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Two experiments were conducted to determine the total tract digestibility of energy and the DE and ME values of 10 European wheat dried distillers grains with solubles (DDGS) fed to growing pigs and adult sows. The wheat DDGS were obtained from European ethanol plants and selected to get a large variability. One control diet, based on wheat (87.2%), soybean meal (10.0%), and minerals and vitamins, and 10 experimental diets prepared from the control diet and 25% each of the 10 sources of DDGS, were fed to 66 crossbred barrows (6 per diet) according to a factorial arrangement or 6 adult sows according to a pseudo Latin square design. Animals were placed in metabolism cages that allowed for the total, but separate, collection of feces and urine for 8 to 10 d after a 7- to 11-d adaptation period. By subtracting the contribution from the control diet in the DDGS-containing diets (i.e., difference method), N and GE digestibilities and DE and ME values for each source of DDGS were calculated. The energy digestibility in wheat DDGS averaged 66.5% (56.3 to 76.0%) and 71.2% (59.7 to 78.2%) in growing pigs and adult sows, respectively. Consequently, average (range) DE values of DDGS were 14.0 (11.8 to 16.2) and 14.9 (12.5 to 16.4) MJ/kg of DM for growing pigs and adult sows, respectively. Our data show that DE content of wheat DDGS can be predicted from their ADF content or from the lightness score (L). By excluding the dark and overheated samples (L Key words: adult sow, digestibility, energy value, growing pig, predictive equation, wheat dried distillers grains with solubles doi: 10.2527/jas.2009-2510

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.sup.+] (high RFI) line consumed more feed than predicted from performance compared with the [RFI.sup.-] (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.sup.+] 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 RFIpigs compared with [RFI.sup.+] 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.sup.+] pigs than in [RFI.sup.-] pigs (1,497 vs. 1,383 kJ x kg of [BW.sup.-0.60] x [d.sup.-1]; P < 0.01), with no subsequent line effect on energy retention. The activity-related HP tended to be greater in [RFI.sup.+] pigs than in [RFI.sup.-] pigs (250 vs. 218 kJ x kg of [BW.sup.-0.60] x [d.sup.-1]; P = 0.09), and the fasting HP was 10% greater (P = 0.04) in [RFI.sup.+] pigs than in [RFI.sup.-] pigs (846 vs. 771 kJ x kg of [BW.sup.-0.60] x [d.sup.-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.sup.+] pigs are energetically less efficient because of their greater HP related to physical activity and basal metabolic rate. Key words: energy utilization, fasting heat production, growing pig, heat production, residual feed intake doi: 10.2527/jas.2009-2395

Eighty-six mixed-parity Large White sows were used to determine the effect of diets with reduced CP content or supplemented with essential AA on 28-d lactation performance under humid tropical climatic conditions. This experiment was conducted in Guadeloupe (West French Indies, latitude 16[degrees]N, longitude 61[degrees]W) between February 2007 and January 2008. Two seasons were distinguished a posteriori from climatic measurement variables continuously recorded in the farrowing room. The average minimum and maximum ambient temperatures and average daily relative humidity for the warm season were 20.5 and 28.2[degrees]C, and 93.8%, respectively. The corresponding values for the hot season were 22.7 and 29.4[degrees]C, and 93.7%, respectively. The dietary experimental treatments were a normal protein diet (NP), a low protein diet (LP), and a NP diet (NP+) supplemented with essential AA. The NP and LP diets supplied the same levels of standardized digestible Lys (i.e., 0.80 g/MJ of NE), and the NP+ diet supplied 0.95 g/MJ of NE. No interaction between season and diet composition was noted on any response variable evaluated. The ADFI was decreased (P < 0.05) in the hot season (i.e., 3.69 vs. 4.72 kg) and therefore decreased by 500 g per [degrees]C increase of ambient temperature under high relative humidity conditions. The ADFI tended to be greater with the LP and NP+ diets when compared with the NP treatment (i.e., +10%, P = 0.08). Litter BW gain and mean BW of piglets at weaning were greater (P < 0.05) during the warm season than during the hot season (2.3 vs. 1.8 kg/d and 7.5 vs. 7.1 kg, respectively). Milk production and composition were not affected by dietary treatments but were affected by season (8.1 vs. 6.8 kg/d, for warm and hot seasons, respectively; P < 0.01). The sows fed LP and NP+ diets tended to have decreased backfat thickness losses (3.3 and 3.8 mm, respectively; P > 0.08). In conclusion, the hot season in humid tropical climates, which combines high levels of temperature and humidity, has a pronounced negative impact on performance of lactating sows. Diets with low CP content or supplemented with essential AA can attenuate the effects of hot and humid season by increasing ADFI in lactating sows. Key words: feed intake, lactation, lysine, protein, sow, tropical climate doi: 10.2527/jas.2008-1176

Forty-seven mixed-parity Large White sows were used to determine the effect of diets with reduced CP content or supplemented with essential AA on 28-d lactation feeding behavior under humid tropical climatic conditions. The study was conducted at the INRA experimental facilities in Guadeloupe, French West Indies (latitude 16[degrees] N, longitude 61[degrees] W) between February 2007 and January 2008. Two seasons were distinguished a posteriori from climatic measurements continuously recorded in the open-front farrowing room. The average ambient temperature and average daily relative humidity for the warm season were 23.6[degrees]C and 93.8%, respectively. The corresponding values for the hot season were 26.1[degrees]C and 93.7%. The dietary experimental treatments were a normal protein diet (17.3%), a low protein diet (14.1%), and a normal protein diet supplemented with essential AA (17.6%). No interaction between season and diet composition was found for all criteria. Average daily feed intake was less (P < 0.01) during the hot season (4,559 [+ or -] 161 vs. 5,713 [+ or -] 204 kg/d). Meal size was reduced during the hot season (542 [+ or -] 37 vs. 757 [+ or -] 47 g/meal; P < 0.01). Daily ingestion time (45.5 [+ or -] 3.2 vs. 55.8 [+ or -] 4.0 min/d; P < 0.05) was less in the hot season. Meal size was reduced during the hot season at night (P < 0.01). In both seasons, daily feed intake, feed ingestion, and rate of feed intake were less (P < 0.01) during the nocturnal period than during the diurnal period. The number of meals per day was not affected (P > 0.10) by season or diet composition. Daily feed intake was greater for the sows fed the low protein diet when compared with normal protein treatments (P < 0.05). Duration of standing was not affected by diet or season (P > 0.05), and averaged 126 [+ or -] 35 min/d. This study confirms that feeding behavior variables of the lactating sow are affected by seasonal pavariations of the tropical climate. Irrespective of season, the reduction of CP content improved feed consumption under tropical conditions. Key words: dietary protein, feeding behavior, lactation, sow, tropical climate

Little knowledge on the digestive and metabolic utilization of solid feed in veal calves is available. The objectives of the study were to determine the effects of 2 solid feeds offered at 2 feeding levels (FL90 and FL105) in addition to a milk replacer on heat production (HP) and protein and fat deposition in veal calves. Sixteen calves (148.0 [+ or -] 3.7 kg) received milk replacer (75% of a reference DE allowance) and solid feeds that consisted of corn grain and pelleted hydrolyzed wheat gluten without (CO) or with (CS) chopped wheat straw. The solid feed supply provided 15 or 30% of the reference DE allowance to achieve FL90 or FL105, resulting in 4 treatments: CO90, CS90, CO105, and CS105. A fifth treatment consisted of using the milk replacer alone at FL90 (treatment M90) and was measured in 4 other calves. All calves were kept individually for 7 d in a respiration chamber to estimate energy and N balances and fasting HP. The digestibility coefficients of DM, OM, GE, and major nutrients were at least 94% for M90 and decreased when solid feed was added (P < 0.05). Methane production was negligible in M90 calves and increased when solid feed was given (ranging 8 to 23 L/d between CO90 and CS105, P < 0.01), indicative of ruminal fermentation. The provision of increasing amounts of solid feed decreased urinary energy in connection with a tendency (P = 0.09) for a reduction of urinary glucose excretion. The metabolizability of DE was greater with the milk replacer (95.6%) and decreased when straw was added (P < 0.01). Neither CO90 or CS90 affected HP and total energy retention (P > 0.05). Dietary treatment had no effect (P > 0.05) on activity HP (53 kJ/kg of [BW.sup.0.85] daily) but did affect thermic effect of feeding; efficiency of utilizing ME for maintenance and growth was greatest for the M90 calves (84.5%, P = 0.02). Fasting HP tended (P = 0.09) to increase at the greatest FL (308 vs. 298 kJ/kg of [BW.sup.0.85] daily). Maintenance ME requirement increased (P = 0.04) from 364 to 382 kJ/ kg of [BW.sup.0.85] daily when feeding level increased (P = 0.04) but was not affected by ingestion of solid feed. The provision of solid feed to veal calves was associated with a reduced efficiency of N retention (P = 0.04), and energy retained as protein tended to decrease (P = 0.08), probably as a result of an imbalanced AA supply of the solid feeds. The data were used to calculate the energy contents of solid feed. The utilization of energy from solid feed differed from that of milk replacer. Key words: digestibility, heat production, protein and fat retention, solid feed, veal calf

Data were collected over the first 4 generations of a divergent selection experiment for residual feed intake of Large White pigs having ad libitum access to feed. This data set was used to obtain estimates of heritability for residual feed intake and genetic correlations ([r.sub.a]) between this trait and growth, carcass, and meat quality traits. Individual feed intake of group-housed animals was measured by single-space electronic feeders. Upward and downward selection lines were maintained contemporarily, with 6 boars and 35 to 40 sows per line and generation. Numbers of records were 793 for residual feed intake (RFI1) of boar candidates for selection issued from first-parity (P1) litters and tested over a fixed BW range (35 to 95 kg) and 657 for residual feed intake (RFI2) and growth, carcass, and meat quality traits of castrated males and females issued from second-parity (P2) litters and tested from 28 to 107 kg of BW. Variance and covariance components were estimated using REML methodology applied to a series of multitrait animal models, which always included the criterion for selection as 1 of the traits. Estimates of heritability for RFI 1 and RFI2 were 0.14 [+ or -] 0.03 and 0.24 [+ or -] 0.03, respectively, whereas the estimate of [r.sub.a] between the 2 traits was 0.91 [+ or -] 0.08. Estimates of [r.sub.a] indicated that selection for low residual feed intake has the potential to improve feed conversion ratio and reduce daily feed intake, with minimal correlated effect for ADG of P2 animals. Estimates of [r.sub.a] between RFI2 and body composition traits of P2 animals were positive for traits related to the amount of fat depots ([r.sub.a] = 0.44 [+ or -] 0.16 for carcass backfat thickness) and negative for carcass lean meat content ([r.sub.a] = -0.55 [+ or -] 0.14). There was a tendency for a negative genetic correlation between RFI2 and carcass dressing percent ([r.sub.a] = -0.36 [+ or -] 0.21). Moreover, selection for low residual feed intake is expected, through lower ultimate pH and lighter color, to decrease pork quality ([r.sub.a] = 0.77 [+ or -] 0.14 between RFI2 and a meat quality index intended to predict the ratio of the weight of ham after curing and cooking to the weight of defatted and boneless fresh ham). Key words: carcass composition, growth, meat quality, pig, residual feed intake

The impact of dietary fiber on fecal digestion is well-known and provides a comprehensive approach toward nutrient digestibility and availability. Little quantitative information is available on digestion of fiber in the different segments of the gastrointestinal tract (GIT). The objectives of this study were to obtain a method allowing the quantification of the digestive process in different segments of the GIT and to study the impact of dietary fiber on nutrient digestibility. Six barrows (average initial BW of 30 kg and fitted with a simple T-cannula at the proximal duodenum and caudal ileum) were used in a replicated 3 x 3 Latin square design. In each period, pigs were offered 1 of 3 diets differing in fiber content (low, medium, and high). Differences in fiber content were created by replacing wheat and barley with wheat bran. Titanium dioxide was included in the diet as an indigestible marker to determine the apparent digestibility coefficients in different segments of the GIT. The apparent digestibility of ash, CP, DM, and OM increased in the different segments of the GIT. Duodenal digestibility coefficients were negative for ash (e.g., -39.9% for the mediumand high-fiber diets), indicating important endogenous mineral secretions by the stomach and digestive glands. The duodenal digestibility of other nutrients and OM were positive but close to zero and numerically lower in the diets with the greater fiber contents. The fiber content in the diet did not affect the apparent ileal digestibility of nutrients. Increasing the fiber content in the diet affected the fecal digestibility of CP, ether extract, and energy (P < 0.01). The method used for studying sites of digestion in the digestive tract provides promising results, but it is limited due to the high variability that is likely caused by sampling limitations and variation between animals. Key words: dietary fiber, digestion, endogenous secretion, pig

The effect of breed [Creole (CR) vs. Large White (LW)] on performance and physiological responses during acclimation to high ambient temperature was studied in 2 experiments involving 24 (12/ breed) growing pigs each. Pigs were exposed to 24 [degrees]C for 10 d (d -10 to -1) and thereafter to a constant temperature of 31 [degrees]C for 16 d (d 1 to d 16) in Exp. 1 and for 20 d (d 1 to d 20) in Exp. 2. For both experiments, the temperature change was achieved over 4 h on d 0. The first experiment began at 105 d of age, and the average BW of CR and LW pigs was 36.6 [+ or -] 2.5 kg and 51.7 [+ or -] 3.0 kg, respectively. The second experiment was designed to compare both breeds at a similar BW (about 52 kg on d 0). Pigs were individually housed and given ad libitum access to feed. At 24 [degrees]C, ADG was lower (P < 0.01) in CR than in LW (602 vs. 913 g/d and 605 vs. 862 g/d in Exp. 1 and 2, respectively), but the ADFI was not affected by breed (190 and 221 g*[d.sup.-1] * [kg.sup.-0.60] in Exp. 1 and 2, respectively). Short-term thermoregulatory responses during the 4-h transition from 24 to 31 [degrees]C (d 0) were analyzed according to a linear plateau model to determine the break point temperature, above which rectal temperature (RT), cutaneous temperature (CT), and respiratory rate (RR) began to change. The CT increased linearly with temperature increase (0.22 [degrees]C/ [degrees]C) and was less (P < 0.05) in CR than in LW (by -0.3 [degrees]C on average). In both experiments, the break point temperature for RT was not affected by breed (27.6 [degrees]C on average), whereas for RR it was greater (P < 0.05) in CR than in LW (27.5 vs. 25.5 [degrees]C, P < 0.01). On average, ADFI declined by about 50 g*[d.sup.-1] * [kg.sup.-0.60] from d -1 to d 1 (P < 0.01), and thereafter at 31 [degrees]C, it gradually increased (23 g * [d.sup.-1] * [kg.sup.-0.60]; P < 0.05), suggesting an acclimation to high exposure. This response was not influenced by breed. After the day that marked the beginning of the acclimation response (i.e., the threshold day), RR, CT, and RT declined over the duration of exposure to 31 [degrees]C (P < 0.05) in both experiments. During this period, RT and CT were less in CR than in LW pigs (39.6 vs. 39.9 [degrees]C and 37.9 vs. 38.2 [degrees]C, respectively; P < 0.05), whereas RR was not affected by breed. The threshold day at which RT began to decline was less in CR than in LW pigs (0.18 vs. 1.17 d and 0.39 vs. 0.93 d in Exp. 1 and 2, respectively; P < 0.05). In conclusion, this study suggests that short- and long-term physiological reactions during heat acclimation differed when CR and LW pigs were compared at the same age or BW. Key words: acclimation, breed, heat stress, pig, thermoregulation

An experiment was carried out to evaluate the metabolic utilization of energy in crossbred barrows during feed restriction and subsequent refeeding. Ten pigs, initially weighing 52 kg, were used in 5 blocks of 2 littermates each. A 7-d adaptation period (P1) was used in which pigs were offered feed at 2.60 MJ of ME*kg of B[W.sup.-0.60] x [d.sup.-1]. This adaptation period was followed by a 7-d period (P2), in which 1 pig of each block continued to receive feed at the same level of feeding, whereas for its littermate a 40% reduction in feed intake was imposed (i.e., 1.55 MJ of ME*kg of B[W.sup.-0.60] x [d.sup.-1].). During the subsequent 7-d period (P3), both pigs were offered feed at 2.60 MJ of ME*kg of B[W.sup.-0.60] x [d.sup.-1]. After P3, pigs were fasted for 1 d. Heat production (HP) was measured for all pigs during the last 3 d of P1 and on all days for P2 and P3. Heat production was measured using an open-circuit respiration chamber. Energy and N balances were determined for P1, P2, and P3. The HP was partitioned into HP due to physical activity, the short-term thermic effect of feeding, and resting HP. Feed restriction during P2 decreased (P < 0.01) total HP, resting HP, short-term thermic effect of feeding, and retained energy, whereas HP due to physical activity was not affected by feed restriction (P = 0.50). Likewise, fecal and urinary N loss, protein gain, lipid gain, and ADG were reduced during feed restriction (P < 0.01). There were no differences in components of HP and metabolic utilization of energy between the 2 groups during P1 and P3. Nevertheless, urinary N loss was decreased (P < 0.05) and ADG increased (P < 0.01) during P3 for pigs that were restricted in P2. Compensatory growth after a period of feed restriction does not seem to be related to a change in the metabolic utilization of energy for gain but more likely is due to gain in water and gut contents. Key words: compensatory growth, feed restriction, heat production, pig

A total of 179 lactations obtained on 71 multiparous sows [30 Creole (CR) and 41 Large White (LW)] between June 2001 and July 2004 were used to determine effects of breed (CR vs. LW) and season (hot vs. warm) in a tropical humid climate on performance during a 28-d lactation period. Mean daily ambient temperature was greater during the hot season than during the warm season (26.0 vs. 23.8[degrees]C), and relative humidity was similar in both seasons (85% on average). For both breeds, ADFI was reduced (-700 g/d, P < 0.01), sow BW loss was greater (17 vs. 12 kg, P < 0.01), and piglet growth was reduced (197 vs. 210 g/d, P < 0.05) during the hot vs. the warm season. At farrowing, LW sows were heavier (255 vs. 186 kg, P < 0.01) and had less backfat (21 vs. 40 mm, P < 0.01) than CR sows. The growth rate of CR piglets was lower than that of LW piglets (192 vs. 215 g/d, P < 0.01). A breed x season interaction was observed (P < 0.05) for ADFI and sow BW loss. During the hot season, the reduction of ADFI was more pronounced in LW than in CR sows (-910 vs. -470 g/d). Regardless of the season, BW loss of CR sows remained constant (14.2 kg), whereas it increased during the hot season for LW sows (10 kg). The weaning-to-estrus and the weaning-to-conception intervals were not affected by breed or season and averaged 4.8 and 6.1 d, respectively. The rectal temperature was greater (0.3[degrees]C) during the hot season than during the warm season and greater in LW than in CR sows (39.1 vs. 38.8[degrees]C, P < 0.10). This study confirms the negative effect of hot season in a tropical humid climate on performance of lactating sows and that breed can have a significant effect on lactation performance. The results also suggest that CR sows are more heat tolerant than LW sows. Key words: breed, feed intake, lactation, performance, sow, tropical climate

The effects of breed and season on performance and feeding behavior were studied during 76 lactations in multiparous Large White (LW; n = 17) and Creole (CR; n = 23) sows reared in a humid tropical climate. The experiment was conducted in Guadeloupe (French West Indies, latitude 16[degrees]N, longitude 61[degrees]W) between May 2002 and July 2004. Average daily ambient temperature was greater during the hot season than during the warm season (26.0 vs. 23.8[degrees]C), but relative humidity was similar in both seasons (85% on average). The daily fluctuations of ambient temperature and relative humidity were similar for both seasons. At farrowing, BW was lower (187 vs. 265 kg) and backfat thickness was greater (40 vs. 22 mm) in CR than in LW sows (P < 0.01). Sows were offered feed ad libitum between the fifth and the 26th day of lactation. There was a breed x season interaction (P < 0.05) for ADFI. During the hot season the reduction of ADFI was more pronounced in LW than in CR sows (-1,100 vs. -300g/ d). Irrespective of breed and season, the daily number of meals was 9.0. The meal size and the rate of feed intake were greater in LW than in CR sows, respectively (555 g and 153 g/min vs. 390 g and 83 g/min; P < 0.01). The diurnal proportion of ADFI was greater in CR than in LW sows (0.60 vs. 0.41; P < 0.01). The reduction in ADFI in LW sows during the hot season was mainly related to a reduction in feed intake during the day rather than during the night (-1.3 vs. -0.2 kg; P < 0.01). Duration of standing was not affected by breed or season, and it averaged 120 min/day. This study confirms the negative effect of the hot season on feeding behavior of lactating sows. It also suggests a better acclimation to daily high temperatures and a greater heat tolerance in CR compared with LW sows, at least for eating behavior. Key words: breed, feeding behavior, feed intake, sow, tropical climate

Twelve multiparous sows with an average initial weight of 182 kg were used in a randomized complete block design to determine the effects of feeding Carnichrome (50 mg of carnitine and 200 [micro]g of chromium picolinate per kilogram of feed, as fed) on energy and nitrogen utilization in early, mid-, and late gestation. All sows were fed a diet with or without Carnichrome for the preceding 28-d lactation, the weaning-to-estrus period, and for the duration of gestation. Daily feeding allowances over pregnancy were based on calculated energy and nutrient requirements to achieve a target sow maternal weight gain of 20 kg and remained constant throughout gestation. Heat production (HP) and its partitioning (activity, thermic effect of feeding short term [TE[F.sub.st]], basal) were determined in early (wk 5 or 6), mid- (wk 9 or 10), and late (wk 14 or 15) pregnancy using indirect calorimetry. Net maternal weight gain and total number of fetuses averaged 21.6 kg and 16.4, respectively. Organic matter and energy digestibility for the Carnichrome diet was greater (P < 0.05), which resulted in greater DE and ME contents (0.6%, P < 0.05) compared with the control diet. The digestibility coefficient of energy in the current experiment for a typical corn and soybean meal diet (92%) was greater than that predicted from DE values of corn and soybean meal in feeding tables (88%). Carnichrome had no effect on total HP, energy retained as protein or lipid, and maternal energy retention in early, mid-, or late gestation. Heat production in late gestation increased linearly (4.0 kJ/[kg B[W.sup.0.75]xd]) for each additional day from d 90 to 110, despite the reduction of ME intake per unit of B[W.sup.0.75]. Metabolizable energy requirement for maintenance was 405 kJ/(kg B[W.sup.0.75]xd). On average, activity HP was 116 kJ/(kg B[W.sup.0.75]xd), which was equivalent to 20% of ME intake; however, this value ranged from 11 to 37% between sows, which corresponds to duration of standing ranging from 210 to 490 min/d. Energy cost of standing activity averaged 0.30 kJ/(kg B[W.sup.0.75]xmin). In conclusion, Carnichrome had no effect on the components of heat production and maternal weight gain during gestation, although it improved energy and organic matter digestibility of the diet. Key Words: Carnitine, Chromium, Gestation, Heat Production, Sows

Two groups of three multiparous Large White x Landrace sows were used to investigate the direct effect of ambient temperature on mammary gland metabolism. Sows from the first group were exposed to temperatures of 28[degrees]C between d 8 and 14 of lactation, and 20[degrees]C between d 15 and 21; treatments were reversed in the second group. Four to six d after farrowing, an ultrasonic blood flow probe was implanted around the right external pudic artery and catheters were fitted in the right anterior mammary vein and in the carotid artery. After surgery all sows were fed 3.8 kg/d of a lactation diet. The arteriovenous (AV, mg/L) plasma samples were obtained every 30 min between 0915 and 1545 on d 5 of exposure to ambient temperature; the same day, milk samples were collected at 1630. Additional arterial samples were obtained between 1000 and 1100 on d 1, 4, and 6 of exposure. Milk yield was estimated from the body weight gain of the litter. Elevated temperature tended to reduce BW loss (2.44 vs 1.82 kg/d, P < 0.10), but did not affect milk yield (11.0 kg/d). Glucagon and leptin arterial concentrations increased (12 and 8%, respectively; P < 0.10), but thyroxin and triiodothyronine concentrations decreased (26 and 16%, respectively; P < 0.01) between 20 and 28[degrees]C. Expressed as a percentage of total nutrients, A--V difference, glucose, amino acids, triglycerides (TG), free fatty acids, and lactate A-V differences represented 60, 20, 11, 8, and 1%, respectively. Exposure to 28[degrees]C increased the extraction rate of glucose, TG, and [alpha]-amino acid N (13, 8, and 2.5%, respectively; P < 0.10). The extraction rates of essential and nonessential amino acids were not affected by temperature. The right pudic artery mammary blood flow increased (872 vs 945 mL/min, P < 0.05) between 20 and 28[degrees]C, whereas milk yield was unaffected by temperature. It is suggested that this apparent inefficiency of the sow mammary gland in hot conditions could be related to an increase of proportion of blood flow irrigating skin capillaries in order to dissipate body heat. Key Words: Mammary Glands, Milk Composition, Nutrient Uptake, Sows, Temperature

The effects of reducing CP level in combination with an increase in ambient temperature (29 vs 22 [degrees] C) on performance and carcass composition were studied in a factorial arrangement of treatments involving 66 Pietrain x (Landrace x Large White) barrows from 27 to 100 kg BW. Animals were fed at each temperature one of three experimental diets that provided 0.85 or 0.70 g of digestible lysine per megajoule of NE, in the growing (27 to 65 kg) and the finishing (65 to 100 kg) phases, respectively. Diet 1 was a corn, wheat, and soybean meal diet formulated without crystalline AA; CP levels were 20.3 and 17.6% for the growing and the finishing phases, respectively. In Diets 2 and 3, CP level was reduced by substituting part of the soybean meal with corn and wheat (Diet 2), or with corn, wheat, and 4% fat (Diet 3). Diets 2 and 3 were supplemented with AA and balanced according to the ideal protein concept. The CP levels of Diets 2 and 3 were, respectively, 15.8 and 16.3% in the growing phase, and 13.4 and 13.8% in the finishing phase. Pigs were housed individually and had free access to feed and water. The ADFI was measured daily, and animals were weighed weekly. Carcass composition was measured at slaughter (100 kg BW). Increasing ambient temperature from 22 to 29 [degrees] C resulted in a 15% reduction in ADFI and 13% lower ADG. Leaner carcasses (P < 0.01) were obtained at 29 [degrees] C (22.8 vs 24.8% carcass fat). At 22 [degrees] C, ADFI was lower (P < 0.05) for the low-CP diets, but daily NE intake, ADG, and carcass composition were not affected (P > 0.05). At 29 [degrees] C, ADFI was not different (P > 0.05) between diets and daily NE intake was higher (P < 0.05) with Diet 3 than with Diet 1, and the difference was more important during the finishing period than during the growing period. Using the model ADFI = a B[W.sup.b], estimates of b were 0.65, 0.53, and 0.53 at 22 [degrees] C and 0.50, 0.44, and 0.50 at 29 [degrees] C, for Diets 1, 2, and 3, respectively. The higher NE intake for Diet 3 at 29 [degrees] C did not improve ADG (P > 0.05) but increased mainly fat deposition. These results indicate that a 4 percentage unit reduction of dietary CP level reduces N excretion (minus 37%) but does not affect growth and carcass composition as long as the ratio between essential AA and NE are kept optimal. In addition, diets with reduced CP limit the effect of high ambient temperature on ADFI. Finally, our results demonstrate the significance of using NE, rather than DE or ME, for formulating diets. Key Words: Body Composition, Dietary Fat, Dietary Protein, Growth, Heat Stress, Pigs

Two replicates of three multiparous crossbred Large White x Landrace lactating sows were used to develop a technique for the continuous direct measurement of the blood flow through the mammary gland using transit time ultrasound. Four to six days after farrowing, an ultrasonic transit time flow probe was implanted around the right external pudic artery in order to measure the short-term variations of mammary blood flow through this vessel in response to postural change (standing vs lying), meal distribution, hand-milking, and weaning. After surgery, all sows were fed 3.8 kg/d of a lactation diet and housed either at 20 or 28 [degrees] C. The implantation of the ultrasonic blood flow probe was successful in all six operated sows. Postmortem examination did not indicate the presence of infection, any collateral bypassing the flow probe, or a reduction of artery diameter. The right pudic artery mammary blood flow (PMBF) was measured for 8.5 h over two periods of three days (d 11 to d 13 and d 18 to d 20 of lactation). The PMBF averaged 910 [+ or -] 238 mL/min but was variable within 1 d. Compared with the lying position, PMBF was decreased (- 6%, P < 0.05) when sows were standing. Between 0 to 15 and 16 to 30 min after oxytocin injection (t = 0) and hand-milking, PMBF remained constant (P = 0.05; 801 vs 767 mL/ min) and increased (P = 0.02), respectively, in comparison with the mean calculated over the preceding 30-min period (982 vs 784 mL/min). The PMBF increased (P < 0.05) after meal distribution and reached a peak 65 min later (i.e., 980 mL/min). The PMBF decreased regularly after separation of piglets at weaning; at 8 and 16 h after weaning, PMBF was 60 and 40% of the value recorded before weaning, respectively. Assuming that PMBF drains one-quarter of the whole mammary gland, it can be calculated that blood flow through the entire mammary gland averages 3.6 L/min and that about 470 L of blood are required to produce 1 kg of milk. The proposed methodology constitutes a new technique to measure direct mammary blood flow and its short-term factors of variation. Key Words: Blood Flow, Lactation, Mammary Glands, Sows

To quantify the utilization of ME by growing pigs, a factorial analysis method is often used in which the ME intake is regressed on protein (PD) and lipid deposition (LD) rates. The approach has been criticized because there often is a strong correlation between PD and LD, which makes accurate estimation of model parameters difficult. The current study describes a nonlinear multivariate analysis procedure in which PD and LD are the result of variation in ME intake. The approach requires a hypothesis concerning the partitioning of ME intake above maintenance between PD and LD. The method was evaluated using data for growing pigs of different genotypes and sex and weighing between 20 and 107 kg that were offered a diet close to ad libitum. Energy, nitrogen, and fat balances were determined at regular intervals over the growing period. The maintenance energy requirement was expressed as a function of BW (with group-specific parameters) or as a function of muscle and visceral mass. The maintenance energy requirements ranged from 913 to 1,070 kJ ME/([(kg BW).sup..60][multiplied by]d) for obese castrates and boars of a synthetic line, respectively. Viscera contributed 1,558 kJ ME/([(kg tissue).sup..70][multiplied by]d) to the maintenance energy requirement, whereas muscle contributed only 555 kJ ME/([(kg tissue).sup..70] [degrees] .d). It was assumed that the proportion of ME intake (above maintenance) designated for PD declined linearly with increasing BW. At 20 kg of BW, 49% of ME intake above maintenance was designated for PD in lean genotypes, whereas this was only 34% in obese genotypes. In general, with increasing BW, less energy was designated for PD, but this relationship depended on genotype and sex. Extremely lean male genotypes maintained a constant partitioning of energy between PD and LD for all BW. The energetic efficiencies varied (depending on the model used to express the maintenance requirement) between .58 and .60 for PD and .77 and .82 for LD. Extrapolation of results suggested that animals fed at maintenance energy level would still deposit protein at the expense of body lipid. It is argued that this finding requires nonbiological efficiencies of lipid catabolism and protein synthesis and illustrates the limitation of the maintenance concept for growing animals. The multivariate analysis method proposed here circumvents many of the problems associated with the factorial regression analysis of ME intake on PD and LD. The method can be used to further refine nutritional models describing growth in pigs. Key Words: Growth, Pigs, Energy, Energy Requirements, Maintenance, Statistical Analysis

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 ([ME.sub.m]) and was represented either as a function of body weight with group-specific parameters ([ME.sub.m] = [a.sub.i] [BW.sup.b]) or as a function of the muscle and visceral mass with an additional additive group effect ([ME.sub.m] = [a.sub.M] [muscle.sup.b] + [a.sub.v] [viscera.sup.b] + [G.sub.i]). With BW as dependent variable, the exponent b was close to .60 and differed significantly from .75. The regression coefficient ([a.sub.i]) averaged 1.02 MJ ME/[kg.sup..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 MEre. Viscera contributed three times more to MEre (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 MEre was lower than that of viscera for most groups. Key Words: Growth, Pigs, Energy Metabolism, Energy Requirements, Maintenance

A total of 94 pigs from seven groups considered as lean (boars from a synthetic line and the Pietrain breed), conventional (boars, gilts, and barrows from the Large White breed), fat (barrows from the Meishan x Large White cross), or obese (Meishan barrows) were serially slaughtered between 12 and 110 kg BW. Carcasses were dissected into muscle, bone, skin, and fat, which was further separated into subcutaneous, intermuscular, and kidney fats. Subcutaneous fat accounted for 60 to 70% of body fat and intermuscular fat for 20 to 35% of body fat. Relative to total rat, intermuscular fat grew more slowly (allometric growth coefficients generally < 1), subcutaneous fat at the same rate (b close to 1), and kidney fat more rapidly (1.12 < b < 1.33). The leaner the animals genetically, the higher the proportion of intermuscular fat in total rat. The ratio of intermuscular to subcutaneous fat varied from .31 in Meishan barrows to .66 in Pietrain boars. Overall, the ratio of intermuscular fat to muscle weight or body weight was positively related to the development of total fat. However, Pietrain pigs were unique in having a high development of intermuscular fat. The present results suggest that 1) the genetic controls of the development of intermuscular and subcutaneous fat are partially independent and 2) the development of intermuscular fat may be determined at an early stage, before 20 kg BW. Key Words: Pigs, Breeds, Subcutaneous Fat, Body Fat, Growth

Using 73 Large White gilts, we studied the lysine requirement during lactation. Sow and pig performance and nitrogen balance of sows were measured during the total 21-d lactation period. Variation in body composition of sows between farrowing and weaning was determined by the comparative slaughter technique. Two levels of crude protein (15.5 and 17.1%) were combined with two levels of L-lysine HCl supplementation (0 and. 16%), resulting in four diets termed P1L1, P1L2, P2L2, and P2L3, containing .66, .77, .77, and .87% crude lysine, and 15.5, 15.5, 17.1, and 17.1% crude protein, respectively. Sows' feed intake, litter growth rate, and milk energy and protein output were not affected by the diet. Nitrogen balance over the total lactation increased (P < .001) with an increase in lysine and(or) protein (-11.7, -7.0, -3.4, and .4 g N/d for P1L1, P1L2, P2L2, and P2L3 diets, respectively). The losses of body weight and muscle weight were higher in P1L1 gilts (P < .01 and .05, respectively) than in gilts on other treatments, whereas the loss of adipose tissue and backfat was similar for the four groups. Multiple linear relationships between lysine intake and milk nitrogen output as predictors and nitrogen balance (N balance = -15.8 + 1.22 lysine - .63 N milk, [R.sup.2] = .89) or variation of muscle weight (Vm = -477 + 30.1 lysine - 14.7 N milk, [R.sup.2] = .70) as predicted values were calculated to estimate lysine requirement according to production performance of sows. Calculations show that for achieving a zero protein balance, 45 to 55 g/d of crude lysine are required for normal to high-yielding sows, respectively. Key Words: Sows, Lactation, Lysine, Requirements, Protein

Measurements of heat production(HP; indirect calorimetry) and its partition between maintenance, physical activity, thermoregulation, and thermic effect of feed or energy gain were carried out in sows maintained in different situations: primiparous or multiparous; pregnant or nonpregnant; thermoneutral or cold conditions; varied feeding levels; and varied body weights (BW). Metabolizable energy requirements for maintenance average 420 kJ/kg [BW.sup..75] at thermoneutrality and moderate physical activity. This value is not significantly affected by parity, pregnancy, and stage of pregnancy. Physical activity is a major factor causing differences in energy balance between sows because activity is variable and its energy cost (27 kJ.kg [BW.sup.-.75][multiplied by]100 [min.sup.-1] standing) is four to five times higher than in other species. Lower critical temperature (LCT) is approximately 20 [degrees] C in pregnant and individually housed sows, and daily HP is increased by approximately 15 kJ/kg [BW.sup..75] for each degree Celsius decrease of ambient temperature below LCT. Efficiencies of utilization of ME for meeting energy requirements for maintenance, maternal gain, and uterine gain are 77, 75, and 50%, respectively. Equations for predicting energy deposition in the uterus and mammary gland are proposed. In addition to activity and thermoregulation, energy requirements of pregnant sows depend on body reserves of energy. Studies with newborn pigs indicate that they are quite sensitive to ambient temperature (i.e., +25 J[multiplied by]kg [BW.sup.-.75][multiplied by][min.sup.-1] for each degree Celsius decrease of temperature), and their LCT is 32 to 34 [degrees] C. The energy demand of pigs for thermoregulation just after birth relies mainly on carbohydrates from glycogen reserves or colostrum. Survival of newborn pigs is highly dependent on the supply of colostrum. Key Words: Sow Pregnancy, Neonates, Pigs, Energy Metabolism

Multiparous Large White sows were used in two experiments to determine the effects of energy intake on the reconstitution of body reserves during pregnancy. In Exp. 1, 21 sows received one of three different energy levels during pregnancy: 7.4, 8.8, or 10.4 Mcal DE/d. In Exp. 2, two energy levels (7.9 and 9.2 Mcal DE/d) were fed to 36 sows that mobilized low or high amounts of body reserves during the previous lactation (6 or 12 pigs per litter, respectively). Nitrogen balances were conducted during five 7-d periods at 11, 32, 53, 82, and 104 d of gestation. All the experimental sows were slaughtered and dissected at the end of pregnancy; 24 control sows were similarly slaughtered at mating in order to estimate composition of BW gain, according to the comparative slaughter technique. In the two experiments, average nitrogen (N) retention increased linearly with energy supply from 9.9 to 14.5 g/d in Exp. 1 (P < .001) and from 10.2 to 12.5 g/d in Exp. 2 (P < .05). Nitrogen retention was not affected by the extent of mobilization of body reserves during the previous lactation in Exp. 2. In both experiments, carcass weight (P < .001), muscle weight (P < .01), and dissectable fat weight (P < .001, Exp. 1; P < .01, Exp. 2) increased with energy supply. We conclude that in high-producing modern multiparous sows, energy supply during gestation is a limiting factor for N retention and muscle weight gain and should be approximately 8,500 kcal DE/d to ensure adequate restoration of body reserves. Key Words: Sows, Pregnancy, Nitrogen, Energy Intake, Body Condition

Tissular and chemical body composition were measured for 85 pigs that were serially slaughtered between 15 and 110 kg BW and considered lean (boars from a Synthetic Line and the Pietrain breed), conventional (boars, gilts, and barrows from the Large White breed), or obese (Meishan barrows). These six groups were expected to be quite different with regard to their body composition. Tissular body composition was predicted from chemical body composition, according to nonlinear regression models. Common relationships were obtained for lean and conventional pigs (Group effect: P > .05). Empty body weight and the weight of adipose tissues were predicted directly from the amounts of body protein and lipid, whereas for estimation of weights of carcass, muscle, and lean, the prediction was improved when the weight of offals (visceral organs and blood) was also included in the model. Validation of prediction models on literature data indicated good agreement between calculated and measured values ([R.sup.2] > .90). These relationships were not applicable to Meishan barrows. In pig growth modeling approaches, proposed equations can be used in order to predict the tissular composition of body weight gain and commercial value at slaughter. Key Words: Pigs, Body Composition, Prediction, Growth Models

Digestible (DE), metabolizable (ME), and net (NE) energy values of seven diets were measured in castrated male pigs of 45 (Stage 1), 100 (Stage 2), or 150 (Stage 3) kg BW. Diets were prepared from a basal diet supplemented with cornstarch, or sucrose, or a protein mixture (referred to here as protein), or rapeseed oil, or a mixture of fibrous ingredients (referred to as fiber), or rapeseed oil + fiber. Diets were fed at similar levels (x maintenance) at the three stages. Heat production at different feeding levels, as measured by indirect calorimetry, allowed calculation of energy retained by each pig (equal to ME intake minus heat production) and an estimate of fasting heat production of all pigs (360 kcal/kg [BW.sup..42]). Net energy intake was then calculated for each pig as retained energy plus 360 x [BW.sup..42]. The amounts of DE digested before the end of the ileum (DEi) and in the hindgut (DEh) were measured. Formulation of diets allowed calculation of energy values of the ingredients added to the basal diet. Digestibility and metabolizability of diets increased significantly from Stages 1 to 3, with higher variations for low-energy diets. The NE:ME ratio (k, %) and dietary NE content were not affected (P >.05) by stage of growth. On average, k was 75%, with higher values for diets containing rapeseed oil or starch (77%) and lower estimates for the fiber diet (72%). As a consequence, k was approximately 90, 82, 80, 72, and 60% for rapeseed oil, cornstarch, sucrose, protein, and fiber, respectively. These values are consistent with the lower k value for ME from DEh (57 vs 78% for DEi). Present data confirm that the hierarchy between feeds is dependent on the energy system (DE vs ME vs NE) and that the NE concept is superior in predicting the 'true' energy value. The present results combined with previous ones show that, under practical conditions, the same NE prediction equations based on digestible nutrient contents, or preferably DE or ME contents, can be applied at all stages of growth in pigs. However, attention should be paid to factors such as BW or feeding level that affect digestibility and metabolizability of feeds markedly. The effects are the most important for ingredients.

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 B|W.sup..60~ plus fasting heat production estimated from data of the present experiment as 179 kcal/kg B|W.sup..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.

The DE and ME values and digestible nutrient contents of 114 diets were measured in 45-kg growing pigs (four to five animals per diet) fed approximately 500 kcal of ME/kg |BW.sup..60~. Diets differed widely with regard to their chemical characteristics and their ingredients. Chemical composition of each diet was measured by at least four laboratories. The results were used to establish prediction equations of DE or ME values, digestible nutrient contents, and digestibility coefficients of energy and nutrients from chemical characteristics. Digestibility coefficients of energy (range: 65 to 95%) and CP (range: 64 to 94%) were highly dependent on dietary fiber and mineral contents. The digestibility coefficient of ether extract increased curvilinearly (from 2 to 84%) with the dietary fat content. The digestibility of fiber was lower (45% for NDF) than for the other chemical constituents. The ME:DE ratio averaged 96.3% and was negatively correlated to the dietary protein content. The DE and ME values could be accurately predicted (|R.sup.2~ |is greater than~ .90 and CV |is less than~ 2%) from chemical characteristics; the best equations were obtained when the following predictors were combined in a linear model: ash, ether extract, crude protein, and an estimate of dietary fiber. The accuracy of the prediction was higher with NDF than with ADF or Weende crude fiber. The results suggest that even a rather large proportion of dietary fiber (approximately 50%) is degraded in the digestive tract, the amount of available energy from fiber digestion is negligible in connection with increased endogenous protein and fat losses. The equations obtained in the present study represent a basis for the prediction of the energy values of mixed diets with a composition of unknown ingredients.

Three litters of four pigs from each of four different groups were used to evaluate the effect of porcine somatotropin (pST) on growth performance, body gain composition, energy and N metabolism, and in vitro cytochrome oxydase (final enzyme of the respiratory chain) activity of tissues. The four groups included boars from a synthetic line (SG1) or the Large White breed (SG2) and barrows from the Large White breed (SG3) or crossbred between Large White and Meishan breeds (SG4). Inherent capacity for daily lean tissue growth (LTG) decreased from SG1 to SG4. Within a litter, one pig was slaughtered and dissected at the beginning of the experiment (55 kg BW) and the three others were fed the same daily supply of protein and amino acids (26 g of lysine/d) but relative daily energy levels were either 113 (without pST: E1/0), 100 (3 mg of pST/d: E2/pST) or 87 (3 mg of pST/d: E3/pST). The 100 energy level corresponded to the ad libitum intake of E2/pST pigs. Two energy and N balances were carried out in respiration chambers during the experimental period. Pigs were slaughtered and dissected at approximately 95 kg BW and composition of gain was estimated using the comparative slaughter technique. In E1/0 pigs, daily BW, lean, and N gain were affected (P < .01) by group; 566, 471, 374, and 315 g/d of lean tissue gain in SG1, SG2, SG3, and SG4 pigs, respectively. At high ME intake (E2/pST vs E1/0), pST increased daily BW (+14%), lean (+27%), or N (+26%) gain and reduced adipose tissue (-50%) gain, but the pST effect was inversely related to LTG: for N, the improvement was 2.8, 7.1, 7.0, and 11.1 g/d in SG1, SG2, SG3, and SG4 groups, respectively. Energy restriction (E3/pST vs E2/pST) reduced (P < .001) adipose tissue gain in all groups but did not affect lean tissue or N gains in SG1, SG2, and SG3 pigs. In the pST-treated pigs of the SG4 group, the lean tissue or N gains were reduced (P < .01) by energy restriction. Energy restriction combined with pST treatment (E3/pST) led to negligible amounts of fat deposited (40 g/d for SG1 + SG2 + SG3 pigs) and a gain:feed ratio higher than 500 g/kg (580 in SG1 pigs). The increased heat production measured in pST-treated pigs was due to its maintenance component: 275 vs 257 kcal of ME kg [BW.sup.-.60] [d.sup.-1] (P < .01). The increased ME requirement for maintenance would be related to the higher mass of liver, kidneys, and heart and the higher metabolic activity per unit of tissue (estimated by the in vitro cytochrome oxidase activity) in the liver. Key Words: Pigs, Somatotropin, Growth Rate, Energy Metabolism, Body Composition, Liver, The administration of porcine somatotropin was found to increase the rate of lean tissue gain and lean tissue lipid deposition in all groups of pigs. Fat deposition was reduced to almost zero when energy restriction was added to pST treatment. Hence, pST may be used as a method of manipulating body fat. Heat production was found to increase, possibly due to metabolic effects in different body compartments to varying degrees. Although little is known about pST effects at the tissue level, a 40% increase in liver oxidative capacity was detected.