Digestible lysine requirement of starter and grower pigs

Three experiments were conducted to determine the digestible lysine requirement of starter (6 kg BW initially) and of grower (21 kg BW initially) pigs. Experiment 1 used 294 starter pigs and lasted 28 d; Exp. 2 used 182 grower pigs and lasted 35 d. Protein and total lysine contents of the basal corn-peanut meal diets were 20 and .8% for Exp. 1 and 16 and .54% for Exp. 2. Basal diets were fortified with five incremental additions of lysine.HCl to provide lysine contents ranging from .8 to 1.3% in Exp. 1, and .54 to .94% in Exp. 2. Diets contained crystalline tryptophan, threonine and isoleucine (Exp. 1 only) to provide dietary concentrations equal to 18, 70 and 60% of the highest lysine level fed. Average daily gain and gain/feed of both starter and grower pigs increased (P less than .05) linearly and quadratically as dietary lysine level increased. For starter pigs, ADG and gain/feed were optimized at 1.1 to 1.2% total lysine. For grower pigs, ADG and gain/feed were optimized at .86% total lysine. In Exp. 3, barrows fitted with an ileal T-cannula were used in a 4 X 4 Latin square design. Basal diets and diets with added lysine were evaluated. Apparent lysine digestibility of the basal starter and grower diets and lysine.HCl were 79.9, 74.1 and 96.7%, respectively. Based on these values and the total lysine contents found to optimize performance, the digestible lysine requirements of starter and grower pigs are 1.03 and .71%, respectively.     

Serum haptoglobin concentration as a marker of clinical signs in finishing pigs

A case-control study of 340 finishing pigs aged 10 to 25 weeks in 15 commercial Danish pig herds was carried out to investigate serum haptoglobin concentration as an objective marker of clinical signs of disease. Pigs with different clinical signs were matched to control pigs without clinical signs with respect to herd, pen, estimated weight and gender, and each pig was subjected to a standard clinical examination. In 86 of the case-control pairs, the rectal temperature was also recorded. There was a significantly higher mean haptoglobin concentration in the serum of lame pigs (P<0.0001), pigs with respiratory disease (P=0.0004), pigs with tail or ear bites (P=0.0004) and pigs with diarrhoea (P=0.02). Similarly, a higher mean rectal temperature was recorded in lame pigs (P<0.0001), pigs with respiratory disease (P=0.002) and pigs with tail or ear bites (P=0.0003). There was a significant but low correlation between rectal temperature and haptoglobin concentration in serum (P=0.003, r=0.20). The area under the receiver-operating-characteristic curve was between 0.67 and 0.78 for the different clinical signs. The maximum simultaneous levels of sensitivity (0.61 to 0.71) and specificity (0.61 to 0.77) of serum haptoglobin for the different clinical signs were obtained at a cut-off value of 1.1 mg/ml. At a cut-off value of 1.8 mg/ml, the sensitivity decreased to 0.31 to 0.60, and the specificity increased to 0.82 to 0.86. It was not possible to define a cut-off value which classified individual pigs according to their clinical signs.     

Further assessment of the dietary lysine requirement of finishing gilts

A cooperative research study involving 635 gilts was conducted at eight research stations to further estimate the lysine requirement of finishing gilts. Dietary crude protein levels of the five dietary treatments ranged from 16.0 to 24.4% with calculated lysine levels of .80, .95, 1.10, 1.25, or 1.40%. Each station contributed a minimum of two replicate pens of pigs per treatment. Average initial and final weights were 53.6 and 116.4 kg, respectively. At the end of the experimental period, pigs were killed and hot carcass weight, 10th-rib fat depth, and longissimus muscle area were measured. Carcass fat-free lean percentage and fat-free lean gain were estimated from these data. Daily lysine intakes averaged 21.8, 25.9, 30.5, 34.3, and 37.8 g/d for the five treatment groups, respectively. Increasing the dietary lysine from .80 to .95% numerically increased weight gain and gain:feed, but these increases were not maintained at higher levels of dietary lysine. Overall, rate and efficiency of gain decreased (cubic, P < .01) with increasing dietary lysine. Carcasses were leaner at the two higher levels of dietary lysine as evidenced by reduced 10th rib backfat (linear, P < .01), increased longissimus area (quadratic, P < .04), and increased percentage of estimated fat-free lean (linear, P < .01). Carcass fat-free lean gain was not influenced by dietary lysine except for a small numerical improvement (P < .11) at the .95% level of dietary lysine that paralleled the improvement in body weight gain. The results indicate that the dietary lysine requirement of finishing gilts with a mean carcass fat-free lean growth rate of 306 g/d from 54 to 116 kg body weight is probably no higher than .80% of the diet to achieve maximum rate and efficiency of body weight gain and carcass lean growth rate. The results also indicate that higher dietary lysine levels may increase carcass leanness in finishing gilts, possibly due to reduced intake of NE. Whether this response is due to the effects of lysine alone, protein (i.e., other amino acids), or soybean meal is unknown.     

Effects of dietary threonine:lysine ratioes and sanitary conditions on performance,plasma urea nitrogen,plasma-free threonine and lysine of weaned pigs

Two 21 d-experiments were conducted to determine the optimum standardized ileal digestible(SID)threonine:lysine ratio(Thr:Lys) for weaned piglets reared under clean(Exp. 1) or unclean(Exp. 2) sanitary conditions and fed antibiotic-free diets. In each experiment, 90 mixed-sex pigs(Duroc × [Yorkshire × Landrace]; initial BW 7.2 ± 0.3 kg) were randomly assigned to 5 dietary treatments each with 6 replicates(3 pigs per pen). The dietary treatments were 5 graded levels of SID Thr:Lys(55,59, 63, 67 and 71%). Diets were corn-wheat-soybean meal-based with a constant SID Lys of 1.18% that was set to be second limiting amino acid. In Exp. 1 and Exp. 2, plasma-free Thr increased(P = 0.05) with increasing dietary SID Thr:Lys. In Exp. 1, the SID Thr:Lys for gain-to-feed ratio(G:F) was optimized at 65%.In Exp. 2, the estimated optimal SID Thr:Lys for overall G:F was 66.5%. In conclusion, an average optimal SID Thr:Lys of 65 and 66.5% could be used to optimize feed efficiency for weaned pigs under clean and unclean sanitary conditions, respectively.     

Serum haptoglobin concentration as an indicator of weight gain in pigs.

Serum haptoglobin concentration was investigated as an indicator of weight gain in commercially-reared pigs. The serum haptoglobin concentrations and weights of 40 pigs were monitored on a weekly basis, from weaning to 13 weeks of age. All data were ranked based on the week 13 weights, and divided into high, middle and low weight gain groups. By the fourth week of the study, when the pigs were seven weeks old, serum haptoglobin concentrations could be used to differentiate pigs that would have a high weight gain at the end of the study from those which would have a low weight gain.     

Estimation of dietary lysine requirement using plasma amino acid concentrations in mature thoroughbreds

Four experiments were conducted to estimate dietary lysine (Lys) requirements using plasma amino acid concentrations as a criterion in mature thoroughbreds. In each experiment four adult thoroughbreds were used. The changes in plasma Lys concentration after feeding were observed in Experiment 1. Blood samples were taken from the cervix vein 0.5 h before, and 1, 3, 5.5, and 10 h after feeding. The plasma Lys concentration increased and remained constant until 3 h after feeding, decreased until 5.5 h and remained constant after then. Therefore, the bleed was done at 3 h after feeding in all later experiments. To make sure of the response speed of the plasma Lys to changes of dietary Lys levels, dietary Lys levels were changed from high to low, and low to high levels in Experiment 2. Blood samples were taken just on the changing day and 1, 2 and 3 days after changing diets. The plasma Lys concentration decreased until 2 days after changing the diet, and then remained constant with advancing days after changing the diet from high Lys to low Lys. On the other hand, the plasma Lys increased until one day after changing the diet, and then remained constant with advancing days after changing dietary Lys levels. Thus, blood samples were taken 3 days after feeding in the next experiments. The possibility of estimating the Lys requirement for maintenance using plasma Lys concentration was elucidated by two methods in Experiments 3 and 4. In Experiment 3, the horses were fed a diet containing 0.33 percent Lys for 3 days. After this the diet was changed to diets containing higher levels of Lys to 0.40, 0.47, 0.54, and 0.61 percent every third day. The Lys requirement was estimated to be 0.46 percent of diet from the response of plasma Lys concentration of five Lys levels. In Experiment 4, a 4 × 4 Latin square design was used for four dietary Lys levels. The Lys requirement was estimated to be 0.47 percent of the diet with a plasma Lys concentration of four Lys levels.     

Influence of dietary lysine level on whole-body protein turnover, plasma IGF-I, GH and insulin concentration in growing pigs

Four growing pigs (initial liveweight 25.9 ± 0.54 kg, final liveweight 43.0 ± 1.06 kg) were used to study the effect of dietary lysine level on nutrient digestibility, whole-body protein turnover, plasma insulin-like growth factor-I (IGF-I), growth hormone (GH), insulin, glucose, and urea nitrogen (PUN). Four diets, containing 7.0 g (L1), 9.5 g (L2), 12.0 g (L3) and 14.5 g (L4) lysine per kg diet respectively, were formulated as experimental treatments. The animals and diets were allocated in a 4 × 4 Latin square design. Nitrogen (N) metabolism and whole-body protein turnover were measured by classical method and single-dose ¹⁵N end-product method, respectively. The blood samples were taken at the end of each experimental period. Results showed that N retention (NR) and N biological value (NBV) were significantly increased from L1 to L4 (P < 0.05). However, differences in NR and NBV between L2, L3 and L4 were not significant (P > 0.05). There was no significant difference on dry matter (DM) digestibility, organic matter (OM) digestibility and N digestibility between different treatments (P > 0.05). Whole-body protein synthesis, protein degradation and protein accretion increased markedly from L1 to L2 (P < 0.05), but did not increase further from L2 to L4. Whole-body protein accretion (y, g/kg W^0.75/d) increased with dietary lysine (x, g/kg) in a quadratic manner: y = − 0.09x² + 2.12x − 5.14 (r² = 0.96, n = 4, P < 0.05).The results also showed that differences in plasma IGF-I, GH, glucose and PUN concentration between different treatments were not significant (P > 0.05). Plasma insulin concentration (y, μIU/ml) was increased with dietary lysine (x, g/kg) in a quadratic manner: y = 0.23x² − 4.10x + 32.25 (r² = 0.99, n = 4, P < 0.05), but it was not found that plasma insulin concentration was related to NR. A significant correlation was found between NR (y, g/d) and plasma IGF-I (x, ng/ml): y = − 3.1 × 10^− 3x² + 1.31x − 122.28 (r² = 0.99, n = 4, P < 0.05).It was concluded that dietary lysine level had a significant influence on NR and whole-body protein turnover but not on plasma IGF-I and GH concentration. Plasma IGF-I may be an important factor controlling N metabolism of growing pigs. Further research was needed to study the mechanism.     

Effects of dietary lysine levels on the concentrations of selected nutrient metabolites in blood plasma of late‐stage finishing pigs

Lysine is the first‐limiting amino acid (AA) in typical swine diets and plays very important roles in promoting growth performance of pigs. This research was conducted to study the effects of dietary lysine on blood plasma concentrations of protein, carbohydrate, and lipid metabolites of pigs. Eighteen crossbred finishing pigs (nine barrows and nine gilts; initial BW 92.3 ± 6.9 kg) were individually penned in an environment controlled barn. Pigs were assigned to three dietary treatments according to a randomized complete block design with gender as block and pig as experimental unit (6 pigs/treatment). Three corn and soybean meal‐based diets were formulated to contain total lysine at 0.43%, 0.71%, and 0.98% (as‐fed basis) for Diets I (lysine deficient), II (lysine adequate), and III (lysine excess) respectively. After 4 weeks on trial, jugular vein blood was collected and plasma was separated. The plasma concentrations of total protein, albumin, urea nitrogen (UN), triglyceride, total cholesterol, and glucose were determined using an ACE Clinical Chemistry System (Alfa Wassermann, Inc., West Caldwell, NJ, USA). Data were analysed using the GLM Procedure with PDIFF (adjust = T) option of SAS. No differences (p > 0.10) were found between barrows and gilts for any of the metabolites measured. While there were no differences (p > 0.10) between pigs fed Diets II and III in plasma concentrations of UN, albumin, and total cholesterol, the concentration of albumin in these pigs was higher (p < .05) than that of pigs fed Diet I, and the concentrations of UN and total cholesterol in these pigs were lower (p < .05) than that of pigs fed Diet I. There were no differences (p > 0.10) among the three dietary treatments in plasma concentrations of total protein, triglycerides, and glucose. These findings indicated that the plasma metabolite profile can be affected by changing dietary lysine content only. Thorough understanding how the plasma metabolite profile is alternated by dietary lysine will facilitate nutrient management for more sustainable swine production.     

日粮蛋白质与赖氨酸水平对断奶仔猪益生素添加效果的影响

为探讨不同日粮养分浓度对益生素添加效果的影响 ,将 4 8头 2 8日龄断奶仔猪随机均分 4组 ,以常规日粮为对照组 ,经 2 8d试验 ,结果发现 :益生素 (0 .1% )在常规日粮中添加 ,能提高断奶仔猪 9.0 3%的增重速度 (P<0 .0 5 )和 6 .3%的饲料转化率 ;而在低蛋白质日粮 (低赖氨酸水平和理想赖氨酸水平 )中的添加 ,能比对照组分别提高 16 .4 3%和 17.97%的增重速度(P<0 .0 1) ,以及 11.2 %和 11.7%的饲料转化率 ,腹泻率也比对照组有明显降低。     

Effect of dietary concentration of metabolizable lysine on finishing cattle performance

A finishing trial and a metabolism trial were conducted to determine the effect of supplemental metabolizable Lys level on finishing calf performance and to estimate the metabolizable Lys requirement of finishing calves. The finishing trial included 60 individually fed crossbred beef steer calves (237 kg; SD = 20 kg) supplemented with either incremental amounts of rumen-protected Lys and Met, or Met alone. Addition of Lys and Met improved gains and efficiencies (quadratic; P < .02) during the first 56 d. There was no response to supplemental Met alone, suggesting that supplemental Lys rather than Met was responsible for the improvement in performance. Using nonlinear analyses to compare gain relative to supplemental Lys intake, maximum gain was determined to be 2.10 kg/d, or .27 kg/d above the zero Lys control, at a supplemental Lys intake of 2.56 g/d. Steers supplemented with 3 and 4 g of Lys had a weight advantage over the control steers of 16 kg at 56 d and 32 kg at the end of the 161-d trial. However, there were no statistical responses to Lys or Met during any periods after 56 d. During a separate metabolism trial, four steers fed the control finishing diet were slaughtered, and abomasal contents were collected for amino acid analyses. The predicted (Level 1 NRC, 1996) metabolizable protein flow to the abomasum for the control diet was 715 g/d, and the predicted Lys flow was 37.9 g/d. A supplemental Lys intake of 2.56 g/d would increase the Lys flow to 40.5 g/d. Feedlot diets low in ruminal escape protein may be deficient in metabolizable Lys, especially early in the feeding period. The metabolizable Lys requirement of steer calves gaining 2.10 kg/d is estimated to be 40.5 g/d.     

Effects of protein concentration on responses to dietary lysine by chicks

Chicks were fed on diets varying in crude protein (CP) content (140 to 280 g/kg diet) in either 8 steps, experiment 1, or 6 steps, experiment 2. Protein composition was held constant in each experiment. At each protein concentration, 5 (experiment 1) or 6 (experiment 2) concentrations of lysine were tested, ranging from 40 to 60 g/kg CP. Growth rate and efficiency of food utilisation to 21 d of age responded to increasing dietary protein contents up to about 230 g CP/kg. An estimate of lysine requirement at each protein concentration was obtained by fitting a quadratic curve to the response data and calculating the dose of lysine (g/kg CP) needed to maximise either growth rate or gain/food ratio. Although no growth response to dietary protein was obtained between 240 and 280 g CP/kg, the amount of lysine needed to maximise growth and gain/food ratio over this range increased systematically when expressed as g/kg diet, but remained constant if expressed as g/kg CP. The regression of lysine required (g/kg diet) for maximum performance (growth or food efficiency) on CP (g/kg diet) was strictly linear for both responses in both experiments throughout the entire range studied (140 g CP/kg to 280 g CP/kg). The estimated lysine requirement was 0.053 of the CP in experiment 1 and 0.055 of the CP in experiment 2. It is concluded that a fixed ratio of lysine to protein should be specified in practical diet formulation, rather than a minimum dietary concentration of lysine. This would ensure that, if the dietary protein content rises above a prescribed minimum value in least-cost formulation, an appropriate adjustment will automatically be made to the lysine content of the solution.     

Commercial validation of the true ileal digestible lysine requirement for eleven- to twenty-seven-kilogram pigs

Five experiments utilizing 3,628 pigs were conducted to determine the true ileal digestible (TID) Lys requirement for 11- to 27-kg pigs fed corn-soybean meal diets. In Exp. 1, 216 barrows (initial BW = 11.5 kg) were used, with dietary TID Lys levels from 1.05 to 1.40% TID Lys (0.07% increments). All diets were isocaloric (3.42 Mcal of ME) and contained the same inclusion of soybean meal (33.1%). Dietary Lys content was increased by adding graded levels of L-Lys.HCl (0.0 to 0.445%), with other crystalline AA supplied to meet minimum AA-to-Lys ratios. For the 21-d period, ADG and G:F increased linearly (P < 0.001) with increasing Lys levels. Experiments 2 through 5 were each conducted in different commercial research facilities. In Exp. 2, a 5-point titration (1.05 to 1.41% TID Lys; 0.09% increments) was used containing the same level of soybean meal (34.3%), with graded levels of L-Lys.HCl addition as in Exp. 1 for a 16-d period. Exp. 3 used similar diets, but was a 28-d period from 11.8 to 28 kg. There were linear increases in ADG (P < 0.01) and G:F (P < 0.01) with increasing dietary Lys in both experiments. On the basis of these results, 2 additional 28-d experiments were conducted with similar diets, except for 1 additional level at 1.50% TID Lys. In Exp. 4, linear increases (P < 0.01) in ADG and G:F were observed from d 0 to 14. From d 14 to 28, there were quadratic increases (P < 0.04) in ADG and G:F, which resulted in quadratic increases (P < 0.01) in ADG and G:F with increasing dietary Lys for the entire 28-d period. Similarly, in Exp. 5, there were linear increases (P < 0.01) in growth performance from d 0 to 14, but there were quadratic increases in G:F (P < 0.001) with increasing dietary Lys for the overall period. Data from all 5 experiments yielded a single-slope, broken-line response, with requirement estimates for TID Lys of 1.33 and 1.35% for 11- to 19-kg pigs. The 5 experiments gave requirement estimates of 1.30% TID Lys (3.80 g of TID Lys/Mcal of ME) for 11- to 27-kg pigs, equivalent to 19 g of TID Lys/kg of gain.     

基于协方差分析对20～40 kg生长猪真可消化赖氨酸需要量研究

试验选用35头体重为20kg左右的杜×(长×大)三元杂交阉公猪,采用完全随机单因子试验设计,随机分为5个处理,单栏饲喂,自由采食,试验期为35d。分别饲喂真可消化赖氨酸水平(TLys)为1.15%、1.05%、0.95%、0.85%和0.75%的等能(14.23MJ/kg)、等氨基酸模式的玉米-豆粕型日粮。基于协方差分析校正生长猪始重差异,通过测定不同TLys水平对生产性能的影响,确定真可消化赖氨酸需要量。结果表明,当TLys为0.95%时,平均日增重最高(P<0.01),料重比最低(P<0.05);经回归分析,TLys含量为0.95%时,平均日增重达到最大值,而料重比最低。上述结果提示,20～40kg生长猪的TLys需求量为0.95%。     

The effect of dietary lysine restriction during the grower phase and subsequent dietary lysine concentration during the realimentation phase on the performance, carcass characteristics and nitrogen balance of growing–finishing pigs

Two experiments (exp.) were conducted to determine the effect of dietary lysine restriction during the grower phase and subsequent dietary lysine concentration during realimentation on the performance, carcass characteristics and nitrogen (N) balance of growing–finishing pigs. Seventy-two pairs of crossbred [meatline sires × (Large White × Landrace) dams] pigs (36 pairs entire male, 36 pairs female) were used in a 2 × 4 factorial performance study (exp. 1, 35 to 96 kg). The two factors were Diet1 (two lysine levels: LO or HI, day (d) 0 to 35) and Diet2 (four lysine levels: LO, M1, M2 and HI, d36 to slaughter). A further 30 boars were used in a 2 × 3 factorial N-balance study (exp. 2, 31 to 42 kg; Diet1: LO or HI; Diet2: LO, M3 and HI). The crude protein (CP) and lysine contents of the five isoenergetic (14.0 MJ DE/kg) diets were: LO (139 g/kg CP, 8.1 g lysine/kg), M1 (162 g/kg CP, 9.7 g lysine/kg), M2 (190 g/kg CP, 11.4 g lysine/kg), M3 (180 g/kg CP, 10.7 g lysine/kg) and HI (217 g/kg CP, 13.1 g lysine/kg). Diets were based on barley, wheat and soyabean meal with added vitamins, minerals and amino acids. Ratios of amino acids relative to lysine were similar for all diets. From d0 to 35 in exp. 1, pigs fed LO had lower daily gains (ADG: 785 vs. 939 g/day; P < 0.001), daily lysine intakes (DLYIN: 14.4 vs. 22.6 g/day; P < 0.001) and poorer feed conversion ratios (FCR: 2.28 vs. 1.84 kg/kg; P < 0.001) than pigs fed HI. From d36 to slaughter, pigs initially fed LO had higher ADG than those initially fed HI (948 vs. 879 g/day; P < 0.01). However, from d0 to slaughter, pigs initially fed LO had lower ADG (868 g/day; P < 0.01) and DLYIN (19.1 g/day; P < 0.001) than those fed HI (913 g/day and 23.3 g/day respectively). There was a Diet1 × Diet2 interaction for FCR from d36 to slaughter and d0 to slaughter (P < 0.05). FCR of pigs previously fed LO improved with each increase in dietary lysine concentration up to 13.1 g/kg (HI), but improvement was only evident for lysine concentrations up to 11.4 g/kg (M2) for pigs previously fed HI. In exp. 2, Diet1 was fed for an initial 5-day collection period (after adjustment to crate; C1). Diet2 was then fed and immediately there were 2 successive 5-day collection periods (C2 and C3). A Diet1 × Time interaction (P < 0.001) indicated that although N retention (NRET) during C1 was lower for pigs fed LO, there was no difference during C2 and C3 in NRET of pigs initially fed either LO or HI (14.5 vs. 25.0 g/day; 23.2 vs. 23.0 g/day; 26.0 vs. 26.6 g/day, for C1, C2 and C3, respectively). However, a similar interaction indicates that although N excretion (NEX) was 23% lower for LO compared with HI pigs during C1, there was no residual reduction in NEX of pigs initially fed LO (P < 0.01: 8.9 vs. 11.6 g/day; 12.3 vs. 12.7 g/day; 13.8 vs. 14.0 g/day, for C1, C2 and C3, respectively). Exp. 1 indicated improved performance and an ability to respond positively to higher lysine concentrations during realimentation for previously restricted compared with unrestricted pigs, however, overall performance was reduced. However, exp. 2 indicated that although NRET of initially restricted pigs increased during realimentation, it did not surpass that of unrestricted pigs. This apparent discrepancy may have been due to the time period of the N balance study.     

Development of a model to describe the compositional growth and dietary lysine requirements of pigs fed ractopamine

The objective of this research was to use recent ractopamine research data to develop an updated mathematical model to describe the daily compositional growth of pigs fed ractopamine. Mean increases of 18.2, 23.1, and 25.0% for daily protein accretion were assumed for 5, 10, and 20 ppm of ractopamine for an overall gain of 40 kg of BW gain during the feeding period. The relative effect of ractopamine described the rapid increase and subsequent decrease in the effect of ractopamine as a function of BW gain or days on test and ractopamine concentration (RC, ppm). The reduction in ME intake produced by ractopamine was described as 0.036 x (RC/20)(0.7) multiplied by the ME intake for the first 20 kg of BW gain, and then increasing to 0.078 x (RC/20)(0.7) at 40 kg of BW gain feeding period. The ratio of fat-free muscle gain to protein accretion increased by 14 to 16% with the feeding of ractopamine, depending on the dietary lysine/essential AA levels. The ratio of carcass fat gain to empty body lipid gain was increased when lysine and essential AA requirements were met. Daily protein accretion and fat-free lean growth were described as functions of dietary lysine/essential AA intakes. The percentage of lysine in protein accretion increased with the feeding of ractopamine from 6.80 to 7.15%, depending on ractopamine concentration. Equations predicting carcass measurements, such as fat and longissimus muscle depths from carcass weight and composition, were modified to incorporate prediction biases produced by ractopamine. For the four concentrations of ractopamine (0, 5, 10, and 20 ppm, respectively) during a 78 to 110 kg of BW feeding period, the model predicted performance levels for ADG (1.03, 1.15, 1.16, and 1.16 kg/d), gain:feed (kg of ADG/kg of ADFI; 0.360, 0.401, 0.412, and 0.425), dressing percentage (75.1, 76.0, 76.3, and 76.4), percentage fat-free lean (48.7, 51.0, 51.5, and 52.2), longissimus muscle area (38.8,41.8,42.5, and 43.5 cm2), 10th-rib fat depth (22.1, 19.8, 19.3, and 18.7 mm), and fat-free lean gain (321, 446, 467, and 495 g/d), comparable to recent research data. The model allows the effect of ractopamine to be added to farm specific pig growth curves. It can be used to evaluate ways to optimize the use of ractopamine, including duration of ractopamine feeding, concentration of ractopamine, and dietary lysine concentration.     

Meta-analysis of the relationship between ractopamine and dietary lysine levels on carcass characteristics in pigs

A meta-analysis was carried out to evaluate the relationship between ractopamine and dietary lysine levels on carcass characteristics in pigs. The database was composed by 29 articles published in international journals from 1990 to 2007, totalizing 155 treatments and 3786 pigs. Average inclusion of ractopamine was 15.3 ppm (ranging from 0 to 30 ppm) and daily average intake of ractopamine was 24.9 mg. Ractopamine addition increased (P < 0.05) hot carcass weight in 4%, loin area in 12% and lean meat content in 4%. Pigs supplemented with ractopamine presented decrease (P < 0.05) of 8% in backfat thickness at the tenth rib, 3% in backfat thickness at the last rib and 5% in mean backfat thickness. Each increase in 1 mg of ractopamine intake represented a reduction of 0.3 mm in tenth-rib (Y = 29.61-0.308 RAC + 0.025 RAC², R² = 0.81, RAC: ractopamine intake expressed in mg) and 0.5 mm at last-rib backfat thickness (Y = 30.52 + 0.519 RAC-0.0054 RAC², R² = 0.94). The use of ractopamine affected (P > 0.05) neither carcass length and dressing, nor meat marbling and color. Loin area was positively correlated (r = 0.27, P < 0.05) and mean backfat thickness was negatively correlated (r = − 0.27, P < 0.05) to dietary lysine concentration. Pigs supplemented with ractopamine whose daily intake of lysine per unit of metabolic weight was more than 195 mg presented (P < 0.05) loin area 4% higher and backfat thickness 10% lower than other animals. Supplemented pigs that received diets with lysine content superior to their calculated amino acid requirement presented weight gain 14% higher, lean meat content 17% higher, leaf fat 34% lower and loin area 6% higher when compared to other supplemented animals. Ractopamine increases lean meat content and reduces backfat thickness in carcass, however, the interaction between additive and nutritional components must be considered in diet formulation.     

Effects of dietary lysine levels and lighting conditions on intramuscular fat accumulation in growing pigs

This study was conducted to test our hypothesis that intramuscular fat (IMF) accumulation increases in pigs fed on a low lysine diet during the dark period than those fed on the same diet during the light period. Using barrows aged 6 weeks, we monitored whether serum glucose and insulin levels were affected by light conditions. Two diets with different levels of lysine, 0.78% (LL diet) and 1.37% (control diet) were prepared. Eight pigs were fed on the diet during the light period, while the remaining pigs were fed during the dark period. The pigs were fed either the LL diet or the control diet. Although IMF contents of Longissimus dorsi (LD) muscle were higher in the pigs fed on a LL diet (p < .05), the light conditions had no effect. Low dietary lysine caused reduction in serum glucose levels (p < .05) and serum insulin levels (p = .0613). However, they were also unaffected by the lighting conditions. To gain further insights, we determined the messenger RNA levels of insulin receptor, insulin receptor substrate 1, acetyl CoA carboxylase, and fatty acid synthase in LD and Rhomboideus muscles and in the liver.     

Activity and requirement of selected amino acids in growing female pigs. 4. Combination of protein sources with lysine, methionine/cystine and threonine limitation

On the basis of the results of 3 previous articles on the efficiency of amino acids in single protein sources a total of 16 protein sources was tested maintaining the limitation relations of the combination partners with regard to the additivity of the efficiencies of lysine, methionine/cystine and threonine. The results of the N metabolism measurements with a total of 60 female pigs of the country breed type (30...55 kg live weight) allow the conclusion that additive relations and thus suitable correction possibilities exist for the gross amino acid content through the amino acid efficiency for the calculation of requirement and requirement meeting. The N utilization model used (GEBHARDT 1963) is in its further development confirmed as the basis of amino acid efficiency.