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This study investigates the effects of different lipids on growth, body composition and lipid metabolism of largemouth sea bass fish Micropterus salmoides. A total of 360 juvenile M. salmoides (mean ± SD mass = 33.83 ± 0.15 g) were randomly stocked into 12 tanks of 0.5 m3 volume for 8 weeks. Four replicates were made in each group, which were fed one of three diets containing fish oil (FO), soybean oil (SO) or lard oil (LO). The weight gain rate and specific growth rate did not differ among the groups (p > 0.05). Fish oil fish had the lowest condition factor (p < 0.05) and highest serum glucose content (p < 0.05). Crude lipid contents in the whole body and in the liver and muscle of FO fish were significantly lower than in the SO and LO groups (p < 0.05). The fatty acid composition of whole‐body lipids was closely correlated with that of the diet. The carnitine palmitoyltransferase 1 (cpt1) activity in the FO group was significantly higher than those in the SO and LO groups (p < 0.05). No significant differences in fatty acid synthase (fasn) activity were observed among the groups (p > 0.05). The Cpt1 and fasn gene expression levels in the FO group were significantly higher than those of the SO and LO groups (p < 0.05). The apolipoprotein B100 gene expression level was significantly higher in the SO group than in the FO group (p < 0.05). Fatty acid‐binding protein 1 gene expression levels in the FO and SO groups were not different (p > 0.05) but were both higher than that of the LO group (p < 0.05). The delta‐6 fatty acyl desaturase gene expression level in the LO group was significantly higher than that in the FO group (p < 0.05), but lower than that in the SO group (p < 0.05). It can be concluded that FO can be completely replaced by SO or LO in the M. salmoides diet, at least within the 8‐week culture period. Different types of dietary lipids significantly affect body condition and hepatic lipid metabolism in M. salmoides.  相似文献   

3.
An 8‐week growth trial was conducted to evaluate effects of dietary oil sources on growth, enzymes activity and genes expression levels related to lipid metabolism of hybrid grouper (♀Epinephelus fuscoguttatus × ♂E. lanceolatu) juveniles. Seven iso‐lipid (97 g/kg of dry matter) and iso‐protein (503.5 g/kg of dry matter) experimental diets were formulated containing 50 g/kg fish oil (FO; acting as controls) or various vegetable oils (VOs): corn oil (CO), sunflower oil (SO), tea oil (TO), olive oil (OO), rice oil (RO) and mixed oil (MO; comprising equal amounts of these oils). Each diet was fed to triplicate groups of 40 fish for per repetition (15.09 ± 0.01 g) for 56 days. The results show that (a) alternative dietary oils had no significant effects on final weight compared with control group (p > .05); (b) compared with FO group, VOs significantly changed the contents of serum lipoproteins, cholesterol, triglycerides and the activity of liver lipid‐metabolizing enzymes (p < .05); (c) CO group had the least effect on the serum lipoproteins, triglycerides and cholesterol of grouper compared with control; the activity of liver lipid‐metabolizing enzymes in RO and control group was the closest; (d) the mRNA levels of Δ6 Fatty acid desaturase (Δ6Fad), hormone‐sensitive lipase (HSL) and lipoprotein lipase (LPL) were not significantly effected by lipid sources, but CO, TO, OO and MO significantly down‐regulated the expression of fatty acid synthetase (FAS) mRNA level in liver, while RO opposite (p < .05); (e) vegetable oil significantly up‐regulated peroxisome proliferator‐activated receptor α (PPARα) and peroxisome proliferator‐activated receptor β (PPARβ) mRNA levels, while TO and RO down‐regulated peroxisome proliferator‐activated receptor γ (PPARγ) mRNA levels (p < .05); and 6) MO significantly increased the mRNA levels of heart‐type fatty acid‐binding protein (H‐FABP) and adipocyte‐type fatty acid‐binding protein (A‐FABP) (p < .05), while other VOs had no effect on them (p > .05). In conclusion, dietary substitution of FO by VO in diet affected lipid metabolism of grouper, which may be regulated by PPARs.  相似文献   

4.
This study investigated the effect of two lipid sources on reproduction performance and growth in pearl gourami. For this purpose, 180 fish (3.32 ± 0.25 g) were fed with three isoenergetic (19.80) and isonitrogenous diets (480 g/kg protein) including FO (80 g/kg fish oil), FS (40 g/kg fish oil and 40 g/kg soybean oil) and SO (80 g/kg soybean oil) for 10 weeks before maturation. At the end of the trial, there was no significant difference in weight gain, feed conversation ratio and body composition between fish fed FO and FS diets. Individuals fed dietary FO had significantly higher levels of n‐3 long‐chain polyunsaturated fatty acids in the muscle (130.5 g/kg lipid) and ovary (140.4 g/kg lipid) as compared with those fed SO diet (64.5, 103.6 g/kg, respectively) (p < .05). Feeding pearl gourami with FO and FS diets enhanced regarding absolute fecundity, relative fecundity, the fertilization rate, larvae total length and survival at 3 day posthatch (p < .05). Also, 17 beta‐estradiol in plasma of fish fed dietary FO (6.2 ng/L) was higher than those fed SO diet (1.7 ng/L) (p < .05). In conclusion, we suggest FS diet for broodstock nutrition of pearl gourami as a model for asynchronous multi‐batch spawning fish.  相似文献   

5.
A 10‐week feeding trial was conducted to evaluate the effects of dietary lipid sources on the growth and immune responses of Chinese mitten crab Eriocheir sinensis. Six isonitrogenous and isoenergetic diets were formulated with fish oil (FO), linseed oil (LO), soybean oil (SO), rapeseed oil (RO), coconut oil (CO) and beef tallow (BT) as the sources of lipid with five replicates each. Thirty crabs (2.35 ± 0.14 g) were stocked into each tank and fed twice daily. Weight gain and specific growth rate of crab fed the FO diet were significantly lower than those fed other diets (P < 0.05), except for crabs fed LO diet (P < 0.05). Crab fed the SO diet weighed more than those fed FO diets (P < 0.05). Serum superoxide dismutase and malondialdehyde of crab fed the FO diet were significantly higher than in other groups (P < 0.05). Crab fed the FO diet had the highest activities of serum phenoloxidase, acid phosphatase, alkaline phosphatase and lysozyme (P < 0.05). The fatty acid composition in the liver of crab reflected the change in test diets. Our results indicate that the use of dietary vegetable or animal oils can achieve similar growth performance to the use of dietary FO in Chinese mitten crab, but non‐FOs may impair crab immunity. Soybean oil is recommended as a suitable replacer for FO in Chinese mitten crab diet.  相似文献   

6.
The optimum water temperature required for the normal growth of Nile tilapia is 25–30°C. In this study, tilapia was reared under suboptimal temperature (21.50 ± 1.50°C) and fed four diets with fish oil (FO), corn oil (CO), sunflower oil (SFO) and linseed oil (LnO) for 8 weeks. The results revealed improved final weight, average daily gain and intestinal amylase activity in the LnO group compared to FO and SFO groups (p < .05). The feed intake was increased significantly in FO and LnO groups compared to CO and SFO groups, while the feed conversion ratio was increased in the FO group (p < .05). The CO, SFO and LnO diets resulted in higher carcass lipids than fish fed FO, while CO decreased the ash content (p < .05). The growth hormone was significantly lowered by LnO, followed by SFO, while CO improved the serum alkaline phosphatase activity (p < .05). Glutathione peroxidase enhanced in fish fed SFO, while the lowest activities were recorded in fish fed FO (p < .05). Total superoxide dismutase was significantly elevated by CO and LnO when compared with fish fed FO and SFO (p < .05). Substituting FO with vegetable oils had normal intestinal and liver histological appearance. It could be concluded that substituting FO with either CO or LnO for Nile tilapia could maintain the normal growth performance and feed utilization with enhanced antioxidant capacity under suboptimal temperature.  相似文献   

7.
An 8‐week trial was conducted to determine the effects of total replacement of 12.9% fish oil (FO) with soybean oil (SBO), peanut oil (PNO), sunflower seed oil (SFSO), corn oil (CO) and canola oil (CNO) on growth performance, health status and fillet fatty acid composition of hybrid sturgeon (194.28 ± 0.14 g). Compared to the FO group, dietary SBO decreased growth performance (p < .05), increased serum glucose and hepatic lipid content (p < .05). No obvious adverse effects on growth performance and health status were observed in PNO, SFSO and CO groups (p > 0.05). The fish fed with CNO had increased growth performance (p < .05), reduced serum ALT, AST, LDL‐C (p < .05) and enhanced serum GSH‐Px, T‐AOC, and LZM, MPO, C4 (p < .05). The contents of C18:1n9, C18:2n6, and ∑n‐3 PUFA and ∑n‐6 PUFA in fillets showed a positive linear correlation with the diets (p < .05). In summary, PNO, SFSO and CO are probable alternative lipid sources to fully replace FO. Hybrid sturgeon prefers to use CNO as a lipid source with improved growth performance and health status. The fillet fatty acid composition mirrors the dietary fatty acid composition.  相似文献   

8.
In order to investigate the effects of dietary fish oil replacement, the turtles (Mauremys sinensis) were fed four experimental diets for 10 months: FO (100% fish oil), FSO (70% fish oil and 30% soybean oil), SFO (30% fish oil and 70% soybean oil) and SO (100% soybean oil), sampled at pre‐vitellogenesis, vitellogenesis and post‐vitellogenesis. The results showed that plasma gonadotropin‐releasing hormone (GnRH) levels were the highest at pre‐vitellogenesis, which promoted the secretion of gonadotropin and sex steroids. Therefore, plasma luteinizing hormone (LH) and estrogen (E2) levels were significantly increased at post‐vitellogenesis (< 0.05), while follicle‐stimulating hormone (FSH) levels increased at vitellogenesis (< 0.05). The FO and FSO groups had significantly higher GnRH and E2 levels than the other two groups (< 0.05). In addition, plasma vitellogenin (Vtg) levels significantly increased at vitellogenesis and post‐vitellogenesis (< 0.05), which were significantly higher in the groups of FO and FSO than SO (< 0.05). Moreover, the expression levels of hepatic estrogen receptor α (Erα) mRNA were significantly increased at vitellogenesis and post‐vitellogenesis while ovarian Cyp19α1α mRNA were significantly increased at post‐vitellogenesis (< 0.05), and both were the lowest in SO. Taken together, the replacement of fish oil with 66.7% soybean oil is feasible.  相似文献   

9.
A 66‐d feeding experiment was conducted to investigate the utilization of vegetable oils in Japanese seabass (initial weight: 10.09 ± 0.70 g). In experimental diets, linseed oil (LO) or soybean oil (SO) was used to replace 1/3, 2/3, and 3/3 of fish oil (FO) (Diets F2L1, F1L2, and LO, respectively, or Diets F2S1, F1S2, and SO, respectively). A diet with FO alone was used as the control diet. LO or SO supplementation did not reduce the specific growth rate (3.06–3.29%/d) and feed efficiency ratio (0.75–0.83) of fish, but group F2L1 showed significantly better growth (P < 0.05) and feed utilization (P < 0.01) than group SO. Total replacement of FO with LO or SO significantly reduced certain non‐specific innate immune responses. Total replacement of FO by LO significantly increased the lipid content of fish. Concentrations of long‐chain polyunsaturated fatty acids (LC‐PUFAs) in whole fish and tissues were significantly reduced by LO or SO supplementation. In conclusion, LO or SO supplementations did not reduce the growth of Japanese seabass but reduced the immune responses and LC‐PUFA concentrations. LO was a better lipid source than SO for Japanese seabass in terms of fish growth and immune responses.  相似文献   

10.
This study was conducted to evaluate the effect of linseed oil (LO) replacing different levels of fish oil (FO) on growth, muscle fatty acid composition and metabolism of gift tilapia (Oreochromis niloticus) (mean initial weight 22 ± 0.5 g) in indoor recycle aquarium tanks for 8 weeks. Fish fed the diet with 50% of the oil as LO had higher final body weight (FWG), specific growth rate (SGR) and protein efficiency ratio (PER) than the other groups (P < 0.05). Hepatopancreas lipid content of fish fed 50% LO was lower than the other groups. Total n‐3 and n‐6 PUFA contents in the dorsal muscle and superoxide dismutase (SOD) activity in serum increased with increasing dietary LO level. Fish fed 50% LO had higher alanine transaminase (ALT), aspartate transaminase (AST) and lipoprotein lipase (LPL) activities in hepatopancreas and total antioxidant capacity (T‐AOC) and alkaline phosphatase (AKP) activities in serum than the other groups (P < 0.05). However, malate dehydrogenase (MDH) activities and malondialdehyde (MDA) contents in hepatopancreas were lower than other groups (P < 0.05) with a 50% substitution level. Results of this study indicated that LO could substitute <50% FO without influencing the growth of tilapia. The higher substitution levels of LO induced negative influences on growth, feed utilization and antioxidant ability of tilapia, but could promote DHA synthesis in tilapia muscle.  相似文献   

11.
Three groups of juvenile golden pompano, Trachinotus ovatus (54.75 ± 0.25 g), were each fed one of three diets containing different lipid sources: fish oil (FO), soybean oil (SO) and lard oil (LO). Fish were reared in sea cages for 8 weeks, and the fish fed the FO diet had significantly higher specific growth rate (SGR) but lower condition factor (CF) than the other treatments. The fatty acid (FA) composition of whole‐body lipids was closely correlated with those in the diets. Although no differences can be found in hepatic fatty acid synthase (fasn) activity, the carnitine palmitoyl transferase 1 (cpt1) activity in fish fed the FO diet was significantly higher compared with other treatments. In addition, the relative gene expression of lipid metabolism‐related enzymes, such as cpt1, fas, apolipoprotein B100 (apoB100), delta‐6 fatty acyl desaturase (fadsd6) and fatty acid‐binding protein 1 (fabp1), was also influenced by the different dietary lipid sources. Serum triglyceride (TG) and glucose content in fish fed the LO and FO diets were significantly higher than those in the SO group. Accordingly, it can be concluded that FO could not be completely replaced by SO or LO in golden pompano diets. The lipid sources of a diet could impose significant influence on body condition factor and hepatic lipid metabolism of golden pompano.  相似文献   

12.
A 6‐week study was conducted to determine the effects of different lipid sources in pelleted diets on juvenile mud crab Scylla paramamosain. Five isonitrogenous and isolipidic diets containing 8% level of fish oil (FO), lard (LD), safflower oil (SO), perilla seed oil (PO) or mixture oil (MO; VFO:VSO:VPO = 1:1:1), and a live food of marine bivalve Potamocorbula rubromuscula as the control diet (CF), were fed to groups of 25 juvenile crabs (average initial weight 7.4 g, carapace width 3.5 cm) in triplicate. The results showed that crabs fed MO had the highest survival (< 0.05). The moisture content was significantly higher in crabs fed LD, SO and PO (< 0.05). Crabs fed SO exhibited the lowest crude protein and lipid (< 0.05). Ash contents were obviously lower in LD group (< 0.05). Highest total lipid in the hepatopancreas and muscle was in LD and FO group respectively. Glucose, total cholesterol and low‐density lipoprotein were higher while high‐density lipoprotein was lower (< 0.05) in LD group. Tissue fatty acid compositions were consistent with those in diets. FO and MO diets had the same depression effect like CF on fatty acid synthase activity and mRNA expression in the hepatopancreas. The results of this study indicated that FO and mixed oil are suitable for preparation of pelleted diets with better effects for juvenile S. paramamosain compared with live food, and the ratio of n‐6/n‐3 fatty acids in pelleted diets must be <1.  相似文献   

13.
A nutrition trial with meagre, Argyrosomus regius was assessed to determine the effect of dietary replacement of fish oil (FO) by soybean oil (SO) on the growth, feed utilization, body composition, fatty acid composition and basic haematological parameters. Six isonitrogenous (47% crude protein) and isoenergetic (gross energy 22 kJ/g) experimental diets were formulated by replacing 0 (FO), 20 (S20), 40 (S40), 60 (S60), 80 (S80) and 100 (S100) % of the FO with SO. Fish were fed three times daily to near satiation for 14 weeks. The specific growth rate (SGR) of fish fed S100 diet was significantly lower than the other treatments, except SO80 diet. The fish fed SO100 diet displayed significantly higher feed conversion ratio than that of other diets (P < 0.05). It was observed that fish fed the SO100 and SO80 diets displayed haemoglobin (HGB) levels significantly lower (P < 0.05) than fish fed the SO20 diet. Packed cell volume (PCV) of fish fed SO20 diet was significantly higher compared to SO100. The white blood cell (WBC) and red blood cell (RBC) remained unaffected by dietary treatment. The docosahexaenoic acid (22:6n‐3, DHA) and eicosapentaenoic acid (20:5n‐3, EPA) levels of meagre were significantly reduced by the substituting of dietary SO by FO at the end of the feeding period. The level of linoleic acid (18:2n‐6, LA) and linolenic acid (18:3n‐3, LNA) significantly raised in fish fed with SO diets (P < 0.05). The results of this study showed that SO could be replaced FO up to 80% in meagre diet without negative effect on growth performance and basic haematological parameters. Furthermore, the maximum level of FO replacement with SO determined by second order polynomial regression analysis, was 30.1% on the basis of maximum SGR.  相似文献   

14.
A feeding trial was conducted to investigate the complete substitution of either fish oil (FO) or squid liver oil (SLO) with crude palm oil (CPO), canola oil (CO) sunflower oil (SFO) or linseed oil (LO), as the sole added lipid source in diets fed to triplicate groups of giant freshwater prawn, Macrobrachium rosenbergii (initial weight = 0.42 ± 0.01 g) for 6 weeks. Prawns fed the CO or SLO diets showed significantly higher (< 0.05) specific growth rate than those fed the FO or CPO diets. The feed conversion ratio of the prawns was significantly better when fed the CO diet, compared with the FO, CPO, SFO and LO diets. The muscle eicosapentaenoic acid content of prawns fed the vegetable oil (VO) diets were not significantly different (P > 0.05) from those fed the FO diet, although all VO‐based diets led to a significantly lower docosahexaenoic acid content compared with prawns fed the FO or SLO diet. The whole‐body total carotenoid content was significantly lower for prawns fed the SLO diet compared with prawns on the CO or CPO diets. The successful use of VO instead of marine‐based oils in prawn diets will likely reduce feeding costs associated with M. rosenbergii aquaculture.  相似文献   

15.
The effect of different dietary oil sources on the innate immunity and resistance of Nile tilapia, Oreochromis niloticus, to Streptococcus agalactiae infection were evaluated. Fish were fed with diets containing different lipid sources (soybean oil [SO], corn oil, linseed oil [LO], fish oil [FO], and olive oil [OO]). Fish fed SO presented the highest (P < 0.05) hematocrit and serum protein. LO and FO diets increased (P < 0.05) the erythrocyte resistance to osmotic lysis in comparison with other treatments. Fish fed OO showed the highest (P < 0.05) iron‐binding capacity and the lowest serum lysozyme and bactericidal activities (P < 0.05). No difference (P > 0.05) was found between diets in alternative complement activity. Fish fed the SO diet had the highest (P < 0.05) survival rate against S. agalactiae challenge. In conclusion, diets with LO oil and FO, rich in ω‐3 fatty acids, and OO, rich in ω‐9 fatty acids, have an immunomodulatory effect in Nile tilapia juveniles. The use of SO in the Nile tilapia diet improved immune function and resistance against S. agalactiae.  相似文献   

16.
In order to study the effects of linseed oil substitution on the growth, body composition, tissue fatty acid composition, flesh nutritional value and immune indices of juvenile Manchurian trout, five feed types containing different levels of linseed oil (LO) mixed with fish oil (FO) were prepared: 0 (0 LO); 250 g/kg (25 LO); 500 g/kg (50 LO); 750 g/kg (75 LO); and 1000 g/kg (100 LO); and fed to juvenile Manchurian trout (initial weight 6.43 ± 0.02 g) for 9 weeks. The results showed that substitution of FO with 750 g/kg LO did not affect the growth of juvenile trout, with protein content in the dorsal muscle, and lipid content in the liver not showing any significant difference (p > 0.05). The highest lipid content found in muscle samples occurred for the 25 LO diet. The fatty acid composition found in the dorsal muscle and the liver of the Manchurian trout reflects the fatty acid composition in the diet, where the relative amount of linolenic acid (ALA), linoleic acid (LA) and docosahexaenoic acid (DHA) found in these organs has a positive linear correlation with their relative composition in the diet (p < 0.05). As the amount of LO in the diet was increased, the composition of ALA found in the sampled organs increased, while the composition of DHA and eicosapentaenoic acid (EPA) decreased. At the same time, the index of atherogenicity (IA) and thrombogenicity (IT) of the muscle samples from the 75 LO and 100 LO diets was significantly lower than for the 0 LO and 25 LO diets (p < 0.05), while the flesh lipid quality (FLQ) in the 100 LO diet was significantly lower than for the other diets (p < 0.05). The aspartate transaminase (AST) activity decreased initially, and then increased, as the level of LO replacement for FO was increased, with the 25 LO diet being significantly lower than for other groups (p < 0.05). The alanine aminotransferase (ALT) activity in serum samples from the 100 LO diet was higher than that from other diets. The lysozyme (LZM) activity in both serum and liver tissue first increased to a peak for the 25 LO and 50 LO diets, respectively, and then decreased as the level of LO was further increased. There was no significant change in the alkaline phosphatase (AKP) activity in the liver samples; however, the acid phosphatase (ACP) activity decreased significantly from the highest value for 0 LO feed group. In conclusion, the composition of fatty acids in the dorsal muscle and the liver was found to be modified by the diets, and with the diet containing less than 750 g/kg LO, being both beneficial for growth, and improved immunity, while maintaining the nutritional value of the lipid content in the dorsal muscle during the 9‐week period.  相似文献   

17.
This study was carried out to investigate and compare the effects of various dietary lipid sources on growth performance, body composition, fatty acid profiles, and hepatic and plasma antioxidant enzyme activities of juvenile rockfish, Sebastes schlegeli. Three replicate groups of fish (initial mean weight, 1.7 ± 0.04 g) were fed four isonitrogenous and isolipidic diets containing either fish oil (FO), soybean oil (SO), linseed oil (LO), or a mixture of SO and LO (SO + LO) for 8 wk. There were no significant differences in survival, weight gain, feed efficiency, and protein efficiency ratios of fish fed the diets containing different lipid sources (P > 0.05). The fatty acids compositions of the liver and muscle tissues reflected the dietary fatty acid compositions. Liver and muscle of fish fed the SO diet had high concentration of linoleic acid, whereas those of fish fed the LO diet were rich in linolenic acid. Liver and muscle of fish fed the FO diet had significantly (P < 0.05) higher levels of eicosapentaenoic acid and docosahexaenoic acid than those of fish fed the SO and LO diets. Dietary lipid source had no significant effect on the hepatic and plasma enzyme activities of superoxide dismutase and glutathione peroxidase. The results of this study suggest that SO and LO can be used as a replacement for FO in the diets of juvenile rockfish without incurring any negative effects on growth, feed utilization, and antioxidant enzyme activity, when the dietary essential fatty acid requirements are satisfied for rockfish.  相似文献   

18.
To investigate the impact of different dietary lipid sources on fillet composition and lipid transport, we conducted a feeding trial and evaluated the proximate composition of muscle tissue, fatty acid profiles, total cholesterol (in muscle and plasma), triglycerides, and lipoprotein concentrations in Nile tilapia, Oreochromis niloticus. Five semi‐purified diets, containing different oils (soybean – SO, corn – CO, linseed – LO, fish – FO, and olive – OO), were supplied to tilapia for 160 d. Fish fed with LO and FO diets had a lower percentage of total lipids in muscle compared with the others (P < 0.05). The highest percentage of protein was found in fish fed with FO diet (P < 0.05). The muscle fatty acid profile was influenced differently by diets (P < 0.05). The group supplemented with SO and CO had a higher concentration of 18:2n‐6, whereas the fish fed with LO diet had a higher level of 18:3n‐3 and those that received the FO diet had more 22:6n‐3 in comparison with those supplemented with vegetable oils. Plasma lipid transport was also affected by the diets: the fish fed with FO diet had higher total cholesterol and high‐density lipoprotein and lower very‐low‐density lipoprotein concentrations (P < 0.05).  相似文献   

19.
Adult Atlantic salmon (Salmo salar; approximately 800 g start weight) were fed diets with a high replacement of fish meal (FM) with plant proteins (70% replacement), and either fish oil (FO) or 80% of the FO replaced by olive oil (OO), rapeseed oil (RO) or soybean oil (SO) during 28 weeks in triplicate. Varying the lipid source only gave non‐significant effects on growth and final weight. However, a significantly reduced feed intake was observed in the SO fed fish, and both feed utilization and lipid digestibility were significantly reduced in the FO fed fish. Limited levels of dietary 18:3n‐3, precursor to EPA and DHA, resulted in no net production of EPA and DHA despite increased mRNA expression of delta‐5‐desaturase and delta‐6‐desaturase in all vegetable oil fed fish. Net production of marine protein, but not of marine omega‐3 fatty acids, is thus possible in Atlantic salmon fed 80% dietary vegetable oil and 70% plant proteins resulting in an estimated net production of 1.3 kg Atlantic salmon protein from 1 kg of FM protein. Production of one 1 kg of Atlantic salmon on this diet required only 800 g of wild fish resources (Fish in ‐ Fish out < 1).  相似文献   

20.
A feeding experiment was conducted to develop non‐fish meal and non‐fish oil diet for red seabream by using plant protein source and Schizochytrium meal which is rich in 22:6n‐3 (DHA). Three iso‐nitrogenous and iso‐lipidic experimental diets were prepared (CP 41.2% ± 0.4%, CL 16.4% ± 1%). Control diet contained both fish meal (40%) and fish oil (6%). In the second diet, fish meal was replaced by plant meals (soy protein concentrate, soybean meal, corn gluten meal) [FO]. In the third diet, fish meal and fish oil were replaced by algae meal (Schizochytrium sp. powder) and plant proteins [AO]. Duplicated groups of juvenile red seabream (8.8 g ± 1.5) were fed the experimental diets for 12 weeks to near satiation. There was no statistical difference among treatment in specific growth rate. Feed conversion ratio of AO diet group was higher than that of control. In wet basis, whole body protein level was significantly higher in AO diet than FO group while lipid content was lower than control group. In fatty acid profile, AO group had significantly lower 18:4n‐3, 20:4n‐3, 22:5n‐3 and 20:5n‐3 (EPA) level, but significantly higher 18:3n‐3 and DHA level than the other two diet fed fish. The results might suggest that further developments in microalgae diet offer a promising lipid source of n‐3 PUFA as essential fatty acid on marine fish. And it showed possibility to develop non‐fish meal and non‐fish oil feed for marine aquaculture fish by using microalgae.  相似文献   

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