement. Duodenal samples were collected for 4 d following 10-d diet adaptation periods. Data were analyzed with animal, period, forage level, sunflower oil level, and two-way interaction between forage and sunflower oil level in the model. Dry matter intake showed a quadratic response (P < 0.04), with an increase in DMI as forage level increased from 12 to 24% followed by a decrease in DMI when 36% forage was fed. Flow of fatty acids at the duodenum was higher (P < 0.03) for 4 vs. 2% sunflower oil diets, and similar among forage levels. Apparent ruminal digestibility of NDF increased in a linear manner (P < 0.04) as dietary forage level increased. Ruminal BH of dietary unsaturated 18-C fatty acids, oleic acid, and linoleic acid increased linearly (P < 0.05) as dietary forage level increased. Linoleic acid BH tended (P < 0.07) to be greater for 4 than 2% sunflower oil level. Duodenal flow of pentadecyclic, stearic, linolenic, and arachidic acids increased linearly (P < 0.05) as dietary forage level increased from 12 to 36%. Duodenal flow of linoleic acid decreased in a linear manner (P < 0.03) with increasing dietary forage level. Flow of trans-10 octadecenoate decreased linearly (P < 0.03) as dietary forage level increased, whereas trans-11 vaccenic acid flow to the duodenum increased (P < 0.01) linearly with increased dietary forage. Dietary forage or sunflower oil levels did not alter the outflow of cis-9, trans-11 CLA. Flows of cis-11, trans-13, and cis-9, cis-11 CLA increased linearly (P < 0.05) with increased dietary forage. Flows of cis-11, cis-13, and trans-11, trans-13 CLA decreased linearly (P < 0.05) with increased dietary forage. Increasing dietary forage levels from 12 to 36% in beef cattle finishing diets increased BH of unsaturated 18-C fatty acid and outflow of trans-11 vaccenic acid to duodenum without altering cis-9, trans-11 CLA outflow.     

Effects of virginiamycin and monensin plus tylosin on ruminal protein metabolism in steers fed corn-based finishing diets with or without wet corn gluten feed

Six ruminally cannulated steers (345 +/- 20 kg initial BW) were used in a 6 x 6 Latin square to evaluate effects of diet and antibiotics on ruminal protein metabolism. Two diets and three antibiotic treatments were arranged factorially. One diet contained (DM basis) 72% dry-rolled corn, 12% soybean meal, 10% alfalfa hay, and 4% molasses (SBM), and the other contained 63% dry-rolled corn, 30% wet corn gluten feed, and 5% alfalfa hay (WCGF). Antibiotic treatments included control, virginiamycin (175 mg/d; VM), and monensin/tylosin (250 and 100 mg/d, respectively; MT). Steers were fed at 12-h intervals at a rate of 2.4% of empty BW daily. Each period included 18 d of adaptation and 3 d of ruminal fluid collections. Samples were collected at 0, 2, 4, 6, 8, and 10 h after the morning feeding on d 19 and 20. On d 21, rumens were dosed 2 h after the morning feeding with 350 g of solubilized casein to evaluate in vivo ruminal protease and deaminase activities. Ruminal fluid samples were collected 1, 2, 3, 4, and 6 h after the casein dose. On d 19 and 20, antibiotics had no effect on ruminal pH or concentrations of VFA, lactate, ammonia, ciliated protozoa, alpha-amino nitrogen (AAN), or peptide N, but VM reduced (P < 0.01) the concentration of isovalerate compared to MT and control. After casein dosing (d 21), peptide N concentration was unaffected by antibiotics, but AAN were higher (P < 0.01) for VM than MT and control. Relative to MT and control, VM reduced ruminal isovalerate (P = 0.05) and increased ruminal propionate (P < 0.01) on d 21. Ruminal pH was lower (P < 0.01) in steers fed SBM than in steers fed WCGF, but lactate concentrations were unaffected by diet. Steers fed SBM had higher (P < 0.05) ruminal concentrations of total VFA and propionate. Ammonia concentrations were lower before feeding and higher after feeding for steers fed WCGF (P < 0.01). Steers fed WCGF had higher counts of total ciliated protozoa than steers fed SBM (P < 0.05) due to greater Entodinium sp. (P < 0.05). Steers fed WCGF had higher (P < 0.01) ruminal AAN and peptide N concentrations than those fed SBM on d 19 and 20. After casein dosing, ruminal peptide N concentrations were similar, but AAN were lower (P < 0.01) for WCGF than SBM. Overall, VM appeared to depress ruminal deaminase activity, and MT had minimal effects on ruminal fermentation products. The protein in WCGF appeared to be more readily degradable than that in SBM.     

Steam-rolled wheat diets for finishing cattle: effects of dietary roughage and feed intake on finishing steer performance and ruminal metabolism

Two experiments were conducted to determine the influence of dietary roughage concentration and feed intake on finishing steer performance and ruminal metabolism. In Exp. 1, 126 steers (334 kg) were used in a completely randomized design and fed (120 d) diets of steam-rolled wheat without roughage or containing 5, 10 or 15% roughage (50% alfalfa hay:50% corn silage). Steers fed 5 or 10% roughage gained faster (quadratic, P less than .05) and were more efficient (quadratic, P less than .05) than steers fed 15% or no roughage. In Exp. 2, six ruminally cannulated steers (447 kg) were used in a 6 x 6 latin square design and fed (twice daily) diets of steam-rolled wheat without roughage or containing 5 or 15% alfalfa hay at twice or three times NE required for maintenance. Increasing dietary roughage increased (linear, P less than .01) ruminal liquid passage 38%, indigestible ADF passage 63%, Yb-labeled wheat passage 75% and fiber fill 31%. The rate of in situ starch digestion tended to increase (linear, P = .16), and ruminal VFA concentration was 40 mM higher (P less than .01) at 4 h after feeding with increased roughage. Increased feed intake increased (P less than .05) ruminal starch fill, fiber fill, liquid fill and liquid passage 23%, Yb-labeled wheat passage 50% and Dry-labeled hay passage 20%. It reduced protozoa five- to sixfold (P less than .01) but doubled total bacterial counts (P less than .01). Ruminal NH3N was lower (P less than .01) and total VFA concentration was 50 mM higher (P less than .01) at 4 h after feeding. The acetate:propionate ratio was reduced from 2.3 to 1.3 (P less than .01) with increased intake. Adding roughage to a steam-rolled wheat diet increased passage and tended to increase rate of starch digestion; increased feed intake with its associated effects on ruminal fill and passage dramatically shifted the microbial population and fermentation end products.     

Effect of soybean lipid on growth and ruminal nitrogen metabolism in cattle fed soybean meal or ground whole soybeans

Three experiments were conducted to determine the effect of soybean lipid on ruminal proteolysis of soybean meal (SBM) and ground whole soybeans (GSB). Experiment 1 was a 92-d growth experiment using 120 calves (206 kg) allotted to 12 pens of 10 calves each. Three replicate pens were assigned to each of the treatment supplements: low SBM (LSBM), low GSB (LGSB), high SBM (HSBM) and high GSB (HGSB). Calves received ad libitum amounts of corn silage top-dressed with the respective supplement (.81 kg/head). High protein supplements produced greater (P less than .05) gains than low protein supplements, with HSBM calves gaining faster (P less than .05) than HGSB calves and LSBM and LGSB calves having similar (P greater than .10) gains. In Exp. 2, 15 ruminally cannulated Angus X Hereford heifers (380 kg) fed corn silage were used to determine ammonia-N release from the treatment supplements: ground corn (control), GSB, SBM and SBM coated with soybean oil (SBMO). Heifers fed the control supplement had lower (P less than .05) ruminal NH3-N concentrations than those consuming soybean protein. Ruminal NH3-N concentrations were similar (P greater than .10) for GSB and SBM; whereas, SBMO had lower (P less than .10) concentrations than SBM through 3 h. In Exp. 3, two ruminally cannulated Angus X Jersey steers (250 kg) were used to determine in situ disappearance of SBM, GSB and SBMO. Total and feed N disappearances were greater (P less than .001) for GSB than SBM or SBMO.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of dietary copper on the expression of lipogenic genes and metabolic hormones in steers

An experiment was conducted to determine the effects of Cu supplementation on performance, subcutaneous adipose tissue mRNA expression of acetyl CoA carboxylase (ACC), stearoyl CoA desaturase (SCD), uncoupling protein 2 (UCP2), and leptin in growing and finishing steers. Forty-eight purebred Angus steers were allotted to one of five treatments: 1) control (no supplemental Cu); 2) 10 mg Cu/kg DM from CuSO4; 3) 10 mg Cu/kg DM from a Cu amino acid complex (Availa Cu); 4) 20 mg Cu/kg DM from CuSO4; 5) 20 mg Cu/kg DM from Availa Cu. Steers were fed an alfalfa hay corn-based diet for 56 d (basal diet contained 7.1 mg Cu/kg DM) and switched to a high-concentrate diet for 144 d (basal diet contained 6.1 mg Cu/kg DM). Blood samples were obtained every 28 d throughout the entire experiment. On d 112 of the finishing period, subcutaneous adipose tissue biopsies were obtained from the tailhead of three animals per treatment and analyzed for ACC, SCD, UCP2, and leptin mRNA expression. Animal performance was not affected by Cu supplementation during the growing phase. Steers receiving 10 mg Cu/kg DM from Availa Cu had higher (P < 0.05) ending body weights and tended (P < 0.10) to have higher ADG than steers receiving 10 mg Cu/kg DM from CuSO4 during the finishing phase. Serum concentrations of nonesterified fatty acid and insulin were not affected by Cu supplementation. Steers receiving supplemental Cu tended (P < 0.11) to have less backfat relative to controls. However, dietary Cu did not influence the level of subcutaneous adipose tissue ACC and SCD mRNA. Neither UCP2 nor leptin gene expression was affected by Cu supplementation. These results indicate that dietary Cu supplementation (10 to 20 mg Cu/kg DM diet) may alter lipid metabolism of subcutaneous adipose tissue; however, it does not seem to affect expression of certain lipogenic genes.     

Influence of dietary cobalt source and concentration on performance, vitamin B12 status, and ruminal and plasma metabolites in growing and finishing steers

Sixty Angus steers, averaging 274 kg, were used to evaluate the effects of Co source and concentration on performance, vitamin B12 status, and metabolic characteristics of steers. Treatments consisted of 0 (control, analyzed 0.04 mg Co/kg), 0.05, 0.10, and 1.0 mg of supplemental Co/kg of DM from CoCO3 or 0.05 and 0.10 mg of supplemental Co/kg of DM from Co propionate. Steers were individually fed a growing diet for 56 d followed by a high-concentrate finishing diet. Performance was not affected by Co supplementation during the growing phase. During the finishing phase, ADFI (DM basis) and ADG were higher (P < 0.05) for the entire finishing phase, and gain:feed was higher (P < 0.10) over the first 56 d for Co-supplemented steers. Steers supplemented with 0.10 mg Co/kg as Co propionate had higher (P < 0.05) ruminal propionate and lower (P < 0.05) acetate molar proportions than steers receiving 0.10 Co/kg as CoCO3 during the growing phase. Supplemental Co increased (P < 0.10) molar proportion of propionate during the finishing phase. Plasma vitamin B12 was higher (P < 0.05) in Co-supplemented steers by d 56 of the growing phase and remained higher (P < 0.10) throughout the study. Control steers had higher (P < 0.05) plasma methylmalonic acid on d 56 of the growing phase and on d 28, 56, and 112 of the finishing phase than steers receiving supplemental Co. Steers supplemented with Co had higher plasma glucose at d 56 (P < 0.01), 84 (P < 0.10), and 112 (P < 0.01) of the finishing phase. Steers supplemented with 0.10 mg Co/kg as Co propionate had higher plasma glucose than those receiving 0.10 mg Co/kg as CoCO3 at d 28 of the growing phase (P < 0.05) and d 28 of the finishing phase (P < 0.10). Final body weight and hot carcass weight were lower (P < 0.10) in steers receiving the control diet, whereas other carcass characteristics were not affected by dietary Co. Average daily gain and feed efficiency for the entire finishing phase did not differ among Co-supplemented steers. However, increasing supplemental Co above 0.05 mg/kg DM (total diet Co = 0.09 mg/kg) resulted in increased (P < 0.01) plasma (linear) and liver (quadratic) vitamin B12 concentrations and decreased (quadratic, P < 0.10) plasma methylmalonic acid concentrations toward the end of the finishing phase. These results suggest that finishing steers require approximately 0.15 mg Co/kg of DM. Vitamin B12 status was not affected by Co source; however, the two Co sources seemed to affect certain metabolites differently.     

Nitrogen utilization and ruminal fermentation in steers fed soybean meal treated with formaldehyde

Four rumen-fistulated steers averaging 400 kg in body weight were used in a 4 X 4 Latin square arrangement with 18-d periods to investigate the effect of treating soybean meal (SBM) with formaldehyde on nitrogen (N) utilization and ruminal fermentation. Experimental diets, on a dry matter basis, consisted of 42% corn silage, 48.5% cracked corn-mineral mixture and 9.5% SBM treated with 0, .3, .6 or .9% formaldehyde by weight. Dry matter and organic matter digestibilities were not affected by treatment. Formaldehyde treatment of SBM resulted in a linear decrease in N digestibility (P less than .005) and urinary N excretion (P less than .01) and a quadratic increase (P less than .05) in N retention. The depression in apparent N digestibility was small when SBM was treated with .3% formaldehyde. This level of formaldehyde treatment also had little effect on in vitro enzymatic hydrolysis of SBM. Ruminal ammonia-N concentrations were lower (P less than .05) in steers fed formaldehyde-treated SBM. Ruminal pH was lower (P less than .05) at 6 and 8 h postfeeding while volatile fatty acid concentrations were higher (P less than .05) at 8 and 12 h postfeeding for steers fed untreated SBM. Propionic acid (mol/100 mol) decreased linearly (P less than .05) with increasing level of formaldehyde treatment. Urea-N concentrations in plasma were decreased (P less than .001) and plasma-free essential amino acid concentrations were increased (P less than .10) by formaldehyde treatment. Ruminal disappearance of N from polyester bags containing the SBM supplements was greatly reduced (P less than .005) by formaldehyde treatment.(ABSTRACT TRUNCATED AT 250 WORDS)     

Effects of dietary nonprotein nitrogen on performance, digestibility, ruminal characteristics, and microbial efficiency in crossbred steers

Two trials were conducted to evaluate the effects of dietary NPN levels on animal performance, diet digestibility, ruminal characteristics, and microbial efficiency. Experiment 1 was conducted with 24 Holstein x Nellore crossbred steers (350 +/- 20 kg of BW) distributed in 6 blocks to evaluate intake and digestibility of nutrients and performance. The diets consisted of 70% corn silage and 30% concentrate (DM basis) and were formulated to contain 12.5% CP (DM basis). Treatments consisted of 0, 15.5, 31, and 46.5% of dietary N as NPN. There were no treatment differences in the daily intakes of DM (P = 0.47), OM (P = 0.60), CP (P = 0.24), nonfiber carbohydrates (NFC; P = 0.74), or TDN (P = 0.63); however, NDF intake decreased linearly as NPN increased (P = 0.02). Additionally, no effects of NPN were observed on apparent total tract digestibility of DM (P = 0.50), OM (P = 0.53), NDF (P = 0.63), or NFC (P = 0.44). The apparent total tract digestibility of CP increased linearly (P = 0.01), but ADG (1.14 kg/d) was not influenced (P = 0.96) as NPN increased. In Exp. 2, 4 ruminally and abomasally cannulated steers (300 +/- 55 kg of BW) were fed the same diet used in Exp. 1 to evaluate the effects of NPN levels on intake and digestibility of nutrients, ruminal characteristics, and microbial efficiency. There were no differences in the daily intakes of DM (P = 0.22), OM (P = 0.17), CP (P = 0.31), NDF (P = 0.29), or TDN (P = 0.49). However, NFC intake increased linearly (P = 0.02), and there was a quadratic effect (P = 0.01) on intake of ether extract as NPN increased. Ruminal digestibility of CP increased linearly (P = 0.01) with the increase of dietary NPN. There were no differences (P >or= 0.28) in microbial protein synthesis and microbial efficiency among the treatments. The results of these trials suggest that dietary NPN levels (up to 46.5% of total N) can be fed to crossbred steers receiving corn silage-based diets without affecting their growth performance or ruminal protein synthesis.     

Influence of level and source of dietary fat on its comparative feeding value in finishing diets for feedlot steers: metabolism

Six crossbred steers (315 kg) with cannulas in the rumen, proximal duodenum and distal ileum were used to study the influence of level and source of dietary fat on characteristics of digestion. Dietary treatments consisted of a steam-rolled barley-based finishing diet containing 1) no supplemental fat; 2) 4% yellow grease (YG); 3) 4% blended animal-vegetable fat (BVF); 4)8% YG; 5) 8% BVF or 6) 6% BVF and 2% crude lecithin. Increasing level of fat supplementation resulted in linear decreases (P less than .01) in ruminal and total tract digestion of OM and ADF and intestinal digestion of fat (P less than .05). At the 4 and 8% levels of supplementation, intestinal true digestibility of fat averaged 80.1 and 69.3%, respectively. Ruminal molar proportions of acetate decreased, and propionate molar proportion, as well as DE and ME values of the diet, increased linearly (P less than .01) with level of fat supplementation. The DE and ME values for fat were 8.17 and 9.76 at the 4% level and 7.35 and 8.72 Mcal/kg at the 8% level of supplementation, respectively. Yellow grease supplementation resulted in greater (P less than .05) ruminal fiber digestion and greater ruminal molar proportions of propionate than BVF. Intestinal fat digestion was similar (P greater than .10) for YG and BVF. Adding 25% lecithin to BVF resulted in greater ruminal fiber digestion and greater ruminal molar proportions of acetate; however, lecithin tended (P less than .10) to have a lower ME value than BVF.     

Effect of ruminal protein degradability on growth and N metabolism in growing beef steers

The objective of two experiments was to correlate plasma levels of urea N (PUN) and the percentage of urine N in the form of urea (UUN) to weight gain in response to different dietary protein regimens for growing Angus steers. In Exp. 1, 60 steers (302 kg BW) were assigned to various levels of dietary N (control plus supplemental N to provide from 100 to 400 g more crude protein daily) within two sources of supplemental N (soybean meal [SBM] or a mixture of two parts corn gluten meal:one part blood meal [CGM:BM]). In Exp. 2, 27 steers (229 kg BW) were fed two levels of SBM, and half of the steers received growth-promoting implants. Steers were housed in groups of 12 and fed individually for 84 d in both experiments. Corn silage was fed at a restricted rate to minimize orts. Jugular blood and urine samples were collected during the experiments. In Exp. 1, maximal ADG of steers fed SBM (1.0 kg) was reached with 671 g/d total crude protein, or 531 g/d metabolizable protein. Maximal ADG of steers fed CGM:BM (0.91 kg) was reached with 589 g/d total crude protein, or 539 g/d metabolizable protein. The DMI was higher (P < 0.07) for steers fed SBM (6.37 kg/d) than for steers fed CGM:BM (6.14 kg/d). Increasing ruminal escape protein from 36% (SBM) to 65% (CGM:BM) of CP decreased (P < 0.05) endogenous production of urea, as evidenced by lower concentrations of urea in blood and lower UUN. In Exp. 2, increasing supplemental protein from 100 to 200 g/d increased (P < 0.05) ADG and PUN. Implants lowered (P < 0.05) UUN, particularly at the higher level of supplemental protein. Protein supplementation of growing steers can be managed to maintain acceptable ADG yet decrease excretion of urea in the urine.