This study aimed to evaluate the nutritional value of pasta enriched with legume or wheat gluten proteins and dried at varying temperature. A total of four isonitrogenous experimental diets were produced using gluten powder/wheat semolina (6/94, g/g) pasta and faba bean flour/wheat semolina (35/65, g/g) pasta dried at either 55°C (GLT and FLT, respectively) or 90°C (FVHT and GVHT, respectively). Experimental diets were fed to ten 1-month-old Wistar rats (body weight=176 (sem 15) g) for 21 d. Growth and nutritional, metabolic and inflammatory markers were measured and compared with an isonitrogenous casein diet (CD). The enrichment with faba bean increased the lysine, threonine and branched amino acids by 97, 23 and 10 %, respectively. Protein utilisation also increased by 75 % (P<0·01) in FLT in comparison to GLT diet, without any effect on the corrected faecal digestibility (P>0·05). Faba bean pasta diets' corrected protein digestibility and utilisation was only 3·5 and 9 %, respectively, lower than the CD. Growth rate, blood composition and muscle weights were not generally different with faba bean pasta diets compared with CD. Corrected protein digestibility was 3 % lower in GVHT than GLT, which may be associated with greater carboxymethyllysine. This study in growing rats clearly indicates improvement in growth performance of rats fed legume-enriched pasta diet compared with rats fed gluten–wheat pasta diet, regardless of pasta drying temperature. This means faba bean flour can be used to improve the protein quality and quantity of pasta.

Nutritional requirements of the Iberian pig, a slow-growing, obese porcine breed, are not well defined and seem to differ from those of conventional or high-performing pigs. The effects of the dietary protein content and the feeding level on the utilisation of metabolisable energy (ME) and the rates of gain, protein, and fat deposition were studied with 81 Iberian castrates growing from 50 to 100 kg body weight (BW) by using the comparative slaughter technique. The animals were fed 4 diets providing 145, 120, 95, and 70 g ideal crude protein (CP) per kg dry matter (DM), and containing 13.94, 14.29, 14.56, and 14.83 MJ ME per kg DM, respectively. Three levels of feeding were evaluated: 0.60, 0.80, and 0.95 × ad libitum intake. Growth rate increased (linear and quadratic, P < 0.001) as the dietary ideal CP content decreased. It also increased with the feeding level (linear, P < 0.001; quadratic, P < 0.05). Gain:feed and gain:ME intake improved by decreasing the ideal CP content in the diet (linear, P < 0.001 and P < 0.05, respectively; quadratic P < 0.001 for both variables). Increasing the feeding level improved linearly gain:feed and gain:ME intake ( P < 0.001). Protein deposition (PD):ME intake ranged between 1.23 and 1.44 g/MJ, and it showed a tendency to reach the maximum value when the diet providing 95 g ideal CP per kg DM was fed (quadratic, P = 0.078). When this diet was offered at 0.95 × ad libitum, PD reached a maximum value of 71 g/day. This dietary treatment resulted in average values for average daily gain and retained energy (RE) of 854 g/day and 21.4 MJ/day, respectively. The average rate of gain was 19.93 g/MJ increase in ME intake, equivalent to an energy cost of 50.2 kJ ME per g gain, irrespective of the dietary ideal CP content. Also, the overall marginal efficiency of protein deposition (ΔPD:ΔME; g/MJ) was 1.34. Increasing the feeding level led to increases in PD (linear, P <  0.001) and RE (linear, P <  0.001; quadratic, P <  0.01) irrespective of the dietary ideal CP concentrations. Between 50 and 100 kg BW, the chemical composition of 1 kg gain averaged 78, 592, 28.7, and 284 g for CP, fat, ash, and water respectively. The net efficiency of use of ME for growth ( kg) and the maintenance energy requirements were 0.606 and 396 kJ/kg BW 0.75 per day, respectively. The results support earlier findings that the genotype has marked effects on protein and energy metabolism of growing pigs and underline important compositional differences of the Iberian pig compared with conventional or modern porcine genotypes.

Twenty-four castrated males were used to study the effect of breed (Large White v. Creole (LW v. CR)) and feeding level (0·70, 0·80, 0·90, and 1·00 ad libitum) on growth performance and protein deposition (PD) and lipid deposition (LD) between 30 and 60 kg in growing pigs under tropical climatic conditions; the CR pigs are raised in the Caribbean area and can be qualified as fat and slow growing pigs. Daily protein and amino acids supplies were calculated to be non-limiting for protein gain. Total PD and LD were measured according to the comparative slaughter technique. Digestibility coefficients of energy and nutrients were estimated over a 10-day period at 45 kg live weight. Neither the breed nor the feeding level influenced the apparent digestibility coefficients of dietary nutrients; only energy digestibility was increased at reduced feeding levels (P<0·05). Average daily gain increased linearly with the increase of metabolizable energy (ME) intake and the slope of the relationship was lower in CR than in LW pigs (30·4 v. 36·6 g per additional MJ ME). The food conversion ratio was not affected by feeding level but it was significantly higher in CR than in LW pigs (2·88 v. 2·36 kg /kg; P<0·001). Daily PD increased with ME intake according to a linear relationship in both breeds and the slope was significantly affected by breed (3·1 v. 4·2 g/MJ ME in CR and LW pigs, respectively; P<0·001). In contrast, the increase of LD and total energy retained with ME were higher in CR than in LW pigs (8·4 v. 6·4 g/MJ and 0·40 v. 0·36 MJ/ MJ ME, respectively; P<0·001).

In pigs the quantification of breakdown and synthesis by powers of body protein led to the estimation of turn-over related protein retention efficiency by the equation kP = {1 + [1 − (P/α) (2/9)Q]−1/6}−1, with α the limit value of whole body protein (P) maturity, so that 0 ≤(P/α)≤1. The factor 2/9 is derived from diffusion attributes indicated by cell and nucleus geometries α and Q represents a scaled transformation of intake, 0 ≤ Q ≤ 1, such that a value of Q = 1 may represent ad libitum intake and Q = 0 the intake at the maintenance requirement. Published observations on finishing steers provide estimates of whole body protein synthesis and breakdown at pre-determined levels of intake in confirmation of the theoretical (2/9)Q power associated with (P/α) in kP. Further confirmation of the (2/9)Q power in cattle follows from satisfactory agreement between an estimate of conventional multiple regression retention efficiency and the turn-over related retention efficiency calculated at the given level of intake, for the mid point of the body mass interval covered by the regression estimate. In addition, a simulation experiment on cattle from the literature gives power estimates of protein breakdown and synthesis in general agreement with those accepted for pigs. Examples on both fine and coarse diets are employed to suggest a general rule for prediction on diets causing submaximal efficiency due to suboptimal intakes.

In sheep, evidence derived from estimates of conventional multiple regression efficiencies suggests that the rule (a-b) = (2/9) Q for the calculation of kP should be reserved for the description of compensatory growth. Protein retention efficiency for ordinary growth should be described by an adaptation of the rule derived for suboptimal intakes.

The magnitude of the discrepancy between conventional regression estimates of protein retention efficiency and theoretical estimates of synthesis efficiency indicates a major contribution ascribable to protein turn-over in the generally accepted estimates. As protein turn-over is known to be influenced by diet, feeding level and degree of maturity, this suggests the development of an estimator of protein efficiency that can be adapted for such differences. Therefore, based on generally accepted formulas for growth description, a method of estimating protein retention efficiency was developed which is flexible enough to accommodate different diets, feeding levels and degrees of maturity. Moreover, a formula was derived to convert one type of estimate to the other by regarding constant efficiency as equivalent to variable efficiency at the mid point of the estimation interval. Increase in scientific depth to this descriptive approach is provided by a theoretical consideration of a possible mechanism of hormonal control of protein synthesis and breakdown, ultimately expressed as proportionalities to powers of whole body protein (P). Molecular considerations on cellular synthesis and breakdown indicate a difference between breakdown and synthesis powers equal to (2/9)Q. The factor (2/9) is indicated by an argument based on insulinlike growth factor derived activator diffusion attributes by nucleus and body tissue geometries, while Q is equal to the proportion of nuclei activated by insulin-like growth factor. This proportion is likely to be a function of the concentration of growth factor in the blood. Hence, a linear relationship between intake and blood insulin-like growth factor concentration suggests that Q can be represented by a scaled transformation of intake, 0 ≤ Q ≤ 1, such that a value of Q = 1 represents ad libitum intake on a suitable diet and Q = 0 intake at the maintenance requirement. The quantification of breakdown and synthesis power differences by (2/9)Q leads to kP = {1 + [1 − (P/α)(2/9)Q]−1/6}−1, for turn-over related protein retention efficiency (kP), with α the limit value of P at maturity, so that 0 ≤ (P/α) ≤ 1. Experimental estimates, derived from direct estimates of whole body protein synthesis and breakdown at predetermined levels of intake, are in excellent agreement with the theoretical (2/9)Q in the power associated with (P/α) in kP. Furthermore, conventional multiple regression retention efficiencies satisfactorily approximate the turn-over related retention efficiency that can be calculated at a given level of intake for the mid point of the interval covered by the regression estimates.

Two experiments were carried out on cattle nourished entirely by intragastric infusion, to determine the extent to which glucose or a glucose precursor determines the response to protein infusion in energy-undernourished animals. In order to determine the requirement for glucose in 1-year-old fasting cattle, glucose was infused at increments to supply 0, 1·5, 2·5, 3·5, 4·5, 5·5 and 6·5 g/kg metabolic body weight (W0·75) and the effects on plasma β-hydroxybutyrate and N excretion were measured. At 5·5 g glucose/kg W0·75 plasma β-hydroxybutyrate was reduced to a basal level of 1·65 mmol/l and fasting N excretion reduced from 529 to 280 mg N/kg W0·75. No further reduction was observed with the higher level of 6·5 g glucose/kg W0·75. In the second trial, three steers were used in a 3 × 3 Latin square design and infused with a volatile fatty acid mixture of 65, 27 and 8 mol acetic, propionic and butyric acids respectively/100 mol, either at an estimated maintenance energy level of 450 kJ/kg W0·75 and supplying a calculated glucose equivalent level of 13·0 g/kg W0·75 (M1A), or at 1·5 × maintenance supplying a glucose equivalent of 20 g/kg W0·75 (M1·5A). Another mixture infused at the maintenance energy level contained 49, 43 and 8 mol acetic, propionic and butyric acids respectively/100 mol but with a glucose equivalent of 20 g/kg W0·75 (M1P). Casein was infused at each of these energy treatments to supply 0, 200, 400, 800, 1600 and 2500 mg N/kg W0·75 daily, and N balance and blood metabolites were measured. N retention increased linearly (r 0·98) with casein infusion. The coefficients for N retention were 0·55, 0·57 and 0·64 for M1A, M1·5A and M1P respectively. The mean efficiency of N utilization was 0·58. The results suggest that provided the glucose need is met there is no relationship between energy supply and efficiency and level of protein retention. However, the results also indicate that glucose requirement in cattle may be higher than that previously observed in sheep.

The common dentex (Dentex dentex) is a sparid fish which is considered a suitable candidate for Mediterranean aquaculture. A seven-weeks feeding trial was conducted over the summer period with common dentex, sea bream (Sparus aurata) and sea bass (Dicentrarchus labrax). All three species were fed to visual satiety with two practical diets with varying crude protein and crude fat levels (55 % protein, 9 % lipids; 46 % protein, 17 % lipids). The initial body weights were 8.2, 11.6 and 17.3 g for common dentex, sea bass and sea bream, respectively. In all cases, specific growth rates were not significantly affected by dietary treatment, but they varied among species (sea bass 1.7-1.8 %; sea bream 2.1-2.3 %; common dentex 3.1-3.2 %). When comparisons between fish species were made, we observed that the increase in growth rates was linked to a decrease of the whole body fat content, as a consequence of a greater utilisation of dietary lipids as energy substrates. Furthermore, in common dentex, the 17 % lipid diet was able to improve protein retention, but this diet effect was less significant in sea bream and sea bass. In contrast to sea bream, the 17 % lipid diet did not up-regulate plasma GH levels in common dentex, which provides additional evidence for a more efficient utilisation of dietary lipids.

An experiment was conducted to evaluate the feeding characteristics and the productive responses of lamb diets containing increasing levels of dried brewers' grains (DBG). Five groups of six 70-day-old Bergamasca lambs were housed in individual pens and given ad libitum for 9 weeks pelleted diets containing 200 g/kg of concentrate and 800 g/kg of a mixture of DBG and lucerne hay in the ratios of 0:80 (DBG0), 20:60 (DBG20), 40:40 (DBG40) 60:20 (DBG60) and 80:0 (DBG80). During the last 12 days of the experimental period, a digestibility trial was carried out for each diet. After this, all the lambs were slaughtered and the composition of the empty body weight was determined. The initial composition of the empty body was estimated from the composition of a sixth group of lambs slaughtered at the beginning of the trial.

The apparent digestibility of dry matter (DM), organic matter, crude protein, ether extract, neutral-detergent fibre and energy increased with the proportion of DBG. The daily DM intake relative to metabolic body weight (M0·75) diminished significantly with the increasing proportion of DBG in the diet, from 127 g/kg M0·75 for diet DBG0 to 83 g/kg M0·75 for diet DBG60. The daily live-weight gain and food DM conversion efficiency were highest with the intermediate diets (414 g/day with diet DBG40 and 240 g/kg DM with DBG60), showing a quadratic trend, an indication of a positive interaction between DBG and lucerne hay. The fat content of the live-weight gain was particularly high in the lambs given the diet with the highest proportion of DBG. It was concluded that DBG may be profitably used in growing-fattening diets for lambs in a proportion not exceeding about 400 g/kg DM.

Between 45 and 100 kg body weight, Large White castrated males (cLW), and crossbred Pietrain × Large White castrated males fcPP×) and boars (bPP×) were either given food ad libitum in experiment 1 or allocated to four energy levels (0·70, 0·80, 0·90, 1·00 ad libitum) in experiment 2. Daily protein and amino acid supplies were calculated to be non-limiting for growth. Protein (PD) and lipid (LD) deposition rates were measured according to the comparative slaughter technique over the whole experimental period (experiments 1 and 2) and according to the nitrogen and energy balance technique at four stages of growth: 48, 64, 79 and 94 kg mean body weight (experiment 2). Average daily gain increased linearly with metabolizable energy (ME) intake, the slope of the relationship being significantly different between types of pig (from −28 to +36 g per additional MJ ME). Daily PD increased with ME intake above maintenance (MEp) according to a linear-plateau relationship in the three types of pig: the slope was significantly affected by type of pig (from +3·4 to 6·0 g per extra MJ MEp) but not by stage of growth. Daily LD increased linearly with MEp intake; neither the type of pig nor the stage of growth affected its slope (+13-5 g per extra MJ MEp). The LD/PD ratio in the extra body-weight gain associated with increased energy intake was affected only by the type of pig.

Protein accretion curves were derived using food intake, growth and body composition data from a total of 320 pigs, which comprised castrated males and gilts from five genotypes. The 32 pigs from each genotype/sex subclass were offered ad libitum a series of isoenergetic diets (13·8 MJ metabolizable energy per kg) designed to provide a non-limiting intake of nutrients and to allow maximum protein deposition rates. Four pigs from each subclass weren slaughtered at each of the live weights (kg) 25, 44, 65, 85, 100, 115, 130 and 150. Daily food intake (dF/dt) was described as an increasing exponential function of age (t), live weight (W) as an increasing exponential function of cumulative food consumed (F), and protein weight (Pr) as an allometric function of live weight (W). The rate of protein accretion in the body of pigs [d(Pr)/dt] was calculated as d(Pr)/dt = (dF/dt).(dW/dF).(dPr)/dW). Bootstrap procedures were used to estimate standard errors for the food intake, growth and compositional parameters and to obtain the confidence bands for the dependent variables (dF/dt, W, Pr and d(Pt)/dt).

Protein accretion rate as a function of live weight was curvilinear, increasing to a maximum, then decreasing with increasing live weight. There were significant differences between subclasses in the maximum rate of protein accretion, although there was no relationship between this rate and the live weight, stage of maturity, or age at which maximum protein accretion occurred. Describing protein accretion as a multiplicative function of food intake, food efficiency and the partitioning of nutrients in the body allowed changes in the magnitude and shape of the protein accretion curve to be ascribed to one, or a combination, of the above mechanisms.

The objective of the present experiment was to define the form of the relationship between varying levels of energy intake at constant, high protein intake and the performance of young pigs. By doing so it was expected that we could distinguish between four models that predict the pig's responses to its diet as rates of protein and lipid retention. Forty young pigs were assigned at 12 kg live weight either to an initial slaughter group (n 8) or to one of four allowances of starch intake at a constant intake of a high-protein feed (with 345 g crude protein (nitrogen x 6.25)/kg food). Half the pigs were killed after 4 weeks and half after 8 weeks on the treatments; at each slaughter point on each treatment half the pigs were entire males and half were females. Increasing the intake of starch (energy) resulted in significant increases in the rates of live weight, empty-body, protein and lipid gains of pigs slaughtered at both stages. There was no minimum positive lipid: protein ratio in the gain of the pigs. Male pigs deposited more protein and less lipid than females but this effect of sex on protein and lipid retention was seen only on the two highest allowances of starch intake. The calculated efficiency of protein utilization increased with increasing starch intake up to a maximum of 0.81, when probably the energy: protein in the diet became non-limiting. The results led to the rejection of two of the models that predict the rates of protein and lipid retention as responses to protein and energy intake, but the two remaining models could not be rejected, at least qualitatively.

The objective of the experiment was to define the form of the relationship between varying levels of protein and energy intake and the performance of young pigs. Forty-four young pigs were assigned at 12 kg live weight for 6 weeks either to an initial slaughter group (n 8) or to one of the nine feeding treatments (n 4); three allowances of a high-protein food with 355 g crude protein (nitrogen × 6.25; CP)/kg (P1, P2, P3) at three levels of feeding (L, M and H). Each feeding level was met by supplementing the allowance of feed P with the appropriate amount of starch and each treatment had two males and two females. The rate of protein deposition was not affected by feeding level at the two lowest allowances of basal feed P (P1 and P2), but it increased with increasing the feeding level for the pigs on treatment P3. Males deposited more protein than females, but this effect was more pronounced with treatment P3. The rate of lipid deposition increased with each increase in the level of feeding and decreased with increasing the allowance of feed P. The calculated efficiency of protein utilization (ep) was expressed as a function of the energy: protein ratio in the feed (MJ metabolizable energy/kg digestible CP). The best model to describe the relationship was a linear-plateau model, with the maximum value for ep of 0.814 at 73 MJ/kg. This relationship provided the basis of a model that could predict the response of a growing pig to its diet as rates of protein and lipid retention