Digestible (DE), metabolizable (ME), and net (NE) energy values of 61 diets were measured in 45-kg growing Large White boars. Net energy was calculated as energy retained at an average ME intake equivalent to 540 kcal/kg BW.60 plus fasting heat production estimated from data of the present experiment as 179 kcal/kg BW.60. Retained energy was measured as the difference between ME intake and heat production obtained in respiration chambers. The amounts of DE digested before the end of the ileum (DEi) and in the hindgut (DEh) were also measured for each diet. Regression equations for predicting dietary NE content from digestible nutrient levels or from DE or ME and chemical characteristics or from chemical composition only were calculated. Efficiencies of utilization of ME for NE (k, %) were also obtained. The mean k value for the 61 diets was 74% (range: 69 to 77). Digestible nutrients were used differently for NE: k values varied from approximately 60% for digestible CP or digestible cell wall fractions to 82% for starch and 90% for digestible ether extract. Accordingly, k for ME associated with DEh was lower than ME from DEi (58 vs 76%). Equations for predicting NE content are proposed. Their applicability, the comparison with other available NE prediction equations, and the effects of energy system on diet formulation are discussed.
An experiment was conducted in which the metabolic utilization of energy was measured in individually penned pigs from seven groups that differed in genotype and(or) sex and ranged in body weight between 20 and 107 kg. The animals were fed a diet containing, on a DM basis, 14.7 MJ ME and at least 21% CP. Heat production was measured in an open-circuit calorimeter, and energy, nitrogen, and fat balances were determined at regular intervals over the growing period; a total of 177 measurements were performed. Body composition of the animals was measured by serial slaughter, and these data were used for estimating the body composition of an animal at a given weight through allometric regression. A factorial analysis procedure was used to estimate the utilization of ME by regressing the ME intake on the observed protein and lipid deposition rates. The intercept of this equation is the maintenance energy requirement (MEm) and was represented either as a function of body weight with group-specific parameters (MEm = a(i) BWb) or as a function of the muscle and visceral mass with an additional additive group effect (MEm = aM muscle(b) + a(v) viscera(b) + G(i)). With BW as dependent variable, the exponent b was close to .60 and differed significantly from .75. The regression coefficient (a(i)) averaged 1.02 MJ ME/kg.60 but it was different for most groups, indicating that different groups of animals have different maintenance requirements. Fixing the exponent to .75 consistently underestimated the maintenance requirement. When the exponent b was not fixed to .75 but estimated, the partial efficiencies for protein and lipid deposition were .62 and .84, respectively. Body muscle and visceral mass could explain a large part of the variation in MEm. Viscera contributed three times more to MEm (per kilogram of mass raised to the .70 power) than did muscle. Even though the muscle mass exceeds to a large extent the visceral mass in animals, the contribution of muscle to MEm was lower than that of viscera for most groups.
Genetic selection on residual feed intake (RFI) can be used as an alternative method to G:F to improve feed efficiency in pigs. The objective of this study was to determine the effects of selection for RFI on digestive and metabolic utilization of energy in 2 lines of purebred French Large White castrated male pigs obtained from a divergent selection experiment over 6 generations. The RFI(+) (high RFI) line consumed more feed than predicted from performance compared with the RFI(-) (low RFI) line. Digestibility of energy and nutrients, total heat production (HP), HP related to physical activity, and energy and N balance were measured in respiration chambers for a 6-d period in pigs offered feed ad libitum. Pigs remained in the chamber for an additional day and did not receive any feed to estimate the fasting HP and calculate the thermic effect of feeding. Five pairs of 2 littermates from the same farrowing batch were used in each line. Because 2 respiration chambers were available for the trial, pigs were measured regularly during the 25- to 95-kg growing period. Two pigs per chamber were used until pigs reached 45 kg of BW, and 1 pig per chamber was used thereafter. Individual feed intake and BW gain were measured continuously from weaning to the end of the trial. Pigs were fed 3 diets with decreasing CP contents during the 25 to 45 (period 1), 45 to 65 (period 2), and 65 to 95 (period 3) kg of BW periods. Average daily feed intake was greater in RFI(+) pigs than in RFI(-) pigs between 25 and 65 kg of BW (2,128 vs. 1,891 g/d; P < 0.01) and G:F was 8% greater in RFI(-) pigs compared with RFI(+) pigs (P < 0.01). There was no line effect on digestibility coefficients or N retention, irrespective of the experimental period studied. Nitrogen retention was 31.2, 28.7, and 20.8 g/d at periods 1, 2, and 3, respectively (P < 0.001). The HP was greater in RFI(+) pigs than in RFI(-) pigs (1,497 vs. 1,383 kJ.kg of BW(-0.60).d(-1); P < 0.01), with no subsequent line effect on energy retention. The activity-related HP tended to be greater in RFI(+) pigs than in RFI(-) pigs (250 vs. 218 kJ.kg of BW(-0.60).d(-1); P = 0.09), and the fasting HP was 10% greater (P = 0.04) in RFI(+) pigs than in RFI(-) pigs (846 vs. 771 kJ.kg of BW(-0.60).d(-1)). The thermic effect of feeding, expressed as a percentage of ME intake, was the same for both lines of pigs (average, 14.7%). In conclusion, the RFI(+) pigs are energetically less efficient because of their greater HP related to physical activity and basal metabolic rate.
To assess the acclimation of pigs to heat stress, the effects of high (338C) or thermoneutral (238C) constant temperatures on feeding behaviour and components of energy balance were studied in group-housed young pigs. Three groups of five pigs were used at each temperature. After 1 week of adaptation, voluntary feed intake (VFI) and heat production (HP) were recorded for thirteen consecutive days. Animals were fed ad libitum. Fasting HP was measured on the last day. Average initial body weights (BW) were 21´4 and 20´9 kg at 23 and 338C respectively. Feeding behaviour was measured individually and rate of feed intake and characteristics of feeding behaviour were calculated. The O 2 consumption, CO 2 production and physical activity of the group were used to calculate total HP (HP tot ) and its components, i.e. fasting HP (HP fas ), HP due to physical activity (HP act ) and thermic effect of feed (TEF). The BW gain and VFI were reduced by 37 and 30 % respectively at 338C. The decrease in VFI corresponded to reduced consumption time (234 %) and size of the meals (232 %). Feeding behaviour was mostly diurnal (66 % of the VFI), and the rate of feed intake (28 g/min) was not affected by temperature. Daily HP tot , HP fas and TEF, expressed per kg metabolic weight (BW 0´60 ), were significantly decreased at 338C by 22, 18 and 35 % respectively, whereas HP act was not affected; TEF expressed per g feed was not affected (2 kJ/g). The decrease in HP tot at 338C was caused by a reduction in TEF and HP fas (kJ/d per/kg BW 0´60 ), which are both related to reduction in VFI.
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