Prediction of net energy of feeds for broiler chickens.

Net energy (NE) enables the prediction of more accurate feed energy values by taking into account the heat increment which is approximately 25% of apparent metabolizable energy (AME) in poultry. Nevertheless, application of NE in poultry industry has not been practiced widely. To predict the NE values of broiler diets, 23 diets were prepared by using 13 major ingredients (wheat, corn, paddy rice, broken rice, cassava pellets, full-fat soybean, soybean meal, canola meal, animal protein, rice bran, wheat bran, palm kernel meal and palm kernel oil). The diets were formulated in order to meet the birds' requirements and get a wide range of chemical compositions (on DM basis; 33.6% to 55.3% for starch; 20.8% to 28.4% for CP, 2.7% to 10.6% for ether extract [EE] and 7.0% to 17.2% for NDF), with low correlations between these nutrients and low correlations between the inclusion levels of ingredients allowing for the calculation of robust prediction equations of energy values of diets or ingredients. These diets were fed to Ross 308 broilers raised in 12 open-circuit respiratory chambers from 18 to 23 d of age (4 birds per cage) and growth performance, diet AME content and heat production were measured, and dietary NE values were calculated. The trial was conducted on a weekly basis with 12 diets measured each week (1 per chamber), 1 of the 23 diets (reference diet) being measured each week. Each diet was tested at least 8 times. In total, 235 energy balance data values were available for the final calculations. Growth performance, AME (15.3 MJ/kg DM on average) and AME/GE (79.4% on average) values were as expected. The NE/AME value averaged 76.6% and was negatively influenced by CP and NDF and positively by EE in connection with efficiencies of AME provided by CP, EE and starch for NE of 73%, 87% and 81%, respectively. The best prediction equation was: NE = (0.815 × AME) - (0.026 × CP) + (0.020 × EE) - (0.024 × NDF) with NE and AME as MJ/kg DM, and CP, EE and NDF as % of DM. The NE prediction equations from this study agree with other recently reported equations in poultry and are suitable for both ingredients and complete feeds.

Re-evaluation of recent research on metabolic utilization of energy in poultry: Recommendations for a net energy system for broilers.

Different energy systems have been proposed for energy evaluation of feeds for domestic animals. The oldest and most commonly used systems take into account the fecal energy loss to obtain digestible energy (DE), and fecal, urinary and fermentation gases energy losses to calculate metabolizable energy (ME). In the case of ruminants and pigs, the net energy (NE) system, which takes into account the heat increment associated with the metabolic utilization of ME, has progressively replaced the DE and ME systems over the last 50 years. For poultry, apparent ME (AME) is used exclusively and NE is not yet used widely. The present paper considers some important methodological points for measuring NE in poultry feeds and summarizes the available knowledge on NE systems for poultry. NE prediction equations based on a common analysis of three recent studies representing a total of 50 complete and balanced diets fed to broilers are proposed; these equations including the AME content and easily available chemical indicators have been validated on another set of 30 diets. The equations are applicable to both ingredients and complete diets. They rely primarily on an accurate and reliable AME value which then represents the first limiting predictor of NE value. Our analysis indicates that NE would be a better predictor of broiler performance than AME and that the hierarchy between feeds is dependent on the energy system with a higher energy value for fat and a lower energy value for protein in an NE system. Practical considerations for implementing such an NE system from the commonly used AME or AMEn (AME adjusted for zero nitrogen balance) systems are presented. In conclusion, there is sufficient information to allow the implementation of the NE concept in order to improve the accuracy of feed formulation in poultry.

Corrigendum to "Methodologies for energy evaluation of pig and poultry feeds: A review" [Animal Nutrition volume 8 (2022), 185-203].

[This corrects the article DOI: 10.1016/j.aninu.2021.06.015.].

Methodologies for energy evaluation of pig and poultry feeds: A review.

The cost of feed represents an important part of the total cost in swine and poultry production (>60%) with energy accounting for at least 70% of feed cost. The energy value of ingredients or compound feeds can be estimated as digestible (DE), metabolisable (ME) and net energy (NE) in pigs and ME and NE in poultry. The current paper reviews the different methods for evaluating DE, ME and NE of feeds for monogastric animals and their difficulties and limits, with a focus on NE. In pigs and poultry, energy digestibility depends on the chemical characteristics of the feed, but also on technology (pelleting, for instance) and animal factors such as their health and body weight. The ME value includes the energy losses in urine that are directly dependent on the proportion of dietary N excreted in urine resulting in the concept of ME adjusted for a zero N balance (MEn) in poultry. For poultry, the concept of true ME (TME, TMEn), which excludes the endogenous fecal and urinary energy losses from the excreta energy, was also developed. The measurement of dietary NE is more complex, and NE values of a given feed depend on the animal and environmental factors and also measurement and calculation methods. The combination of NE values of diets obtained under standardised conditions allows calculating NE prediction equations that are applicable to both ingredients and compound feeds. The abundance of energy concepts, especially for poultry, and the numerous feed and animal factors of variation related to energy digestibility or ME utilisation for NE suggest that attention must be paid to the experimental conditions for evaluating DE, ME or NE content. This also suggests the necessity of standardisations, one of them being, as implemented in pigs, an adjustment of ME values in poultry for an N retention representative of modern production conditions (MEs). In conclusion, this review illustrates that, in addition to numerous technical difficulties for evaluating energy in pigs and poultry, the absolute energy values depend on feed and animal factors, the environment, and the methods and concepts. Finally, as implemented in pigs, the use of NE values should be the objective of a more reliable energy system for poultry feeds.

Postprandial insulin and nutrient concentrations in lipopolysaccharide-challenged growing pigs reared in thermoneutral and high ambient temperatures1.

The aim of this study was to evaluate the associated effects of ambient temperature and inflammation caused by repeated administration of Escherichia coli lipopolysaccharide (LPS) on insulin, energy, and AA metabolism. Twenty-eight pigs were assigned to one of the two thermal conditions: thermoneutral (24 °C) or high ambient temperature (30 °C). The experimental period lasted 17 d, which was divided into a 7-d period without LPS (days -7 to -1), and a subsequent 10-d LPS period (days 1 to 10) in which pigs were administered 5 repeated injections of LPS at 2-d intervals. Postprandial profiles of plasma insulin and nutrients were evaluated through serial blood samples taken on days -4 (P0), 4 (P1), and 8 (P2). Before the LPS-challenge (P0), postprandial concentrations of glucose, lactate, Gln, Ile, Leu, Phe, Tyr, and Val were greater in pigs kept at 24 °C than at 30 °C (P < 0.05). In contrast, Arg, Asp, Gly, His, and Met postprandial concentrations at P0 were lower at 24 °C than at 30 °C (P < 0.05). At both 24 and 30 °C conditions, pigs had greater postprandial concentrations of insulin (P < 0.01) and lower concentrations of NEFA (P < 0.01) and α-amino nitrogen (P < 0.05) at P1 and P2 than at P0. Compared with P0, postprandial concentrations of glucose were greater (P < 0.05) at P1 in pigs kept at 24 °C, and at P1 and P2 in pigs kept at 30 °C. At both ambient temperatures, pigs had lower (P < 0.05) postprandial concentrations of Ala, Gly, His, Ile, Leu, Pro, Ser, Thr, Trp, and Val at P1 and P2 than at P0. Arginine postprandial concentration at P1 was lower than at P0 in pigs kept at 24 °C (P < 0.05), whereas no difference was observed in pigs at 30 °C. Relative to P0, Gln and Tyr concentrations were lower at P1 and P2 in pigs kept at 24 °C (P < 0.01), whereas lower Gln concentration was observed only at P2 (P < 0.01) and lower Tyr only at P1 (P < 0.01) in pigs kept at 30 °C. Our study shows a hyperglycemic and hyperinsulinemic state in LPS-challenged pigs and a greater magnitude of this response in pigs kept at 30 °C. Furthermore, LPS caused important changes in BCAA, His, Thr, and Trp profiles, suggesting the role these AA in supporting the inflammatory response. Finally, our results suggest that LPS-induced effects on postprandial profiles of specific AA (Arg, Gln, Phe, and Tyr) may be modulated by ambient temperature.

Metabolizable energy of corn, soybean meal and wheat for laying hens.

Feed formulation using apparent metabolizable energy (AME) corrected to zero nitrogen retention (AMEn) is widely used by poultry nutritionists. Most available tabulated data are from experiments using adult cockerels or growing broilers. Specific values are rarely available for laying hens. A study was conducted to evaluate AME, AMEn, and AMEs (AME adjusted to 50% nitrogen retention) of corn, soybean meal (SBM) and wheat in laying hens using the reference diet substitution and regression methods. Forty eight 42-wk-old Hy-Line Brown hens were used, 2 birds per cage with six replicates per diet. Test diets contained 30% test ingredient (as is basis) and 65.7% reference diet (as is basis) with limestone, other minerals, vitamins, and amino acids held constant across the reference and test diets. Using the reference diet substitution method, AME values obtained for corn, SBM, and wheat were 3,791, 2,621, and 3,565 kcal/kg (DM), respectively. The corresponding AMEn values were 3,722, 2,496, and 3,479 kcal/kg (DM), and AMEs were 3,784, 2,835, and 3,562 kcal/kg (DM), respectively. Calculation of AME, AMEn, and AMEs of ingredients using regression based on the inclusion rate (DM) of dietary ingredients and reference diet gave identical values to those obtained by the reference diet substitution method. In addition, the measured AMEn values of ingredients using laying hens in this study were close to those calculated from proximate composition using the European Union prediction equation based on adult cockerels.

Net energy prediction and energy efficiency of feed for broiler chickens.

Global consumption of chicken meat has increased at a faster rate than any other animal protein source, and thus refinements in energy formulation techniques for feed have continued to gain importance. Formulation of animal feed based on net energy (NE) has been implemented in ruminants and pigs but not in poultry. A closed-circuit respiratory calorimetry system was employed on 25- to 28-day-old broilers fed 19 diets formulated with varying nutrient composition to produce equations to predict NE and apparent metabolizable energy (AME) efficiency of feed for broiler chickens. Performance, energy and N balance, respiratory quotient, and energy utilization were measured in the birds. Linear regression analysis was performed to generate prediction equations for dietary energy content and AME efficiency. The NE content was positively related to AME and ether extract, but negatively to crude protein. The study generated equations that can accurately predict NE, and NE/AME using AME value and chemical composition of feeds. The NE prediction equations were further validated on a separate set of diets with high correlation (r = 0.99) and accuracy. The outcomes are an important step for the broiler industry to adapt to an NE system in place of AME systems for the formulation of broiler chicken feeds following robust validation experiments.

Net energy content of rice bran, corn germ meal, corn gluten feed, peanut meal, and sunflower meal in growing pigs.

OBJECTIVE: The objective of this experiment was to determine the net energy (NE) content of full-fat rice bran (FFRB), corn germ meal (CGM), corn gluten feed (CGF), solvent-extracted peanut meal (PNM), and dehulled sunflower meal (SFM) fed to growing pigs using indirect calorimetry or published prediction equations. METHODS: Twelve growing barrows with an average initial body weight (BW) of 32.4±3.3 kg were allotted to a replicated 3×6 Youden square design with 3 successive periods and 6 diets. During each period, pigs were individually housed in metabolism crates for 16 d, which included 7 days for adaptation. On d 8, the pigs were transferred to the respiration chambers and fed one of the 6 diets at 2.0 MJ metabolizable energy (ME)/kg BW0.6/d. Total feces and urine were collected and daily heat production was measured from d 9 to d 13. On d 14 and d15, pigs were fed at their maintenance energy requirement level. On the last day pigs were fasted and fasting heat production was measured. RESULTS: The NE of FFRB, CGM, CGF, PNM, and SFM measured by indirect calorimetry method was 12.33, 8.75, 7.51, 10.79, and 6.49 MJ/kg dry matter (DM), respectively. The NE/ME ratios ranged from 67.2% (SFM) to 78.5% (CGF). The NE values for the 5 ingredients calculated according to the prediction equations were 12.22, 8.55, 6.79, 10.51, and 6.17 MJ/kg DM, respectively. CONCLUSION: The NE values were the highest for FFRB and PNM and the lowest in the corn co-products and SFM. The average NE of the 5 ingredients measured by indirect calorimetry method in the current study was greater than values predicted from NE prediction equations (0.32 MJ/kg DM).

Net energy of corn, soybean meal and rapeseed meal in growing pigs.

BACKGROUND: Two experiments were conducted to estimate the net energy (NE) of corn, soybean meal, expeller-pressed rapeseed meal (EP-RSM) and solvent-extracted rapeseed meal (SE-RSM) using indirect calorimetry and to validate the NE of these four ingredients using pig growth performance. METHODS: In Exp.1, 24 barrows (initial BW = 36.4 ± 1.6 kg) were allotted to 1 of 4 diets which included a corn basal diet, a corn-soybean meal basal diet and two rapeseed meal diets containing 20% EP-RSM (9.5% ether extract) or SE-RSM (1.1% ether extract) substituted for corn and soybean meal. The design allowed the calculation of NE values of corn, soybean meal and rapeseed meals according to the difference method. In Exp.2, 175 growing pigs (initial BW = 36.0 ± 5.2 kg) were fed 1 of 5 diets for 28 d, with five pigs per pen and seven replications (pens) per treatment in order to validate the measured energy values. Diets were a corn-soybean meal diet and four diets including 10% or 20% EP-RSM and 10% or 20% SE-RSM. RESULTS: The NE of corn, soybean meal, EP-RSM and SE-RSM were 12.46, 11.34, 11.71 and 8.83 MJ/kg DM, respectively. The NE to ME ratio of corn (78%) was similar to tabular values, however, the NE to ME ratios of soybean meal (70%) and rapeseed meal (76%) were greater than tabular values. The greater NE value in EP-RSM than in SE-RSM is consistent with its higher EE content. Increasing EP-RSM or SE-RSM did not affect the growth performance of pigs and the caloric efficiency of NE was comparable for all diets. CONCLUSIONS: The NE of EP-RSM was similar to soybean meal, and both were greater than SE-RSM. The DE, ME and NE values measured in Exp.1 are confirmed by results of Exp. 2 with comparable caloric efficiencies of DE, ME or NE for all diets.

High ambient temperature alleviates the inflammatory response and growth depression in pigs challenged with Escherichia coli lipopolysaccharide.

Pig production has increased in hot climate countries over recent years, but the effect of exposure to high temperatures on the health status of farm animals has not been investigated thoroughly. It is not clear how the ambient temperature (Ta) might influence responses to inflammatory challenge in pigs. The aim of the present study was to evaluate the effects of high Ta on performance and physiological parameters of growing pigs, subjected to repeated administration of Escherichia coli lipopolysaccharide (LPS). Thirty-seven pigs, each fitted with a jugular catheter, were assigned to one of two Ta conditions: thermo-neutral (TN, 24 °C) or high (HT, 30 °C). After a 14-day adaptation period, and a 7-day measurement period, pigs were administered five repeated injections of LPS at 48 h intervals. Irrespective of Ta, the LPS challenge reduced feed consumption and increased plasma pro-inflammatory cytokines, haptoglobin and cortisol. However, the extent of these responses was greater in pigs at TN than HT. In both groups, plasma thyroxine and triiodothyronine concentrations decreased, following the first LPS injection and thereafter returned to baseline, which occurred faster at HT than at TN. Moreover, the LPS challenge decreased growth and feed efficiency in pigs kept at TN, which was not observed in pigs kept at HT. The results suggest a greater capacity of pigs to limit the physiological and metabolic disturbances caused by inflammatory challenge, when kept at HT, compared to TN.

Thermoregulatory responses during thermal acclimation in pigs divergently selected for residual feed intake.

The objective of this study was to evaluate the performance and thermoregulatory responses during acclimation to high ambient temperature (Ta) of pigs from two lines selected for high (RFI(+)) or low (RFI(-)) residual feed intake with the hypothesis that RFI(-) pigs producing less heat would better tolerate high Ta. Pigs (50 kg initial body weight; 17 per line among which 10 of them were catheterized) were individually housed in a climatic-controlled room where Ta was maintained at 24.2 ± 0.4 °C during 7 days and thereafter at 30.4 ± 0.7 °C during 14 days. Irrespective of Ta, RFI(-) pigs had lower feed intake (ADFI) and similar average daily gain (ADG) than RFI(+) pigs. Whatever the line, ADFI, ADG, and feed efficiency decreased with increased Ta. Overall, the Ta increase resulted in an increase in rectal temperature (RT), skin temperature (ST), and respiratory rate (RR) within the first 24-48 h and, subsequently, in a decrease followed by stabilization. The RT decrease during acclimation occurred 24 h earlier in RFI(-) pigs than in RFI(+). Thyroid hormones and cortisol decreased at high Ta and it was similar in both lines. Based on performance and RT, ST, and RR responses, it seems that selection for low RFI tends to ameliorate pigs' tolerance to high Ta. Nevertheless, this selection does not induce significant differences between lines in endocrine and metabolite responses during thermal stress.

Partitioning of heat production in growing pigs as a tool to improve the determination of efficiency of energy utilization.

In growing pigs, the feed cost accounts for more than 60% of total production costs. The determination of efficiency of energy utilization through calorimetry measurements is of importance to sustain suitable feeding practice. The objective of this paper is to describe a methodology to correct daily heat production (HP) obtained from measurements in respiration chamber for the difference in energy expenditure related to physical activity between animals. The calculation is based on a preliminary published approach for partitioning HP between HP due to physical activity (AHP), thermic effect of feeding (TEF) and basal metabolic rate (fasting HP; FHP). Measurements with male growing pigs [mean body weight (BW): 115 kg] which were surgically castrated (SC), castrated through immunization against GnRH (IC), or kept as entire male (EM) were used as an example. Animals were fed the same diet ad-libitum and were housed individually in two 12-m(3) open-circuit respiration chambers during 6 days when fed ad-libitum and one supplementary day when fasted. Physical activity was recorded through interruption of an infrared beam to detect standing and lying positions and with force transducers that recorded the mechanical force the animal exerted on the floor of the cage. Corrected AHP (AHPc), TEF (TEFc), and HP (HPc) were calculated to standardize the level of AHP between animals, assuming that the ratio between AHPc and ME intake should be constant. Inefficiency of energy utilization (sum of AHPc and TEFc) was lower than the inefficiency estimated from the slope of the classical relationship between HPc and ME intake but was associated with higher requirements for maintenance. Results indicate that EM pigs had higher FHP but lower TEFc than IC and SC pigs. These results agree with the higher contents in viscera of EM pigs that stimulate their basal metabolic rate and with the reduced utilization of dietary protein to provide energy for maintenance energy requirements and fat deposition (FD).

Maintenance energy requirements of growing pigs and calves are influenced by feeding level.

The conventional regression method for partitioning heat production (HP) in growing animals between HP associated with either maintenance or growth assumes maintenance HP to be independent of feeding level (FL). However, there are indications that this assumption is not correct and an alternative method is proposed in this study from a reanalysis of 3 trials. In trial 1, 73-, 152-, and 237-kg calves received one milk replacer at 77, 84, 92, and 100% of their ad libitum metabolizable energy (ME) intake. In trial 2, 70-kg barrows received one diet at 60, 80, and 100% of their ad libitum ME intake {2600 kJ ME/[kg body weight (BW)(0.60) · d]}. In trial 3, 60-kg barrows received a basal diet [1700 kJ ME/(kg BW(0.60) · d)] or 4 diets consisting of the basal diet plus 850 kJ ME/(kg BW(0.60)·d) of starch alone or starch with corn gluten, casein, or vegetable oil. In the 3 trials (n = 48, 18, and 28, respectively), HP and activity-related HP were measured on individuals pigs and calves in respiration chambers for 6 d (fed state) and fasting HP (FHP; at zero activity) was calculated as the asymptotic value of HP kinetics on d 7 (feed-deprived state). The FHP changed by 0.22 kJ in calves and 0.14 kJ in pigs/kJ ME intake change during the previous days. The efficiency of using ME for maintenance and growth [k(mg); 1- (HP - FHP)/ME] was not affected by FL (calves: 84%, pigs in trial 2: 74%). In trial 3, k(mg) varied between diets in connection with variations in efficiencies between nutrients (from 55% for corn gluten to 85% for lipid). This new method of representing partitioning of ME intake considers FHP as variable with FL, does not require estimates of maintenance ME requirements, includes efficiencies that depend on diet characteristics, and is not biased by metabolic adaptations of the animal to FL.

Fasting heat production and energy cost of standing activity in veal calves.

Metabolic body size of veal calves is still calculated by using the 0.75 exponent and no data were available to determine energy cost of physical activity during the whole fattening period. Data from two trials focusing on protein and/or energy requirements were used to determine the coefficient of metabolic body size and the energy cost of standing activity in male Prim'Holstein calves. Total heat production was measured by indirect calorimetry in ninety-five calves weighing 60-265 kg and was divided using a modelling approach between components related to the BMR, physical activity and feed intake. The calculation of the energy cost of standing activity was based on quantifying the physical activity by using force sensors on which the metabolism cage was placed and on the interruption of an IR beam allowing the determination of standing or lying position of the calf. The best exponent relating zero activity fasting heat production (FHP 0) to metabolic body size was 0.85, which differed significantly from the traditionally used 0.75. Per additional kJ metabolizable energy (ME) intake, FHP 0 increased by 0.28 kJ; at a conventional daily 650 kJ/kg body weight (BW)0.85 ME intake, daily FHP 0 averaged 310 kJ/kg BW 0.85. Calves stood up sixteen times per day; total duration of standing increased from 5.1 to 6.4 h per day as animals became older. The hourly energy cost of standing activity was proportional to BW 0.65 and was estimated as 12.4 kJ/kg BW 0.65. These estimates allow for a better estimation of the maintenance energy requirements in veal calves.

Digesta transit in different segments of the gastrointestinal tract of pigs as affected by insoluble fibre supplied by wheat bran.

Digestibility is the result of two competing processes: digestion and digesta transit. To develop or parameterise mechanistic models of digestion, both processes have to be quantified. The aim of this study was to determine the effect of insoluble dietary fibre on the transit in the gastrointestinal tract of pigs. Six barrows (33 kg initial body weight and fitted with two simple T-cannulas at the proximal duodenum and distal ileum) were used in a double 3 x 3 Latin square design. Pigs were offered diets differing in total dietary fibre content (170, 220 and 270 g/kg DM) at 4 h intervals. A single meal marked with YbO2 and Cr-EDTA was used to determine the kinetics of markers concentrations of the solid and liquid phases, respectively. The mean retention time (MRT), calculated by the method of the moments, averaged 1, 4 and 38 h in the stomach, small intestine and large intestine, respectively. Increasing the insoluble fibre content in the diet had no effect on MRT in the stomach and decreased the MRT of both phases in the small intestine (P < 0.05). In the large intestine, increasing the insoluble fibre content decreased the MRT of the liquid phase (P = 0.02) and tended to decrease the MRT of the solid phase (P = 0.06). Transit of the solid phase in the large intestine was 4-8 h slower than transit of the liquid phase. Analysis of marker excretion curves indicated that the small and large intestine should be represented mathematically to have both a tubular (propulsion) and compartmental (mixing) structure.

Evaluation of energy systems in determining the energy cost of gain of growing-finishing pigs fed diets containing different levels of dietary fat.

Two experiments were conducted to evaluate the impact of different energy systems in predicting the energy cost of gain of growing-finishing pigs fed diets containing different levels of dietary fat. The diets in both experiments were based on wheat, corn and soybean meal and supplemented with 0, 1.75, 3.50 and 5.25% tallow. In Experiment 1, 24 crossbred barrows (Duroc x Landrace x Yorkshire) were randomly allocated to one of the four dietary treatments to determine the digestible (DE) and metabolizable (ME) energy content of the diets and net energy (NE) was calculated from DE and ME values. In Experiment 2, 96 crossbred barrows (Duroc x Landrace x Yorkshire) were used to evaluate the effectiveness of the energy systems in predicting the energy cost of gain for growing-finishing pigs fed ad libitum. There were six pens per treatment and four pigs per pen. The results obtained in trial 1 were used for calculating the energy cost of gain in trial 2. During the growing period, there was a linear decrease (p < 0.05) in the DE and ME cost of gain, while the NE cost of gain was not influenced by level of fat. During the finishing period, neither DE, ME or NE cost of gain were influenced by the dietary fat level. For the total experiment, the DE and ME cost of gain decreased (linear effect; p = 0.001), but there was no significant decrease in the NE cost of gain. It is concluded that the NE system can predict the performance of growing-finishing pigs more precisely for diets differing in fat content than can the DE and ME systems.

Deposition of dietary fatty acids, de novo synthesis and anatomical partitioning of fatty acids in finishing pigs.

Predicting aspects of pork quality becomes increasingly important from both a nutritional and technological point of view. The aim of the present study was to provide quantitative information on the relation between nutrient intake and whole-body fatty acid (FA) depositions. This information is essential to develop mechanistic models predicting the FA content of tissues. A serial slaughter study was carried out in which thirty pigs were slaughtered between 90 and 150 kg. The diet included 15 g/kg soyabean oil and contained 44 g/kg fat. Only 0.31 and 0.40 of the digested n-6 and n-3 FA were deposited, respectively. Approximately one-third of the n-3 supply that was deposited resulted from the conversion of 18:3 to other metabolites (i.e. EPA, docosapentaenoic acid and DHA). This proportion was affected by the pig genotype. De novo-synthesised FA represented 0.86 of the total non-essential FA deposition, and its average composition corresponded to 0.017, 0.286, 0.025, 0.217 and 0.454 for 14:0, 16:0, 16:1, 18:0 and 18:1, respectively. Although the average whole-body FA composition was relatively constant during the finishing period, this was not so for the tissues. In the carcass (without backfat), the content of 18:1 increased during the finishing period, whereas that of 16:0 and 18:0 decreased. Backfat captured a proportionally greater fraction of 18:2 than did the carcass of the residual tissues. In contrast, a proportionally greater fraction of the dietary 18:3 supply was deposited in the carcass compared to other tissues.

Previous feeding level influences plateau heat production following a 24 h fast in growing pigs.

Factorial approaches to estimate energy requirements of growing pigs require estimation of maintenance energy requirements. Heat production (HP) during fasting (FHP) may provide an estimate of maintenance energy requirements. Six barrows were used to determine effects of feeding level on components of HP, including extrapolated plateau HP following a 24 h fast (FHPp). Based on a cross-over design, each pig was exposed to three feeding levels (1.55, 2.05 and 2.54 MJ metabolisable energy/kg body weight (BW)(0.60) per d) between 30 and 90 kg BW. Following a 14 d adaptation period, HP was estimated using indirect calorimetry on pigs housed individually. Dynamics of HP were recorded in pigs for 5 d during the fed state and during a subsequent 24 h fast. Metabolisable energy intake was partitioned between thermal effect of feeding (HPf), activity HP (HPa), FHPp and energy retention. Feeding level influenced (P<0.05) total HP during the fed state, HPf and activity-free FHPp (609, 644 and 729 (SE 31) kJ/kg BW(0.60) per d for low, medium and high ME intakes, respectively). The value of FHPp when expressed per kg BW(0.60) did not differ (P=0.34) between the three subsequent experimental periods. Feeding level did not (P=0.75) influence HPa. Regression of total HP during the fed state to zero metabolisable energy intake yielded a value of 489 (SE 69) kJ/kg BW(0.60) per d, which is a lower estimate of maintenance energy requirement than FHPp. Duration of adaptation of pigs to changes in feeding level and calculation methods should be considered when measuring or estimating FHPp, maintenance energy requirements and diet net energy content.

Deposition of dietary fatty acids and of de novo synthesised fatty acids in growing pigs: effects of high ambient temperature and feeding restriction.

Predicting aspects of pork quality becomes increasingly important from both a nutritional and a technological point of view. Little information is, however, available concerning the quantitative relation between nutrient intake and fatty acid (FA) deposition at the whole-animal level. In this study, eight blocks of five littermate barrows were used in a comparative slaughter trial. At 24 kg body weight (BW), one pig from each litter was slaughtered to determine the initial FA composition. The other littermates were assigned to one of four feeding levels (ranging from 70 % to 100 % of intake ad libitum) and were given a diet containing 0.36 g/kg lipid and 0.22 g/kg FA. The temperature for each block was maintained at either 23 or 30 degrees C. At 65 kg, the pigs were slaughtered and the body lipid and FA composition was determined. Seventy per cent of the digested n-6 FA and 50 % of the n-3 FA were deposited. The average composition of de novo synthesised FA corresponded to 1.7, 30.3, 2.4, 19.7 and 45.9 % for 14 : 0, 16 : 0, 16 : 1, 18 : 0 and 18 : 1 FA, respectively. At 23 degrees C and for feeding ad libitum, 33 % of 16 : 0 FA was deposited, 1.7 % shortened to 14 : 0, 63 % elongated to 18 : 0 and 2.8 % unsaturated to 16 : 1. Twenty-eight per cent of 18 : 0 FA was deposited and 72 % unsaturated to 18 : 1. At 30 degrees C, 18 : 0 FA desaturation was reduced by 3.5 %. Feed intake and temperature independently affected the elongation of 16 : 0 FA. A reduction in feed intake increased the elongation rate, whereas the increase in temperature reduced the elongation rate.