The applicability of body composition as estimated by the bioimpedance method to predict energy expenditure (EE) was studied. Ten healthy subjects underwent measurement of body composition and 24-h energy expenditure (24-h EE) twice in a respiration chamber on a fixed program. The 24-h EE and its components, sleeping EE (SEE), basal EE (BEE), and daytime EE, for an individual were very reproducible (coefficient of variation 2.3%, 1.4%, 5.0%, & 3.1%, respectively). The variability of 24-h EE among subjects was 11.4% but only 4.1% when adjusted for differences in lean body mass (LBM). LBM was the best determinant of 24-h EE, BEE, and SEE and accounted for 91-93% of the interindividual variance of EE. The prediction equations were 24EE (kcal/d) = 390 + 33.3 LBM (r2 = 0.93, P = 0.000001), SEE (kcal/h) = 9.8 + 1.1 LBM (r2 = 0.92, P = 0.000001), and BEE (kcal/h) = -3.1 + 1.35 LBM (r2 = 0.91, P = 0.000002). In conclusion, 24EE, BEE, and SEE can be predicted with a high degree of precision from LBM as estimated by bioimpedance in normal-weight subjects.

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Zusammenfassung Die Oxidation von Nährstoffen und Retention von Kohlenhydraten, Protein und Fett hei wachsenden Schweinen Die Oxidation von Nährstoffen sowie deren Beitrag zur Fettretention wurde an Hand von 185 individuellen Bilanzstudien mit wachsenden Schweinen (40–100 kg Lebendgewicht) beurteilt. Der Respirationskoeffizient ohne Berücksichtigung des Proteins (RQnp) lag entweder unter oder über 1. Die beschriebene Methode basierend auf Gasaustausch sowie Kohlenstoff‐Stickstoffbilanz zur Berechnung der Oxidation von Nährstoffen und Lipogenese ist in beiden Fällen gültig (RQnp > 1 und RQnp < 1). Bei einer den Wachstumsbedarf deckenden Energiezufuhr (ME ≥ 1,2 MJ/kg0.75) ist die Oxidation von Nährstoffen im Bezug auf die Proteinretention abhängig von der Menge und Qualität des verdauten Proteins. Weiterhin besteht eine Abhängigkeit von der Menge an verdaulichen Kohlenhydraten. Die Versorgung mit Fett spielt dagegen keine Rolle. Die Oxidation von Kohlenhydraten trägt mit 85%, die von Protein mit 15% zur anfallenden Wärmeenergie bei. Eine Fettoxidation findet auch bei hohem Fettgehalt der Nahrung nicht statt. Die Lipogenese aus Kohlenhydraten stellt die Hauptquelle für die Körperfettretention dar. Da keine Fettoxidation stattfindet, wird das gesamte Nahrungsfett im Körper reteniert. Bei einer für das Wachstum zu geringen Energiezufuhr werden Nahrungsfett und Körperfett oxidiert. Um Protein für die Retention zu erhalten, ist die Oxidation von Protein vermindert. Selbst bei Mobilisierung von Körperfett und Oxidation von Nahrungsfett wird ein Teil der Kohlenhydrate und des Proteins für die Lipogenese vermutlich zum Aufbau von Strukturfett verwendet.

Energy metabolism and substrate oxidation was measured in 12 growing pigs by means of indirect calorimetry and nutrient balances. The measurements were carried out during 5 days of feeding followed by 4 days of starvation and 5 days of re-feeding. During the feeding period, dietary carbohydrates were the main energy source, sufficient to cover energy requirements without oxidation of fat. Starvation reduced the total heat production and affected the oxidation pattern by reducing protein oxidation and shifting from carbohydrate to fat oxidation. On the second day of starvation, the main energy source was body fat and there was no oxidation of carbohydrate. On the second day of re-feeding, the heat production reached the same level as during the feeding period. Also, during the second day of re-feeding, the pattern of nutrient oxidation was similar to the feeding period with oxidation of carbohydrate providing 90% and oxidation of protein providing 10% of the total heat production. There was no fat oxidation. The results demonstrated that the growing pigs were able to re-establish oxidative patterns already 2 days after re-alimentation.

Oxidation of protein (OXP), carbohydrate (OXCHO) and fat (OXF) was investigated with 12 growing bulls treated with beta-agonist (L-644, 969) during two 6 weeks trials (Section A and B) at a mean live weight of 195 and 335 kg. Heat production and nutrient oxidation was calculated from gas exchange, with CO2 reduced for CO2 from fermentation processes, and nitrogen excretion in urine. The beta-agonist had no effect on the level of rumen fermentation as indicated by the same methane production for control and treated animals. Heat Production (HE, RQx) increased by the treatment of beta-agonist corresponding to the increment in the protein retention. OXP/HE,RQx was reduced to about 10% in treated animals, indicating that in order to supply amino acids for an increased protein deposition oxidation of protein is decreased. OXF/HE,RQx were markedly higher in treated animals, but as indicated by the same CH4 production the level of the short chain fatty acids (SCFA) production was the same. Therefore, it was concluded that the increase in OXF was not caused by an increase in SCFA but by a direct influence of beta-agonist on mobilization and oxidation of body fat.