An experiment was carried out to study the effect of changes in either the quality or the quantity of dietary protein intake on the free essential amino acid profiles in plasma, muscle or liver of growing chickens. Following a randomized paired-feeding design based on metabolic body weight (kg M0·75), White Rock male broilers were allocated to one of three isoenergetic (14·5 kJ metabolizable energy per g dry matter (DM)) semisynthetic diets containing different levels of protein (60, 120, 180 or 240 g/kg DM). All diets were based on soya-bean meal, as the sole source of protein, either unsupplemented (diets S) or supplemented with 20 g/kg L-lysine (diets SL) or 2 g/kg DL-methionine (diets SM). Samples of blood, biceps muscle and liver were taken and amino acid analysis was determined by high performance liquid chromatography. Plasma was only adequate to detect the effect of the supplementation with methionine to balance the dietary amino acid (AA) profile. Plasma concentrations of free methionine significantly increased as a result of the supplementation with methionine (P < 0·001) and remained unaffected by the amount of protein ingested. When lysine was added to diets S to induce an AA imbalance, a significant increase in muscle concentrations of free valine, isoleucine and phenylalanine (P <0·05) and a significant decrease in liver concentrations of free arginine and phenylalanine were observed (P<0·05). The supplementation with DL-methionine gave rise to a significant fall in the concentrations of free histidine, glycine and threonine (P < 0·05) and increased those of isoleucine and methionine in the skeletal muscle (P < 0·05), while in liver it significantly lowered the concentrations of free arginine, valine, leucine, phenylalanine and methionine (P < 0·001 to P < 0·05) and raised that of free glycine (P < 0·001). The ratios lysine: phenylalanine, lysine: valine and methionine: glycine in muscle together with that of methionine: glycine in liver seem to be appropriate indexes of the adequacy of the dietary AA profile to requirements.

An experiment was carried out to study the effect of changes in either the quality or the quantity of dietary protein intake on the excretion of nitrogen (N) compounds in the chicken. Thirty-two White Rock male broilers (1 day old) were raised in batteries and fed a commercial starter diet for 9 days. Then they were randomly divided into eight groups each of four birds, of similar body weight (mean live weight: 178 (s.e. 1·9) g), and individually housed in metabolism cages. Following a paired-feeding design based on metabolic body weight (kg M0·75), each group of birds was given, for an experimental period of20 days, each of four levels of protein (60, 120, 180 or 240 g/kg: 5 days each) in two groups of isoenergetic (14·5 kj metabolizable energy per g dry matter) and semisynthetic diets based on soya-bean meal, known to be first limiting in methionine, either unsupplemented (diets S) or supplemented with 2 g/kg DL-methionine (diets SM). Excreta were collected every 3 days for 48 h, frozen and stored at −20°C. The excreta samples were subjected to chemical analysis for uric acid by a rapid high-performance liquid chromatographic method, for urea and ammonia by a colorimetric method, and for total N by the Kjeldahl procedure. In general, the excretion of major N compounds was markedly affected by either the quality or the content of dietary protein. Overall, the excretion of total N, uric acid-N, ammonia-N and urea-N significantly (P < 0·05) decreased with improvement in dietary protein quality and significantly (P < 0·05) increased with increase in protein intake. Regression equations were obtained relating the excretion of uric acid, urea, ammonia and total N on protein supply. For the partition ofN compounds output, the ratios of uric acid-N and ammonia-N to total N significantly (P < 0·05) decreased on improving dietary protein quality and increased or remained unchanged, respectively, with the increase in dietary protein content. The use of the ratio of ammonia-N to total N is recommended as a rapid, easy and accurate indicator of dietary protein adequacy, as an alternative to measures based on total N balance, without the need for separation of urine and faeces.

Free amino acid (AA) levels in plasma, muscle and liver were measured in growing chickens given either high or low protein diets varying in quality. In experiment 1, they were force-fed once a day (09.00 h), for 4 days, at about 1·5 × M level, a nitrogen-free (NF) diet and then, on day 5, they were given either diet NF or isoenergetic (13·1 kj metabolizable energy (ME) per g dry matter (DM)) and isonitrogenous high protein diets (200 g crude protein (CP) per kg) based on casein (C), lupin (L), soya bean (SB), faba bean (FB), field pea (FP), vetch (V) or bitter vetch (B) as the sole source of protein. In experiment 2, chickens were force-fed twice a day (09.00 h and 18.00 h), for 3 days, at about 1·9 × M level, with four isoenergetic (13·1 k) ME per kg DM) and isonitrogenous low protein diets (120 g CP per kg) based on SB, FP, V or B as the sole source of protein. On days 5 (experiment 1) and 4 (experiment 2) samples of plasma, muscle and liver were taken for AA analysis over 3 to 4h after morning meal.

In general, within experiments, no significant differences in AA concentrations in plasma, muscle or liver among diets were found. However, there was a qualitative but not a quantitative agreement between the AA abundance in tissues and the AA rank of dietary protein. Moreover, when pooling data from experiments 1 and 2, significant regressions were found between the levels of threonine, aspartic acid, glutamic acid, glycine and proline in plasma, of lysine, alanine, glutamic acid, glycine and proline in muscle or that of proline in liver and the corresponding amounts ingested with the different diets. Under the conditions of these experiments, however, it was not possible to establish conclusively a direct relationship between the level of free amino acids in tissues and dietary protein quality.