Use of Standard or Modified Plant-Derived Lipids as Alternatives to Fish Oil in Feeds for Juvenile Nile Tilapia

In support of developing sustainable aquafeeds, production performance and fillet fatty acid profile were assessed in juvenile Nile tilapia (0.61 ± 0.0 g/fish mean ± SE) raised for 16 weeks on diets containing fish oil or 50:50 blends of fish and plant-derived lipids. Standard, low 18:3n-3, or saturated fatty acid (SFA)-enriched soybean oils, palm oil, or low 18:3n-3 canola oil may be used to partially spare fish oil in feeds for Nile tilapia without impairing production performance, though use of hydrogenated soybean oil appears to impair growth and conversion efficiency. Of the plant lipids evaluated, palm and SFA-enriched soybean oil appear to be the best alternatives in terms of maintaining fillet long-chain polyunsaturated fatty acid content and the nutritional value of tilapia fillets.     

Effects of dietary fish oil substitution with mixed vegetable oils on growth and fillet fatty acid composition of juvenile Caspian great sturgeon (Huso huso)

The objective of this study was to determine the effects of fish oil replacement with dietary vegetable oils on growth performance, chemical composition and fatty acids profiles in fillets of farmed Caspian great sturgeon juveniles Huso huso (26.97 ± 0.49 g). Five isonitrogenous and isolipidic diets were formulated, containing 10 % of added oil. The diet with 100 % kilka fish oil (Caspian tyulka, Clupeonella caspia) was the control. Fish oil was substituted by 50 % of vegetable oils consisting of an equal share of sunflower and soybean oils (diet A), sunflower and canola oils (diet B) and soybean and canola oils (diet C). In diet D, 100 % of fish oil was replaced with vegetable oil (1:1:1 ratio of sunflower oil, soybean oil and canola oil). Significant differences (P > 0.05) were not detected during 60 days feeding trial in final body weight, weight gain, condition factor, specific growth rate, feed conversion rate, protein efficiency ratio and the chemical composition of fillet (crude protein, crude lipid, moisture and ash). Generally, the fatty acids composition of fish fillets was reflective of the dietary lipid sources. These results indicate the feasibility of substituting fish oils with the mixture of vegetable oils in diets of juvenile H. huso without negative influence on growth providing optimum ratios of n-3/n-6 and n-3/18:1n-9 is met in the diet.     

Nutritional regulation of hepatocyte fatty acid desaturation and polyunsaturated fatty acid composition in zebrafish (Danio rerio) and tilapia (Oreochromis niloticus)

The desaturation and elongation of [1-¹⁴C]18:3n-3 was investigated in hepatocytes of the tropical warm freshwater species, zebrafish (Danio rerio) and Nile tilapia (Oreochromis niloticus). The hepatocyte fatty acid desaturation/elongation pathway was assayed before and after the fish were fed two experimental diets, a control diet containing fish oil (FO) and a diet containing vegetable oil (VO; a blend of olive, linseed and high oleic acid sunflower oils) for 10 weeks. The VO diet was formulated to provide 1% each of 18:2n-6 and 18:3n-3, and so satisfy the possible EFA requirements of zebrafish and tilapia. At the end of the dietary trial, the lipid and fatty acid composition was determined in whole zebrafish, and liver, white muscle and brain of tilapia. Both zebrafish and tilapia expressed a hepatocyte fatty acid desaturation/elongation pattern consistent with them being freshwater and planktonivorous fish. The data also showed that hepatic fatty acid desaturation/elongation was nutritionally regulated with the activities being higher in fish fed the VO diet compared to fish fed the FO diet. In zebrafish, the main effect of the VO diet was increased fatty acid Δ6 desaturase activity resulting in the production of significantly more 18:4n-3 compared to fish fed the FO diet. In tilapia, all activities in the pathway were greater in fish fed the VO diet resulting in increased amounts of all fatty acids in the pathway, but primarily eicosapentaenoic acid (EPA; 20:5n-3) and docosahexaenoic acid (DHA; 22:6n-3). However, the fatty acid compositional data indicated that despite increased activity, desaturation of 18:3n-3 was insufficient to maintain tissue proportions of EPA and DHA in fish fed the VO diet at the same level as in fish fed the FO diet. Practically, these results indicate that manipulation of tilapia diets in commercial culture in response to the declining global fish oil market would have important consequences for fish fatty acid composition and the health of consumers. Scientifically, zebrafish and tilapia, both the subject of active genome mapping projects, could be useful models for studies of lipid and fatty acid metabolism at a molecular biological and genetic level. This revised version was published online in August 2006 with corrections to the Cover Date.     

Comparison of effects of vegetable oils blended with southern hemisphere fish oil and decontaminated northern hemisphere fish oil on growth performance, composition and gene expression in Atlantic salmon (Salmo salar L.)

Replacement of fish oil with sustainable alternatives, such as vegetable oil, in aquaculture diets has to be achieved without compromising the nutritional quality, in terms of n-3 highly unsaturated fatty acid (HUFA) content, of the product. This may be possible if the level of replacement is not too high and oil blends are chosen carefully but, if high levels of fish oil are substituted, a fish oil finishing diet prior to harvest would be required to restore n-3HUFA. However, a decontaminated fish oil would be required to avoid increasing undesirable contaminants. Here we test the hypotheses that blending of rapeseed and soybean oils with southern hemisphere fish oil will have a low impact upon tissue n-3HUFA levels, and that decontamination of fish oil will have no major effect on the nutritional quality of fish oil as a feed ingredient for Atlantic salmon. Salmon (initial weight ~ 0.8 kg) were fed for 10 weeks with diets in which 60% of fish oil was replaced with blends of soybean, rapeseed and southern hemisphere fish oil (SVO) or 100% decontaminated northern fish oil (DFO) in comparison with a standard northern fish oil diet (FO). Decontamination of the oil was a two-step procedure that included treatment with activated carbon followed by thin film deodorisation. Growth performance and feed efficiency were unaffected by either the SVO or DFO diets despite these having lower gross nutrient and fatty acid digestibilities than the FO diet. There were also no effects on the gross composition of the fish. Liver and, to a lesser extent flesh, lipid levels were lower in fish fed the SVO blends, due to lower proportions of neutral lipids, specifically triacylglycerol. Tissue lipid levels were not affected in fish fed the DFO diet. Reflecting the diet, flesh eicosapentaenoic acid (EPA) and total n-3 fatty acids were higher, and 18:1n-9 lower, in fish fed DFO than FO, whereas there were no differences in liver fatty acid compositions. Flesh EPA levels were only slightly reduced from about 6% to 5% although docosahexaenoic acid (DHA) was reduced more severely from around 13% to about 7% in fish fed the SVO diets. In contrast, the liver fatty acid compositions showed higher levels of n-3 HUFA, with DHA only reduced from 21% to about 18% and EPA increased from under 8% to 9–10% in fish fed the SVO diets. The evidence suggested that increased liver EPA (and arachidonic acid) was not simply retention, but also conversion of dietary 18:3n-3 and 18:2n-6. Increased HUFA synthesis was supported by increased hepatic expression of fatty acyl desaturases in fish fed the SVO diets. Flesh n-3HUFA levels and desaturase expression was significantly higher in fish fed soybean oil than in fish fed rapeseed oil. In conclusion, partial replacement of fish oil with blends of vegetable oils and southern hemisphere fish oil had minimal impact on HUFA levels in liver, but a greater effect on flesh HUFA levels. Despite lower apparent digestibility, decontamination of fish oil did not significantly impact its nutritional quality for salmon.     

Effects of total replacement of dietary fish oil on growth performance and fatty acid compositions of hybrid tilapia (Oreochromis niloticus × O. aureus)

The aim of this study is to evaluate the effects of total replacement of fish oil (FO) with pork lard (PL), soybean oil (SO), or tea seed oil (TO) on growth and fatty acid compositions of hybrid tilapia (Oreochromis niloticus × O. aureus). Four diets were formulated to contain 4.5 % of each of the different lipid sources. Each diet was assigned to triplicate groups of 15 hybrid tilapia with the same initial body weight (4.6 ± 0.5 g). After a 10-week feeding, the FO, SO, and TO groups had similar final body weight. The mean hepatosomatic index in the FO group was significantly lower than the other groups (2.5 vs 2.9–3.0; P < 0.05). Whole-body lipid levels were highest in the TO group (5.2 ± 0.4 %) and lowest in the FO group (4.3 ± 0.5 %). Total n-3 polyunsaturated fatty acids (PUFA) concentrations were greater in the SO and FO groups (5.5 ± 0.1 and 7.1 ± 0.2, respectively) than in the PL and TO groups (1.7 ± 0.1 and 1.4 ± 0.1, respectively). The FO group had a 2- to 4-fold reduction in the n-6/n-3 PUFA ratio relative to the other groups. The concentrations of both docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) were significantly (P < 0.05) higher in the FO group than in the other groups. Our data demonstrate that total replacement of dietary FO with SO or TO has little effects on growth of hybrid tilapia but reduces the contents of health-benefiting DHA and EPA in fish body.     

Administration of two oils rich in n-3 long-chain polyunsaturated fatty acids to rat pups of dams fed a diet high in fat and low in n-3 polyunsaturated fatty acids

Long-chain polyunsaturated fatty acids (LCPUFA) with 20 or 22 carbons are considered important to the development of infants and sometimes added to infant formulae. In this study, two characteristic sources of n-3 LCPUFA (fish oil and microalgal oil) were orally administrated to rat pups of mildly n-3 PUFA — deficient dams to compare the consequences of the administration. The milk from the dams fed a n-3 PUFA — restricted diet contained less n-3 LCPUFA than that of the dams fed a control diet. Pups were administered 1 mg/g weight of the test oil at the age of 5–7 days. At the age of 7 days, they were sacrificed before or after the administration and fatty acid compositions of the stomach and serum lipid were studied. The administration changed docosahexaenoic acid (DHA; 22:6n−3) levels in the stomach contents and serum lipids with time. Eicosapentaenoic acid (EPA; 20:5n−3) levels increased immediately after the administration of fish oil. The administration of microalgal oil also affected the serum lipid EPA level, in spite of a lack of EPA. In this study, both oils effectively supplemented DHA. Fish oil returned the serum EPA level close to the control value while microalgae oil had little effect.     

Effects of dietary lipids on the fatty acid composition of triglycerides and phospholipids in tissues of white sturgeon

Eight purified diets were fed to juvenile white sturgeon, Acipenser transmontanus Rick, for 9 weeks to investigate the effect of dietary lipids on the fatty acid composition of phospholipids and triglycerides from muscle, liver and brain. The diets contained 150 g kg^?1 of oils from canola, corn, cod liver, lard, linseed, soybean, safflower, or a control mixture (corn oil/cod liver oil/lard, 1:1:1, by wt). Dietary lipids significantly (P≤ 05) affected the composition of tissue triglycerides and phospholipids. Tissue triglyceride fatty acid composition ranged widely, in parallel with the dietary lipids, while phospholipids changes were more conservative. Brain phospholipid fatty acid composition was less responsive to diet compared with that in muscle and liver. Considerable amounts of n-6 and n-3 long chain polyun-saturated fatty acids (> C₂₀) were found in triglycerides and phospholipids with all diets, demonstrating that white sturgeon can desaturate and elongate linoleic acid (18:2n–6) and linolenic acid (18:3n–3). Further, the products of the Δ6 desaturase, i.e. 18:3 n–6 and 18:4n–3, were relatively abundant in triglyceride, suggesting that the Δ6 desaturase might not be a limiting step in the process in white sturgeon. Nevertheless, accumulation of both EPA and DHA was greater in the sturgeon fed fish oil than those fed linseed oil, indicating that muscle triglyceride EPA and DHA levels are best enhanced by diets rich in preformed EPA and DHA.     

豆油替代鱼油对圆斑星鲽幼鱼生长和肌肉脂肪酸的影响

本实验旨在研究饲料中豆油替代鱼油对圆斑星鲽(Verasper variegatus)幼鱼生长和肌肉脂肪酸组成的影响。用豆油分别替代0、25%、50%和75%的鱼油,配制4组等氮、等脂肪的饲料。选择初始体重为(65.47±1.57)g的圆斑星鲽幼鱼360尾,随机分为4组,每组3个重复,每个重复30尾鱼,养殖56 d。结果显示,(1)随着豆油替代水平的升高,增重率(WGR)呈现降低的趋势(P0.05),饲料系数(FCR)呈现升高的趋势(P0.05),25%替代组的WGR高于鱼油组(P0.05)。(2)豆油替代鱼油对圆斑星鲽肌肉的粗蛋白、粗脂肪、灰分和水分含量无显著性影响(P0.05),对肝体比(HSI)、脏体比(VSI)和肥满度(CF)无显著性影响(P0.05),豆油替代组肝脏的脂肪含量显著高于鱼油组(P0.05)。(3)随着饲料中豆油水平的增加,圆斑星鲽幼鱼肌肉亚油酸(C18:2n-6)和亚麻酸(C18:3n-3)显著升高(P0.05),而二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)则显著降低(P0.05)。研究结果表明,在该实验条件下,饲料中高比例的豆油替代鱼油会降低鱼体的生长性能和肌肉脂肪酸营养品质。     

Effect of Dietary Fish Meal Replacement by Canola Meal on Growth Performance and Hepatic Intermediary Metabolism of Genetically Improved Farmed Tilapia Strain of Nile Tilapia,Oreochromis niloticus,Reared in Fresh Water

An 8‐wk feeding trial was conducted to evaluate the potential of replacing fish meal with canola meal in experimental diets for genetically improved farmed tilapia (GIFT) strain of Nile tilapia, Oreochromis niloticus (mean initial weight: 20.0 ± 0.62 g, means ± SD), reared in fresh water. Six isonitrogenous (30% crude protein) and isolipidic (10%) diets were formulated with canola meal included at six levels of 0 (control), 11, 22, 33, 44, and 55%, replacing 0, 15, 30, 45, 60, and 75% fish meal, respectively. Growth performance and feed utilization showed no significant differences among the treatments. In general, dietary canola meal supplementation showed significant effect on hepatic composition of tilapia, but not muscle composition. Viscerosomatic index tended to increase with increasing dietary canola meal levels from 0 to 44%, and then declined when dietary canola meal levels further increased from 44 to 55%. Dietary fish meal replacement by canola meal significantly influenced several hepatic enzymatic activities, including succinate dehydrogenase, lactate dehydrogenase, malic dehydrogenase, lipoprotein lipase, and hepatic lipase, suggesting that dietary fish meal replacement by canola meal had significant effects on nutrient metabolism in the liver. Based on the information above, 75% of dietary fish meal could be replaced by canola meal with no effect on growth performance of GIFT strain of Nile tilapia. Use of canola meal in practical diets for GIFT stain of Nile tilapia may allow producers and feed mills to formulate more economical diets.     

Interactions between dietary docosahexaenoic acid and other long-chain polyunsaturated fatty acids on performance and fatty acid retention in post-smolt Atlantic salmon (Salmo salar)

A study with varying dietary inclusion levels (1, 5, 10, 15 and 20 g kg^?1) of docosahexaenoic acid (DHA; 22:6n-3) was conducted with post-smolt (111 ± 2.6 g; mean ± S.) Atlantic salmon (Salmo salar) over a 9-week period. In addition to the series of DHA inclusion levels, the study included further diets that had DHA at 10 g kg^?1 in combination with either eicosapentaenoic acid (EPA; 20:5n-3) or arachidonic acid (ARA; 20:4n-6), both also included at 10 g kg^?1. An additional treatment with both EPA and DHA included at 5 g kg^?1 (total of 10 g kg^?1 long-chain polyunsaturated fatty acids, LC-PUFA) was also included. After a 9-week feeding period, fish were weighed, and carcass, blood and tissue samples collected. A minor improvement in growth was seen with increasing inclusion of DHA. However, the addition of EPA further improved growth response while addition of ARA had no effect on growth. As with most lipid studies, the fatty acid composition of the whole body lipids generally reflected that of the diets. However, there were notable exceptions to this, and these implicate some interactions among the different LC-PUFA in terms of the fatty acid biochemistry in this species. At very low inclusion levels, DHA retention was substantially higher (~250 %) than that at all other inclusion levels (31–58 %). The inclusion of EPA in the diet also had a positive effect on the retention efficiency of DHA. However, EPA retention was highly variable and at low DHA inclusion levels there was a net loss of EPA as this fatty acid was most likely elongated to produce DHA, consistent with increased DHA retention with additional EPA in the diet. Retention of DPA (22:5n-3) was high at low levels of DHA, but diminished with increasing DHA inclusion, similar to that seen with DHA retention. The addition of EPA to the diet resulted in a substantial increase in the efficiency of DPA retention; the inclusion of ARA had the opposite effect. Retention of ARA was unaffected by DHA inclusion, but the addition of either EPA or ARA to the diet resulted in a substantial reduction in the efficiency of ARA retention. No effects of dietary treatment were noted on the retention of either linolenic (18:3n-3) or linoleic (18:2n-6) acids. When the total n-3 LC-PUFA content of the diet was the same but consisted of either DHA alone or as a combination of EPA plus DHA, the performance effects were similar.     

Deposition of tocopherol and tocotrienol in the tissues of red hybrid tilapia, Oreochromis sp., fed vitamin E-free diets supplemented with different plant oils

Vitamin E, a potent antioxidant consisting of four isomers each (α, β, γ, δ) of tocopherol (T) and tocotrienol (T3), is found naturally in plant oils at different concentrations. In this study, four semi-purified isonitrogenous and isolipidic (10 %) diets containing canola oil, cold-pressed soybean oil, wheat germ oil, or palm fatty acid distillates (PFAD) as the sole vitamin E source were fed to triplicate groups of red hybrid tilapia (Oreochromis sp.) fingerlings (14.82 ± 0.05 g) for 45 days. Vitamin E concentrations and composition were measured in the muscle, liver, skin, and adipose tissue. Deposition of α-T (53.4–93.1 % of total vitamin E) predominated over deposition of other isomers, except in the liver of fish fed the SBO diet, where α-T and γ-T deposition was in the ratio 40:60. T3 deposition (2.6–29.4 %) was only detected in tissues of fish fed the PFAD diet; adipose tissue was the major storage depot. Fish fed the SBO diet contained significantly more (P < 0.05) muscle thiobarbituric acid-reactive substances. Muscle fatty acid composition reflected dietary fatty acid profile. This is the first study to compare the deposition in fish tissues of the naturally occurring vitamin E isomers present in plant oils. The type and concentration of endogenous vitamin E and the fatty acid composition of plant oils can affect the oxidative stability of tilapia tissues.     

Oil extraction From the Copepod Calanus finmarchicus Using Proteolytic Enzymes

The limited amount of fish oils available has led to extensive search for alternative sources of oils rich in long-chain n-3 polyunsaturated fatty acids (PUFA). The zooplankton Calanus finmarchicus is present in large amounts in the North Atlantic and have lipid-rich stages which can be harvested. The main objective of this study was to investigate if the use of food grade proteolytic enzymes, Alcalase® and Flavourzyme®, could improve oil recovery in an industrial-like process, and to characterize the oil obtained. The results showed a substantially higher oil yield with the use of proteolytic enzymes compared to standard fish oil production technology. The oil from C. finmarchicus had a high content of n-3 PUFA mainly comprised of stearidonic acid (18:4 n-3), eicosapentaenoic acid (EPA), and docosahexaenoic acid (DHA). Wax esters were the dominating lipid class in the oil.     

Enhancing highly unsaturated ω‐3 fatty acids in phase‐fed rainbow trout (Oncorhynchus mykiss) using Alaskan fish oils

Rainbow trout, average weight 185–187 g, were fed feeds containing menhaden oil, canola oil or fish oils (pollock, pink salmon or rockfish) produced from Alaskan seafood processing waste as the added oil for 8 weeks, at which time the fish weighed 391–411 g (average 404 g, pooled SE = 5.7). The fish were previously fed from 75 g average weight fed commercial feed containing poultry oil as the added oil. No significant differences were measured in final weight or feed conversion ratio among dietary treatment groups. Significant differences were found in fillet ω‐3 fatty acid (FA) levels from fish receiving fish oil‐supplemented feeds compared to those from fish receiving feeds containing canola oil. Fillet contents of eicosapentaenoic acid (EPA; 20:5ω3) and decosahexaenoic acid (DHA; 22:6ω3) were highest in the pollock oil treatment group, although all fish oils increased highly unsaturated ω‐3 FA contents (mg 100 g^?1) of fillets. Fish oil used through the production cycle was reduced by 25% by supplementing feeds with poultry oil during the middle phase of production (75–175 g) compared to using feeds containing fish oil throughout the production cycle. Fish oils recovered from Alaskan seafood processing waste were suitable alternatives to conventional fish oil as ingredients in rainbow trout production feeds.     

微粒饲料中以微藻粉替代鱼油对牙鲆(Paralichthys olivaceus)稚鱼生长存活和脂肪酸组成的影响

以18日龄的牙鲆(Paralichthys olivaceus)稚鱼为研究对象,通过11 d 的生长实验,研究了添加不同比例的微藻粉替代鱼油对牙鲆稚鱼生长、存活率和脂肪酸组成的影响。以鱼油组(FO)为对照组,以裂壶藻粉(Schizochytrium sp.)、微绿球藻粉(Nannochloropsis sp.)和橄榄油替代不同比例的鱼油,配制成5组等氮等能的实验饲料,分别命名为鱼油组(FO),50%混合替代组(M50)、100%混合替代组(M100)、100%裂壶藻橄榄油替代组(S100)、100%微绿球藻橄榄油替代组(N100)。结果显示,微藻粉替代鱼油对牙鲆稚鱼的生长无显著影响;含有裂壶藻的各饲料组(M50、M100、S100)成活率显著高于 FO 组和 N100组(P?0.05);微藻粉替代鱼油不影响牙鲆稚鱼主要脂肪酸的组成;Person相关性分析发现,C14：0、C16：1n-7、C18：2n-6、C20：0、C18：3n-3、C22：0、C20：4n-3、EPA、C22：5n-6和 DHA 的百分含量均与其饲料中的百分含量呈显著正相关(P<0.05);总饱和脂肪酸、总单不饱和脂肪酸、n-3多不饱和脂肪酸的百分含量以及 DHA/EPA 比率均与其饲料组成表现出显著正相关(P<0.05)。综上所述,微藻作为脂肪源替代鱼油完全可以满足牙鲆稚鱼的生长和发育,各种脂肪酸均可以被牙鲆稚鱼充分消化和吸收,并且添加两种微藻后提高了稚鱼的 DHA 含量和 DHA/EPA 比率,与鱼油对照组相比显著提高了牙鲆稚鱼的成活率。因此,以微藻替代鱼油在牙鲆稚鱼的培育中是可行的。     

Evaluation of canola oils as alternative lipid resources in diets for juvenile red seabream, Pagrus auratus

This study examined three potential oil resources, crude and refined canola oil and refined soybean oil as replacements for added dietary fish oil in diets for juvenile red seabream. These oil resources were evaluated for their potential to replace added fish oil (40 g kg^?1) in fishmeal based (600 g kg^?1) diets, with 100 g kg^?1 of total lipids. Each of the three plant oils was used to replace 25%, 50%, 75% or 100% of the added dietary fish oil. Each of the three plant oils showed potential as a replacement for dietary fish oil, although a significant reduction in growth and feed utilisation was observed with the complete (100%) replacement of added fish oil by crude canola oil. No other significant effects of oil type or inclusion level on growth were apparent. A negative control (no added fish oil or plant oil, 60 g kg^?1 of total lipid) yielded poorer growth than all treatments except the diet containing 40 g kg^?1 of added crude canola oil (100% replacement). This observation confirmed that the added oils were utilized by the fish. A positive control diet containing 80 g kg^?1 of added fish oil (140 g kg^?1 total dietary lipid) sustained the best growth in the study, confirming that the 13 experimental diets were energy limiting as planned. Notably, few effects of the alternative oils were seen on the proximate composition of the fish. However, the influence of the alternative oils on the tissue fatty acid composition was considerable, irrespective of plant oil type or processing grade. Particularly notable was the overall increase in the level of polyunsaturated fatty acids in the tissues of the fish fed the plant oil diets, with these trends becoming more apparent with the greater levels of fish oil replacement. Minimal reductions in the levels of the long‐chain polyunsaturated fatty acids of eicosapentaenoic (20:5n‐3) and docosahexaenoic (22:6n‐3) acid were observed from any of the plant oil treatments. Sensory assessment, by an Australian taste panel, of the fish fed the fish oil reference, or the 100% replacement by refined canola or refined soybean diets showed a preference in order of canola oil > soybean oil > fish oil fed fish. Clearly, both canola and soybean oils have considerable potential as replacements of fish oils in diets for this species.     

Relationship between dietary lipid source, oxidative stress, and the physiological response to stress in sub-yearling chinook salmon (Oncorhynchus tshawytscha)

Relationships between dietary lipid source, stress, and oxidative stress were examined in juvenile chinook salmon (Oncorhynchus tshawytscha). Four different experimental diets were used: menhaden oil (MHO; elevated 20:5n-3 and 22:6n-3), soybean oil (SBO; elevated 18:2n-6), linseed oil (LSO; elevated 18:3n-3), and a mixture of 55% linseed oil and 45% soybean oil (MIX; approximately equal levels of 18:2n-6 and 18:3n-3). Juvenile salmon (initial body weight of 16.0 g) were fed experimental diets for 12 weeks (early March to early June). At the end of feeding, fish subjected to a low-water stressor for 96 h had greater liver and brain lipid peroxidation compared to unstressed controls; peroxidation was not influenced by diet. Diet and stress affected plasma cortisol levels. Stressed fish fed SBO had the greatest cortisol concentrations, followed by MIX, MHO, and LSO (mean concentrations for the SBO and LSO diets differed significantly). The cortisol response to stress may have been influenced by the ratio of prostaglandin 1- and 2-series to prostaglandin 3-series precursor fatty acids provided by the different diets. The results of this study suggest a connection between the physiological response to stress, dietary lipid quality, and oxidative stress. This is the first evidence of such a relationship in fish. Abbreviations: AA - arachidonic acid; ACTH - adrenocorticotropin; BHT - butylated hydroxytoluene; BLPO - brain lipid peroxidation; dGLA - dihomo-γ-linolenic acid; DHA - docosahexanoic acid; EPA - eicosapentanoic acid; FER - feed efficiency ratio; FOX - ferrous oxidation-xylenol orange; GLA -γ-linolenic acid; LA - linoleic acid; LCO3 - long-chain n-3 polyunsaturated fatty acids; LLPO - liver lipid peroxidation; LN - linolenic acid; LPO - lipid peroxidation; LSO - linseed oil; MHO - menhaden oil; MIX - 55% linseed oil + 45% soybean oil; PC - plasma cortisol; PG - prostaglandin(s); PGE₂- prostaglandin E₂; PUFA - polyunsaturated fatty acid; SBO - soybean oil. This revised version was published online in July 2006 with corrections to the Cover Date.     

Effect of Dietary Safflower and Canola Oil on Growth Performance,Body, and Fatty Acid Composition of Rainbow Trout (Oncorhynchus mykiss)

The objective of the present study was to evaluate the effects of the diets enriched with safflower and canola oil on growth, feed utilization, body composition, liver, and muscle fatty acid composition of rainbow trout (Oncorhynchus mykiss). Rainbow trout having approximate initial weight of 97.03 ± 0.10 g were fed the experimental diets containing only fish oil (Group 0SFO), safflower oil (50% safflower oil, Group 50SFO and 33% safflower oil, Group 33SFO), and vegetable oil blend (33% safflower and 33% canola oil, Group 66SFCO) for 45 days. Twenty-five fish were randomly assigned for triplicate treatments and offered the test diets two times daily to apparent satiation. At the end of the experiment, survival was 100% in all treatments. No significant differences in the weight gain, specific growth rate, feed conversion ratio, and protein efficiency ratio were found between fish fed with the different experimental diets. The highest hepatosomatic index (HIS) and viscerasomatic index (VSI) was obtained in 50SFO and 33SFO groups, respectively. The moisture, protein, lipid, and ash content in the body composition of the fish increased in all experimental groups. The lipid content was not significantly different among the groups (p > 0.05); however, there was a significant difference in ash content between the control and the other groups (p < 0.05). The experimental diets containing vegetable oil (50SFO and 33SFO groups) and vegetable oil blend (66SFCO group) had significantly higher concentrations of n-6 fatty acids, predominantly in the form of linoleic acid (LA). The n-3 fatty acids were present in significantly higher concentration in the control treatment (0SFO). The fatty acid composition of fish fillet and liver were reflective of the dietary lipid source. While the fillet and liver of fish fed the 50SFO diet was high in linoleic acid (18:2 n-6), fish fed the 66SFCO diet had high concentrations of oleic acid (OA; 18:1 n-9). The present study suggests that fish oil can be replaced by up to 50% with safflower oil and by up to 66% with safflower + canola oil blend in rainbow trout diets with no significant effect on growth.     

HUFA content and DHA/EPA improvements of Artemia sp. with commercial oils during different enrichment periods

Several commercial oils of plant and animal origin were tested in order to improve the HUFA content and the DHA:EPA ratio of Artemia sp. metanauplii. The relationship between the n-3 and n-6 fatty acid series, and more recently, the DHA:EPA ratio seem to be indicators for better survival and growth of marine fish larvae. The tested plant oils were derived from linseed, peanut and sunflower, and the animal oils came from squid, sardine, cod liver and Selco emulsion. For each oil emulsion tested, four different enrichment periods (9, 24, 33 and 48 h) were evaluated in the same Artemia sp. strain (Artemia EG from Artemia Systems Inc., Baasrode, Belgium). The results show that oil emulsions of plant origin give very poor results in relation to either HUFA content or DHA:EPA ratio. All the oil emulsions from animal origin resulted in HUFA incorporation. Sardine oil was the poorest and squid oil the best. The HUFA content and the DHA:EPA ratio increased with enrichment periods up to 33 h, followed by a negligible variation up to the final 48 h.     

Effects of safflower oil supplementation in diet on growth performance and body fatty acid composition of turbot (Psetta maxima)

The aim of the study was to investigate the effects of the diets that contain safflower oil and fish oil as lipid sources, on growth, feed conversion and body composition in turbot (Psetta maxima). Two iso-nitrogenous and iso-lipidic diets (55 % protein and 14 % lipid) were prepared that include 100 % fish oil (FO group) and 100 % safflower oil (SFO group) for turbots with average weight of 62.21 ± 1.28 g, and fish were fed with these diets for 104 days. At the end of the experiment, the weight gain, specific growth rate and feed conversion ratio were the highest in SFO group than in FO group (p < 0.05). Fatty acid composition of fish body reflected the fatty acid composition determined in the experimental diets. The amounts of palmitic acid (PA; C16:0), oleic acid (OA; C18:1n-9), linoleic acid (LA; C18:2n-6) and docosahexaenoic acid (DHA; C22:6n-3) were dominant fatty acids in fish body. It was confirmed that the usage of safflower oil instead of fish oil in turbot feed did not generate any negative effects on growth, feed conversion and the values regarding the growth performance.