Chick responses to dietary arginine and methionine levels at different environmental temperatures.

1. Two experiments were conducted with broiler chicks in battery brooders from 1 to 21 d to determine the broiler chicks' responses to arginine (Arg) and methionine (Met) combinations at control (22 to 25 degrees C) and warm (32 to 35 degrees C) temperatures. 2. In Experiment 1, two levels of Arg (15.2 and 25.2 g/kg of the diet) and two levels of Met (3.5 and 5.5 g/kg) of a maize-soy based diet were fed at two temperatures, 22 or 32 degrees C. Results of Experiment 1 were similar to those of Experiment 2, but most treatment differences were not significant. 3. In Experiment 2, chicks were randomly allotted to 9 dietary treatments: 3 levels of Arg (15.2, 25.2 and 35.2 g/kg of the diet) x 3 levels of Met (3.5, 5.5 and 7.5 g/kg of the diet) at 25 or 35 degrees C. At the warmer temperature, chick growth depression from supplemental Arg was not as severe as at the control temperature (significant Arg x temperature interaction); neither were growth increases as large from supplemental Met (significant Met x temperature interaction). 4. Kidney and breast muscles were collected for arginase activity and creatine analysis, respectively. Remaining chicks were fasted for 10 h and re-fed. Excreta from the next 24 h were collected for total creatine and creatinine analysis. There were no effects of either Arg or Met on muscle creatine concentration at either control or warm temperatures. Chicks raised at 25 degrees C excreted more creatine and creatinine than those raised at 35 degrees C. 5. These results confirm that temperature affects responses to dietary Arg and Met and suggest that the higher temperature slowed the Arg metabolism of chicks through the creatine synthesis pathway.

Dietary interrelationships among arginine, methionine, and lysine in young broiler chicks.

Since excess dietary lysine (Lys) can increase the chick's arginine (Arg) requirement and excess Arg can increase the chick's methionine (Met) requirement, experiments were conducted to test the hypothesis that responses to dietary Lys and Met are also interrelated. Day-old Ross x Ross chicks were fed a maize-soyabean meal-based diet supplemented with four levels of L-Arg (0, 5, 10 or 20 g/kg), factorially arranged with four levels of supplemental DL-Met (0, 1, 2 or 3 g/kg). Three replicate pens of ten chicks each were randomly assigned to each treatment and fed for 14 d. An increase in Arg in the diet caused growth and feed-intake depression (P=0.0001), but increasing Met in the diet enhanced growth and feed intake (P=0.0001). Arg toxicity was dependent on the Met level of the diet (Arg x Met interaction; P=0.0153). Experiment 2 was conducted to study interrelationships among Arg, Met, and Lys. Eight treatments were factorially combined: two levels of supplemental L-Arg (0 or 10 g/kg), two levels of supplemental DL-Met (0 or 2 g/kg), and two levels of supplemental L-Lys (0 or 6 g/kg). Six replicate pens of eight chicks per treatment were used. A three-way interaction among Arg, Met, and Lys was observed for body-weight gain and feed intake (P<0.023). As expected, kidney arginase activity increased as dietary Lys increased (P=0.0004). No interactions were found for kidney arginase activity. Muscle creatine increased when chicks were fed the higher Arg (25.2 g/kg) diet (P=0.0047). A three-way interaction among Arg, Met, and Lys was found for muscle creatine (P=0.0075). Excess dietary Lys depressed muscle creatinine concentration, but only in the presence of the lower concentrations of Arg and Met. To conclude, an interrelationship among Arg, Met, and Lys was demonstrated, and it was probably related to creatine biosynthesis.

The influence of labile dietary methyl donors on the arginine requirement of young broiler chicks.

Two experiments were conducted with Ross x Ross boiler chicks in battery brooders from 1 to 14 d of age to determine the influence of dietary methyl donors on the Arg requirement of young broiler chicks. Experiment 1 had a 6 x 2 factorial design, with six levels of Arg supplementation (0, 0.1, 0.2, 0.3, 0.4, and 0.5%) and two levels of DL-Met supplementation (0 and 0.2% of the diet). The design of Experiment 2 was identical to Experiment 1, except that a second source of labile methyl groups was added, 0.2% betaine (6 x 3 factorial arrangement). Both experiments had four replicate pens of 10 chicks each per treatment. The basal diet was based on corn (34.52%), whey (26.96%), corn gluten meal (16.53%), soybean meal (11.74%), and poultry fat (23% CP and 3.20 kcal/g of ME). At 14 d, three chicks per replicate were randomly killed, and breast muscle was collected and pooled for creatine analysis. The broken-line linear model was used to estimate the Arg requirements of the chicks. There were no differences in Arg requirements due to methyl source so the data were pooled. In Experiment 1, the Arg requirements were 1.17 +/- 0.04% for gain, 1.23 +/- 0.03% for feed conversion ratio (FCR), and 1.18 +/- 0.03% for muscle creatine, when the diet contained 0.45 or 0.65% Met. In Experiment 2, the Arg requirements were 1.20 +/- 0.05% for gain, 1.23 +/- 0.03% for FCR, and 1.26 +/- 0.02% for muscle creatine. There was no apparent difference in the Arg requirement of young broilers due to methyl donor supplementation.

Determination of the methionine requirement of male and female broiler chicks using an indirect amino acid oxidation method.

The methionine requirement of 250-to-300-g broiler chicks was estimated from the oxidation of L-[1-14C] phenylalanine of chicks given meals containing graded levels of DL-methionine. L-[1-14C] phenylalanine was used as an indicator amino acid for amino acid oxidation and, indirectly, protein synthesis. Four experiments were conducted using an incomplete block design with three replications each. Chicks were crop intubated with semifluid diets at a ratio of 1 g of diet per 45 g of bird weight. Two feedings 2 h apart were used to reduce variability, and the sample collection period was 3 h after the second feeding. Regression analysis of 14CO2 release from L-[1-14C] phenylalanine was used to estimate the methionine requirement. The model was as follows: response = max + rc x (req - x) x I, where max = plateau, rc = rate constant, req = requirement, and I = 1 when x < req, otherwise I = 0. The methionine requirements of Ross x Ross chicks were 0.57 +/- 0.03% and 0.52 +/- 0.08% for male and female chicks, respectively in Experiment 1 and 0.55 +/- 0.05% and 0.52 +/- 0.04%, respectively, in Experiment 2. In the third experiment (Arbor Acre High-Yield), phenylalanine oxidation stabilized at a low rate when dietary methionine levels reached 0.54 +/- 0.03% and 0.53 +/- 0.04% for males and females, respectively. In a growth trial covering a longer period (Experiment 4), the methionine requirements of male and female Ross x Ross chicks, based on feed conversion, were 0.52 +/- 0.05% and 0.45 +/- 0.02%, respectively, and based on body gain were 0.54 +/0.09% and 0.48 +/- 0.04%, respectively. The results suggested that the methionine requirement of male chicks tended to be higher than that of females in both strains. However, differences were small and not significant.

Transfer of dietary conjugated linoleic acid to egg yolks of chickens.

There is interest in increasing the conjugated linoleic acid (CLA) content of foods because of purported benefits of CLA for human health. Two experiments were conducted to determine the influence of dietary CLA concentration on CLA content of eggs. In Experiment 1, diets containing 0, 0.5, 2.5, or 5.0% CLA were fed to 26-wk-old White Leghorn hens (Hy-Line W-77) for 29 d. No CLA was detected in the yolk lipids of hens fed the control diet. Concentration of CLA in the yolk lipids linearly increased as dietary CLA increased. The maximum concentrations of CLA in the yolk lipids of hens fed 0.5, 2.5, or 5.0% CLA occurred 11 d after the start of the experiment and were 0.82, 5.82, and 11.20% of the total fatty acids, respectively. Concurrent decreases were observed in concentrations of C18:1, C18:2, C18:3, C20:4, and C22:6. Rate of egg production, body weight gain, and feed intake were not affected by dietary CLA. Average weights of eggs and yolks were decreased for hens fed 5.0% CLA compared with other dietary treatments. In Experiment 2, 62-wk-old hens were fed diets containing 0 or 5.0% CLA. Maximum CLA concentration in the yolk lipids of hens fed 5.0% CLA was less (7.43%) than that observed in Experiment 1. Feeding 5.0% CLA decreased feed intake but did not affect rate of egg production, weight of eggs, albumens, or yolks, or body weight gain through 36 d. Results of these experiments show that eggs produced by hens fed 5.0% CLA will contain 310 to 365 mg of CLA per egg. Such eggs could provide a substantial amount of CLA source in human foods.

Effect of dietary conjugated linoleic acid on the quality characteristics of chicken eggs during refrigerated storage.

Twenty-four, 79-wk-old White Leghorn hens were assigned randomly to three diets containing 0, 2.5, or 5.0% conjugated linoleic acid (CLA). The diets were fed for 4 wk to determine the effect of dietary CLA on quality characteristics of eggs. Eggs were collected daily and stored at 4 C for 1, 7, 21, or 49 d. At the designated times, the eggs were processed to evaluate water content, fatty acid composition, color, proportions and pH of yolk and albumen. Firmness of yolk after the eggs were hard-cooked was also determined. The proportions of myristic, palmitic, stearic, CLA (9-cis, 11-trans CLA and 10-trans, 12-cis CLA isomers), and unidentified fatty acids in egg yolk lipids were increased as dietary CLA increased, but those of palmitoleic, oleic, linoleic, linolenic, arachidonic, and docosahexaenoic acid were decreased. Duration of refrigeration increased the proportion of egg yolk but decreased the contents of albumen and yolk lipids after 21 d or longer of storage. Egg yolk pH increased as refrigeration time increased, regardless of dietary treatment, but the increase was greater in the eggs produced by hens fed the CLA diets. Albumen pH increased significantly after 7 d of storage but remained unchanged until 21 d and then decreased by 49 d. Dietary CLA had no effect on the pH of albumen until 49 d of storage. After 49 d storage, egg albumen pH from hens fed CLA diets was lower than that of albumen from hens fed the control diet. Yolk color was not influenced by the dietary CLA and storage, but the egg yolk surface from hens fed CLA diets sometimes had relatively dark color with light spots. Dietary CLA and storage of CLA eggs increased the firmness of hard-cooked egg yolk. The texture of yolks from hard-cooked CLA eggs was rubbery and elastic, and the yolks were more difficult to break using an Instron. It was speculated that the quality changes of CLA eggs were related to the increase of yolk water content, the movement of ions between yolk and albumen through yolk membrane, and the changes of egg yolk pH during storage.