RATE OF CO2 PRODUCTION (RaCO2) AND ESTIMATES OF ENERGY EXPENDITURE (EE) IN WRESTLING PRACTICE 271

1997 ◽  
Vol 29 (Supplement) ◽  
pp. 47 ◽  
Author(s):  
C. A. Horswill ◽  
D. G. Curby ◽  
W. P. Bartoli ◽  
R. Murray
2018 ◽  
Vol 36 (09) ◽  
pp. 918-923
Author(s):  
Sourabh Verma ◽  
Sean M. Bailey ◽  
Pradeep V. Mally ◽  
Heather B. Howell

Objective To determine longitudinal measurements of resting energy expenditure (REE) by indirect calorimetry (IC) in healthy term infants during the first 2 months of life. Study Design An outpatient prospective pilot study was performed in healthy term infants to estimate REE by measuring expired gas fractions of oxygen (O2) and carbon dioxide (CO2) with IC in a respiratory and metabolic steady state. Results A total of 30 measurements were performed. Fourteen subjects completed measurements at both 1 and 2 months of life, and two subjects had only measurements made at 1 month of life. Mean REE values were 64.1 ± 12.7 and 58.4 ± 14.3 kcal/kg/d at 1 and 2 months of age, respectively. Mean O2 consumption and CO2 production measurements were 9.3 ± 2.0 and 7.7 ± 1.2 mL/kg/min and 8.1 ± 2.2 and 6.4 ± 1.1 mL/kg/min at 1 and 2 months of age, respectively. Conclusion This pilot study demonstrates longitudinal measurements of REE by IC in healthy term infants during the first 2 months of life. We also demonstrate that, overall, there is consistency in REE values in this population, with a likely decrease in individual longitudinal measurements over the first 2 months of life.


Rangifer ◽  
2000 ◽  
Vol 20 (2-3) ◽  
pp. 211 ◽  
Author(s):  
Geir Gotaas ◽  
Eric Milne ◽  
Paul Haggarty ◽  
Nicholas J.C. Tyler

The doubly labelled water (DLW) method was used to measure total energy expenditure (TEE) in three male reindeer (Rangifer tarandus tarandus) aged 22 months in winter (February) while the animals were living unrestricted at natural mountain pasture in northern Norway (69°20'N). The concentrations of 2H and l8O were measured in water extracted from samples of faeces collecred from the animals 0.4 and 11.2 days after injection of the isotopes. Calculated rates of water flux and CO2-production were adjusted to compensate for estimated losses of 2H in faecal solids and in methane produced by microbial fermentation of forage in the rumen. The mean specific TEE in the three animals was 3.057 W.kg-1 (range 2.436 - 3.728 W.kg1). This value is 64% higher than TEE measured by the DLW method in four captive, non-pregnant adult female reindeer in winter and probably mainly reflects higher levels of locomotor activity in the free-living animals. Previous estimates of TEE in free-living Rangifer in winter based on factorial models range from 3.038 W.kg-1 in female woodland caribou (R. t. caribou) to 1.813 W.kg-1 in female Svalbard reindeer (R. t. platyrhynchus). Thus, it seems that existing factorial models are unlikely to overestimate TEE in reindeer/caribou: they may, instead, be unduly conservative. While the present study serves as a general validation of the factorial approach, we suggest that the route to progress in the understanding of field energetics in wild ungulates is via application of the DLW method.


1992 ◽  
Vol 263 (3) ◽  
pp. R685-R692 ◽  
Author(s):  
C. L. Jensen ◽  
N. F. Butte ◽  
W. W. Wong ◽  
J. K. Moon

The doubly labeled water (2H(2)18O) method used to estimate total energy expenditure (EETotal) is particularly sensitive to analytic error in preterm infants, because of their high percentage of body water and the high ratio of water flux to CO2 production. To evaluate further use of this method, the EE of 12 preterm infants was measured by indirect calorimetry and 2H(2)18O simultaneously and continuously for 5 days. Initial infant weight, age, and postconceptional age were (means +/- SD) 1,674 +/- 173 g, 4.4 +/- 2.6 wk, and 34.6 +/- 1.6 wk, respectively. The indirect calorimeter system included an air-temperature-controlled chamber and heart rate monitor. EE was measured by indirect calorimetry for 85.6 +/- 4.7% of study time and estimated from the linear regression of heart rate on EE for 14.4 +/- 4.7% of study time. The 2H(2)18O method entailed an initial dose of 100 mg 2H2O and 250 mg 18O/kg and a final dose of 75 mg 18O/kg; urine was collected twice daily. 2H and 18O enrichments were measured by gas-isotope-ratio mass spectrometry. EE was calculated from measured 2H and 18O dilution spaces (NH, NO), turnover rates (kH, kO), and measured respiratory quotient. The ratio of 2H to 18O dilution spaces was 1.01 +/- 0.01 and the ratio of kO to kH was 1.16 +/- 0.04. Estimation of EE from 2H(2)18O and indirect calorimetry agreed within 1%, although individual variability in methods was large.


1990 ◽  
Vol 259 (4) ◽  
pp. E576-E585 ◽  
Author(s):  
M. I. Goran ◽  
E. J. Peters ◽  
D. N. Herndon ◽  
R. R. Wolfe

Total energy expenditure (TEE) was measured in 15 burned children with the doubly labeled water technique. Application of the technique in burned children required evaluation of potential errors resulting from nutritional intake altering background enrichments during studies and from the high rate of water turnover relative to CO2 production. Five studies were discarded because of these potential problems. TEE was 1.33 +/- 0.27 times predicted basal energy expenditure (BEE), and in studies where resting energy expenditure (REE) was simultaneously measured, TEE was 1.18 +/- 0.17 times REE, which in turn was 1.16 +/- 0.10 times predicted BEE. TEE was significantly correlated with measured REE (r2 = 0.92) but not with predicted BEE. These studies substantiate the advantage of measuring REE to predict TEE in severely burned patients as opposed to relying on standardized equations. Therefore we recommend that optimal nutritional support will be achieved in convalescent burned children by multiplying REE by an activity factor of 1.2.


1993 ◽  
Vol 44 (7) ◽  
pp. 1423
Author(s):  
LR Giles ◽  
JM Gooden

The paper reviews the current methods available for the measurement of heat exchange in pigs. The cost of construction of automated open-circuit respiration chambers, in association with climate-controlled facilites, has restricted continuous measurement of energy expenditure in pigs to a small number of laboratories around the world. Ventilated hoods and face mask techniques are not viable alternatives because of difficulties in maintaining a uniform environment around the animal and restriction of food intake. Indirect techniques, including carbon dioxide (CO2) entry rate and doubly-labelled water are only applicable when other technique are not available because of the errors involved when energy expenditure is based on CO2 production alone. An alternative procedure is described for the measurement of energy expenditure in the growing pig. Whole-body oxygen (O2) consumption is calculated from the product of cardiac output and the arteriovenous difference in blood O2 concentration across the lungs (Fick principle). Oxygen consumption recorded with the new procedure was compared with the ventilated hood and CO2 entry-rate techniques, and used to examine the heat exchange of growing pigs maintained at high ambient temperatures


1996 ◽  
Vol 270 (1) ◽  
pp. E164-E169 ◽  
Author(s):  
P. Ritz ◽  
T. J. Cole ◽  
C. Couet ◽  
W. A. Coward

Accuracy and precision of the the doubly labeled water (DLW) measurements of energy expenditure are commonly estimated with models that do not account for 2H and 18O natural abundance variation. A new and simple treatment that completes the ratio-product model is derived in the present study. It uses both linear regression of multipoint data with time and information on within-subject 2H and 18O natural abundance variation. Use of this treatment is demonstrated in a group of seven subjects in whom 2H and 18O natural abundance variation was assessed by collecting predose samples for 6-8 days before dosing. In this set of 16 measurements, the precision (coefficient of variation) of individual DLW estimates of CO2 production was 4.90 +/- 2.14%, of which 3.23 +/- 1.20% arose from natural abundance variation.


1992 ◽  
Vol 263 (4) ◽  
pp. E676-E687 ◽  
Author(s):  
M. Elia ◽  
N. J. Fuller ◽  
P. R. Murgatroyd

Bicarbonate turnover and energy expenditure were assessed in six healthy male volunteers, by the use of a constant infusion of radiolabeled bicarbonate (NaH14CO3) administered over 36 h, while the volunteers were confined to a whole body indirect calorimeter. Recovery and dilution of isotope were assessed from measurements made on continuous collections of CO2, entering and leaving the calorimeter, urine, and intermittent spot breath and saliva samples. Mean recovery of infused label in gaseous CO2 was 95.6 +/- 1.1% (SD) between 12 and 36 h. Applying a 95% mean recovery of label to each subject individually enabled the use of integrated mean specific activity of CO2 in spot breath and urine samples to predict measured net CO2 production and energy expenditure to within about +/- 6%. Estimates based on urinary measurements were compromised slightly by the exchange of label through the bladder wall (this was dependent on pH and volume of urine). It is concluded that this constant-infusion labeled bicarbonate method offers a potentially useful means of assessing net CO2 production and total energy expenditure over the short term (e.g., 1-3 days).


1991 ◽  
Vol 260 (1) ◽  
pp. E75-E88 ◽  
Author(s):  
M. Elia

Carbon dioxide production in free living animals and humans can be measured using tracer techniques, but the prediction of energy expenditure also requires an estimate of the energy equivalents of CO2 (energy expended/CO2 produced; EeqCO2). This work is concerned with assessing the variation in EeqCO2 with the use of dietary information, indirect calorimetry, and theoretical concepts. The EeqCO2 for diets (EeqCO2 diet) ingested by 63 individuals living in a Cambridgeshire village, UK, was found to vary by less than 10%. The EeqCO2 diet for different populations varied by greater than 10% and for artificial enteral feeds by approximately 20%. Alcohol increases this variability because it has a particularly high EeqCO2. Variation in the nitrogenous end products of metabolism may also have a substantial effect on the EeqCO2 for a subject (EeqCO2 body), especially when a large proportion of energy expenditure is derived from protein oxidation, as in strict carnivores. Nutrient/energy imbalances such as those associated with growth, hypercaloric feeding, or starvation may also have major effects on EeqCO2 body. It is concluded that the calculation of energy expenditure from CO2 production should not employ a universal value for EeqCO2 body. The value should take into account the physiological and clinical state under investigation. Practical recommendations are suggested.


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