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1.
In an experiment with broilers (origin Tetra B) and with rats (albino, Wistar line) with 2 animals each, heat production was ascertained by measuring CO2 production and O2 consumption over 20 minutes after their feeding 18 h and 1 h before the beginning of measuring at ambient temperatures of 30, 25, 20, 15 and 10 degrees C. Every variant was followed through over 6 h/d in 12 measuring sections. The feed amount/ánimal and day was adapted to energy maintenance requirement. At the beginning of the experiments the broilers and rats were 14 and 21 weeks old resp. and weighed 2.2 kg and 220 g resp. The variation of the ambient temperature did not influence the heat production of the broilers. In contrast to this, the time of feeding in relation to the beginning of measuring had a distinct effect on heat production. Whereas a heat production of 342 +/- 34 kJ/kg LW0.75.d was ascertained in the postabsorptive state 18 h after the last feed intake, it increased by 11% to 393 +/- 32 kJ/kg LW0.75.d when measuring began 1 h after feeding. The very act of feed intake increased heat production by 75%. Rats showed a distinct increase of heat production caused by a decreasing ambient temperature. In the temperature range of 30-25 degrees C the increase was shallower than in the range of 25-10 degrees C. Per 1 degrees C below 25 degrees C heat production increased by 30 kJ/kg LW0.75.d. The increase was independent of the metabolism level, which was influenced by the feeding variants. The results are discussed in connection with Rubner's theory of heat compensation.  相似文献   

2.
The heat production of 4 rats was measured by means of indirect calorimetry over 20 h/d at intervals of 4 min at ambient temperatures of 30, 25, 20 and 15 degrees C and feed intakes of 0, 4, 8 and 12 g/d. When the rats were hungry, their heat production was reduced by between 8 and 44 kJ/kg LW0.75.d. Feed intake increased heat production by between 54 and 102%. In the temperature range between 20 and 30 degrees C the rats required 0.36 kJ or 2.4% resp. of the metabolizable energy for the intake of 1 g feed. At 15 degrees C the corresponding values were 0.48 kJ or 3.2% resp. The activity-conditioned quota of heat production was estimated as 31 +/- 10%. In the temperature range of between 30 and 25 degrees C thermoregulatory heat production amounted to 5 and that in the temperature range between 25 and 15 degrees C to 20 kJ/kg LW0.75.d.K. No compensation of thermoregulatory heat by heat from increase of energy intake could be proved in the temperature range between 15 and 30 degrees C.  相似文献   

3.
In two experiments with fully-grown albino rats (Wistar strain) the energetic utilization of glucose, sunflower oil and casein in the maintenance metabolism was determined under thermoneutral conditions of keeping the animals. The relative requirement of metabolizable energy for maintenance was, with either glucose, sunflower oil or casein being the sole energy source of the feed, in experiment 1 100:105:133 and in experiment 2 100:102:135. The absolute values of the maintenance requirement of metabolizable energy were in experiment 1 347 +/- 26, 364 +/- 61 and 460 +/- 33 resp., and in experiment 2 330 +/- 11, 337 +/- 21 and 446 +/- 27 kJ/kg LW 0.75 resp. The results are discussed in connection with the efficiency of ATP synthesis (metabolizable energy/mol ATP gain) in the oxidative decomposition of nutrients.  相似文献   

4.
Albino rats bred in the institute (Wistar line) divided into 3 groups of 9 animals each received, beginning at the age of 4 weeks, feed mixtures with 10, 40 and 70% protein in the rations over a period of 24 weeks divided into 14 subperiods of study. The feed mixture changed cyclically for the groups of animals after each sub-period. Every period was divided into a growth period (8 days) with the rats kept in metabolism cages and a period of feeding on maintenance level (4 days) with the rats kept in respiration chambers. In both periods the temperature was kept constant at 30 degrees C. On 3 days of feeding on the maintenance level the metabolism parameters of energy, C and N metabolism were measured and energy maintenance requirement was ascertained. Both the energy maintenance requirement of the growing rats (up to 200 g live weight) and that of the nearly fully grown and fully grown rats resp. (greater than 200 g live weight) significantly depended on the nutrient composition of the feed mixtures supplied. It increased with the increasing protein and simultaneously decreasing carbohydrate quotas in the feed. On an average of the studies the rats had, in the sequence of 10, 40 and 70% protein content, an energy maintenance requirement of 383 +/- 31 (n = 105), 415 +/- 31 (n = 106) and 459 +/- 36 kJ metabolizable energy/kg LW0.75.d (n = 102). Energy maintenance requirement behaved relatively like 100:108:120. Based on the fact that energy maintenance requirement may be considered the requirement of ATP, relative expectancy values for energy maintenance requirement can be calculated with the energetic efficiency of the ATP synthesis (kJ metabolizable energy/Mol ATP gain) in nutrient catabolism from the relation of the experimentally ascertained nutrient metabolism at a variant supply of protein of 100:110:118. The hypothesis that the efficiency of ATP synthesis in the catabolism of the main nutrients supplying energy can be considered a relative measure of the dependence of the energy maintenance requirement on nutrient composition has been confirmed in this experiment. Different findings in earlier experiments raise the question if those findings were influenced by adaptation effects. An experimental solution of this question is considered important.  相似文献   

5.
8 experiments were carried out with 9 albino rats each (Wistar line, bred at the institute) in the live weight range between 70 and 200 g and at environmental temperatures (ET) of 34, 32, 30, 28, 26, 24, 22 and 20 degrees C. In the course of each individual experiment the rats were alternatively fed for maintenance and weight gain (semi ad libitum) with feed mixtures containing 10, 25 and 40% crude protein (3 animals/variant). Energy metabolism was measured according to the method of indirect calorimetry over a total of 780 metabolism periods. In the temperature range studied there was no compensation between thermoregulatory heat and heat from other processes of the metabolism. The partial utilization of metabolizable energy for energy retention in the body was independent of ET and ranged between 73 and 80% for the 7 experiments with ET between 32 and 20 degrees C. Energy utilization depended on the protein content of the feed and decreased from 81 to 79 or 73 resp. when the protein content increased from 10 to 25% or to 40% resp. Energy requirement for protein retention varied between 1.61 and 2.09 kJ metabolizable energy/kJ and was independent of ET. Energy maintenance requirement (measured at 28, 30 and 32 degrees C) increased with the growing protein content from 415 to 439 and 447 kJ/kg LW0.75.d resp. (regression analysis) and from 411 to 420 and 432 kJ/kg LW0.75.d (measuring at maintenance level). The relative weight gain with the increased protein content of the feed largely corresponds to the expected values according to the efficiency of ATP synthesis in the oxidative degradation of nutrients. The relationship between heat production and ET is parabolic. In the live weight range studied the average thermoneutral temperature (TNT) was 32 degrees C. It decreased during the course of development from 34 to 30 degrees C. TNT decreased with the growing protein content of the feed. Thermoregulatory heat production depended on both environmental temperature and the stage of development. Its average value in the development range studied decreased with an increase of the environmental temperature by 2 K each, starting from 20 degrees C and rising to 32 degrees C, in the following linear sequence: 23.3, 21.0, 16.8, 12.5, 8.3, 4.0 and 0.3 kJ/kg LW0.75.d.K.  相似文献   

6.
In two experiments with male Wistar rats energy metabolism was measured on the feeding level of maintenance in the course of growth and in various adult periods after the application of feed mixtures with various protein-carbohydrate quotas (10, 40 and 70% crude protein) according to two different feeding regimes. While there was a change of protein levels between the animal groups in periods 1 to 3 and 8 to 10 from one period to the other, the protein levels in periods 4 to 7 and 11 to 13 remained the same for each animal group. Irrespective of the feeding regime, a dependence of the energy maintenance requirement on the nutrients according to the expected values was measured, which result from the different efficiency of ATP synthesis in the oxidative degradation of the nutrients. On an average of the periods maintenance requirement amounted to 357 +/- 21, 399 +/- 16 and 443 +/- 28 kJ/kg LW0.75.d (experiment 1) and 350 +/- 29, 383 +/- 34 and 442 +/- 30 kJ/kg LW0.75.d (experiment 2) for 10, 40 and 70% crude protein in the feed. The relation between the maintenance requirement values was 100:112:124 and 100:109:126. This contrasts with the relative expected values of 100:108:115 and 100:109:116.  相似文献   

7.
In 2 experiments with young broiler chickens, origin Tetra B, heat production was measured in dependence on ambient temperature indirectly and with the gas exchange both over 24 h and in 20-minute periods beginning on their 5th day of live. The chickens, divided into 2 X 2 groups according to sex, were constantly kept in a climatic chamber changed in to a respiration chamber during the 8- or 11-week-long experiments. The maximum variation of the temperature was between 5 and 35 degrees C. In the periods of 24-h measurements over 4 days each, the ambient temperature was changed from day to day in steps of 5 degrees C. Heat production was influenced by the age of the chickens, energy intake and ambient temperature. The results of the measurements at the same age and the same energy intake and a temperature variation between 5 and 35 degrees C can well be described by polynomes of the 3rd degree up to the 8th week of live. The thermoregulatory conditioned heat production per 1 degree C below the critical temperature decreased with the age of the chickens. In the first few weeks of life it was 20 kJ, in the 6th and 7th weeks of life 10-15 kJ and then decreased to 4-5 kJ/kg life weight 0.75.d. degrees C. Based on the temperature of minimal heat production, the heat production of 16- to 30-day-old chickens increased to 60-80% at an ambient temperature of 5 degrees C; the metabolism of chickens older than 7 weeks was only increased by about 20%. For the first 2 weeks 35 degrees C were ascertained as critical temperature, for the 3rd to 6th weeks 30 degrees C and for the 7th and 8th weeks 25 degrees C.  相似文献   

8.
7 experiments with 6 chickens each (origin Tetra B) in the live weight range between greater than 100 and less than 300 g and up to 1800 g were carried out at environmental temperatures (ET) of 35, 30, 25 (2 experiments) 20 (2 experiments) and 15 degrees C. In the course of each experiment the chickens alternatively received feed mixtures containing 20 and 40% crude protein (3 animals/variant) for maintenance and weight gain (semi ad libitum). Energy metabolism was measured according to indirect calorimetry over a total of 645 metabolism periods. In the temperature range studied there was no compensation between thermoregulatory heat and heat from other metabolic processes. The partial utilization of metabolizable energy for energy retention in the body was independent of ET and remained in the limits between 71 and 73%. Energy utilization was dependent on the protein content of the feed. It decreased from 75 to 69% with the increase of the protein content from 20 to 40%. Energy requirement for protein retention varied between 1.67 and 1.89 kJ metabolizable energy/kJ and was independent of ET. Energy requirement (metabolizable energy) for the maintenance of the energy balance was independent of the protein content of the feed. It increased from 433 kJ/kg LW0.75.d at 35 degrees C to 693 kJ/kg LW0.75.d at 15 degrees C ET. The relationship between heat production and ET is parabolic. The thermoneutral temperature decreased from 35 to 25 degrees C in the course of development. In the live weight range of 300-500 g thermoregulatory heat production had its maximum with 19 kJ/kg LW0.75.d.K and decreased in the further development to 10-13 kJ/kg LW0.75.d.K.  相似文献   

9.
In addition to earlier experiments with growing rats on the protein levels 10, 25 and 40% crude protein in the dry matter of the feed (Hoffmann et al., 1982 a), two groups of nine male Wistar rats each received feed mixtures with 6 or 25% crude protein resp. and energy metabolism on the energy maintenance level in an N equilibrium or with a positive N balance resp. were measured on 6 levels of live weight between 65 and 250 g and additionally also at subsequent fasting day. Energy maintenance requirement on average of the 6 periods amounted to 381 and 377 kJ metabolizable energy/kg W 0.75 X d on a low or middle protein level resp. and thus did not show changes at the decrease of N retention to values of about zero even with regard to different ATP formation capacities of the nutrients.  相似文献   

10.
1. Data from 30 published experiments have been analysed to examine the relationships between environmental temperature and the long-term, adapted responses of laying pullets, measured as metabolisable energy intake, egg output and body weight change. Heat production was also estimated indirectly from the other three variables. 2. The majority of experiments employed White Leghorns, but there were 8 large trials in which brown crossbred pullets had been compared directly with White Leghorns. These trials were used to estimate differences in energy intake and heat output between brown and white birds. 3. A total of over 26,000 birds was involved in the analysis. Individual trials varied in scale from 9 birds to 2,280 birds per treatment and in duration from 8 to 61 weeks. The constant temperatures investigated ranged from 10 degrees C to 34 degrees C, but there were no data for brown pullets beyond 30 degrees C. 4. The relationship between temperature and metabolisable energy intake is curvilinear, with food intake declining more steeply as ambient temperature approaches body temperature. Adapted heat production per bird is also a curvilinear function of temperature, tending towards a value of zero when extrapolated to the point at which ambient temperature equals normal body temperature. However no satisfactory data are available for fully adapted responses in the range 34 to 42 degrees C because egg production declines continuously when these temperatures are maintained for long periods. 5. When energy intake and heat output are expressed as functions of metabolic body size (kg 0.75) they can be represented as linear functions of temperature within the range 15 to 30 degrees C, but the slope must change outside this range. 6. It is calculated that the energy available for production is at a maximum at 23 degrees C for brown birds and at 24 degrees C for White Leghorns. Gross energetic efficiency is at a maximum at 30 degrees C, but egg output is reduced at this temperature. The optimum operating temperature for laying houses will depend upon the local cost of modifying ambient temperature and on the cost of supplying diets of appropriate protein content.  相似文献   

11.
Forty 3-week old male Wistar rats (initial weight 45-50 g) were used. After weaning they were fed ad libitum for four weeks (I to IV) on 6 isocaloric and isonitrogenous semisynthetic diets based on soya bean meal (diet SBM) or on ground lupin seed (diet LS) alone or autoclaved (A) or not at 120 degrees C and supplemented with DL-methionine (diets ALSm or LSm, respectively) or with DL-methionine + L-lysine (diets ALSm + l or LSm + l). The diets differ in their protein quality and were formulated in order to provide the adequate experimental conditions to determine the biological value (10% crude protein). Then over the fifth and sixth weeks (V and VI) the rats were fed on the same diets but restricted to 60% of the voluntary feed intake. In a parallel experiment, a group of eight rats previously fed ad libitum on diet SBM for four weeks was fasted for 72 h and then fed on the same diet at a level of intake slightly below maintenance. After a 24 h adaptation period, irrespective of the level of intake and type of diet, a series of 24 h gas-exchanges measurements were carried out in open-circuit respiration chambers. Measurements of energy balance were used to calculate ME for maintenance (MEm) and the efficiency of utilization of ME, using a linear regression of energy retention (RE) on ME. The estimates for MEm derived from energy balances of rats fed above maintenance ranged from 564 to 621 kJ/kgW0.75 per d. No significant differences between diets were observed. From pooled data MEm was found to be 599 kJ/kgW0.75 per d, a value not significantly different from that calculated from measurements at fasting and below maintenance levels (598 kJ/kgW0.75 per d). The efficiency of utilization of ME for maintenance was 81.1% and the efficiencies of utilization of ME for RE ranged from 36.6 to 59.9%. It is concluded that no variations in MEm requirements in growing rats attributable to variations in dietary protein quality have been found. Nevertheless, these results should be taken with caution because of limitations inherent of statistical modelling approaches of partitioning ME.  相似文献   

12.
Heat production (indirect calorimetry) and motor activity were measured continuously with 4 repetitions at 8 male albino rats (24 h fasting) over 21 h (4 minute cycle of measured value registration). The average difference between maximum and minimum heat production in a 4-minute measuring period amounted to 82 +/- 14% (68 to 139%). There was a significant connection between heat production and activity. 7.9 +/- 1.2% of the heat production of the hungry rat could be ascribed to activity. In the course of the day of fasting (24 h) an average metabolism reduction of 15 kJ/kg LW0.75 could be observed.  相似文献   

13.
1. The objective of this study was to determine a metabolisable energy (ME) requirement model for broiler breeder hens. The influence of temperature on ME requirements for maintenance was determined in experiments conducted in three environmental rooms with temperatures kept constant at 13, 21 and 30 degrees C using a comparative slaughter technique. The energy requirements for weight gain were determined based upon body energy content and efficiency of energy utilisation for weight gain. The energy requirements for egg production were determined on the basis of egg energy content and efficiency of energy deposition in the eggs. 2. The following model was developed using these results: ME = kgW0.75(806.53-26.45T + 0.50T2) + 31.90G + 10.04EM, where kgW0.75 is body weight (kg) raised to the power 0.75, T is temperature ( degrees C), G is weight gain (g) and EM is egg mass (g). 3. A feeding trial was conducted using 400 Hubbard Hi-Yield broiler breeder hens and 40 Peterson males from 31 to 46 weeks of age in order to compare use of the model with a recommended feeding programme for this strain of bird. The application of the model in breeder hens provided good productive and reproductive performance and better results in feed and energy conversion than in hens fed according to strain recommendation. In conclusion, the model evaluated predicted an ME intake which matched breeder hens' requirements.  相似文献   

14.
In connection with the measuring of parameters of the protein metabolism in parallel experiments, the energy metabolism of 6 chickens (origin Tetra B) in the live weight range between approximately 100 and 1,800 g was determined under conditions of restricted energy supply. 3 animals each received a feed mixture containing 20% (animal group 1) and 38% (animal group 2) crude protein. The amount of feed was daily increased by 1.5 g DM. The digestibility of energy and nitrogen was independent of the age. 66.3 +/- 3.3% and 64.0 +/- 5.0% resp. of the metabolisable energy were utilised for protein and fat retention. The energy maintenance requirement, determined at a live weight of 2,000 g, was independent of protein supply and averaged in the two animal groups 434 +/- 40 kJ metabolisable energy/kg live weight 0.75 . d. The result of multiple regression was, for the growth period investigated, an energy maintenance requirement of 403 +/- 32 kJ metabolisable energy/kg live weight 0.75 . d. 1.77 and 1.38 J metabolisable energy resp. were required for 1 J protein or fat retention. The energy requirement for protein retention was independent of the degree of protein supply. The results from the measuring of energy metabolism are discussed in connection with the kinetic parameters of protein metabolism ascertained in parallel experiments.  相似文献   

15.
Six animals each out of 12 female fattening hybrids (150 X (L X E] were given rations containing 17 or 45% crude protein resp. 4 periods of growth feeding alternated with 5 periods of maintenance feeding in the live weight range between 33 and 146 kg. The feeding level did not have an influence on the level of digestibility. From the experiments with 17% crude protein in the ration 1004 and from those with 45% crude protein 947, on average 977 kJ metabolizable energy per kg LW0.62 in the maintenance periods and 980 in the growth periods were derived as maintenance requirement of metabolizable energy. These values for maintenance requirement are by 50% higher than those in previous experiments of our work team. In contrast to expectations, energy maintenance requirement did not grow due to the increase of the protein content of the rations. The utilization of metabolizable energy for retention was 73% for rations with a normal protein content and 66% for those with a high protein content. The partial utilization of metabolizable energy for fat retention was ascertained as 83% and as 49% for protein retention by means of multiply regressive evaluation.  相似文献   

16.
Investigations were carried out about nitrogen and energy metabolism feeding rations with 17-24 and 44-47% crude protein content on maintenance and growing level to castrated male hybrid pigs of line 150. In growing periods the N deposition amounted to 10 g/animal.d (15 kg live weight), 18 g/animal.d (30 kg LW) and 21 g/animal.d (greater than 40 kg LW) on lower protein feeding level. In experiments with higher protein feeding level the corresponding results were 17, 22 and 22 g N deposition/animal.d. The partial utilization of metabolizable energy for deposition amounted to 70% for the rations with 17-24% protein content and to 59% for the rations with 44-47% protein content, without correlation to the animals development and the alternation in the protein feeding level. The results of regression analysis about maintenance requirement were 814, 775 and 806 kJ metabolizable energy/kg LW0.62.d in trials feeding rations with 17-24% crude protein content as well as 764, 846 and 818 kJ metabolizable energy/kg LW0,62.d in trials feeding rations with 44-47% crude protein content. 1,5-1,8 MJ metabolizable energy were used per MJ protein energy deposition and 1,3-1,4 MJ per MJ fat energy deposition respectively. The energy deposition per kg live weight gain amounted to values between 9 (10 kg LW) and 18 MJ (60 kg LW).  相似文献   

17.
The effect of temperature (23 or 33 degrees C) and feeding level on components of energy balance was studied in seven groups of individually reared Piétrain x (Landrace x Large White) littermate piglets. Within each litter, one pig was reared at 23 degrees C and given a predefined feeding level close to ad libitum (23AL pigs), one was reared at 33 degrees C and also fed close to ad libitum (33AL), and one was reared at 23 degrees C and pair-fed to the 33AL pig (23PF). Piglets of one litter were acclimated during 2 to 4 wk to their experimental temperature in temperature-controlled rooms before being transferred (one per week) to a respiration chamber for measurement of nitrogen and energy balances. The average initial BW was 22.4 kg. The data on O2 consumption, CO2 production, and physical activity were collected over seven consecutive days and used to calculate total heat production (HPtot) and its components: fasting heat production (FHP), heat production due to physical activity (HPact), and thermic effect of feed (TEF). A preliminary trial was conducted in which heat production was measured in three piglets according to a Latin square design at 23, 25, and 27 degrees C. Total heat production was, but activity-free heat production was not, affected by temperature, and no firm conclusions could be drawn as to whether 23 degrees C was within the thermoneutral zone of fed piglets. In Trial 2, the combination of increased temperature and reduced feed intake resulted in a 20% lesser heat production in 33AL than in 23AL pigs. This was due to a reduction in both TEF (-39%) and FHP (0.642 vs 0.808 MJ x d(-1) x kg BW-0.60). Despite the shorter duration of standing activity, HPact was slightly higher at 33 degrees C, probably due to hyperventilation at this temperature. With similar feeding levels (23PF vs 33AL), HPtot and activity-free heat production were less at 33 degrees C and energy retention as protein (+6%) and fat (+31%) was increased. Because HPact was similar for both treatments, the greater energy retention for 33AL seemed to be due to a greater utilization of feed energy or to a reduced maintenance requirement (i.e., reduced FHP). However, the type of stress imposed on 23PF and 33AL pigs was different and may have affected energy metabolism. The results suggest that the reduction in heat production of piglets at high ambient temperatures is caused by a reduction in voluntary feed intake and differences in energetic efficiency. The mechanisms for the lesser efficiency at 23 degrees C compared to 33 degrees C (at the same level of feed intake) remain unclear.  相似文献   

18.
Energy retention was measured alternately at 12 barrows, fattening hybrids of line 150 (150 X (L X E], at maintenance level (4 periods) and growth feeding (5 periods) in the live weight range between 32 and 134 kg, 6 animals each received rations with 17 and 45% crude protein resp. during the complete experimental period. The nutrition level did not have a significant influence on the digestibility level of the feed. The experiments carried out at maintenance level showed that the maintenance requirement of metabolizable energy in the experiments with 17% crude protein in the ration was 941, in the experiments with 45% crude protein in the ration 913kJ ME/kg LW0.62 and on average 927 kJ ME/kg LW0.62. Including the experiments with growth feeding one can conclude from a regression analysis, largely in agreement with the measured values, that 955 kJ ME/kg LW0.62 is the energy maintenance requirement. These values of maintenance requirement are by 50% higher than those derived from previous measurings. In contrast to expectations, the increase of protein concentration in the ration did not result in a higher energy maintenance requirement. The utilization of metabolizable energy for retention amounted to 74% for rations with a normal protein content and to 65% for those with a high protein content. The multiply regressive evaluation showed a utilization of metabolizable energy for fat retention of 79% and for protein retention of 53%.  相似文献   

19.
1. Mature domestic drakes of 7 genotypes, ranging in live weight from 1.1 to 5.1 kg, were each given a daily allowance of feed just below the level of recorded ad libitum intake. 2. House temperature was maintained at 26 degrees C for 16 weeks and then at 10 degrees C for a further 8 weeks. 3. Under these conditions, live weight quickly adjusted to the level of feed supplied and then remained stable. 4. Regression of metabolisable energy intake on live weight (W) yielded estimates of maintenance requirement of 583 kJ/kgW(0.75).d at 10 degrees C and 523 kJ/kgW(0.75).d at 26 degrees C.  相似文献   

20.
Energy metabolism-by means of indirect calorimetry-and kinetic parameters of the protein metabolism on the basis of the 3-compartment model were measured with 4 groups of 4 or 5 male Wistar rats in the growth range of between 70 and 230 g live weight in a total of 5 alternately successive periods at the feeding levels growth and energy maintenance as well as 4 different levels of protein supply (6, 10, 17 and 26% crude protein in the feed). The partial energy requirement values for protein retention (bp) for every animal and every period are calculated from the data of energy metabolism. On an average of the 3 growth periods they amounted to 1.75 +/- 0.37 kJ/kJ. A statistically significant linear relation with a slope of approximately 1 could be derived regressively between the protein synthesis rate and the protein retention rate, including all 5 test periods. There was no proven relation between the bp values and the corresponding individual values of the ratio of protein synthesis rate-diminished by the regressively derived protein synthesis rate in the N balance-to the protein retention rate. The results do not permit proven statements on the quantitative relations between protein turnover and energy requirement for protein retention, which is first of all due to methodical shortcomings in measuring both protein metabolism and energy metabolism. They indicate, however, that the heat production from protein synthesis has only a relatively low share in the additional energy expenditure for protein retention and does not considerably surpass the necessary minimal cost for the synthesis of the deposited protein in growing rats.  相似文献   

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