The maximum metabolizable energy intake and the relationship with basal metabolic rate in the striped hamsterCricetulus barabensis

2002 ◽  
Vol 47 (4) ◽  
pp. 417-423 ◽  
Author(s):  
Zhi-Gang Song ◽  
De-Hua Wang
1982 ◽  
Vol 34 (3) ◽  
pp. 355-357 ◽  
Author(s):  
R. T. Cowan ◽  
J. J. Robinson ◽  
I. McDonald

ABSTRACTData from three comparative slaughter experiments involving a total of 73 ewes were used to study the influence of body fat content at the start of lactation (X1 kg) and of metabolizable energy intake (X2, MJ/day), on the rate of loss of body fat by lactating ewes over the first 6 weeks of lactation (Y, g/day). The relationship was described by the equation:Thus the rate of fat loss was greater for ewes with higher initial fat contents, but the differential became less as metabolizable energy intake increased. Since increases in body fatness depress food intake it was not possible to prevent loss of body fat during early lactation in fat ewes given high concentrate diets ad libitum. The likely response in milk yield to increase in body fatness at parturition is therefore strongly dependent on the relative levels of body fatness and metabolizable energy intake. The value of any improvement in condition of the ewe at parturition may be considerable when metabolizable energy intake during lactation is low but much less when it is expected to be high.


2005 ◽  
Vol 34 (3) ◽  
pp. 1006-1016 ◽  
Author(s):  
Douglas Sampaio Henrique ◽  
Ricardo Augusto Mendonça Vieira ◽  
Pedro Antônio Muniz Malafaia ◽  
Maurício Cordeiro Mancini ◽  
André Luigi Gonçalves

Data of 320 animals were obtained from eight comparative slaughter studies performed under tropical conditions and used to estimate the total efficiency of utilization of the metabolizable energy intake (MEI), which varied from 77 to 419 kcal kg-0.75d-1. The provided data also contained direct measures of the recovered energy (RE), which allowed calculating the heat production (HE) by difference. The RE was regressed on MEI and deviations from linearity were evaluated by using the F-test. The respective estimates of the fasting heat production and the intercept and the slope that composes the relationship between RE and MEI were 73 kcal kg-0.75d-1, 42 kcal kg-0.75d-1 and 0.37. Hence, the total efficiency was estimated by dividing the net energy for maintenance and growth by the metabolizable energy intake. The estimated total efficiency of the ME utilization and analogous estimates based on the beef cattle NRC model were employed in an additional study to evaluate their predictive powers in terms of the mean square deviations for both temperate and tropical conditions. The two approaches presented similar predictive powers but the proposed one had a 22% lower mean squared deviation even with its more simplified structure.


1969 ◽  
Vol 20 (2) ◽  
pp. 375 ◽  
Author(s):  
Graham N McC

Energy, carbon, and nitrogen balances were determined in adult wether sheep given a diet of lucerne hay and whole oats at several planes of nutrition between fasting and ad libitum. Four sheep were studied when their weight was c. 30 kg (10% fat) and later when they weighed c. 75 kg (33% fat); another four were studied at c. 70 kg (30% fat) and later at c. 45 kg (16% fat). The most obvious effect of fatness was loss of appetite. Voluntary food intake began to decline when body weight approached 60 kg and was half of the maximal amount when the sheep weighed 70 kg or more; one very fat sheep ate only 100–200 g food/day for several weeks. 1n addition, environmental changes such as transfer from a pen to a cage or respiration chamber often caused temporary inappetence when the sheep were in fat condition but seldom when they were lean. Fasting metabolic rate increased with body weight in accordance with the relationship generally applicable to adult sheep except when the sheep were in the anorectic phase of obesity, at which time their metabolic rate was 30–40% above normal. The digestibility of the diet was not dependent on the fatness of the sheep, nor was the relationship between metabolizable and digestible energy. At each level of feeding, the heaviest sheep produced most heat, but differences were less than at fasting; oxidation of fat, rather than protein, was responsible. When daily heat production and metabolizable energy were both expressed as multiples of the fasting energy loss, all sheep conformed to one relationship; the same held for the relation between energy balance and metabolizable energy. Net efficiency (change of energy balance divided by change of metabolizable energy intake) was 78% for maintenance and 55% for production, irrespective of body condition. Gross efficiency (energy storage divided by gross energy intake) was strongly influenced by body condition. When fed ad libitum, thin sheep achieved an efficiency of c. 26 % and fat sheep reached 21 % whereas anorectic very fat sheep never exceeded 10%. Thin, fat, and very fat sheep required 400, 500 and 650 g dry matter/day respectively for maintenance (zero gross efficiency).


2003 ◽  
Vol 140 (4) ◽  
pp. 451-459 ◽  
Author(s):  
H. DARMANI KUHI ◽  
E. KEBREAB ◽  
S. LOPEZ ◽  
J. FRANCE

Data from six studies with male broilers fed diets covering a wide range of energy and protein were used in the current two analyses. In the first analysis, five models, specifically re-parameterized for analysing energy balance data, were evaluated for their ability to determine metabolizable energy intake at maintenance and efficiency of utilization of metabolizable energy intake for producing gain. In addition to the straight line, two types of functional form were used. They were forms describing (i) diminishing returns behaviour (monomolecular and rectangular hyperbola) and (ii) sigmoidal behaviour with a fixed point of inflection (Gompertz and logistic). These models determined metabolizable energy requirement for maintenance to be in the range 437–573 kJ/kg of body weight/day depending on the model. The values determined for average net energy requirement for body weight gain varied from 7·9 to 11·2 kJ/g of body weight. These values show good agreement with previous studies. In the second analysis, three types of function were assessed as candidates for describing the relationship between body weight and cumulative metabolizable energy intake. The functions used were: (a) monomolecular (diminishing returns behaviour), (b) Gompertz (smooth sigmoidal behaviour with a fixed point of inflection) and (c) Lopez, France and Richards (diminishing returns and sigmoidal behaviour with a variable point of inflection). The results of this analysis demonstrated that equations capable of mimicking the law of diminishing returns describe accurately the relationship between body weight and cumulative metabolizable energy intake in broilers.


2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 158-159
Author(s):  
Phillip A Lancaster

Abstract Metabolizable energy required for maintenance varies with diet and empty body chemical composition. The objective was to quantify the relationships of dietary characteristics and empty body chemical composition with heat production. A literature search was performed to compile data (31 studies, 214 treatment means) on metabolizable energy intake (MEI) and composition of empty body gain in growing steers and heifers. Data analysis were performed using R statistical package for mixed models with study as random variable. Nonlinear regression of energy gain (EG) on MEI indicated the relationship was not curvilinear in this data set, likely due to lack of negative values of EG. Further analyses were conducted using a linear model. Dietary characteristics of roughage level (0–100% of diet DM) and CP (10–25% diet DM), metabolizable energy concentration (1.3–3.3 Mcal/kg DM), and roughage type were evaluated in the model. Roughage sources were categorized into no roughage, silage, hay, pellets, silage + pellets, and hay + pellets. Of the empty body chemical components, proportion of fat in the empty body (EBFp) and in the gain (EBFgp) had a significant (P < 0.001) interaction with MEI on HP. Of the dietary characteristics, roughage level and type had a significant (P < 0.001) interaction with MEI on HP; however, when both were included in the model, roughage type was not significant (P > 0.10). The final model was 47.01 ± 12.54 + 0.630 ± 0.05*MEI – 132.3 ± 64.7*EBFp + 0.0007 ± 0.0001*MEI*Roughage level + 0.753 ± 0.24*MEI*EBFp – 0.268 ± 0.032*MEI*EBFgp with an R2 of 0.919 and an AIC of 1614 compared with 0.867 and 1695 for the simple linear regression model of HP on MEI. In conclusion, greater empty body fat decreased the intercept, and greater empty body fat proportion and levels of roughage in the diet increased the slope between HP and MEI, whereas greater percentage of fat in the empty body gain decreased the slope between HP and MEI.


2014 ◽  
Vol 43 (1) ◽  
pp. 139-148 ◽  
Author(s):  
Helena Moreira ◽  
Betânia Passos ◽  
Josiane Rocha ◽  
Vivianne Reis ◽  
André Carneiro ◽  
...  

Abstract The object of the study was to analyze the relationship between aerobic fitness and body composition in postmenopausal women. We hypothesized that postmenopausal women that had higher adiposity had lower cardiorespiratory capacity, regardless of the characteristics of menopause. The sample included 208 women (57.57 ± 6.62 years), whose body composition and the basal metabolic rate were evaluated by octopolar bioimpedance (InBody 720) and the oxygen uptake by the modified Bruce protocol. Most of the sample showed obesity and a high visceral fat area. The visceral fat area and the basal metabolic rate explained 30% of the variation of oxygen uptake, regardless of age, time, nature or hormone therapy. The values of the latter variables were reduced in the presence of high central adiposity (-6.16 ml/kg/min) and the basal metabolic rate of less than 1238 kcal/day (-0.18 ml/kg/min). The women with oxygen uptake above 30.94 ml/kg/min showed lower values of total and central adiposity when compared with other groups. With an increase of aerobic fitness, there was a growing tendency of the average values of the soft lean mass index, with differences between the groups low-high and moderate-high. These results suggest worsening of the cardiorespiratory condition with an increase of central adiposity and a decrease of the BMR, regardless of age and menopause characteristics.


2015 ◽  
Vol 99 (6) ◽  
pp. 1025-1030 ◽  
Author(s):  
M. Thes ◽  
N. Koeber ◽  
J. Fritz ◽  
F. Wendel ◽  
B. Dobenecker ◽  
...  

2002 ◽  
Vol 138 (2) ◽  
pp. 221-226 ◽  
Author(s):  
A. ALLAN DEGEN ◽  
B. A. YOUNG

Body mass was measured and body composition and energy requirements were estimated in sheep at four air temperatures (0 °C to 30 °C) and at four levels of energy offered (4715 to 11785 kJ/day) at a time when the sheep reached a constant body mass. Final body mass was affected mainly by metabolizable energy intake and, to a lesser extent, by air temperature, whereas maintenance requirements were affected mainly by air temperature. Mean energy requirements were similar and lowest at 20 °C and 30 °C (407·5 and 410·5 kJ/kg0·75, respectively) and increased with a decrease in air temperature (528·8 kJ/kg0·75 at 10 °C and 713·3 kJ/kg0·75 at 0 °C). Absolute total body water volume was related positively to metabolizable energy intake and to air temperature. Absolute fat, protein and ash contents were all affected positively by metabolizable energy intake and tended to be related positively to air temperature. In proportion to body mass, total body water volume decreased with an increase in metabolizable energy intake and with an increase in air temperature. Proportionate fat content increased with an increase in metabolizable energy intake and tended to increase with an increase in air temperature. In contrast, proportionate protein content decreased with an increase in metabolizable energy intake and tended to decrease with an increase in air temperature. In all cases, the multiple linear regression using both air temperature and metabolizable energy intake improved the fit over the simple linear regressions of either air temperature or metabolizable energy intake and lowered the standard error of the estimate. The fit was further improved and the standard error of the estimate was further lowered using a polynomial model with both independent variables to fit the data, since there was little change in the measurements between 20 °C and 30 °C, as both air temperatures were most likely within the thermal neutral zone of the sheep. It was concluded that total body energy content, total body water volume, fat and protein content of sheep of the same body mass differed or tended to differ when kept at different air temperatures.


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