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.
Omega-3 polyunsaturated fatty acids (n-3 PUFA) enriched eggs have a growing market share in the egg industry. This study examined the stability of n-3 PUFA enriched eggs fortified with antioxidants (vitamin E or organic Selenium [Sel-Plex] or both) following cooking and storage. The total fat content was not affected by cooking or simulated retail storage conditions, whereas, n-3 fatty acids were reduced. The content of n-3 fatty acids in boiled eggs was higher than in fried eggs. Lipid oxidation was significantly affected by the different cooking methods. Fried eggs contained higher levels of malondialdehyde (MDA, 2.02 μg/kg) and cholesterol oxidation products (COPs, 13.58 μg/g) compared to boiled (1.44 and 10.15 μg/kg) and raw eggs (0.95 and 9.03 μg/kg, respectively, for MDA and COPs). Supplementation of antioxidants reduced the formation of MDA by 40% and COPs by 12% in fried eggs. Although the content of MDA was significantly increased after 28 days of storage, COPs were not affected by storage. Our study indicated that the n-3 PUFA in enriched eggs was relatively stable during storage and home cooking in the presence of antioxidants.
The influence of vitamin E and selenomethionine (SeMet) on lipid oxidation in frozen-raw and cooked omega-3 enriched dark chicken meat was evaluated. Feed was supplemented with 2 levels of vitamin E (250 and 50 IU/kg of feed) and selenium (0.1 mg of sodium selenite/kg of feed and 0.3 mg of SeMet/kg of feed). An extruded linseed product was used as the alpha-linolenic acid source. Fatty acid (FA) profile, oxysterols, and thiobarbituric reactive acid substances (TBARs) were analyzed in frozen-raw, boiled, pan-fried, and roasted meat. After 6 mo of storage, oxysterols in frozen-raw meat remained stable with either high or low levels of dietary antioxidants. During cooking, high levels of vitamin E reduced oxysterol formation, whereas high levels of SeMet were inconsistent and even increased oxysterols during roasting. TBARs in frozen-raw meat stored for 6 mo were inhibited by high levels of either antioxidant. Conversely, no protective effect during cooking was observed at this time of storage. After 12 mo at -30 degrees C no antioxidant protection was observed.
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