Consumers are becoming more aware of the effect of the food they eat on their health. One of the ways they hope to reduce their risk of cardiovascular disease is by consuming more foods enriched with n-3 polyunsaturated fatty acids (PUFA). Due to the high content of alpha-linolenic acid (LNA), dietary flaxseed is a good source for increasing n-3 PUFA in poultry meat. A study was conducted with 2 primary objectives: to establish the distribution of n-3 PUFA between triacylglycerol (TAG) and phospholipid of broiler chicken breast and thigh meat and to determine the duration of dietary flaxseed supplementation required to ensure a level of n-3 PUFA of 300 mg per 100 g of meat necessary to label meat as a source of n-3 PUFA. This experiment was conducted as a 2 x 8 factorial, with 2 dietary levels of ground flaxseed (10 and 17%) and 8 durations of dietary flaxseed before processing [0 (control), 4, 8, 12, 16, 20, 24, and 35 d]. A total of 128 Ross x Ross 308 mixed-sex broilers were evaluated to 35 d of age. Breast and thigh meat fatty acid composition was analyzed on duplicate samples of ground meat pooled from 8 birds per treatment. Broken-stick analysis was used to estimate the duration required to achieve 300 mg of n-3 PUFA per 100 g of breast meat. Results clearly indicated that LNA was mainly deposited in the TAG fraction of both breast and thigh meat. Enriching the chicken breast meat with 300 mg of n-3 PUFA per 100 g of meat was achieved in 11.3 and 26.2 d with a 17 and 10% level of flaxseed in diet, respectively. Although a significant increase of n-3 long-chain PUFA (20:5n-3, 22:5n-3, and 22:6n-3) was found in the phospholipid and TAG fraction of both tissues, the concentration of these functional components was low. More than 95% of n-3 PUFA enrichment was due to LNA.
Consumers are becoming more aware of the impact on their health of the food they eat. One of the ways they hope to reduce their risk of cardiovascular disease is by consuming more foods enriched with polyunsaturated fatty acids (PUFA), particularly n-3 fatty acids. Flaxseed is a good source for increasing the n-3 PUFA in poultry meat because of the high content of alpha-linolenic acid. A study was conducted to identify an optimal process to enrich of broiler diets with n-3 PUFA by using 2 levels of flaxseed fed for various times before processing. The acceptability of broiler meat functional properties was tested to ensure that further processing efficiencies would not be compromised by the enrichment strategy. This experiment was conducted as a 2 x 8 factorial, with 2 dietary levels of ground flaxseed (10 and 17%) fed for 8 lengths of time before processing [0 (control), 4, 8, 12, 16, 20, 24, and 35 d]. Of 650 Ross x Ross 308 mixed-sex broilers reared in this study, 128 were used to evaluate breast and thigh meat functional properties, oxidative stability, and sensory analysis. No statistical interactions were found between treatments for chicken breast meat quality traits. The duration of feeding flaxseed strongly affected meat quality parameters. In particular, feeding flaxseed for 16 d resulted in a final pH of 5.65, compared with 5.93 in the control. The lower ultimate pH found in animals fed flaxseed affected meat cooking loss, drip loss, and shear value (P < 0.0001). Shear value significantly increased after 16 d of feeding flaxseed (P < 0.0001). Susceptibility to oxidation increased in both breast and thigh broiler meat with the duration of feeding flaxseed. Enriching the diet for less than 16 d did not result in perceivable sensory defects. Duration of flaxseed feeding significantly affected the color characteristics, functional properties, and oxidative stability of broiler meat.
An experiment was conducted to study the effect of broiler breeder feeding management practices on pullet performance, BW uniformity, and carcass traits during rearing (to 22 wk of age). At 3 wk of age, 1,200 Ross 308 breeder pullets were assigned to one of 5 treatments: 1) control: standard mash diet, fed daily; 2) high fiber: mash diet containing 25% lower nutrient density, fed daily; 3) scatter: standard diet in pellet form scattered on litter, fed daily; 4) skip-a-day: standard mash diet, fed on alternate days; or 5) grading: standard mash diet, fed daily (birds sorted into low, average, and high BW groups every 4 wk). Birds on the high fiber treatment consumed more feed (P<0.0001) and had the highest feed conversion ratio (FCR; P<0.004) but the lowest ME to gain and CP to gain ratios (P≤0.002). Skip-a-day treatment pullets consumed more ME and CP than birds in any other treatment (P<0.001). Grading yielded the highest BW uniformity at 22 wk of age (CV=6.2%), while control and high fiber treatment groups were least uniform (CV>15%; P<0.0001). Skip-a-day feed restriction produced birds with the significantly lowest breast muscle and highest liver weight compared to all other treatments (P<0.05). Variation in shank length, chest width, and breast muscle was lowest in the grading treatment, whereas the CV for fat pad and liver was lowest in the skip-a-day treatment. In this trial, broiler breeder target BW profiles were achieved using combinations of quantitative and qualitative feed restriction, or preemptive management practices. Qualitative diet dilution and skip-a-day management did little to increase flock uniformity relative to the control during the most intense period of feed restriction (7 to 19 wk). Scatter feeding increased flock uniformity to a small degree, whereas grading yielded the highest increase in BW and carcass trait uniformity.
The time required to reach a plateau of n-3 polyunsaturated fatty acid (PUFA) concentration in plasma and egg yolk and dynamics of the enrichment process were examined in laying hens. A group of 75 Lohmann White Leghorn layers (65 wk) were fed one of 3 diets: control, moderate, or high n-3 PUFA-enriched diet for 18 d. Diets provided similar ME and CP and contained 0, 7.5%, or 15% LinPRO (source of n-3 PUFA), respectively. Prior to dietary treatment, baseline values were established for the BW, fatty acid composition in egg yolk on a whole-egg basis, and in plasma. These measurements were repeated at 6, 12, and 18 d of feeding. Enzymatic conversion rates of linolenic acid (LNA) to long-chain fatty acids were calculated. Data were analyzed with Proc Mixed of SAS, and broken stick analysis was used to determine n-3 PUFA plateau using the NLIN procedure of SAS (P < 0.05). The total egg yolk n-3 PUFA reached a plateau of 343.7 mg/egg and 272.9 mg/egg after 6.6 and 5.9 d on the high and moderate diets, respectively. In blood plasma, the n-3 PUFA concentrations reached saturation in 7.2 d with 0.93 mg/mL and 0.67 mg/mL on high and moderate diets, respectively. The transfer efficiency of total n-3 PUFA from the diet to the egg yolk was calculated as 55.6% in control birds, 30.5% in moderate birds, and 22.2% in high birds, demonstrating reduced transfer efficiency of n-3 PUFA as inclusion in the feed increases. Final egg yolk n-3 PUFA concentrations had a CV of 16.5% compared with 28.5% for plasma. After 12 d, the long-chain n-3 PUFA [eicosapentaenoic acid (EPA), docosapentaenoic acid (DPA), and docosahexaenoic acid (DHA)] were significantly higher in egg yolk from hens on the moderate and high enriched diets compared with those from hens fed the control diet, whereas in plasma values did not differ. Broken stick analysis of egg enrichment indicated that high birds reached the target threshold of 300 mg of total n-3 PUFA/egg in 5 d. A significant increase in EPA, DPA, and DHA and reduction in arachidonic acid content in egg yolks from hens fed enriched diets compared with the control diet confirms competition for enzymes during postabsorptive modification of these fatty acids. This work contributes to the understanding of individual hen effects on n-3 PUFA absorption and the effect of level of dietary enrichment with an extruded flax product on final yolk n-3 PUFA concentration.
The effects of broiler breeder BW and nutrient intake on ovary morphology and plasma reproductive hormone profiles were examined at photostimulation (PS) (21 wk) and at sexual maturity (SM) in standard (STD) and low (LOW), or high (HIGH) BW birds provided either restricted (RF) or ad libitum (AL) access to feed between PS and SM. At PS, 30 Shaver Starbro pullets at target BW were assigned to the STD treatment, and birds either 20% heavier (HIGH) or lighter (LOW) assigned accordingly. Ten birds of each size group were processed immediately for carcass analysis and 10 birds assigned to each size by feed interaction group. Blood samples were taken at 3-d intervals beginning at PS and profiles constructed for estradiol-17beta, luteinizing hormone (LH), and follicle-stimulating hormone (FSH) to examine the relationship between body size, feeding level, and reproduction. Birds were processed for assessment of reproductive traits following SM. The AL birds reached SM with 11.0 large yellow follicles (LYF) (> 10 mm diameter) compared to 7.1 in RF birds. Small follicle atresia (< 5 mm diameter) was low in AL birds (10.3) compared to RF birds (32.3). The extent of small follicle atresia in RF birds was found to be inversely proportional to LYF number by stepwise regression. Increased small follicle atresia was associated with a longer sexual maturation period in RF birds (r = 0.619; P = 0.0003). Plasma estradiol-17beta concentration was greater in HIGH than in STD or LOW birds at PS, suggesting more advanced ovary development in HIGH birds. Estradiol-17beta profiles were similar in shape in all treatments, with the primary difference being the length of time prior to a substantial estradiol-17beta increase. Following PS, plasma LH and FSH concentrations of AL birds increased to levels nearly double that of RF birds, indicating a role for nutrient intake with rate of reproductive development. Plasma LH and FSH concentrations remained elevated for a greater time period in RF birds, however, possibly relating to the development of processes limiting LYF recruitment. This experiment demonstrated a modulation of reproductive hormone concentrations during sexual maturation by feeding level in conjunction with a sensitivity of the ovary to nutritional effects.
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