Lipid and cholesterol oxidation in chicken meat are inhibited by sage but not by garlic

The effects of the addition of sage and garlic in chicken meat on lipid and cholesterol oxidation, having as prooxidant factors the addition of salt, thermal treatment, and frozen storage, were evaluated. The content of unsaturated fatty acids did not change in the presence of sage; on the contrary, with garlic, the content of these fatty acids decreased after cooking and storage. Hexanal and pentanal contents were lower in patties containing sage, and higher in those with garlic. The 7-ketocholesterol was the cholesterol oxide found in higher amount in raw chicken on day 0, while the formation of 7β- and 7α-hydroxycholesterol was verified only from day 30 on. Cooking and storage resulted in increase of total cholesterol oxides and decrease of α- and γ-tocopherol. Sage was effective in controlling lipid and cholesterol oxidation, minimizing the prooxidant effects of salt, cooking, and storage. However, garlic presented no effect as antioxidant and accelerated lipid oxidation. PRACTICAL APPLICATION: The addition of sage to chicken meat (0.1 g/100 g) is a good alternative to prevent and delay the formation of compounds derived from lipid oxidation that are responsible for off-flavors and loss of nutritional quality during long-term frozen storage. Care must be taken when using garlic to seasoning chicken meat products, such as hamburgers and meatballs, especially cooked or precooked due to its potential to promote lipid oxidation and consequently raising the risk of having the product rejected by the consumer.     

Oxidative stability of Atlantic salmon (Salmo salar,L.) fillet enriched in α-, γ-, and δ-tocopherol through dietary supplementation

The purpose of this study was to examine the effect of dietary tocopherols on the oxidative stability of Atlantic salmon fillet. The fish were fed four diets supplemented with 150mg kg⁻¹ α-tocopherol and different combinations of γ- and δ-tocopherol (50 or 100mgkg⁻¹) for 10 months, slaughtered, and stored for 16 days on ice, or 48 weeks at −30 °C. Fillet concentrations of tocopherols at slaughter were 0.101 ± 0.001, 0.091 ± 0.004 and 0.025 ± 0.002 times feed concentration for α-, γ- and δ-tocopherol, respectively. Fillet α-tocopherol, but not γ- and δ-tocopherol, was moderately lowered during iced and frozen storage. The non-α-tocopherols protected the fillet against lipid oxidation in a dose-dependent manner during frozen storage, but appeared to act as prooxidants during storage on ice. It is concluded that α-tocopherol may be better suited than mixed tocopherols as a tool to optimize the oxidative stability of Atlantic salmon fillet.     

Effect of dietary levels of fat, α-tocopherol and astaxanthin on colour and lipid oxidation during storage of frozen rainbow trout (Oncorhynchus mykiss) and during chill storage of smoked trout

 Female rainbow trout (Oncorhynchus mykiss) with an initial weight of 0.8–0.9 kg were raised in two experiments including a total of 2550 fish divided into 17 groups. The fish were raised for 6 months on 13 different feeds (four fish groups were replicates) varying in dietary levels of fat (27% or 32%), astaxanthin (40, 70 or 100 mg astaxanthin/kg feed) and vitamin E (α-tocopherol; 100, 300 or 600 mg all-rac-α-tocopheryl acetate/kg feed). The levels of fat, astaxanthin and α-tocopherol in the fillets all increased with increasing dietary levels of each feed component. Furthermore, astaxanthin deposition was found to be significantly improved by increasing the dietary fat level from 27% to 32%, but was not affected by dietary levels of α-tocopherol. The highest deposition of α-tocopherol was found in fish fed the lowest level of astaxanthin (40 mg/kg), whereas α-tocopherol deposition was unaffected by the dietary fat level. Frozen storage (–28  °C) of gutted, cleaned and glazed raw fish for 18 months significantly reduced astaxanthin and α-tocopherol levels, while lipid oxidation, measured as thiobarbituric acid reactive substances (TBARS) was limited. In the first experiment, the highest TBARS levels were found during frozen storage in fish fed the lowest level of astaxanthin (40 mg/kg versus 70 mg/kg or 100 mg/kg); unaffected by dietary levels of α-tocopherol (100 mg/kg versus 600 mg/kg), whereas the dietary astaxanthin level (70 mg/kg versus 100 mg/kg) did not influence lipid oxidation in frozen fish in the second experiment. After brine injection, fillets of fish were smoked and a vacuum-packed (95%), sliced product in a transparent laminate was produced. The quality (pigmentation and lipid oxidation) during 3 weeks of illuminated, chill storage (3  °C) was compared for smoked products produced from fresh fish and from fish stored at –28  °C for 12 months and 18 months. Smoked fillets from fish fed 32% fat were found to be less red than those from fish fed 27% fat, and the astaxanthin content and surface redness of the smoked product decreased during chill storage. Lipid oxidation was pronounced in smoked trout, but a high level of α-tocopherol in the fillet significantly reduced lipid oxidation during chill storage of the smoked product. Lipid oxidation in smoked fillets from fish fed 32% fat was more pronounced than in fish fed 27% fat, but increasing the dietary α-tocopherol level from 300 mg/kg feed to 600 mg/kg feed effectively counteracted the negative effect of the high-fat diet on lipid oxidation in the smoked product. Astaxanthin did not affect lipid oxidation in the chill-stored smoked product, in contrast to the frozen, raw fish. Astaxanthin seems to protect against the very early stages of lipid oxidation, while α-tocopherol is more important as an antioxidant at more advanced stages of lipid oxidation. Received: 8 January 1998 / Revised version: 23 March 1998     

α-生育酚处理与真空包装对复合鲟鱼糜冻藏期间品质的影响

通过向不漂洗鲟鱼糜（non-rinsed sturgeon surimi，NRSS）添加40%（以鱼糜质量计）的鸡胸肉制备脂肪含量较高的复合鲟鱼糜（composite sturgeon surimi，CSS），为延缓其冻藏过程中品质劣变，分别采用真空包装与添加α-生育酚的处理方式对复合鲟鱼糜进行冻藏处理，并检测冻藏期间的凝胶强度、质构特性、持水性、脂肪氧化程度、脂肪酸组成及挥发性风味物质含量等指标。结果表明：冻藏期间，CSS组的凝胶强度、质构特性均优于NRSS组；真空包装组复合鲟鱼糜凝胶强度的下降程度低于其他各组，但在硬度和弹性方面与α-生育酚处理组无明显差异；冻藏16 周，CSS＋真空包装组和CSS＋α-生育酚组的持水性和亚油酸相对含量的下降程度均明显低于CSS组，且其鱼糜凝胶组织均匀致密、排列整齐，挥发性风味以青草味为主，哈喇味和土腥味较弱；冻藏4 周，真空包装和α-生育酚处理的复合鲟鱼糜硫代巴比妥酸反应物值增加幅度明显低于NRSS组，冻藏16 周，真空包装组的硫代巴比妥酸反应物值增加幅度仍明显低于其他组。综上，真空包装与α-生育酚添加可以有效地保持复合鲟鱼糜质构特性，抑制脂肪氧化，并减缓风味劣变。     

α-Tocopherol and Ascorbate Delay Oxymyoglobin and Phospholipid Oxidation In Vitro

An oxymyoglobin liposome model was used to study the effects of α-tocopherol and/or ascorbate upon oxymyoglobin and lipid oxidation. Both oxidations were delayed (P<0.05) by increased concentrations of α-tocopherol alone and α-tocopherol/ascorbate relative to controls. The 14 μ Mα-tocopherol/140 μM ascorbate treatment resulted in greatest delay in both oxymyoglobin and lipid oxidation. Ascorbate alone delayed oxymyoglobin oxidation; effectiveness diminished as ascorbate increased. Ascorbate showed a prooxidant effect toward lipid oxidation which was unchanged in the presence of EDTA. Results support the hypothesis that α-tocopherol retards lipid oxidation directly and OxyMb oxidation indirectly.     

Meta-analysis of the effects of dietary vitamin E supplementation on α-tocopherol concentration and lipid oxidation in pork

Meta-analyses have been carried out to quantify the effect of dietary vitamin E on α-tocopherol accumulation and on lipid oxidation in porcine M. longissimus. Published results of 13 (vitamin E accumulation) and 10 (lipid oxidation) experiments respectively were used for the analyses. After a number of standardization procedures, a nonlinear relationship was found between the supplementary vitamin E and the accumulation of α-tocopherol in pork which approached a maximum value of 6.4 μg/g tissue. Pork lipid oxidation levels were described in terms of Thiobarbituric Acid Reacting Substances (TBARS) values. The statistical analysis revealed significant effect of vitamin E dose, muscle α-tocopherol concentration and supplementation time on TBARS, resulting in two prediction models for lipid oxidation. Meta-analysis has proven to be a valuable tool for combining results from previous studies to quantify the effects of dietary vitamin E. Further studies, carried out with standardized experimental protocols would be beneficial for model validation and to increase the predictive power of the derived models.     

Effect of rosemary extract, chitosan and α-tocopherol on lipid oxidation and colour stability during frozen storage of beef burgers

The effect of rosemary extract, chitosan and α-tocopherol, added individually or in combination, on lipid oxidation and colour stability of frozen (−18 °C) beef burgers stored for 180 days was investigated. The burgers’ lipid oxidation and appearance were evaluated through measurement of primary (conjugated dienes and peroxide value) and secondary (malondialdehyde) oxidation products, together with visual assessment and instrumental measurement of colour. Chitosan alone and in combination with either rosemary or α-tocopherol had the best antioxidative effect (P ? 0.05) compared to individual use of rosemary or α-tocopherol, while the best results were obtained with the combination of chitosan and rosemary. The differences of antioxidative effects, however, between individual use of rosemary or α-tocopherol as compared to the controls were also significant (P ? 0.05). Chitosan added individually or in combination with either rosemary or α-tocopherol had also a noteworthy effect on the burgers’ appearance as it contributed to red colour retention for a much longer period (P ? 0.05) compared all other treatments and the controls. In conclusion, the best antioxidative effects were obtained with the combination of chitosan and rosemary extract.     

Effect of plant extracts on lipid oxidation during frozen storage of minced fish muscle

The aim of the study is to determine the effect of pomegranate seed extract (PSE) and grape seed extract (GSE) addition to chub mackerel minced muscle on lipid oxidation during frozen storage. Each extract was added to minced fish muscle at 2% concentration and then stored at ?18 °C for 3 months. The effect of plant dietary fibres to control lipid oxidation was compared with untreated samples (control). Formation of lipid hydroperoxides and thiobarbituric acid‐reactive substances (TBARS) was significantly inhibited by PSE and GSE addition when compared with control. Both extracts significantly retarded lipid oxidation according to the results of TBARS. A significant reduction of L* (lightness), a* (redness) and b* (yellowness) values was detected during frozen storage. GSE added samples had the highest redness and the lowest lightness and yellowness. However, samples with PSE showed the lowest redness and highest yellowness and h° (hue angle) values. The results from this study suggest GSE is a very effective inhibitor of primary and secondary oxidation products in minced fish muscle and have a potential as a natural antioxidant to control lipid oxidation during frozen storage of fatty fish.     

Oxymyoglobin and Lipid Oxidation in Phosphatidylcholine Liposomes Retarded by α-tocopherol and β-carotene

An n-3 fatty acid-constructed oxymyoglobin liposome model was used to study the effects of 10 μM α-tocopherol and/or various concentrations of β-carotene on oxymyoglobin and lipid oxidation. Oxidation was delayed by α-tocopherol or β-carotene treatments alone (p < 0.05). β-Carotene at 1.5 μM and 2μM caused greater delay in oxymyoglobin oxidation than α-tocopherol (p < 0.05). For lipid oxidation inhibition, 2 μM β-carotene was similar in effect to α-tocopherol. With α-tocopherol plus 1.5 or 2 μM β-carotene, greater oxidation delaying effect resulted for both oxymyoglobin and lipid oxidations than with 1.5 or 2 μM β-carotene treatment alone (p < 0.05).     

Inhibition of oxidation of omega-3 polyunsaturated fatty acids and fish oil by quercetin glycosides

The antioxidant properties of naturally occurring flavonols, quercetin glycosides, were examined and compared with common food antioxidants butylated hydroxytoluene (BHT) and α-tocopherol. Antioxidants were incorporated into selected polyunsaturated fatty acids (PUFA) or fish oil in aqueous emulsions and bulk oil systems. The effectiveness of quercetin was similar to or greater than quercetin glycosides in inhibiting lipid oxidation in the oil-in-water emulsion systems when oxidation was induced by heat, light, peroxyl radical or ferrous ion. In bulk fish oil, C-3 glycosylation enhanced the antioxidant activity of quercetin. The effectiveness of quercetin and its glycosides was greater than that of α-tocopherol in the emulsions. Quercetin and quercetin-3-O-glucoside exhibited a better antioxidant activity than BHT in bulk fish oil; however, the reverse was observed in the emulsions of omega-3 PUFA and fish oil systems in agreement with the polar paradox theory. Quercetin and its glycosides were more effective than α-tocopherol in emulsion systems.     

The effect of α-tocopherol and butylated hydroxyanisole on the colour properties and lipid oxidation of kavurma, a cooked meat product

Kavurma is a cooked meat product and is consumed sliced. The amount of animal fat in kavurma (30-40%) is higher than in other meat products; therefore, lipid oxidation and colour defects are a major problem during storage and in the market place. To preserve the quality characteristics of kavurma in markets antioxidants must be added and the product must be packaged and stored at low temperature. In this study, the effects of α-tocopherol and butylated hydroxyanisole (BHA) levels on lipid oxidation and colour deterioration of sliced and vacuum-packaged kavurma were investigated. Kavurma was made from beef meat and melted beef fat in 5 groups: No-added antioxidant, 50mg/kg BHA, 100mg/kg BHA, 50mg/kg α-tocopherol and 100mg/kg α-tocopherol. The kavurma produced was sliced (3-4-cm thick) and vacuum packed and stored at 4°C for 300 days, and thiobarbituric acid reactive substance, pH, moisture, lightness, redness and yellowness values of sliced product were determined during storage. The use of antioxidants in kavurma production caused a significant (P<0.01) decrease in the thiobarbituric acid reactive substances (TBARS) values. The lipid oxidative stability effect of the antioxidants was in following order: 100mg/kg BHA>100mg/kg α-tocopherol>50mg/kg BHA=50mg/kg α-tocopherol>no-added antioxidant group. Also, TBARS values did not differ significantly (P>0.05) between 0 and 300 days in the 100mg/kg BHA and 100mg/kg α-tocopherol groups. In addition, the no-added antioxidant group had lower lightness and yellowness values than all the antioxidant groups. Sliced and vacuum-packaged kavurma with added antioxidant showed greater colour and lipid oxidative stability during storage than kavurma to which no antioxidant was added.     

Oxidative stability of frozen pork patties: Effect of fluctuating temperature on lipid oxidation

The mobility of solutes in fat from pork belly, in lean pork belly and in lean pork longissimus dorsi, containing 1% NaCl was characterized by the ESR spin probe technique using the nitroxyl spin probes TEMPO and TEMPOL. The mobility of TEMPO in fat increased for temperature above -60 °C and the mobility of TEMPOL in lean meat increased for temperature above -40 °C. Temperatures for studying the effect of fluctuating temperatures during frozen storage of meat were selected based on the ESR characterization of the mobility of solutes. The oxidative stability of pork patties during frozen storage was measured as thiobarbituric acid reactive substances (TBARS), during storage at -10, -23 and -40 °C and with fluctuations between these temperatures, of pork patties made from pork loin (low fat 1.8%) or pork belly (high fat 22.7%). Lower storage temperatures resulted in less lipid oxidation, and temperature fluctuations between -40 and -23 °C and fluctuations between -23 and -10 °C resulted in oxidation intermediate to oxidation in samples stored at constant low or high temperatures of the fluctuation interval. The level of α-tocopherol was unaffected by the extent of oxidation in the frozen samples, an observation which is discussed in relation to differences in molecular mobility between oxygen and α-tocopherol.     

Porcine oxymyoglobin and lipid oxidation in vitro

The present study was carried out to investigate the effect of dietary α-tocopherol supplementation on porcine oxymyoglobin (OxyMb) and lipid oxidation (TBARS) in model lipid systems, and to determine the influence of 4-hydroxynonenal (4-HNE), a secondary product of lipid oxidation, on porcine OxyMb stability. Porcine metmyoglobin (MetMb) formation was greater in the presence of 4-HNE than the control (P<0.05). Western blot analyses confirmed the covalent modification of myoglobin (Mb) histidine residues by 4-HNE. When combined with microsomes, both equine and porcine OxyMb oxidation increased with time of incubation, and was greater at 37 than at 25?°C (P<0.05). Lower TBARS values were observed in microsomes prepared from vitamin E-supplemented than control pork livers (P<0.05). α-Tocopherol concentration did not affect OxyMb oxidation in microsomes at 25 or 37?°C (P>0.05). These results differ from those observed with beef muscle microsomes where both OxyMb and lipid oxidation were delayed with elevated α-tocopherol levels. These results suggest that the factors affecting Mb and lipid oxidation interactions may be species-dependent.     

EFFECT OF DIETARY VITAMIN E AND SURFACE APPLICATION OF OLEORESIN ROSEMARY ON IRON/ASCORBATE-STIMULATED LIPID OXIDATION IN MUSCLE TISSUE AND MICROSOMES FROM RAINBOW TROUT (Oncorhynchus mykiss)

The effect of dietary α-tocopheryl acetate and surface application of oleoresin rosemary on iron/ascorbate-induced lipid oxidation in rainbow trout ( Oncorhynchus mykiss ) muscle and microsomes was investigated. The 2-thiobarbituric acid-reactive substances (TBARS) values of muscle and microsomes isolated from fish fed the higher concentration of α-tocopherol (500 mg/kg feed) were smaller than those of fish fed the lower concentration (100 mg/kg feed). The protective effect of oleoresin rosemary on lipid oxidation in fish muscle was also observed. Analysis of variance revealed a significant (p < 0.01) interaction between dietary treatments and incubation time. Dietary α-tocopherol supplementation significantly increased the α-tocopherol concentration of muscle microsomal membranes, thereby increasing the oxidative stability of the membrane lipids.     

Effect of carnosine, salt and dietary vitamin E on the oxidative stability of chicken meat

The effect of carnosine on lipid and cholesterol oxidation in salted chicken thigh meat and its relationship to dietary α-tocopherol supplementation was examined. Broilers (Cobb 500) were fed diets with a basal (30 mg kg(-1)) or supplemental (200 mg kg(-1)) level of α-tocopheryl acetate for 6 weeks. Thigh meat patties were prepared with carnosine (1.5%), salt (1%) or salt plus carnosine. Salt accelerated lipid and cholesterol oxidation following cooking and refrigerated storage. However, carnosine inhibited lipid and cholesterol oxidation in salted patties. Dietary α-tocopherol supplementation also reduced the extent of lipid and cholesterol oxidation in salted patties. The combination of carnosine and dietary α-tocopherol resulted in the greatest lipid and cholesterol stability in salted meat.     

Effects of supranutritional dietary vitamin E levels on subcellular deposition of α-tocopherol in the muscle and on pork quality

The influence of three levels of vitamin E in the diet of pigs on the subcellular deposition of α-tocopherol in the muscle and on selected quality characteristics of pork meat (oxidative stability of lipids, colour, drip loss, microbial growth) was studied. The content of α-tocopherol in adipose tissue and L. dorsi muscle as well as in mitochondrial and microsomal fractions of the muscle significantly increased (P < 0.05) with increasing levels of dietary vitamin E. The differences in the concentrations of α-tocopherol in the subcellular fractions were evident in the enhanced stability of the membranes when exposed to metmyoglobin/hydrogen peroxide. The beneficial effect of dietary vitamin E on the oxidative stability of pork lipids during the storage of pork chops and ground pork was also demonstrated. Even though lipid oxidation increased in all cases during storage, the pork products from the pigs receiving the highest level of vitamin E (200 IU kg^?1 feed) exhibited the smallest increase in thiobarbituric acid reactive substances. In addition, increased colour stability and decreased drip loss were observed on keeping pork chops, which had been previously frozen for three months, at 4°C under fluoresent light for 10 days. The possible effect of α-tocopherol on membrane fluidity in this context is discussed.     

Effects of Dietary Antioxidants and Oxidized Oil on Membranal Lipid Stability and Pork Product Quality

The effects of dietary tocopherol and oxidized oil on the oxidative stability of membranal lipids in pig muscles and on the oxidative stability of pork products during refrigerated and frozen storage were evaluated. Membrane-bound α-tocopherol stabilized the membranal lipids and reduced the extent of lipid oxidation occurring in pork patties and pork chops during storage. Oxidized dietary oil had an adverse effect on the stability of both the membranal lipids and pork products. The addition of salt to the pork patties accelerated the oxidative process when the patties were stored under fluorescent light and in the dark.     

Antioxidant mechanism of grape procyanidins in muscle tissues: Redox interactions with endogenous ascorbic acid and α-tocopherol

The present study investigates the antioxidant mechanism of grape procyanidins and, in particular, their aptitude to establish redox interactions with two important components of the endogenous antioxidant system of muscle tissues, α-tocopherol (α-TOH) and ascorbic acid (AA). To this end, the progress of lipid oxidation was monitored in fish muscle supplemented with grape procyanidins at the concentrations usually employed in antioxidant food applications, and then related to the redox stability of the endogenous α-TOH and AA. In addition to the lipid oxidation protective effect, the incorporation of procyanidins also provided an improvement of the redox stability of the endogenous components in a straight procyanidinic concentration-dependent manner. Results showed the capacity of procyanidins to repair oxidised α-TOH at medium-long term, and to delay the AA depletion. Therefore, such cooperative redox interaction of exogenous procyanidins adequately complements the natural α-TOH regenerative system supplied by AA that is efficient at the early post mortem stages.     

Improvement of Pigment and Lipid Stability in Holstein Steer Beef by Dietary Supplementation with Vitamin E

Pigment and lipid oxidation was investigated in fresh ground sirloin from control and vitamin E-supplemented (370 I.U./head/day) Holstein steers. Alpha-tocopherol levels were higher (P<0.05) in muscle from supplemented animals than from controls. During 6 days storage at 4°C, metmyoglobin accumulation and lipid oxidation (TBA) were greater (P<0.05) in beef from control versus supplemented animals. TBA value and % metmyoglobin were highly correlated in the control (r = 0.91) and supplemented (r = 0.72) groups. TBA values of cooked sirloin slices subsequently stored for 2 days at 4°C, and for frozen ground sirloin patties stored at -18°C for 1.5 and 3 months, were lower (P<0.05) in beef from supplemented animals than from controls. Meat which contained in excess of ca. 0.3 mg α-tocopherol/100 g tissue displayed the least oxidation of both pigments and lipids.     

Effects of plant extracts on lipid oxidation in fish croquette during frozen storage

The aim of this study was to investigate the effects of tomato and garlic extracts on lipid oxidation in fish croquette during frozen storage. The fish for croquette was purchased from the main fish market in Antalya, Turkey. Commercial tomato and garlic extracts were added into the croquette formulation. Lipid quality of frozen croquettes was analyzed at monthly intervals. There was no difference in free fatty acids and UV absorbance values of treatment groups. Treatment of tomato and garlic extracts kept oxidation at low levels. The results for thiobarbutiric acid, para-anisidine, and conjugated-diene values showed that tomato extract was the most effective in delaying lipid oxidation than garlic extract.