Effect of dietary electrolyte balance on metabolic rate and energy balance in pigs

2002 ◽  
Vol 74 (2) ◽  
pp. 299-305 ◽  
Author(s):  
Y. Dersjant-Li ◽  
J. W. Schrama ◽  
M. J. W. Heetkamp ◽  
J. A. J. Verreth ◽  
M. W. A. Verstegen

AbstractThe effect of two dietary electrolyte balance (dEB, Na+ + K+ – Cl-) levels (–135 and 145 mEq/kg diet) on heat production, energy and nitrogen retention in piglets was assessed. The experiment consisted of a 13-day adaptation period and a 7-day balance period in two open-circuit climate respiration chambers. Nine groups of three (4 weeks old) crossbred barrows were assigned to one of two diets (five and four groups for –135 and 145 mEq/kg dEB diets respectively). During the balance period, diets were provided at 2·3 times the energy requirement for maintenance in two equal meals daily. Total heat production for each group was determined every 9 minutes from the exchange of CO2 and O2. Faeces and urine mixture was quantitatively collected during the balance period to measure energy and nitrogen balance. Total heat production and metabolizable energy costs for maintenance tended (P 0·10) to be higher in the 145 mEq/kg dEB group (681 and 443 kJ/kg0·75 per day respectively) than in the –135 mEq/kg dEB group (660 and 412 kJ/kg0·75 per day respectively). Differences in total heat production between the two dEB groups mainly occurred in the daytime (light period), when significance level was P 0·01. The respiratory quotient and energy retention as fat were numerically (but not statistically significantly) lower in the 145 mEq/kg dEB group compared with –135 mEq/kg dEB. In conclusion, energy balances were similar for both treatments. However in the daytime (light period), piglets needed more energy for maintenance after ingesting a diet with a dEB level of 145 mEq/kg compared to a diet with a dEB level of –135 mEq/kg at a restricted feeding level.

1998 ◽  
Vol 130 (2) ◽  
pp. 193-198
Author(s):  
G. SEMIADI ◽  
C. W. HOLMES ◽  
T. N. BARRY ◽  
P. D. MUIR

Two experiments each with two rates of feeding (maintenance and twice maintenance) were conducted during summer 1993/94 (Expt 1) and summer 1994/95 (Expt 2), at Massey University, New Zealand. Four sambar and four red deer, including stags and hinds aged 10–14 months, were used in each year. Animals were fed a pelleted diet (total N 30 g/kg DM; NDF 247 g/kg DM). Digestibility and nitrogen (N) balances were determined using deer metabolism cages, whilst methane production and heat production were determined using open circuit respiration calorimetry, with measurements made on each deer at both rates of feeding. Digestibility and metabolizability of energy were greater for sambar than for red deer in Expt 1 but not in Expt 2. Nitrogen retention, expressed as a proportion of N intake, was similar for sambar and red deer. Metabolizable energy required for maintenance (MEm) was 474 kJ kg W−0·75 d−1 for sambar deer and 567 kJ kg W−0·75 d−1 for red deer, whilst the efficiency of utilization of ME above maintenance (kg) was similar for sambar deer and red deer. These studies indicated that the sambar deer had lower rates of maintenance heat production than the red deer, which may explain the sambar's superior feed conversion measured in previous experiments. However, the two species utilized nitrogen with similar efficiency, when fed a high quality ration.


1990 ◽  
Vol 63 (2) ◽  
pp. 155-163 ◽  
Author(s):  
C. Prieto ◽  
J. F. Aguilera ◽  
L. Lara ◽  
J. FonollÁ

Sixteen adult castrated male goats of the Granadina breed, with initial live weights ranging from 26.0 to 33.3 kg were used in two experiments to determine their protein and energy requirements for maintenance. Digestibility, nitrogen and energy balance measurements were made during the experiments. Two diets, which were based on pelleted lucerne (Medicago sativa) hay alone or on this forage and barley, were individually given at about maintenance level once daily. Gas exchange was measured using open-circuit respiration chambers. Fasting heat production was also determined. By regression analysis endogenous urinary N and maintenance requirements for N were estimated to be 119 mg/kg body-weight (W)0.75 per d and 409 mg total N/kg W0.75 per d respectively. Fasting heat production was 324 kJ/kg W0.75. The energy requirement for maintenance was calculated by regression of energy balance on metabolizable energy (ME) intake and a value of 443 kJ/kg W0.75 per d was found. The overall efficiency of utilization of ME for maintenance was 0.73.


1986 ◽  
Vol 42 (2) ◽  
pp. 257-268 ◽  
Author(s):  
G. M. Cronin ◽  
J. M. F. M. van Tartwijk ◽  
W. van der Hel ◽  
M. W. A. Verstegen

ABSTRACTIn response to tethering, many sows develop seemingly non-functional repetitive behaviour (stereotypies), which may be performed for several hours in a day.The quality and quantity of activity performed by sows with different degrees of adaptation to tethering was studied in relation to energy expenditure. Three groups of five sows were recognized: (1) High, sows which showed a high incidence of stereotyped activity after prolonged tethering; (2) T/Low, sows with limited experience of tethers; and (3) G/Low, the same sows as in group 2 after regrouping.High sows were about three times more active than T/Low sows: the proportions of time involved in 24 h were 0·35 and 0·13 respectively. Most of the former sows' activity was in the form of sterotypies. The activity level of the G/Low sows was between that of the two tether treatments (proportionately 0·17 of 24 h). Both tethered treatments spent proportionately about 0·05 of 24 h in using drinkers compared with proportionately less than 0·02 of the time for the G/Low sows.High sows produced proportionately 0·36 more heat than T/Low sows during the 12-h light period in each day. During this period, proportionately 0·40 and 0·20 of heat production from High and T/Low sows was associated with activity. The diurnal activity of the G/Low sows was associated with proportionately 0·24 of heat production.Stereotypies and excessive drinker use accounted for proportionately 0·86, 0·52 and 0·24 of the activity of High, T/Low and G/Low sows. The proportions of metabolizable energy intake required for these activities were 0·23, 0·07 and 0·04 respectively for the three treatments. The study concludes that tethering is stressful when sows develop, and then indulge in frequent coping behavioural patterns which increase metabolic rate.


1999 ◽  
Vol 133 (4) ◽  
pp. 409-417
Author(s):  
D. E. KIRKPATRICK ◽  
R. W. J. STEEN

An experiment was carried out in 1994 to examine energy and nitrogen utilization of lambs offered two contrasting grass-based diets. The two forages, which were from the same parent herbage, were grass silage and grass which was conserved by freezing. They were offered as sole diets or supplemented with either 250 or 500 g concentrates per kg total dry matter intake (DMI) to give a total of six experimental treatments. Seventy-two Dutch Texel × Greyface (Border Leicester × Blackface) lambs, consisting of 36 males which were initially 36 (S.D. 4·9) kg liveweight and 36 females which were initially 34 (S.D. 2·5) kg liveweight were used. Ensiling significantly increased apparent digestibility of dry matter, energy and nitrogen (P<0·001), but had no significant effect on methane energy loss as a proportion of gross energy intake, metabolizable energy intake (MEI), heat production, energy retained, efficiency of utilization of energy for growth (kg) or nitrogen retention. Supplementation of forage with concentrates resulted in a curvilinear decrease in heat production expressed as a proportion of MEI (P<0·05) and a linear increase in energy retention, expressed as an absolute value or as a proportion of MEI (P<0·05). Supplementation of forage tended to increase kg when calculated using Agricultural Research Council estimates of maintenance energy requirements, but had no significant effect when alternative estimates of maintenance were used. It is concluded that ensiling had no effect on efficiency of utilization of energy or nitrogen as measured by indirect calorimetry.


1995 ◽  
Vol 61 (3) ◽  
pp. 581-588 ◽  
Author(s):  
J. Vernet ◽  
M. Vermorel ◽  
W. Martin-Rosset

AbstractSix sport horses were given 1·26 times the measured maintenance energy requirement (MEm) from each of the four following diets: H1, meadow hay in the long form (organic matter digestibility OMD = 0·541); HMI, 700g/kg the same hay and 300 g/kg pelleted maize; HSBPI, 600g/kg hay and 400g/kg pelleted dehydrated sugar-beet pulp; SCFI, 500g/kg wheat straw and 500g/kg pelleted compound food (experiment 1). In experiment 2, eight sport horses were equipped with a portable device for recording feeding behaviour and fed at 1·31 MEm diet HI (meadow hay in the long form: OMD = 0·574).Circadian energy expenditure (EE) of horses was determined by indirect calorimetry using two large open-circuit respiration chambers. Horses were continuously standing. Increase in metabolic rate (IMR) during eating was calculated from the difference between the mean EE obtained during each eatingperiod and the corresponding resting EE. The mean daily ingestion rate of hay H2 amounted to 148 (s.d. 27)mg dry matter per kg metabolic body weight per min. IMR during the two main meals averaged 0·388 (s.d. 0·059) and was not significantly different between diets H1, H2, HM1 and SCF1. Expressed per kg dry matter intake, energy cost of eating (ECE) was similar for diets H2, H1 and SCF1 but significantly lower for HSBP1 and HM1 (P<0·05). ECE of simple foods was calculated from those of the diets and of hay: proportionately 0·010, 0·042, 0·102 and 0·285 metabolizable energy intake for pelleted maize, pelleted SBP, long hay and wheat straw, respectively.


1991 ◽  
Vol 52 (3) ◽  
pp. 499-507 ◽  
Author(s):  
D. S. Rao ◽  
K. J. McCracken

ABSTRACTTwo experiments were conducted each using one batch of six Landrace littermate, entire male, pedigree pigs in a Latin-square change-over study of the effects of energy intake on nitrogen and energy metabolism over the range 33 to 88 kg live weight. One animal from each litter was slaughtered at 33 kg body weight to obtain initial body composition data. Five feeding levels (80, 100, 120, 140 and 160g/kg M0·63) were used during five consecutive metabolism trials each of 11-days duration, excreta being collected during the last 7 days. The pigs were housed in individual metabolism cages and the diets were offered in liquid form (approx. 300 g dry matter (DM) per kg) twice daily at 09.00 and 16.00 h. Heat production was measured for 1 day during each balance period in an open-circuit respiration chamber. The average daily gain, nitrogen retention, heat production and energy retention increased linearly (P < 0·001) with increasing metabolizable energy (ME) intake. The relationship between energy intake and protein deposition was linear up to levels above the normal ad libitum consumption of energy. Protein deposition potential of these high genetic potential pigs was at least 200 g/day, and tended to be constant between 35 and 85 kg live weight. From the combined results of experiments 1 and 2, the energy requirement for maintenance was 0·982 MJ ME per kg M0·63 per day and the decrease in protein deposition was approximately 6 g/MJ reduction in ME within the range of practical energy intakes.


1972 ◽  
Vol 52 (4) ◽  
pp. 751-759 ◽  
Author(s):  
V. D. SHARMA ◽  
L. G. YOUNG ◽  
G. C. SMITH ◽  
R. SAISON

The influence of crossbreeding and sex on digestible (DE) and metabolizable (ME) energy values, fasting heat production (FHP), energy requirement for maintenance and growth, and on the efficiency of utilization of metabolizable energy in young weanling pigs, was investigated by employing a comparative slaughter technique. The pigs obtained by insemination of Yorkshire sows with pooled semen (equal number of sperms) from purebred Yorkshire and Hampshire boars, were identified for genotype by blood-group typing. A total of 37 pigs was used in this study, of which 9 pigs selected at random were killed to provide the initial body composition and energy status of pigs in the feeding experiment. The remaining 28 pigs (16 purebred: 8 male and 8 female; and 12 crossbred: 6 male and 6 female) were allotted at random to a feeding experiment of a randomized complete block design involving a 2 × 2 × 2 factorial arrangement (purebred vs. crossbred, male vs. female, and level of dietary energy input: 130 and 330 kcal ME/Wkg0.75 daily). One metabolism trial with each pig individually kept in a crate was conducted during the 4th week of the 40-day feeding period. The coefficients of DE and ME were 89.2 and 84.2%, respectively, and were not influenced by sex or genotype. An interaction was observed in the estimates of the fasting heat production and energy requirement for maintenance. Purebred Yorkshire males had a greater fasting heat production than Hampshire × Yorkshire males, whereas females of the two breeding groups had similar values. The apparent efficiency of utilization of ME was 76% and the net efficiency of utilization of ME available above maintenance was 66%. The energetic efficiency and the net energy value of the diet were similar for both breeding groups and sex. The mechanism of rapid gains due to crossbreeding was investigated.


2019 ◽  
Vol 97 (Supplement_3) ◽  
pp. 391-392
Author(s):  
Aaron B Norris ◽  
Whitney L Crossland ◽  
Luis O Tedeschi ◽  
Jamie L Foster ◽  
James P Muir ◽  
...  

Abstract Our objective was to evaluate how quebracho tannin (QT; Schinopsis balansae) within a roughage-based diet affected energy partitioning of growing beef steers. Ruminant production is essential to meeting the protein requirements of an increasing global population. However, gaseous byproducts from ruminant production, such as methane (CH4), not only reduce energetic efficiency, it can also be detrimental to the environment. Feed-grade antibiotics have traditionally been utilized for improved feed efficiency; however, consumer perception has prompted the pursuit of natural rumen modulators. Condensed tannins are a potential alternative due to their capacity for enhancing protein efficiency and reducing CH4. In our study, a 4 x 8 Latin rectangle design utilizing four periods and 8 British crossbred steers (236 ± 16 kg) were used to determine the effects of QT fed at 0 (control), 1.5, 3, and 4.5% of DM, within a roughage-based ration. Following 12-d dietary adaptation, animals were relocated to open-circuit respiration calorimetry chambers fitted with metabolism stands for gas exchange measurements and collection of total feces and urine over 48 h. Data were analyzed using a random coefficients model with animal and period as random factors. Inclusion of QT had no effect on intake, fiber digestibility, or nitrogen retention (P &gt; 0.10). Provision of QT increased fecal energy, resulting in reduced digestible energy (DE) (P &lt; 0.01). Urinary energy was not different (P = 0.49) but gas energy decreased (P &lt; 0.01) as QT inclusion increased. Metabolizable energy (ME) decreased linearly as QT increased (P &lt; 0.01), but all treatments maintained a ME-to-DE ratio of 0.86. Heat energy decreased (P = 0.01) with increased QT rate; however, there was no difference in retained energy. Although QT reduced gas and heat energy, this could not compensate for the reduction in digestible energy, leading to decreased energetic efficiency with QT inclusion.


1986 ◽  
Vol 34 (2) ◽  
pp. 173-184
Author(s):  
W. van der Hel ◽  
R. Duijghuisen ◽  
M.W.A. Verstegen

In two experiments, pigs with initial weights of 20 kg were kept in climate-controlled respiration chambers. After a 7-day adaptation period at 22-24 degrees C the temperature was reduced in 4 degrees C steps to 8 degrees C and then increased to 24 degrees C. Each temperature treatment lasted 3 days. Feed contained 12 kJ metabolizable energy per g and was given at 93 and 83 g/kg0.75 per day in experiments 1 and 2, respectively. Lower temperature increased 24 h heat production, but not 24 h activity. The mean activity periods moved from before and after feeding to after feeding, especially in the afternoon. During the afternoon, activity decreased at the lower ambient temperature, whereas metabolic rate remained constant. It is concluded that the effect of ambient temperature on metabolic rate depends on the time of day. (Abstract retrieved from CAB Abstracts by CABI’s permission)


1993 ◽  
Vol 70 (2) ◽  
pp. 381-392 ◽  
Author(s):  
S. B. Cammell ◽  
M. J. Haines ◽  
M. Gill ◽  
M. S. Dhanoa ◽  
J. Frances ◽  
...  

Eight Friesian calves were reared from birth to the start of the experiment at a predetermined growth rate of 1.0 kg/d. Four calves (group 1) commenced the experiment at 22 weeks of age and the remainder (group 2) at 34 weeks, and feed intake was calculated to provide sufficient metabolizable energy to sustain zero energy balance (Em). Between experimental days 30 and 56 at maintenance levels of feeding, respiratory exchange measurements were made using open-circuit calorimetry to provide indirect estimates of heat production (H) simultaneous with measurements of faecal and urinary excretion of energy and N. A datum point for Em and H was established for each animal giving mean values for Em of 491 and 537 and for H of 476 and 511 kJ/kg live weight (LW)0.75 per d for groups 1 and 2 respectively. Treatment levels calculated as 0·25, 0·5, 0·75 and 1·25 of dry matter intake required to sustain the measured Em, were imposed on individual animals after day 56 and further measurements of H and faecal/ urinary balance were made between days 72 and 84 followed by measurements of fasting heat production (FHP) during days 86–90 from the two animals in each group which had received the 0.75 and 1.25 levels of intake. Regression analysis of the treatment levels indicated separate linear models which predicted Em at 419 and 473 kJ/kg LW0·75 per d for groups 1 and 2 respectively. The incorporation of FHP with partitioning of faecal and urinary energy losses measured during fasting altered the relationship but not the predicted Em. Overall predicted Em (days 72–84) from all models were 406 and 478 kJ/kg LW0.75 per d for groups 1 and 2 respectively which were significantly lower (P < 0·05) than Em measured during days 30–56.


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