Jaap van Milgen

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.

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.

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.

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.

A nutritional model of fatty acid composition in the growing-finishing pig

A dynamic model was developed to study the effects of diet composition on lipid deposition and fatty acid (FA) composition in pigs. A basic model of protein and lipid deposition was used. Deposited lipids originate from dietary FA and de novo synthesized FA. It is hypothesised that 0.85 of absorbed FA are deposited as-is, and that the composition of de novo synthesized FA was constant throughout growth. Sensitivity analysis indicated that feed intake, efficacy of dietary FA storage and partitioning of de novo synthesized FA had a major impact on FA composition. Evaluation of the model indicated that predictions of protein, lipid, and backfat mass were insufficient, mainly due to the assumption of a constant ratio of lipid to protein mass in the basic growth model. Nevertheless, predictions of the FA composition of backfat and perinephric tissue were reasonable. Differences in FA composition between different tissues could only partly be explained by differences in tissue development. Development of this conceptually simple model was hampered by the limited availability of experimental data on the contribution of dietary lipids to purposes other than lipid deposition, the composition of de novo synthesized FA and the partitioning of FA between different depot sites.

Models based on variable fractional digestion rates to describe ruminal in situ digestion

Using a first-order model to describe ruminal in situ digestion implies that the rate of digestion is affected only by the quantity of potentially digestible substrate remaining. Other factors, like the microbial efficacy for digesting substrate, are assumed to be constant. However, microbes are not only the cause but also the result of digestion, being one of the digestion end-products. Two sigmoidal models (a logistic and a Gompertz-like model) were derived from a general digestion function in which the rate of digestion equals the product of the quantity of potentially digestible substrate remaining and a non-constant fractional rate of digestion (microbial efficacy function). The models were compared with a first-order model with a discrete lag time. The logistic model specifically accounted for the conversion of substrate mass to microbial mass, but did not describe microbial migration between the substrate and the ruminal fluid. In contrast, the Gompertz-like model assumed that the change in microbial efficacy was only time-dependent. There was little difference between models in estimates of scale parameters, but the asymptotic microbial efficacy was consistently higher for the logistic model than for the other models. Estimates of discrete lag time in the first-order model were biased towards obtaining values identical to the independent variable. Scale estimators appeared to be more robust than kinetic estimators. Lack-of-fit was present for most model-data set combinations. The similar patterns of residuals between models suggested that a four-parameter model may be insufficient to describe the data. It was concluded that if a four-parameter model is to be used, the model with a discrete lag time would be the least biologically appropriate.

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.

A Methionine Deficient Diet Enhances Adipose Tissue Lipid Metabolism and Alters Anti-Oxidant Pathways in Young Growing Pigs.

Methionine is a rate-limiting amino-acid for protein synthesis but non-proteinogenic roles on lipid metabolism and oxidative stress have been demonstrated. Contrary to rodents where a dietary methionine deficiency led to a lower adiposity, an increased lipid accretion rate has been reported in growing pigs fed a methionine deficient diet. This study aimed to clarify the effects of a dietary methionine deficiency on different aspects of tissue lipid metabolism and anti-oxidant pathways in young pigs. Post-weaned pigs (9.8 kg initial body weight) were restrictively-fed diets providing either an adequate (CTRL) or a deficient methionine supply (MD) during 10 days (n=6 per group). At the end of the feeding trial, pigs fed the MD diet had higher lipid content in subcutaneous adipose tissue. Expression levels of genes involved in glucose uptake, lipogenesis but also lipolysis, and activities of NADPH enzyme suppliers were generally higher in subcutaneous and perirenal adipose tissues of MD pigs, suggesting an increased lipid turnover in those pigs. Activities of the anti-oxidant enzymes superoxide dismutase, catalase and glutathione reductase were increased in adipose tissues and muscle of MD pigs. Expression level and activity of the glutathione peroxidase were also higher in liver of MD pigs, but hepatic contents in the reduced and oxidized forms of glutathione and glutathione reductase activity were lower compared with control pigs. In plasma, superoxide dismutase activity was higher but total anti-oxidant power was lower in MD pigs. These results show that a dietary methionine deficiency resulted in increased levels of lipogenesis and lipolytic indicators in porcine adipose tissues. Decreased glutathione content in the liver and coordinated increase of enzymatic antioxidant activities in adipose tissues altered the cellular redox status of young pigs fed a methionine-deficient diet. These findings illustrate that a rapidly growing animal differently adapts tissue metabolisms when facing an insufficient methionine supply.

Oxidation of Dietary Stearic, Oleic and Linoleic Acids in Growing Pigs Follows a Biphasic Pattern

We used the pig as a model to assess the effects of dietary fat content and composition on nutrient oxidation and energy partitioning in positive energy balance. Pigs weighing 25 kg were assigned to either: 1) a low fat-high starch diet, or 2) a high saturated-fat diet, or 3) a high unsaturated-fat diet. In the high-fat treatments, 20% starch was iso-energetically replaced by 10.8% lard or 10.2% soybean oil, respectively. For 7 d, pigs were fed twice daily at a rate of 1200 kJ digestible energy · kg(-0.75) · d(-1). Oral bolus doses of [U-(13)C] glucose, [U-(13)C] α-linoleate, [U-(13)C] stearate, and [U-(13)C] oleate were administered on d 1, 2, 4, and 6, respectively, and (13)CO(2) production was measured. Protein and fat deposition were measured for 7 d. Fractional oxidation of fatty acids from the low-fat diet was lower than from the high-fat diets. Within diets, the saturated [U-(13)C] stearate was oxidized less than the unsaturated [U-(13)C] oleate and [U-(13)C] linoleate. For the high unsaturated-fat diet, oxidation of [U-(13)C] oleate was higher than that of [U-(13)C] linoleate. In general, recovery of (13)CO(2) from labeled fatty acids rose within 2 h after ingestion but peaked around the next meal. This peak was induced by an increased energy expenditure that was likely related to increased eating activity. In conclusion, oxidation of dietary fatty acids in growing pigs depends on the inclusion level and composition of dietary fat. Moreover, our data suggest that the most recently ingested fatty acids are preferred substrates for oxidation when the direct supply of dietary nutrients has decreased and ATP requirements increase.

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-m3 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).