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.

1. Balance trials with respiration measurements were performed with twelve rats and twelve pigs given either low-or high-crude-fibre diets. There were six collection periods with the rats over a live-weight range of 86264 g and three collection periods with the pigs over a live-weight range of 30-55 kg. Measurements were made on the influence of microbial activity in the digestive tract on digestibility and nitrogen and energy metabolism. Dietary inclusion of the antibiotic Nebacitin was the method used to reduce the microbial population.2. The microbial activity in the hind-gut (pmol AT€'/$ air-dry contents) of antibiotic-treated rats was reduced to approximately one-tenth of that of untreated rats.3. Live-weight gain was not significantly affected in either species by a reduction in the microbial activity, in spite of a reduction in dry matter digestibility in animals with reduced microflora. 4.For rats on low-crude-fibre diets, a reduction in microflora reduced digestibility of all nutrients and energy and metabolizability of digestible energy by approximately 5.4%. All differences were highly significant. On high-crude-fibre diets the decrease was approximately 5.9%. In pigs on both crude fibre levels, the digestibility was also influenced by the level of microflora, but the pattern was somewhat different from that obtained with rats, with the Nebacitin treatment increasing the digestibility of N slightly, and the digestibility of fat markedly.5. Retained N in rats reached a maximum when the rats were approximately 60 d old and thereafter decreased with increasing age. However, for pigs daily N retention increased with age. The retained N:digested N value decreased linearly with age in the rats, but varied little with age over the range (104146 d) studied in the pigs.6. The metabolizability of gross energy (metabolizable energy (ME): gross energy) was significantly reduced with an increase in crude fibre level and by the addition of Nebacitin.7. Retained energy (RE) in relation to ME (RE:ME), was not significantly affected either by level of microbial activity or by crude fibre. 8.The ratio, RE as fat (RF):RE as protein (RP) increased as the animals grew. In the rat experiment there was a tendency for RP to be higher for animals with normal microflora than for animals with r e d u d microflora for both crude fibre levels.9. With rats, the regression analyses indicated that the energy requirement for maintenance could be influenced by both the level of microbial activity in the digestive tract and by the level of fibre in the diet. The net availability of ME for maintenance and growth by rats averaged 0.72 for all treatments.10. The net availability of ME for growth in the pigs averaged 0.65 for all treatments.

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Two groups of pigs weighing 90 (Expt A) or 80 (Expt B) kg walked on a horizontal moving rubber belt for a distance of 315 m at a speed of 25.6 ± 0.38 and 28.8 ± 0.35 m/min respectively for 10 min in an open-air-circuit respiration unit. From measurements of VO₂ and VCO₂, heat production and oxidation of carbohydate and fat were calculated 30 min before (I), 10 min during walking (II) and in intervals of 10 min (III, IV) and 30 min (V) after walking. Heat production increased 2-3 times in section II in relation to section I, remained high for 20 min in section III and IV, but reached the basal line in section V. Oxidation of carbohydrate was the main source for heat production.

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