Early primary biliary cholangitis is characterised by brain abnormalities on cerebral magnetic resonance imaging.

BACKGROUND: Brain change can occur in primary biliary cholangitis (PBC), potentially as a result of cholestatic and/or inflammatory processes. This change is linked to systemic symptoms of fatigue and cognitive impairment. AIM: To identify whether brain change occurs early in PBC. If the change develops early and is progressive, it may explain the difficulty in treating these symptoms. METHODS: Early disease brain change was explored in 13 patients with newly diagnosed biopsy-proven precirrhotic PBC using magnetisation transfer, diffusion-weighted imaging and 1 H magnetic resonance spectroscopy. Results were compared to 17 healthy volunteers. RESULTS: Cerebral magnetisation transfer ratios were reduced in early PBC, compared to healthy volunteers, in the thalamus, putamen and head of caudate with no greater reduction in patients with greater symptom severity. Mean apparent diffusion coefficients were increased in the thalamus only. No 1 H magnetic resonance spectroscopy abnormalities were seen. Serum manganese levels were elevated in all PBC patients, but no relationship was seen with imaging or symptom parameters. There were no correlations between neuroimaging data, laboratory data, symptom severity scores or age. CONCLUSIONS: This is the first study to be performed in this precirrhotic patient population, and we have highlighted that neuroimaging changes are present at a much earlier stage than previously demonstrated. The neuroimaging abnormalities suggest that the brain changes seen in PBC occur early in the pathological process, even before significant liver damage has occurred. If such changes are linked to symptom pathogenesis, this could have important implications for the timing of second-line-therapy use.

Valine and isoleucine requirement of 20- to 45-kilogram pigs.

Three experiments were conducted to determine the Val and Ile requirements in low-CP, corn-soybean meal (C-SBM) AA-supplemented diets for 20- to 45-kg pigs. All experiments were conducted for 26 to 27 d with purebred or crossbred barrows and gilts, which were blocked by initial BW. Treatments were replicated with 5 or 6 pens of 3 or 4 pigs per pen. At the beginning of Exp. 1 and the end of all experiments, blood samples were obtained from all pigs to determine plasma urea N (PUN) concentrations. All diets were C-SBM with 0.335% supplemental Lys to achieve 0.83% standardized ileal digestible (SID) Lys, which is the Lys requirement of these pigs. In Exp. 1, 0, 0.02, 0.04, 0.06, 0.08, or 0.10% L-Val was supplemented to achieve 0.51, 0.53, 0.55, 0.57, 0.59, or 0.61% dietary SID Val, and Thr, Trp, Met, and Ile were supplemented to maintain Thr:Lys, Trp:Lys, TSAA:Lys, and Ile:Lys ratios of 0.71, 0.20, 0.62, and 0.60, respectively. Also, supplemental Gly and Glu were added to all diets to achieve 1.66% Gly + Ser and 3.28% Glu, which is equal to the Gly + Ser and Glu content of a previously validated positive control diet that contained no supplemental AA. Treatment differences were considered significant at P < 0.10. Valine addition increased ADG, ADFI, and G:F in pigs fed 0.51 to 0.59% SID Val (linear, P < 0.08), but ADG and ADFI were decreased at 0.61% SID Val (quadratic, P ≤ 0.10). On the basis of ADG and G:F, the SID Val requirement is between 0.56 and 0.58% in a C-SBM diet supplemented with AA. In Exp. 2 and 3, 0, 0.02, 0.04, 0.06, or 0.08% L-Ile was supplemented to achieve 0.43, 0.45, 0.47, 0.49, or 0.51% dietary SID Ile, and Thr, Trp, Met, and Ile were supplemented to maintain Thr:Lys, Trp:Lys, TSAA:Lys, and Val:Lys ratios of 0.71, 0.20, 0.62, and 0.74, respectively. Also, supplemental Gly and Glu were added to achieve 1.66% Gly + Ser and 3.28% Glu as in Exp. 1. Data from Exp. 2 and 3 were combined and analyzed as 1 data set. Daily BW gain, ADFI, and G:F were not affected by Ile additions to the diet; however, ADFI was decreased among pigs fed the diet with 0.45% SID Ile (P < 0.10) compared with pigs fed the 0.43% SID Ile diet. Broken-line analysis requirements could not be estimated for the combined data from Exp. 2 or 3. The results of this research indicate that the SID Val requirement is between 0.56 to 0.58% (0.67 to 0.70 SID Val:Lys), and the Ile requirement is adequate at 0.43% SID Ile (0.52 SID Ile:Lys) for 20- to 45-kg pigs.

Technical note: Effect of determining baseline plasma urea nitrogen concentrations on subsequent posttreatment plasma urea nitrogen concentrations in 20- to 50-kilogram pigs.

Plasma urea N (PUN) has been used as an indicator of AA requirements and efficiency of AA utilization in swine. However, PUN concentrations vary among a population of pigs, even a population with a close range of BW and fed the same diet. Thus, pretreatment or baseline PUN concentrations are used as a covariate to reduce variation of posttreatment PUN. However, this procedure increases experimental costs and stress to the pigs. Data from 14 experiments (26 to 28 d in duration) conducted using PUN as a response variable were compiled into 1 data set. Each experiment had 4 to 6 treatments. The purpose of this technical report was to summarize the effect of determining pretreatment baseline PUN concentrations on subsequent posttreatment PUN concentrations in 20- to 50-kg pigs. In all experiments, pigs were fed corn- and soybean meal-based diets and low-CP diets with various AA additions; pigs were assigned to dietary treatments in a randomized complete block design with a minimum of 4 replicates of 3 to 5 pigs each. Before the start of each experiment, all pigs were fed a common diet for a minimum of 3 d. Blood samples were collected from each pig before allotment to dietary treatments (d 0) and at the end of each experiment. The baseline (d 0) PUN was analyzed as a covariate for posttreatment PUN. Data from each experiment were analyzed without and with baseline PUN in the statistical model. In all experiments combined, there were 768 possible treatment comparisons. The covariate baseline PUN was statistically significant (P < 0.10) in 9 of 14 experiments. However, only 8 treatment differences changed statistical significance as a result of analyzing the data with baseline PUN as a covariate. These 8 treatment differences were in 3 experiments. These results indicate that it is not always necessary to determine baseline PUN concentrations when feeding diets with large differences in AA content.

Growth performance of 20- to 50-kilogram pigs fed low-crude-protein diets supplemented with histidine, cystine, glycine, glutamic acid, or arginine.

The purpose of this investigation was to compare the growth performance of grower pigs fed low-CP, corn-soybean meal (C-SBM) AA-supplemented diets with that of pigs fed a positive control (PC) C-SBM diet with no supplemental Lys. Five experiments were conducted with Yorkshire crossbred pigs, blocked by BW (average initial and final BW were 21 and 41 kg, respectively) and assigned within block to treatment. Each treatment was replicated 4 to 6 times with 4 or 5 pigs per replicate pen. Each experiment lasted 28 d and plasma urea N was determined at the start and end of each experiment. All diets were formulated to contain 0.83% standardized ileal digestible Lys. All the experiments contained PC and negative control (NC) diets. The PC diet contained 18% CP and was supplemented with only DL-Met. The NC diet contained 13% CP and was supplemented with L-Lys, DL-Met, L-Thr, and L-Trp. The NC + Ile + Val diet was supplemented with 0.10% Val + 0.06% Ile. The NC + Ile + Val diet was supplemented with either His (Exp. 1), Cys (Exp. 2), Gly (Exp. 2, 3, and 4), Glu (Exp. 3), Arg (Exp. 4), or combinations of Gly + Arg (Exp. 4 and 5) or Gly + Glu (Exp. 5). Treatment differences were considered significant at P < 0.10. In 3 of the 4 experiments that had PC and NC diets, pigs fed the NC diet had decreased ADG and G:F compared with pigs fed the PC diet. The supplementation of Ile + Val to the NC diet restored ADG in 4 out of 5 experiments. However, G:F was less than in pigs fed the PC diet in 1 experiment and was intermediate between the NC and PC diets in 3 experiments. Pigs fed supplemental Ile + Val + His had decreased G:F compared with pigs fed the PC. Pigs fed supplemental Cys to achieve 50:50 Met:Cys had decreased G:F compared with pigs fed the PC. Pigs fed Ile + Val + 0.224% supplemental Gly had similar ADG, greater ADFI, and decreased G:F compared with pigs fed the PC. Pigs fed Ile + Val + 0.52% supplemental Gly had ADG and G:F similar to that of pigs fed the PC. Pigs fed supplemental Glu had decreased G:F compared with pigs fed the PC. Pigs fed Ile + Val + 0.48% supplemental Arg had decreased G:F compared with pigs fed the PC. Pigs fed the diet supplemented with Gly + Arg had ADG and G:F similar to pigs fed the PC. Pigs fed the low-CP diets had reduced plasma urea N compared with pigs fed PC. The results of these experiments indicate that supplementing Gly or Gly + Arg to a low-CP C-SBM diet with 0.34% Lys, Met, Thr, Trp, Ile, and Val restores growth performance to be similar to that of pigs fed a PC diet with no Lys supplementation.

Effects of glycine supplementation at varying levels of methionine and cystine on the growth performance of broilers fed reduced crude protein diets.

Two experiments were conducted to investigate Gly addition to reduced crude protein corn-soybean meal (C-SBM) diets with varying levels of TSAA achieved by varying Met and Cys. The experiments were conducted with female Ross 708 broilers in brooder batteries from 0 to 18 d posthatching. Treatments had 6 replicates with 6 broilers/pen. Diets in all experiments were fed without or with Gly supplementation to contain 2.32% total Gly + Ser. All diets were C-SBM based and formulated to contained 1.27% standardized ileal digestible Lys supplemented with 0.20% Lys (0.394% Lys·SO(4)) and to meet or exceed the requirement of all nutrients except Met and Cys where appropriate. Experiment 1 consisted of 8 dietary treatments. Three ratios of Met to Cys (60:40, 50:50, and 40:60) were used on a mole for mole basis to achieve 0.063 mol of TSAA/kg of feed and a positive control with Met:Cys of 50:50 at 0.76 TSAA:Lys. Glycine supplementation did not affect ADG or ADFI; however, G:F was increased (P = 0.003) with Gly supplementation. An increase in Cys and a decrease in Met resulted in a decrease (P = 0.028) in ADG but had no effect on ADFI or G:F. In experiment 2, Met was kept constant at a marginal level of 0.45% and Cys was increased in 0.05% increments from 0.35 to 0.50%. Glycine supplementation had no main effect on ADG, ADFI, or G:F; however, Gly increased G:F at the lower levels of Cys but not at the higher levels (Gly × Cys, P = 0.031). A linear decrease (P = 0.071) was found in ADFI with increasing Cys supplementation. These data indicate that Gly increased G:F in female broilers fed suboptimal levels of Met and Cys but not at Cys levels at or above the requirement. This implies that the synthesis of Cys accounts for a portion of the increased G:F observed from Gly supplementation in female broilers fed reduced CP C-SBM diets.

Maximizing the use of supplemental amino acids in corn-soybean meal diets for 20- to 45-kilogram pigs.

Four experiments were conducted to determine the Lys requirement, the maximum amount of supplemental Lys that does not decrease growth performance, and to determine the order of limiting AA beyond Lys, Thr, Trp, and Met in a corn-soybean meal diet for 20- to 45-kg pigs. All experiments were conducted for 27 to 28 d with purebred or crossbred barrows and gilts, which were blocked by initial BW. Treatments were replicated with 4 to 6 pens of 4 to 6 pigs per pen. In all experiments, pigs and feeders were weighed on d 0, 14, and 27 or 28. At the beginning and end of all experiments, blood samples were obtained from all pigs to determine plasma urea N (PUN) concentrations. In Exp. 1, 0.830, 0.872, 0.913, and 0.955% standardized ileal digestible (SID) Lys was fed, whereas 0.747, 0.788, 0.830, 0.872, and 0.913% SID Lys was fed in Exp. 2. Broken-line analysis requirement estimates could not be estimated from any response variable in Exp. 1, but in Exp. 2, using ADG and PUN, the estimated SID Lys requirement was 0.83%. In Exp. 3, 0, 0.118, 0.191, 0.264, and 0.335% supplemental Lys was added to achieve 0.83% SID Lys in all diets, and Thr, Trp, and Met were supplemented to maintain Thr:Lys, Trp:Lys, and TSAA:Lys of 0.65, 0.18, and 0.60, respectively. Based on ADG, ADFI, and G:F, up to 0.23% supplemental Lys can be added along with supplemental Thr, Trp, and Met without negatively affecting growth performance; PUN was linearly decreased (P < 0.001) by supplemental Lys. In Exp. 4, treatments were 1) positive control (PC) without supplemental AA, 2) negative control (NC) with 0.335% supplemental Lys + 0.140% l-Thr + 0.035% l-Trp + 0.117% dl-Met, 3) NC + 0.044% l-Val, 4) NC + 0.021% l-Ile, and 5) NC + 0.044% l-Val + 0.021% l-Ile. Individual addition of Val and Ile did not improve (P > 0.10) ADG or G:F compared with the NC. The combined addition of Val + Ile resulted in ADG that was intermediate between the PC and NC diets but not different from either diet (P > 0.10); G:F was not improved (P > 0.10) to that observed in pigs fed the PC diet. The PUN was not different (P > 0.10) among pigs fed diets with supplemental AA but less (P < 0.10) than pigs fed the PC. The results of this research indicate that the Lys requirement for 20- to 45-kg pigs is 0.83% SID Lys, up to 0.23% supplemental Lys (0.29% l-Lys·HCl or 0.45% l-Lys·SO(4)) can be added along with supplemental Thr, Trp, and Met without negatively affecting growth performance, and another AA besides Val and Ile may be limiting growth performance in a corn-soybean meal diet with 0.335% supplemental Lys.

Phytase supplementation improved growth performance and bone characteristics in broilers fed varying levels of dietary calcium.

An experiment was conducted to investigate the effect of dietary Ca level on the efficacy of phytase. A total of 288 male Ross × Ross 708 broilers with initial and final BW of 37 and 705 g, respectively, were used in brooder batteries from 0 to 21 d posthatch. Each treatment had 8 replications with 6 broilers/replicate pen. All diets were corn-soybean meal based and formulated to contain 1.26% total Lys. The treatments were positive control with 0.45% nonphytate P and 1% Ca and a negative control with 0.20% nonphytate P with 0.67, 1.00, or 1.33% Ca fed with or without 500 phytase units of Optiphos (Escherichia coli-derived phytase; JBS United Inc., Sheridan, IN). Increasing Ca from 0.67 to 1.33% linearly decreased (P ≤ 0.003) ADG, ADFI, bone breaking strength, bone weight, tibia ash weight, and percentage tibia ash; however, quadratic effects were found for ADFI, G:F, percentage tibia ash, and mortality (P ≤ 0.09). Phytase supplementation increased (P < 0.001) ADG, ADFI, bone breaking strength, bone weight, ash weight, and percentage tibia ash and decreased (P = 0.054) mortality. The increase in ADG, ADFI, bone weight, ash weight, and percentage tibia ash (P ≤ 0.026) and decrease in mortality (phytase × Ca linear; P = 0.058) from phytase supplementation was greater in broilers fed the higher levels of Ca. Calcium utilization was linearly decreased (P < 0.002) with increasing Ca. Phosphorus digestibility and utilization were increased with increasing levels of Ca (P ≤ 0.002); however, P utilization decreased at 1% Ca and increased at 1.33% (quadratic; P < 0.070). Phytase supplementation increased Ca utilization (P < 0.024), P digestibility (P < 0.001), and P utilization (P < 0.029). However, the increase in P digestibility (phytase × Ca; P < 0.021) was greater at the lower levels of Ca whereas P utilization (phytase × Ca; P < 0.001) was greater at 1.33% Ca with phytase supplementation. The results of this research indicate that dietary Ca level, within the ranges used in this experiment, does not negatively affect the efficacy of phytase.

Effect of salmon protein hydrolysate and spray-dried plasma protein on growth performance of weanling pigs.

Two experiments, each consisting of 2 trials, were conducted to determine the effect of salmon protein hydrolysate (SPH) and spray-dried plasma protein (SDPP) fed during the first week postweaning and their subsequent effect on the growth performance of weanling pigs. Pigs were fed in a 3-phase feeding program with durations of 7 d for phase 1 in both Exp. 1 and 2; 14 or 15 d for phase 2 in Exp. 1 and 2, respectively; and 7 or 8 d for phase 3 in Exp. 1 and 2, respectively. Dietary treatments were fed only during phase 1, whereas the same diet was fed to all pigs in phases 2 and 3. Pigs were blocked by initial BW and sex, and littermates were balanced across treatments. Data from the 2 trials within each experiment were combined and analyzed together; no treatment × trial interactions (P > 0.10) were observed. In Exp. 1, a total of 324 weanling pigs (10 replications of 5 or 6 pigs per pen) with an average initial BW of 6.4 ± 1.3 kg were assigned to 1) a control diet with no SPH or SDPP, 2) 1.5% SPH, 3) 3.0% SPH, 4) 1.5% SDPP, 5) 3.0% SDPP, or 6) 1.5% SPH + 1.5% SDPP. Experiment 2 was similar to Exp. 1, but red blood cells were removed from all diets to reduce diet complexity. In Exp. 2, weanling pigs (n = 320, 14 replications of 5 or 6 pigs per pen) with an average initial BW of 5.4 ± 1.2 kg were assigned to 1) a control diet with no SPH or SDPP, 2) 1.5% SPH, 3) 1.5% SDPP, or 4) 1.5% SPH + 1.5% SDPP. Three batches of SPH were used, and each batch was analyzed for AA composition. In Exp. 1, the inclusion of SDPP or SPH during phase 1 did not affect (P > 0.10) ADG, ADFI, or G:F compared with those of pigs fed the control diet. No carryover effects on growth performance were observed in any of the subsequent phases. Overall, G:F was greater (P = 0.08) in pigs fed the 1.5% diets compared with those fed the 3.0% diets. In Exp. 2, no differences (P > 0.10) were observed in ADG, ADFI, or G:F among pigs fed the SPH or SDPP diets compared with those of pigs fed the control diet. Pigs fed the combined diet had greater (P < 0.10) overall ADFI compared with that of pigs fed the control diet, but ADFI was similar to that of pigs fed the SPH and SDPP diets. These results indicate that inclusion of up to 3% SDPP or SPH in diets fed during the first week postweaning did not affect the growth performance of weanling pigs, and no subsequent carryover effects were observed. Salmon protein hydrolysate did not affect the growth performance of weanling pigs and may be considered an alternative protein source in diets for weanling pigs.

Additivity of effects from dietary copper and zinc on growth performance and fecal microbiota of pigs after weaning.

Four experiments were conducted to determine the interactive effects of pharmacological amounts of Zn from ZnO and Cu from organic (Cu-AA complex; Cu-AA) or inorganic (CuSO(4)) sources on growth performance of weanling pigs. The Cu was fed for 4 (Exp. 1) or 6 (Exp. 2, 3, and 4) wk after weaning, and Zn was fed for 4 (Exp. 1) or 2 (Exp. 2, 3, and 4) wk after weaning. Treatments were replicated with 7 pens of 5 or 6 pigs per pen (19.0 ± 1.4 d of age and 5.8 ± 0.4 kg of BW, Exp. 1), 12 pens of 21 pigs per pen (about 21 d of age and 5.3 kg of BW, Exp. 2), 5 pens of 4 pigs per pen (20.3 ± 0.5 d of age and 7.0 ± 0.5 kg of BW, Exp. 3), and 16 pens of 21 pigs per pen (about 21 d of age and 5.7 kg of BW, Exp. 4). In Exp. 1 and 2, Cu-AA (0 vs. 100 mg/kg of Cu) and ZnO (0 vs. 3,000 mg/kg of Zn) were used in a 2 × 2 factorial arrangement. Only Exp. 1 used in-feed antibiotic (165 mg of oxytetracycline and 116 mg of neomycin per kilogram feed), and Exp. 2 was conducted at a commercial farm. In Exp. 3, sources of Cu (none; CuSO(4) at 250 mg/kg of Cu; and Cu-AA at 100 mg/kg of Cu) and ZnO (0 vs. 3,000 mg/kg of Zn) were used in a 3 × 2 factorial arrangement. In Exp. 4, treatments were no additional Cu, CuSO(4) at 315 mg/kg of Cu, or Cu-AA at 100 mg/kg of Cu to a diet supplemented with 3,000 mg/kg of Zn from ZnO and in-feed antibiotic (55 mg of carbadox per kilogram of feed). In Exp. 1 and 2, both Zn and Cu-AA improved (P < 0.001 to P = 0.03) ADG and ADFI. No interactions were observed, except in wk 1 of Exp. 2, where Zn increased the G:F only in the absence of Cu-AA (Cu-AA × Zn, P = 0.04). A naturally occurring colibacillosis diarrhea outbreak occurred during this experiment. The ZnO addition reduced (P < 0.001) the number of pigs removed and pig-days on antibiotic therapy. In Exp 3, ADFI in wk 2 was improved by Zn and Cu (P < 0.001 and P = 0.09, respectively) with no interactions. In wk 1, G:F was reduced by ZnO only in the absence of Cu (Cu × Zn, P = 0.03). Feeding Zn decreased fecal microbiota diversity in the presence of CuSO(4) but increased it in the presence of Cu-AA (Cu source × Zn, P = 0.06). In Exp. 4, Cu supplementation improved the overall ADG (P = 0.002) and G:F (P < 0.001). The CuSO(4) effect on G:F was greater (P < 0.001) than the Cu-AA effect. Our results indicate that pharmacological amounts of ZnO and Cu (Cu-AA or CuSO(4)) are additive in promoting growth of pigs after weaning.

Contribution of exogenous dietary carbohydrases to the metabolizable energy value of corn distillers grains for broiler chickens.

The objectives of this study were to determine the ileal digestible energy (IDE), ME, and ME(n) contents of corn distillers grains (CDG) for broiler chickens and to quantify these energy utilization responses to carbohydrase supplementation by the regression method. The CDG sample used in the current experiment contained (by analysis) 936 g/kg of DM, 4,894 kcal/kg of gross energy, 315.1 g/kg of CP, 94.6 g/kg of crude fat, 94.8 g/kg of crude fiber, 495.6 g/kg of neutral detergent fiber, 179.1 g/kg of acid detergent fiber, 0.19 g/kg of Ca, and 4.8 g/kg of P. The studies were conducted at 2 locations (Purdue or Louisiana State University) and CDG were incorporated into a practical corn-soybean meal diet at 3 levels (0, 300, or 600 g/kg) without or with added carbohydrase in a 2 x 3 x 2 factorial arrangement. The carbohydrase premix was added to supply 2,000 U of xylanase + 1,800 U of amylase/kg of feed. The diets were fed to 288 broiler chickens from d 15 to 22 posthatch with 6 birds per cage and 8 replicate cages per diet in a randomized complete block design at each of 2 locations. The broiler chicks were fed a standard broiler starter diet from d 1 to 15 posthatch. The IDE of diets decreased both linearly (P < 0.01) and quadratically (P < 0.05) as CDG increased from 0 to 600 g/kg regardless of carbohydrase supplementation. There was a linear (P < 0.01) decrease in ME of diet from 3,239 to 2,510 kcal/kg as CDG increased from 0 to 600 g/kg in the diets without added carbohydrase, whereas for birds fed the carbohydrase-supplemented diets, there were both linear (P < 0.01) and quadratic (P < 0.01) decreases from 3,398 to 2,613 kcal/kg as CDG increased from 0 to 600 g/kg. Dietary ME(n) linearly decreased (P < 0.01) regardless of carbohydrase supplementation as CDG increased from 0 to 600 g/kg. Supplementation with carbohydrase improved (P < 0.01) IDE, ME, and ME(n). Regressions of CDG-associated IDE, ME, or ME(n) intake in kilocalories against kilograms of CDG intake without added carbohydrase generated the following: IDE = 44 + 2,340X, r(2) = 0.953; ME = 10 + 2,315X, r(2) = 0.993; and ME(n) = 10 + 2,132X, r(2) = 0.991. Corresponding regressions when carbohydrase was added were as follows: IDE = -17 + 2,622X, r(2) = 0.985; ME = -25 + 2,448X, r(2) = 0.979; and ME(n) = -22 + 2,264X, r(2) = 0.978. These data indicate that the respective IDE, ME, and ME(n) values (kcal/kg of DM) of the CDG sample evaluated were 2,340, 2,315, and 2,132 when carbohydrase was not added and 2,622, 2,448, and 2,264 when carbohydrase was added. Comparison using ANOVA procedures indicated that the slope when carbohydrase was added was greater (P < 0.05) than when carbohydrase was not added. This response implies that carbohydrase supplementation improved (P < 0.05) the IDE, ME, and ME(n) of CDG in practical corn-soybean meal-based diets used in this current study by 12, 5.7, and 6.2%, respectively.

Effect of milk chocolate product on week-1 feed intake and growth performance of weanling pigs.

Experiments were conducted to assess the effect of dried whey (DW; 70% lactose) or milk chocolate product (MCP; 20% lactose and 60% sugars) on wk-1 feed intake and growth performance of pigs. Diets contained 1.60, 1.40, 1.40, and 1.20% total Lys for phase 1 (d 0 to 7), 2 (d 7 to 14), 3 (d 14 to 21), and 4 (d 21 to 35), respectively. Pigs were blocked by initial BW; sex and littermates were balanced across treatment; treatments were replicated with a minimum of 5 pens of 4 pigs each. Pigs were weaned at 24, 19, and 24 d of age with an initial BW of 6.5, 6.0, or 6.3 kg for Exp. 1 to 3, respectively. In Exp. 1 and 2, the treatments were 1) negative control (NC), no lactose added, 2) positive control (PC) with DW, 3) 25% replacement of the level of DW of the PC diet with MCP (25MCP), and 4) 50% replacement of the level of DW of the PC diet with MCP (50MCP). The level of DW or combinations of DW and MCP were 20, 10, and 5% for phases 1, 2, and 3 respectively. A common diet with no lactose was fed during phase 4. In Exp. 3, the treatments were 1) NC, 2) PC, and 3) 100% replacement of the level of DW of the PC diet with MCP (100MCP). In the combined data of Exp. 1 and 2, daily collected feed intake during wk 1 was increased (P < 0.10) from d 3 to 7 for the PC pigs; on d 2, 3, 4, and 7 for the 25MCP pigs; and from d 2 to 7 for the 50MCP pigs compared with the NC pigs. There was no difference (P > 0.10) on any day of wk 1 among pigs fed the PC and MCP diets. During phase 1, ADG and ADFI were increased (P < 0.10) for the PC, 25MCP, and 50MCP pigs compared with the NC pigs, but G:F was not affected (P > 0.10). During phases 2, 3, 4, and overall, there were no differences (P > 0.10) in growth performance among pigs fed the PC and MCP diets. In Exp. 3, collected daily feed intake during wk 1 was increased (P < 0.10) from d 2 to 5 for PC pigs and on d 1 and 2 for the 100MCP pigs compared with the NC pigs. However, there was no difference (P > 0.10) on any day of wk 1 between the PC and 100MCP pigs. Growth performance was not affected (P > 0.10) during any phase of the experiment. Combined data from Exp. 1, 2, and 3 using the NC and PC diets indicated that dietary DW increased (P < 0.10) final BW and increased ADG and ADFI during phases 1, 2, 3, and overall. These results indicate that partial or total replacement of DW with MCP had no effect on wk-1 feed intake or growth performance of weanling pigs and that MCP could be considered as a formulation alternative to DW.

Comparison of dried whey permeate and a carbohydrate product in diets for nursery pigs.

Three experiments were conducted to compare dried whey permeate (DWP; 80% lactose) and a carbohydrate product (CHO; 40% lactose, 30% sucrose, and 10% glucose) for nursery pigs. Pigs were fed in a 3-phase feeding program, and diets contained 1.6, 1.4, and 1.2% total Lys for phases 1 (d 0 to 7), 2 (d 7 to 21), and 3 (21 to 28). Dietary treatments included 1) control (no lactose), 2) low level of DWP, 3) high level of DWP, 4) low level of CHO, and 5) high level of CHO. In Exp. 1 (4 reps of 4 pigs per pen; initial BW = 7 kg and 23 d of age), the low and high levels used for each source in each phase were phase 1 (12.5 and 25%), phase 2 (10 and 20%), and phase 3 (6 and 12%). In Exp. 2 (6 reps of 5 pigs per pen; initial BW = 8 kg and 26 d of age) and 3 (4 reps of 4 pigs per pen; initial BW = 6 kg and 21 d of age), the inclusion levels were phase 1 (6 and 12%), phase 2 (3 and 6%), and phase 3 (common diet with no lactose). In Exp. 1, pigs fed diets with DWP or CHO had increased ADG (P = 0.02 and P = 0.01) and ADFI (P = 0.01) compared with pigs fed the control diet during phase 1. Gain:feed was reduced (P = 0.08) for pigs fed diets with CHO. During phases 2, 3, and overall, ADG, ADFI, and G:F were not affected (P > 0.10) by diet. In Exp. 2, pigs fed diets with CHO had increased ADG (P = 0.08 and P = 0.07) and ADFI (P = 0.04 and P = 0.01) compared with pigs fed the control diet during phases 1 and 2. Pigs fed diets with CHO had increased ADFI (P = 0.08 and P = 0.07) in phases 1 and 2 and increased ADG (P = 0.02) in phase 2 compared with pigs fed diets with DWP. Overall, pigs fed diets with DWP and CHO had increased ADFI (P = 0.06 and P = 0.01) compared with pigs fed the control diet, but ADG was increased (P = 0.07) for pigs fed diets with CHO. In Exp. 3, ADG, ADFI, and G:F were not affected (P > 0.10) by DWP or CHO during phase 1. Daily BW gain was increased (P = 0.02 and P = 0.07) for pigs fed diets with DWP or CHO during phase 2 compared with pigs fed the control diet. Overall, ADG was increased (P = 0.05) for pigs fed diets with DWP, but ADFI and G:F were not affected. Results from the combined data of Exp. 2 and 3, indicated that overall ADG (P = 0.05 and P = 0.04) and ADFI (P = 0.04) were increased in pigs fed diets with DWP or CHO compared with pigs fed the control diet. These data suggest that DWP or CHO improve growth performance of weanling pigs.

Uric acid, urea, and ammonia concentrations in serum and uric acid concentration in excreta as indicators of amino acid utilization in diets for broilers.

Five experiments were conducted to determine if serum uric acid, serum urea N (SUN), serum ammonia, and the uric acid content of the excreta (UAE) could be used to determine the efficacy of amino acid (AA) utilization in diets for broilers. All experiments were conducted with Ross x Ross 308 or 708 broilers from 0 to 14 or 0 to 18 d posthatching in brooder batteries. Treatments had 6 or 7 replications with at least 6 broilers per replicate pen. All diets were corn and soybean meal-based and formulated to contain 1.0% Ca and 0.45% nonphytate P and to meet or exceed the requirements of all nutrient requirements except total Lys, Met, and Thr (experiment 1) or Met (experiments 2 to 5). Experiment 1 consisted of 2 dietary treatments. Diet 1 was formulated to be deficient in Lys, Thr, and Met and diet 2 was formulated to be adequate in all nutrients. Broilers fed the AA-adequate diet had increased (P<0.01 to 0.03) ADG, ADFI, and G:F compared with broilers fed the AA-deficient diet. Serum uric acid, SUN, serum ammonia, and UAE were not affected (P=0.34 to 0.70) by dietary treatment. In experiments 2 to 5, diets contained 1.35% total Lys, 2 levels of Met (0.50 or 0.76 TSAA:Lys), and without or with Gly supplementation up to 2.32% Gly+Ser. Broilers fed diets containing supplemental Met in experiments 2 to 5 had increased (P=0.01 to 0.03) ADG, ADFI, and G:F. Gain:feed was increased (P=0.01 to 0.07) in broilers fed supplemental Gly. Serum uric acid and SUN were decreased (P<0.01) after a 2-h fast in broilers fed supplemental Met and Gly. Serum uric acid and SUN also were decreased at other times after fasting, but the 2-h fast gave the most consistent response. Uric acid content of the excreta was decreased (P<0.01) in broilers fed supplemental Met. Serum ammonia was decreased (P<0.01 to 0.02) in experiments 2, 3, and 4 at varying times postfeeding but was not affected by diet in experiment 5. The results of this research indicate that serum uric acid, SUN, and UAE concentrations can be used as an indicator of AA utilization in broilers fed AA-adequate and AA-deficient diets.

Effect of phytase on apparent total tract digestibility of phosphorus in corn-soybean meal diets fed to finishing pigs.

Five experiments were conducted to investigate the ability of different phytase products to improve P digestibility in finishing pigs. A corn-soybean meal basal diet containing 0.50% Ca, 0.32% P, and 0.40% Cr(2)O(3) was used to calculate apparent P and GE digestibility. Pigs were individually penned and fed their respective diet for ad libitum intake for 12 d before fecal sampling on d 13 and 14 and blood collection on d 14 for plasma P determination. Experiments 1 through 4 used gilts with across-trial average initial and final BW of 84 and 97 kg, respectively. Pigs were fed Natuphos (Exp. 1), OptiPhos (Exp. 2), Phyzyme (Exp. 3), or RonozymeP (Exp. 4) at 0, 200, 400, 600, 800, or 1,000 phytase units (FTU)/kg (where 1 FTU is defined as the quantity of enzyme required to liberate 1 micromol of inorganic P per min, at pH 5.5, from an excess of 15 micromol/L of sodium phytate at 37 degrees C). Experiment 5 used barrows with initial and final BW of 98 and 111 kg, respectively, and were fed diets containing 0, 500, or 1,000 FTU/kg of Natuphos, OptiPhos, Phyzyme, or RonozymeP. Pigs fed Natuphos (Exp. 1) and OptiPhos (Exp. 2) exhibited a linear and quadratic (P < 0.01) improvement in P digestibility with increasing levels of dietary phytase, whereas pigs fed Phyzyme (Exp. 3) and RonozymeP (Exp. 4) exhibited a linear (P < 0.01) improvement in apparent P digestibility with increasing levels of dietary phytase. In Exp. 5, the improvement in apparent P digestibility with increasing levels of dietary phytase was linear (P < 0.01) for Natuphos, Phyzyme, and RonozymeP, but was linear and quadratic (P < 0.01) for OptiPhos. Based on regression analysis, inorganic P release at 500 FTU/kg was predicted to be 0.070, 0.099, 0.038, and 0.030% for Natuphos, OptiPhos, Phyzyme, and RonozymeP, respectively. These estimates are comparable with those of pigs in Exp. 5, for which the estimated inorganic P release at 500 FTU/kg was 0.102, 0.039, and 0.028% for OptiPhos, Phyzyme, and RonozymeP, respectively, but not for the 0.034% value determined for Natuphos. The effect of dietary phytase on GE digestibility was inconsistent with a linear (P < 0.01) improvement in GE digestibility noted for OptiPhos (Exp. 2 and 5) and RonozymeP (Exp. 4), but the quadratic (P < 0.01) improvement for Natuphos. There was no effect of dietary phytase on plasma inorganic P. The data presented show clear improvements in P digestibility, with the estimated level of inorganic P release being dependent on phytase source and level.

The effect of chromium as chromium propionate on growth performance, carcass traits, meat quality, and the fatty acid profile of fat from pigs fed no supplemented dietary fat, choice white grease, or tallow.

The purpose of this research was to investigate the effect of Cr as chromium propionate (CrProp) on growth performance, carcass traits, meat quality, and the fatty acid profile of fat from pigs fed no supplemented dietary fat, choice white grease (CWG), or tallow. An experiment was conducted with 108 crossbred Yorkshire gilts assigned in a randomized complete block design based on BW (average initial and final BW were 29 +/- 3 and 109 +/- 7 kg, respectively) and allotted within block to a 2 x 3 factorial arrangement of treatments. The treatment arrangement consisted of 2 levels of Cr supplementation (0 and 200 microg/kg in the form of CrProp) and 3 dietary fat sources (no added fat, CWG, or tallow). Each treatment was replicated 6 times with 3 pigs per replicate pen. The experiment was conducted over time with 3 replicates in each of 2 trials. A 4-phase grower-finisher feeding program was used. Dietary treatments were 1) a corn-soybean meal (C-SBM) diet with no added fat; 2) a C-SBM diet with 4% added tallow; 3) a C-SBM diet with 4% added CWG; 4) diet 1 + 200 microg/kg of Cr as CrProp; and 5) diet 2 + 200 microg/kg of Cr; 6) diet 3 + 200 microg/kg of Cr. Addition of Cr did not affect (P > 0.10) growth performance, but did decrease (P = 0.05) 10th-rib backfat and increase (P = 0.03) percentage of muscle. Gain:feed was increased (P = 0.003) and ADFI was decreased (P = 0.03) by fat addition. Fat addition increased HCW (P = 0.05) and dressing percent (P = 0.03). Average backfat, 9th-rib LM cook loss, and 10th-rib LM drip loss and total loss were decreased (P = 0.02 to 0.04) by tallow. Belly bending on both the teatline and scribe side were increased (P = 0.01 to 0.03) by CWG. Iodine values on belly fat samples were decreased (P = 0.02) by Cr supplementation. In addition, iodine values on belly and loin fat samples were increased (P = 0.001) by CWG. Overall, Cr supplementation decreased backfat and the iodine value of belly fat and increased the percentage of muscle.

Effect of incremental levels of red blood cells on growth performance and carcass traits of finishing pigs.

Three experiments were conducted to determine the effect of incremental levels of red blood cells (RBC; 0 to 4%, Exp. 1; 0 to 2%, Exp. 2 and 3) on growth performance and carcass traits of finishing pigs. Dietary treatments were formulated to meet or exceed the nutrient requirements of barrows and gilts gaining 350 g of lean BW gain per day and were formulated to contain 0.52% apparent ileal digestible (AID) Lys for barrows and 0.59% AID Lys for gilts. In Exp. 1, barrows and gilts (2 replicates of barrows and 2 of gilts; 4 pigs per pen) were fed 0, 1, 2, 3, or 4% RBC. Initial BW (mean +/- SD) was 84.6 +/- 4.9 and 82.42 +/- 4.8 kg, and final BW was 118.7 +/- 6.5 and 120.0 +/- 9.6 kg for barrows and gilts, respectively. Two barrows and 2 gilts per pen were randomly selected and slaughtered for collection of carcass measurements. Experiment 2 was similar to Exp. 1, except 0, 1, or 2% RBC were added. Initial BW was 82.5 +/- 6.4 and 79.2 +/- 7.0 kg, and final BW was 125.5 +/- 6.2 and 119.8 +/- 8.8 kg for barrows and gilts, respectively. Each dietary treatment had 4 replicates per sex with 4 pigs per pen. One barrow and 1 gilt per treatment replicate were randomly selected and slaughtered for collection of carcass traits and viscera weights. Experiment 3 was similar to Exp. 2 except only barrows were used, and the initial and final BW were 86.0 +/- 5.7 and 133.4 +/- 8.4 kg, respectively. Each dietary treatment had 4 replicates with 3 pigs per pen, and all pigs were slaughtered for collection of carcass traits and viscera weights. In Exp. 1, final BW, ADG, and G:F were decreased linearly (P < 0.01 to 0.10) as RBC addition increased, but ADFI was not affected. With increased RBC addition, average backfat increased (P < 0.09) and fat free lean decreased (P < 0.04). There was a quadratic effect (P < 0.04) on dressing percentage (DP); the 2% RBC addition increased DP, but the 3 and 4% additions decreased DP. The RBC addition had no effect (P > 0.10) on any remaining carcass measurements. In Exp. 2, there was a quadratic effect (P < 0.07) of RBC addition on average backfat; the 1% RBC addition decreased backfat, but the 2% addition returned backfat to the level of the control pigs. There was no effect (P > 0.10) on any other response variable. In Exp. 3, with increased RBC addition, average backfat linearly decreased (P < 0.04) and large intestine percentage increased (P < 0.09). There was no effect of RBC addition (P > 0.10) on any other response variable. Our data indicate that feeding 3 or 4% RBC decreases growth performance of finishing pigs. However, feeding 1 or 2% RBC to finishing pigs had no detrimental effects on growth performance and increased DP in one experiment.

The interactive effects of glycine, total sulfur amino acids, and lysine supplementation to corn-soybean meal diets on growth performance and serum uric acid and urea concentrations in broilers.

Four experiments were conducted to determine the interactive effects of Gly, TSAA, and Lys in corn-soybean meal diets on growth performance of broilers. All experiments were conducted with female Ross x Ross 308 or 708 broilers in brooder batteries from 0 to 18 d posthatching. Treatments had 5 to 8 replications with 5 or 6 broilers per replicate pen. Diets in all experiments were fed without or with Gly (2.32% total Gly + Ser). All diets contained 0.25% l-Lys.HCl except in experiment 1, where no crystalline Lys was added. In experiment 1, the total dietary Lys level was 1.26% with TSAA:Lys of 0.72 and 0.76. Increasing TSAA:Lys increased (P < 0.07) G:F. The main effect of Gly was not significant for ADG, ADFI, or G:F; however, G:F was increased by Gly in broilers fed 0.72 but not in those fed 0.76 TSAA:Lys (Gly x TSAA:Lys, P < 0.03). In experiment 2, the total dietary Lys level was 1.26% with TSAA:Lys of 0.51, 0.68, 0.72, and 0.76. Glycine addition did not affect ADG, ADFI, or G:F; however, increasing TSAA:Lys linearly increased (P < 0.01) ADG, ADFI, and G:F and the response was quadratic for ADG and G:F. Experiment 3 was similar to experiment 2 except the total dietary Lys level was 1.35%. Glycine addition increased (P < 0.03) G:F and decreased (P < 0.04) serum uric acid (SUA) and serum urea N concentrations. Also, increasing TSAA:Lys linearly and quadratically (P < 0.02) increased ADG, ADFI, and G:F. In experiment 4, broilers were fed 2 levels of total dietary Lys (1.26 and 1.35%), 3 levels of TSAA:Lys (0.72, 0.76, and 0.80), and without or with Gly supplementation up to a total of 2.32% Gly + Ser. Glycine addition increased ADG (P < 0.02) and G:F (P < 0.01). The increase in G:F with Gly was not the same for all TSAA:Lys (Gly x TSAA:Lys, P < 0.07). Increasing Lys increased (P < 0.01 to 0.10) ADG, ADFI, and G:F. Glycine addition increased ADG and ADFI more in broilers fed 1.35% Lys than in those fed 1.26% Lys (Lys x Gly, P < 0.09). Glycine addition increased SUA in broilers fed 1.26% Lys but decreased SUA in broilers fed 1.35% Lys (P < 0.01). Glycine addition decreased SUA in broilers fed the TSAA:Lys of 0.80 but not at the other TSAA:Lys (P < 0.08). These data indicate that Gly increased G:F and decreased SUA in diets with 1.35% Lys and excess TSAA.

Effect of incremental levels of L-lysine and determination of the limiting amino acids in low crude protein corn-soybean meal diets for broilers.

Research was conducted to determine the level of l-Lys that can be included in corn-soybean meal (C-SBM) diets for broilers before an amino acid (AA) beyond Met, Lys, Thr, or Gly becoming limiting and to determine the order of limiting AA in low CP C-SBM diets. All experiments were conducted with Ross 708 broilers (0 to 18 d of age) in brooder batteries. Treatments contained 7 or 8 replicates with 6 birds per replicate. In all experiments, a control C-SBM diet containing no l-Lys.HCl and a similar diet [positive control (PC) + Gly] with supplemental Gly to provide 2.32% total dietary Gly + Ser were fed. All diets were formulated to contain 1.26% total Lys. All diets with added l-Lys.HCl contained supplemental Gly to provide 2.32% total dietary Gly + Ser. In experiment 1, l-Lys.HCl was added to the diets at 0.02% increments from 0.15 to 0.27%. Compared with the PC + Gly diet, there were no negative effects (P > 0.10) of supplemental Lys on ADG, ADFI, or G:F. In experiment 2, l-Lys.HCl was added to the diets at 0.05% increments from 0.25 to 0.60%. Compared with the PC + Gly diet, ADG and G:F were decreased (P < 0.03) in broilers fed diets containing greater than 0.30% l-Lys.HCl but not (P > 0.10) in the 0.25% l-Lys.HCl diet. In experiment 3, l-Lys.HCl was added to the diets at 0.05% increments from 0.20 to 0.30%. Daily gain was decreased (P < 0.03) in broilers fed 0.30% l-Lys.HCl but not in those fed 0.20 or 0.25% l-Lys.HCl. In experiment 4, the order of limiting AA was determined in a C-SBM diet containing 0.45% L-Lys.HCl. In addition to the PC and PC + Gly diets, diets consisted of a negative control (NC) diet with 0.45% l-Lys.HCl, NC + 0.247% Ile, NC + 0.484% l-Arg.HCl, NC + 0.249% Val, and all possible 2- and l-way combinations of all 3 AA. Compared with the NC diet, addition of Arg and the combination of Arg and the other AA increased ADG and ADFI, indicating that Arg was the limiting AA in this diet. Experiment 5 was conducted in an identical manner to experiment 4 except the diets with the added AA contained the same ratio of corn to soybean meal that is present in a diet with 0.25% l-Lys.HCl. The results of experiment 5 suggest that Arg and Val are equaling limiting in a diet with 0.25% l-Lys.HCl. In summary, 0.25% l-Lys.HCl can be added to C-SBM diets supplemented with Met, Thr, and Gly with no negative effects on growth performance, and Arg and Val are equaling limiting (after Met, Thr, Lys, and Gly) in diets containing 0.25% l-Lys.HCl.

The influence of dietary selenium on common indicators of selenium status and liver glutathione peroxidase-1 messenger ribonucleic acid.

The objective of this research was to determine the influence of dietary Se on various indicators of Se status and relative liver glutathione peroxidase 1 (GPx-1) messenger RNA (mRNA) levels in growing Holstein bull calves. Calves (n = 14, 7/diet) were started 28 d after birth on a Se-adequate (SeA) or Se-deficient diet (SeD) and maintained on the diet until 180 d of age. Blood samples were taken from each calf for determination of erythrocyte GPx-1 and plasma GPx-3 activities and plasma Se concentration on d 28 of age, every 28 d thereafter, and at 180 d of age. To assess liver Se and GPx-1 mRNA, 3 calves were first killed at d 21 of age for baseline (BSL) measurements, and 4 calves from each treatment were killed at trial conclusion. Feed intake and ADG were not affected (P = 0.62) by dietary Se concentrations. However, liver Se concentration was greater (P < 0.05) for BSL calves and SeA calves than SeD calves, but no difference (P = 0.68) was observed between BSL calves and SeA calves. Plasma Se was greater for SeA calves (P < 0.01) than for SeD calves by d 56 of age. The GPx-1 activity was greater in SeA calves (P < 0.01) by d 84 of age, whereas GPx-3 activity was greater in SeA calves, but not until d 180 of age (P < 0.01). There was a 50% decrease in GPx-1 mRNA for the SeD calves (P < 0.05) compared with SeA calves. Thus, relative GPx-1 mRNA transcript level is reflective of Se status in the bovine. Furthermore, 152 d on a semi-purified, SeD diet is adequate to create a Se deficiency in growing Holstein bull calves started on a SeD diet at 28 d of age.

Effects of dietary spray-dried plasma protein on sow productivity during lactation.

Seventy-two primiparous and multiparous sows (36 per dietary treatment) farrowed in 4 groups were used to evaluate the effects of spray-dried plasma protein (SDP) on sow and litter performance during lactation. Dietary lactation treatments consisted of a corn-soybean meal control and a corn-soybean meal diet containing 0.5% SDP. Both diets were formulated to contain 1.0% total Lys and 3.46 Mcal/kg of ME and were fed from d 107 +/- 1.2 of gestation to weaning. Sows were allotted to dietary treatment based on breed, parity, and the date of d 107 of gestation. Litters were standardized within diet, and pigs were weaned at an average age of 19 +/- 2.1 d. Sows were fed 3 times daily during lactation. After weaning, sows were fed a common gestation diet and checked twice daily for estrus. Sows were grouped by parity (young sows, 3) for statistical analysis. The data were analyzed as a 2 x 2 factorial arrangement of treatments; the factors were parity (3) and SDP (0 or 0.5%). Treatment differences were considered significant at P < 0.10. Mature sows had a greater BW on d 107 of gestation, on d 1 postfarrowing, and at weaning; greater lactation ADFI; and greater litter BW after cross-fostering, but pig survival to weaning was decreased. Sows fed SDP had a greater gestation interval, litter BW at weaning, and litter ADG, with 1 less lactation day. The effect of SDP addition was dependent on sow parity, as noted by numerous SDP x parity interactions. The addition of SDP increased lactation ADFI in mature sows but decreased ADFI in young sows. Mature sows fed SDP had a greater number of pigs weaned per litter, litter and pig weaning weights, pig survival to weaning, and number of pigs weaned per litter weighing more than 3.6 kg, but the SDP diet had little to no effect on these responses in young sows. Subsequent farrowing data were collected, but no dietary treatment effects (P > 0.10) were observed. The results of this research indicate that SDP increased productivity of sows in parity 4 or greater.