A standard protocol is required for carrying out routine ileal nitrogen (N) digestibility rat bioassays. The aim of this study was to determine the effects of feeding regimen on ileal N digestibility in rats fed diets containing different protein sources and chromic oxide as an indigestible marker. The experimental design was seven diets (protein-free (PF), enzyme-hydrolysed casein (EHC), lactalbumin (LAC), wheat gluten (GLU), ®sh ®llets (FIS), soy protein isolate (SOY), zein) by three feeding regimens (frequent, meal, ad libitum) with 10 rats per diet. In frequent feeding, food was provided for eight 10 min periods between 09:00 and 16:00; in meal feeding, food was provided for one 3 h period at 09:00; in ad libitum feeding, food was available at all times. Rats were fed for 8 days, killed and digesta were collected from the terminal 20 cm of the ileum. The diets and freeze-dried digesta were then analysed for N and chromium (Cr). There were statistically signi®cant effects of feeding regimen on ileal digesta weight, ileal N/Cr ratio and apparent (AND) and true (PF TND, EHC TND) N digestibility. Mean N digestibilities, averaged over four dietary treatments (LAC, GLU, FIS, SOY), for the frequent, meal and ad libitum feeding regimens respectively were: AND, 88.8, 90.4, 85.8; PF TND, 94.9, 96.4, 97.0; EHC TND, 92.7, 94.0, 95.6. Although the N digestibilities were higher for rats on meal feeding compared with frequent feeding, the only statistically signi®cant differences were for the lactalbumin treatment, and these were small in absolute terms. This study demonstrated that meal feeding was suitable and frequent feeding was unnecessary for most protein sources tested, and that ad libitum feeding was not ideal because of the smaller and more variable quantities of digesta collected and the more variable ileal N/Cr ratios.
INTRODUCTIONThe determination of protein and amino acid digestibility is an integral component of protein quality evaluation procedures. In the past, determination of protein digestibility in monogastric animals has generally been accomplished using nutrient balance techniques to measure the amount of faecal nitrogen (N) that is excreted in relation to dietary N intake. Inaccuracy with this approach has been recognised 1±5 and this arises from microbial metabolism of undigested dietary protein and endogenously secreted, N-containing compounds entering the large bowel from the small intestine. As a consequence, protein digestibility is now frequently given as apparent and true ileal digestibility based on the measurement of N ow at the terminal ileum.