Comparative responses of genetically lean and fat chickens to lysine,arginine and non‐essential amino acid supply. I. growth and body composition

1. Three experiments were performed to study the effects of amino acid imbalance on the growth of genetically lean (LL) or fat (FL) male chickens from 28 to 42 d of age. In experiment 1, five concentrations of digestible lysine were compared (4.75, 6.75, 7.75, 8.75 and 9.75 g/kg). In experiment 2, four concentrations of digestible arginine were compared (6.53, 7.69, 8.84 and 10.0 g/kg). In experiment 3, three diets were compared: a high‐protein diet (189 g CP/kg), a low‐protein diet containing added essential amino acids (EAA) (144 g CP/kg) and this low‐protein diet supplemented with 40 g/kg of non‐essential amino acids (NEAA) (glutamic acid + aspartic acid).

2. LL birds exhibited a lower growth rate than the FL when the diet was deficient in either lysine or arginine. Plotting weight gain against lysine or arginine intake suggested that most of this effect was caused by variations in food intake.

3. When protein gains (body or total proteins) were plotted against lysine or arginine intake, LL chickens appeared more efficient than FL chickens.

4. Similar growth rates, although slightly lower in FL, were obtained with low‐ and high‐protein diets. However, NEAA supplementation of the low‐protein diet reduced adiposity of LL and did not modify that of FL. Increasing crude protein content (all amino acids) was more effective than NEAA supplementation in decreasing the adiposity of both lines.     

Comparative responses of genetically lean and fat broiler chickens to dietary threonine concentration

Genetically lean (LL) or fat (FL) male broiler chicken's were fed on 5 diets containing either 3.80, 4.27, 4.75, 5.22 or 5.70 g true digestible threonine per kg. Threonine deficiency induced a more pronounced reduction in growth in the LL than in the FL but did not influence abdominal fat and breast muscle proportions in either line. Plotting weight gain or protein gain against threonine intake suggests that the requirement of both lines is very similar in terms of mg per g of gain. Thus food intake or appetite should account for differences between genotypes. Requirement for true digestible threonine was estimated as 10.70 mg per g of weight gain or 63.8 mg per g of protein gain, using a linear regression approach. The quadratic polynomial equations suggest that the requirements are 13.9 and 12.4 mg digestible threonine per g of gain for LL and FL respectively.     

Comparative utilisation of sulphur‐containing amino acids by genetically lean or fat chickens

1. Genetically lean (LL) or fat (FL) male chickens were fed from 28 to 47 days of age on 5 experimental diets differing by their methionine + cystine content (5.4, 5.8, 6.2, 6.6 and 7.0 g/kg, respectively).

2. Growth rate of LL chickens was reduced by the lower sulphur‐containing amino acid (SAA) concentrations whereas that of FL was not modified.

3. LL chickens exhibited a larger feather protein gain than FL, which was stimulated by SAA intake.

4. SAA retention, when plotted against SAA consumption, was always greater in LL than in FL.

5. Large differences were observed between genotypes for plasma‐free amino acids. Lysine, glutamic acid, histidine and serine were found at significantly higher concentrations in LL birds. Branched amino acids, aromatic amino acids, SAA and arginine were found at higher concentrations in FL. No differences were observed for aspartic acid, glycine, alanine and total amino acids. Methionine supplementation decreased free amino acid concentrations, with the exceptions of arginine and leucine.

6. It is concluded that lean chickens require a higher dietary concentration of SAA than FL. This is mainly caused by their lower food consumption and their greater feather synthesis. However, LL use SAA more efficiently than FL.     

Protein utilisation and turnover in lines of chickens selected for different aspects of body composition

1. Protein utilisation and turnover were measured in male chickens sampled from a line selected for high breast yield and a randombred control line (lines QL and CL, experiment 1) and in male chickens sampled from lines selected for either high or low abdominal fatness (lines FL and LL, experiment 2). In each experiment, 18 birds per line were given iso-energetic (12.9 MJME/kg) diets containing either 120 or 220 g CP/kg from 21 to 29 d (experiment 1) and 33 to 43 d (experiment 2). 2. Measurements were made of growth rate, food intake, body composition, excreta production and Ntau-methylhistidine excretion as a measure of myofibrillar protein breakdown, and fractional rates (%/d) of protein deposition, breakdown and synthesis were calculated. 3. In experiment 1, there were no significant differences between the line means for the fractional measures of protein turnover, but there was marked differential response in the two lines in the fractional rates of protein deposition, breakdown and synthesis, to increase in protein intake. The positive slope of the regressions of fractional (%/d) protein deposition and synthesis rates on protein intake (g/d/kg BW) were approximately 1.4- and 2.0-fold higher respectively in the QL than the CL line birds, and the negative slope of the regression of fractional breakdown rate on protein intake was approximately threefold greater in the CL than the QL line birds. 4. In experiment 2, fractional deposition rate was 6.2% lower, but fractional breakdown rate 9.4% higher in the LL than the FL birds, whilst there was essentially no difference in response of the FL and LL birds in the components of protein turnover to increase in protein intake. Line differences in deposition and breakdown rates were thus a reflection of the considerably higher (20%) food and hence protein intake in the FL than the LL birds. 5. The differential line responses in protein turnover in the two experiments suggest that selection for increased breast muscle yield and for reduced body fatness manipulate different physiological pathways in relation to protein turnover, but neither selection strategy results in an improvement in net protein utilisation at typical levels of protein intake by birds on commercial broiler diets, through a reduction in protein breakdown rate.     

Are genetically lean broilers more resistant to hot climate?

1. Genetically lean (LL) or fat (FL) male chickens were exposed to either high (32°C) or control (22°C) ambient temperature up to 9 weeks of age. They were fed on one of two isoenergetic diets differing in protein content: 190 or 230 g/kg.

2. At 22°C, weight gain of LL broilers was the same as in FL chickens, but at the high temperature LL birds grew to a greater weight than FL ones.

3. Food conversion efficiency was not affected by ambient temperature in LL chickens but was depressed in FL ones at 32°C.

4. Increasing dietary protein content did not alleviate heat‐induced growth depression irrespective of the genotype.

5. Gross protein efficiency was higher in LL chickens and was less depressed at 32°C than in FL birds.

6. Fat deposition decreased with increasing protein concentration at normal temperature in both genotypes; at high temperature, high protein content enhanced fatness, particularly in LL chickens.

7. Thus, genetically lean broilers demonstrated a greater resistance to hot conditions: this was indicated by enhanced weight gain and improved food and protein conversion efficiencies.     

Combined effects of clenbuterol and various concentrations of protein on performance of broiler chickens

1. The effects of the beta-adrenergic agonist, clenbuterol (1 mg/kg diet) on the growth and muscle composition in female broiler chickens (14 to 32 d of age) fed on diets containing various concentrations of protein (220, 240 or 260 g protein/kg) were examined. 2. Body weight gain over the 18 d period increased linearly with increasing protein intake. The rate of gain was significantly higher in clenbuterol-treated chickens than in control birds. 3. Dietary clenbuterol increased thigh muscle weight and protein concentration of breast and thigh muscle, regardless of dietary protein content. Protein/DNA ratio in thigh muscle was enhanced by clenbuterol feeding, and the magnitude of difference of the ratio was higher in chickens fed on the 240 and 260 g CP/kg diets than in those fed the 220 g CP/kg diet. 4. It was concluded that clenbuterol-treated chickens require increased dietary protein to maintain maximal growth, and that increased protein consumption is an important factor in improving growth in clenbuterolfed broilers.     

Comparative responses of genetically lean and fat chickens to lysine,arginine and non‐essential amino acid supply. II. plasma amino acid responses

1. Three experiments performed to study the effects of amino acid imbalances on the growth of genetically lean (LL) and fat (FL) male chickens from 28 to 42 d of age were described by Leclercq et al. (1994). The plasma amino acid concentrations of birds on selected treatments from that paper are reported here. In experiment 1, three dietary concentrations of digestible lysine were compared (4.75, 6.75 and 7.75 g/kg). In experiment 2, two dietary concentrations of digestible arginine were compared (6.53 and 10.00 g/kg). In experiment 3, three diets were compared: a high‐protein diet (189 g CP/kg), a low‐protein diet containing added essential amino acids (144 g CP/kg), and this low‐protein diet supplemented with 40 g/kg of non‐essential amino acids (NEAA; glutamic and aspartic acids).

2. The present results are compared with two earlier reports on the same genotypes. The LL consistently had lower plasma concentrations of me‐thionine, cystine, phenlyalanine, isoleucine and valine, and higher concentrations of histidine, than the FL chickens. In 4 of 5 experiments, LL leucine concentrations were lower, and glutamic acid, tyrosine, glutamine and alanine were higher, than in the FL. The other amino acids measured; arginine, lysine, aspartic acid, glycine and serine, exhibited variable responses among the experiments.

3. When the limiting essential amino acids, lysine and arginine, were added to a deficient diet, the plasma concentration of the supplemented amino acid increased while the others remained constant or decreased.

4. When glutamic and aspartic acids were added to the low protein diet, plasma amino acid responses were similar to those of adding a limiting amino acid to a deficient diet, except that alanine exhibited a dramatic increase.

5. Although there were genotype by diet interactions for several amino acids, the interactions were caused by differences in the degree of the responses, not in their direction.

6. These results suggest that the FL and LL genotypes do not utilise various amino acids with the same efficiency and, as a consequence, the ideal profile of dietary amino acids should not be the same for both lines. The results support the hypothesis that selection for fatness and leanness changed the amino acid requirements independently of the: effects of food intake.     

Effects of dietary chitosan on fat deposition and lipase activity in digesta in broiler chickens

1. The effect of dietary chitosan on fat deposition and lipase activity in the small intestinal contents was investigated in broiler chickens fed an adequate or high metabolisable energy (ME) diet. 2. Male broiler chickens at 14 d old were fed on the adequate or high ME diet supplemented with 0 or 50 g/kg chitosan, which has a low viscosity, for 3 weeks. 3. Dietary chitosan did not affect food intake, body weight gain or food efficiency in either dietary ME groups. 4. Dietary chitosan reduced the excessive abdominal fat deposition induced by the high ME diet. 5. Dietary chitosan increased the weight of intestinal contents irrespective of dietary ME concentration. 6. Dietary chitosan decreased the lipase activity per g of small intestinal contents. 7. These results suggest that dietary chitosan with low viscosity decreases lipase activity and fat absorption in the small intestine, consequently resulting in a reduction of fat deposition in broiler chickens. 8. It was concluded that dietary chitosan with low viscosity can decrease body fat deposition without reducing food intake and body weight gain in broiler chickens.     

Effect of dietary protein content on episodic growth hormone secretion and on heat production of male broiler chickens.

1. The effect of the crude protein content (200 and 150 g/kg) of isoenergetic diets on episodic growth hormone (GH) release and on heat production was investigated in male broiler chickens. 2. Decreasing the crude protein content of isoenergetic diets from 200 g/kg (HP diet) to 150 g/kg (LP diet) resulted in depressed body weight gain, impaired food conversion efficiency and increased abdominal fat deposition. 3. The pattern of growth hormone secretion was markedly affected by dietary treatment. Broiler chickens fed on the LP diet had higher overall mean, amplitude, baseline and peak frequency than the HP chickens. 4. The LP chickens produced more heat per unit of metabolic body weight than the HP chickens. 5. The hypothesis relating the pattern of GH secretion to protein conversion efficiency was corroborated.     

Lactobacilli counts in crop,ileum and caecum of growing broiler chickens fed on practical diets containing whole or dehulled sweet lupin (Lupinus angustifolius) seed meal

1. Four experiments with growing broiler chickens were carried out to study the effects of the inclusion in their diets of lupin (Lupinus angustifolius ) seed meal on E. coli and lactobacilli counts in crop, ileum and caeca at 3 or 4 weeks of age. 2. Diets were formulated to contain the same amounts of metabolisable energy (12.55 MJ/kg) and protein (210 g/kg). Raw whole (heat-untreated) or dehulled sweet (low in alkaloids) lupin seed meal (400 and 320 g/kg respectively) were used to prepare the lupin-based diets, whose protein content was completed with either defatted soyabean meal or casein. 3. Final body weight and food intake of chickens fed on whole lupin seed meal diets were lower than controls, but gain: food ratios were not different. However, birds given the diet with dehulled lupin seed meal had similar body weight, food intake and gain: food values as those of controls. 4. While E. coli counts were not affected, lactobacilli numbers were consistently increased compared to controls in all intestinal sections of chickens fed on the whole or dehulled lupin-based diets, irrespective of the age of the birds or the presence of soyabean meal or casein in the diet. The lactobacilli species isolated were: Lactobacillus fermentum, L. acidophilus, L. salivarius and L. brevis 5. The results suggest that the use of whole or dehulled sweet lupin seed meal in diets for growing broilers might enhance the growth of lactic acid-fermenting bacteria in the gut.     

Investigations of energy metabolism in weanling barrows: the interaction of dietary energy concentration and daily feed (energy) intake

Much of our understanding of energy metabolism in the pig has been derived from studies in which the energy supply was controlled through regulated feed intake. In commercial situations, where ad libitum feeding is practiced, dietary energy concentration, but not daily feed intake, is under producer control. This study evaluated the interactive effects of dietary energy concentration and feeding level (FL) on growth, body composition, and nutrient deposition rates. Individually penned PIC barrows, with an initial BW of 9.5 +/- 1.0 kg, were allotted to 1 of 9 treatments in a 3 x 3 factorial arrangement plus an initial slaughter group (n = 6) that was slaughtered at the beginning of the trial. Three NE concentrations (low, 2.15; medium, 2.26; and high, 2.37 Mcal of NE/kg) and 3 feeding levels (FL: 100, 80, or 70% of ad libitum access to feed) were investigated. Daily feed allowance for the restricted-fed pigs was adjusted twice per week on a BW basis until completion of the experiment at 25 +/- 1 kg of BW. Average daily gain, ADFI, and G:F were unaffected by NE (mean = 572 g, 781 g, and 0.732 g/g, respectively). Average daily gain and ADFI, but not G:F, increased (P < 0.05) with FL. Empty body lipid concentration increased with dietary NE concentration and with FL; a significant (P < 0.01) interaction revealed that empty body lipid concentration increased most rapidly as ADFI increased on the highest energy diet. Empty body lipid concentration was greatest in pigs with ad libitum access to the high-NE diet. Empty body protein concentration decreased with increasing NE (P < 0.05) but was not affected by FL. Empty body protein deposition (PD) increased with increasing FL (P < 0.001), but not with NE. Empty body lipid deposition (LD) and the LD:PD ratio increased (P < 0.01) in pigs with ad libitum access to the high-NE diet. In conclusion, NE did not interact with FL on growth, body protein concentration, or PD, suggesting that the conclusions regarding energy utilization obtained from experiments using restricted feed intake may not easily be applied to pigs fed under ad libitum conditions. The interactive effects of NE and FL on body lipid concentration, LD, and the LD:PD ratio indicate that changes in dietary energy concentration alter the composition of gain without necessarily changing overall BW gain. Consequently, the composition of gain is an important outcome in studies on energy utilization.     

Effect of exogenous corticosterone in genetically fat and lean chickens

1. The effects of daily injections of corticosterone (1 or 5 mg/bird) on growth, fat deposition, liver lipid and plasma concentrations of uric acid, glucose, insulin and growth hormone were studied using genetically selected lines of fat (FL) and lean (LL) chickens. 2. Both doses of corticosterone depressed body weight gain and increased the liver lipid and the abdominal fat to the same extent in both lines. 3. In both lines, corticosterone caused a dose-dependent increase in the plasma concentrations of uric acid, glucose and insulin in the fasted and refed states. 4. In untreated birds, plasma concentrations of growth hormone (GH) were slightly higher in FL than in LL chickens and slightly decreased during refeeding. The response was not modified by injection of 1 mg corticosterone. Injections of 5 mg decreased plasma GH in both lines in the fasting state and in LL chickens during refeeding. In contrast, the same dose increased GH in FL chickens during refeeding. This contradiction remains unexplained. 5. The results suggest that corticosterone sensitivity is not involved in difference of fattening between FL and LL chickens.     

Nutrient and energy retention in weaned Iberian piglets fed diets with different protein concentrations

Fifty-eight purebred castrated male Iberian (IB) piglets (initial BW 9.9 ± 0.1 kg) were used in an experiment to determine the effect of dietary protein content (PC) and feeding level (FL) on the rates of BW gain, whole body protein deposition (PD), and energy utilization between 10 and 25 kg of BW using the serial slaughter method. Treatments followed a 4 × 2 factorial arrangement with 4 PC (201, 176, 149, and 123 g of CP/kg of DM) and 2 FL (0.95 and 0.70 × ad libitum) and 6 or 7 piglets per combination of treatments. All diets were formulated to have an optimal AA pattern. Six piglets were slaughtered at the start of the trial to estimate initial body composition. The experimental pigs were individually housed in an environmentally controlled room (27 ± 2°C) until they reached 25 kg of BW, when they were slaughtered and analyzed for body composition. Positive linear effects of dietary PC on ADG, G:F, and gain:ME intake were observed (P < 0.001). Piglets fed at the highest FL showed greater ADG, G:F, and gain:ME intake (P < 0.001). An average increase was estimated to be 38.0 g of gain/MJ of ME intake. Protein deposition increased linearly from 35.6 to 50.9 g/d with increasing dietary PC (P < 0.001). A daily increase was estimated to be 0.35 g of PD/g of CP intake. Although the maximal genetic potential for PD of the IB piglet was not attained, a maximal value of 59.9 g/d for whole-body PD was achieved when the diet provided 201 g of CP/kg of DM and was fed at 0.95 × ad libitum. Piglets on the highest FL deposited on average 39% more body protein (P < 0.001) than restricted piglets. An average value of 4.39 g increase in PD/MJ of ME intake was obtained for diets containing 201 and 176 g of CP/kg of DM. Maintenance energy requirements and net efficiency of utilization of ME for growth, calculated by linear regression of ME intake on body retained energy, were 427 kJ/kg of BW(0.75)·d(-1) and 0.552, respectively. The corresponding partial efficiencies of utilization of ME for protein and fat deposition were 0.378 and 0.672, respectively, considerably less than the accepted values for conventional pig breeds. Practical diets of the young IB piglet should contain at least 201 g of ideal CP/kg of DM.     

Effects of feeding growing broiler chickens with practical diets containing sweet lupin (Lupinus angustifolius) seed meal

1. Two experiments with growing broiler chickens were carried out to study the effects of the inclusion in their diets of whole or dehulled lupin (Lupinus angustifolius) seed meal on productive and physiological parameters. The effects of the addition of a commercial protease (1 g/kg, Bio-Feed Pro, Novo. Nordisk, Madrid) were also tested. 2. Diets were formulated to contain the same amounts of energy (12.55 kJ/g) and protein (210 g/kg). Raw whole (not heat treated) or dehulled sweet (low in alkaloids) lupin seed meal (400 and 320 g/kg, respectively) were used to formulate the lupin-based diets, and the protein content was completed with either defatted soybean or casein. 3. Final body weight and feed intake of chickens fed diets containing whole lupin seed meal (400 g/kg) were lower than controls, but gain:feed ratios were not different. The presence of soybean or casein in the diet did not affect productive parameters. Birds fed dehulled (320 g/kg) instead of whole lupin seed meal had similar body weight, feed intake and gain:feed values to controls. The addition of a commercial protease (1 g/kg, Bio-Feed Pro CT) to whole lupin/soy or whole lupin/casein diets tended to increase feed intake and final weight of the birds. 4. Plasma uric acid concentration was higher, and plasma cholesterol and triglycerides lower, in chicks fed whole lupin but not in those fed dehulled lupin seed meal. Plasma amino acid concentrations were not different from controls in birds fed lupin diets. 5. Apparent ileal digestibility of amino acids was not different from controls for the different lupin diets. The relative weight of the liver was higher than controls in lupin-fed birds, but not in those fed enzyme supplemented lupin-based diets. Liver concentrations of DNA tended to rise, while those of glycogen tended to decrease and liver RNA was lower in lupin-fed chicks.     

The effects of dietary protein independent of essential amino acids on growth and body composition in genetically lean and fat chickens

1. Growth performance between 28 and 49 d of age and carcase composition at 49 d in genetically lean (LL) and fat (FL) broilers fed on diets varying in non-essential amino acid (NEAA) concentrations were compared in 2 experiments. In experiment 1, 3 crude protein (CP) contents (133, 155, and 178 g/kg) were compared. In experiment 2, 4 CP levels (131, 150, 170 and 189 g/kg) were compared. All diets were supplemented with synthetic amino acids to cover the EAA requirement of the LL birds. 2. Weight gains of FL chickens were not affected by dietary treatments, while those of LL increased when CP level increased. 3. Reducing CP content always increased body lipids, abdominal fat and food conversion ratio in both lines in both experiments; however, the effect on abdominal fat was more pronounced in the FL birds. 4. Reducing CP concentration always decreased breast muscle proportion in both lines in both experiments, even when growth rate was not affected by CP. 5. It is concluded that LL chickens require diets more concentrated in NEAA than fat chickens and that there seems to be an effect of NEAA on breast muscle development.     

Broiler responses to digestible threonine at different ages: a neural networks approach

Three experiments were conducted with broiler chickens to evaluate the effects of digestible threonine (DThr) and crude protein (CP) on their performance at three different phases of age: 1–14, 15–28 and 29–42 days. The measured traits included the following: average daily gain (ADG), feed intake (FI), feed conversion ratio (FCR), carcass crude protein (CCP), body lipid (BL), feather weight gain (FWG), protein deposited in feather (FCP), carcass plus feather protein (CFCP), carcass Thr deposition (CDThr) and nitrogen excretion (NE). A dilution technique was used to create seven diets (with eight replicates) increasing the DThr content from 1.5 to 10 g/kg of diet for phase 1, 1.3–8.9 g/kg of diet for phase 2, and 1.2–8.2 g/kg of diet for phase 3. Data measured were imported into neural networks (NNs) to: (i) predict the measured traits in response to DThr and CP, (ii) rank the importance of DThr and CP on these traits through sensitivity analysis and (iii) find the optimal levels of DThr and CP that lead to the desired (maximum or minimum) responses. For each trait investigated, 50 different random groups of data were generated using a bootstrapping method. These 50 data groups were then used to develop 50 separate NNs which were subsequently combined to construct the final ensemble NN model. In general, accuracy of the models constructed was acceptable, although models of high (ADG, FCR, CFCP, BL, DThr and NE; 0.64 ≤ R² ≤ 0.99) and low (CCP, FWG and FCP; 0.26 ≤ R² ≤ 0.79) accuracy were obtained. All models developed showed the greatest sensitivity to DThr. This may be explained by the dilution technique diet preparation used in these experiments. Optimization results showed decreases in optimal values of DThr and CP with increasing age for all traits. The highest level of DThr was suggested for minimum BL, followed by minimum FCR, maximum ADG, maximum CFCP, minimum NE and maximum CCP respectively. Results showed that the optimal values of DThr for minimum FCR in phases 1–3 were 8.5, 7.4 and 6.4 g/kg of diet, while these values for maximum ADG were 8.2, 7.2 and 6.4 g/kg of diet respectively.     

Sodium butyrate maintains growth performance by regulating the immune response in broiler chickens

1. The experiment was conducted to investigate the effects of dietary sodium butyrate on the growth performance and immune response of broiler chickens. In experiment 1, 240 1-d-old chickens were allocated into 4 dietary groups (0, 0·25, 0·50 or 1·00 g sodium butyrate/kg) with 6 replicates each. In experiment 2, 120 1-d-old chickens were fed a control diet (without sodium butyrate) or 1·00 g sodium butyrate/kg diet. Half of the chickens fed on each diet were injected intra-peritoneally with 0·5 g/kg body weight of Escherichia coli lipopolysaccharide (LPS) at 16, 18 and 20 d of age. 2. There was no effect of dietary sodium butyrate on growth performance. On d 21, serum interleukin-6 (IL-6) and tumour necrosis factor-alpha (TNF-α) were decreased in chickens given 1·00 g sodium butyrate/kg, serum superoxide dismutase (SOD) and catalase activities were significantly increased, and malondialdehyde (MDA) was decreased by dietary sodium butyrate at 0·50 or 1·00 g/kg. On d 42, serum IL-6 was markedly decreased by dietary sodium butyrate, while 1·00 g sodium butyrate/kg greatly reduced MDA and increased catalase. 3. LPS challenge significantly reduced the growth performance of chickens. Serum IL-1β, IL-6, TNF-α, corticosterone, alpha-1 acid glycoprotein (AGP) and prostaglandin E(2) (PGE(2)) were increased in LPS-challenged chickens. Dietary sodium butyrate supplementation maintained the body weight gain and feed intake. Sodium butyrate supplementation inhibited the increase in IL-6 and AGP in serum at 16 d of age and TNF-α, corticosterone, AGP and PGE(2) at 20 d of age. Similar inhibitory effects of sodium butyrate in serum glucose and total protein concentrations were also found at 20 d of age. 4. The results indicated that dietary sodium butyrate supplementation can improve the growth performance in chickens under stress and that this may be used to moderate the immune response and reduce tissue damage.     

Effect of cooking and methionine supplementation on nutritional value of bitter vetch seed as a feed ingredient for broilers

The present study was conducted to evaluate the adequacy of applying heat treatment and methionine (Met) supplementation to improve the use of bitter vetch (BV) as a feed ingredient in the growth diet of broilers. A total of 540 Ross-308 chicks were fed various BV-supplemented diets between the ages of 35 and 49 days. The chicks were assigned randomly to one of nine experimental treatments, including raw and cooked bitter vetch seeds at two levels (100 and 200 g/kg) with or without Met (210 mg/kg) supplement and a corn–soybean-based diet as control. Results showed that feeding the 200-g/kg raw BV decreased feed intake by 52% in relation to the control diet (P < 0.05). Cooking the BV did not improve the feed intake. Met supplementation of 100 g/kg raw or cooked BV and 200 g/kg cooked BV resulted to a similar feed intake in the control group. Chicks fed with the 200 g/kg raw BV had an average depressed body weight gain of 90% in comparison to the birds fed with the control diet. The combination of cooking and Met supplementation of this diet resulted to a similar body weight gain to the control diet. Feeding 100 g/kg of raw or cooked BV also reduced (P < 0.05) body weight gain, and Met supplementation of these diets resulted in a body weight gain similar to the control group. Chicks fed with 100 g/kg of raw or cooked BV supplemented with Met or 200 g/kg of cooked BV plus Met has similar feed conversion ratio to the control group. In conclusion, heating BV seeds is not sufficient to overcome the limiting effects of BV seeds on feed intake and weight gain, and that Met supplementation does provide some improvement. The combination of cooking and Met supplementation was more efficient.     

Effects of diet acidification and xylanase supplementation on performance, nutrient digestibility, duodenal histology and gut microflora of broilers fed wheat based diet

1. The objective of this experiment was to study the influences of xylanase and citric acid on the performance, nutrient digestibility, digesta viscosity, duodenal histology, and gut microflora of broilers fed on a wheat based diet.

2. The experiment was carried out as a 2?×?3 factorial arrangement with two concentrations of xylanase (0 and 200?mg/kg) and three concentrations of citric acid (0, 20 and 40?g/kg). A total of 408 one-day-old chickens with similar body weight were distributed into 24 pens with 17 birds/pen. Each dietary treatment was given to 4 replicate pens from 0 to 24?d of age. To determine the apparent nutrient digestibility, chromic oxide (3?g/kg) was added to the diets as an indigestible marker.

3. Xylanase significantly increased body weight gain at 24?d of age by 1·4% and improved gain-to-feed (G:F) by 3·6%. The inclusion of 40?g/kg citric acid decreased feed intake and body weight gain by 15·4% and 11·8%, respectively. The inclusion of 20?g/kg of citric acid decreased feed intake, but it did not affect body weight gain of broilers at 24?d of age. The inclusion of 20 and 40?g/kg citric acid improved G:F by 3·8 and 4·3% respectively. Xylanase significantly decreased the viscosity of digesta and improved retention of DM, CP, and energy.

4. Xylanase and citric acid did not have any effect on the histo-morphology of the duodenum and intestinal microbial population.

5. In conclusion, citric acid at 20?g/kg decreased feed intake, did not have a negative effect on body weight gain, and improved G:F. Xylanase decreased digesta viscosity, increased nutrient retention and consequently improved performance of broilers fed on a wheat based diet.