Effects Of Different Dietary Lipids Research Articles

Effects of different dietary lipids on growth, body composition and lipid metabolism‐related enzymes and genes in juvenile largemouth bass, Micropterus salmoides

Effects of different dietary lipids on growth, body composition and lipid metabolism‐related enzymes and genes in juvenile largemouth bass, <i>Micropterus salmoides</i>

Effects of dietary lipid sources on hepatic nutritive contents, fatty acid composition and proteome of Nile tilapia (Oreochromis niloticus)

Dietary oils of varying fatty acid composition have been used in tilapia feeds; nevertheless, investigation of their effects on metabolism and physiological processes has been limited. Therefore, in this study, using proteomic technology, the effects of different dietary lipids (DLs) on hepatic lipid metabolism and physiological processes were investigaed in Nile tilapia (Oreochromis niloticus). Fish were fed with different DL, which included palm oil (PO), linseed oil (LO) and soybean oil (SBO) for 90 days. Growth performance appeared to be similar among the dietary group. Hepatic FA contents were reflected by DL. Dietary PO (source of saturated fatty acids; SFA) led to an increase in the hepatosomatic index as well as lipid and protein contents in liver. Dietary SBO (source of n-6 polyunsaturated fatty acids; n-6 PUFAs) increased hepatic carbohydrate contents, but decreased the hepatic protein. The proteomic analysis showed that these nutritive changes in the liver were mediated by several proteins involved in lipid, carbohydrate, and amino acid metabolism. Dietary SBO showed an increased accumulation in proteins related to oxidative stress, immune and inflammatory processes. Dietary LO (source of n-3 PUFAs) increased abundance of cytoskeleton-related proteins. qRT-PCR was performed to provide supportive information for the result of proteomic study. Similar effects of DLs on mRNA levels were observed for atp5b, krt18, and selenbp1. Combined together, dietary SFA could supply as energy reservoir for regular activites. Dietary n-3 and n-6 PUFAs led to induce vital metabolic and physiologic processes which would contribute to maintaining normal health and/or providing health-related benefits. SignificanceDietary SBO increased hepatic carbohydrate contents, but decreased the hepatic protein. Different dietary lipid led to alter the abundance of several proteins (i.e., DHRS1, ATP5B, PLA2G12B, APO, AMY2A, GRP78, PRSS1, FAH, and PRSS36) involved in lipid, carbohydrate, and amino acid metabolism. Dietary SBO showed an increased accumulation in proteins (i.e., QDPR, CABC1, and PRDX6) that respond to oxidative stress, suggesting that n-6 PUFAs induce oxidative conditions. Dietary SBO led to increase the accumulation of proteins (i.e., NITR26, NCCRP1, and LCN) involved in immune and inflammatory processes. Dietary LO increased the abundant levels of cytoskeleton-related proteins (i.e., ACTB, AHNAK, ERC2, KRT18, and RILP1). Other proteins (i.e., SELENBP1, FAM46C, and ANC1) involved in other physiological processes were also modulated by DL. qRT-PCR was performed to provide supportive information of proteomic study. Similar effects of DLs on mRNA levels were observed for atp5b, krt18, and selenbp1.

Dietary oils influence ovary and carcass composition and embryonic development of zebrafish

To evaluate the effect of different dietary lipids on zebrafish reproduction, we examined parameters including ovary and carcass composition, oestradiol (E2) levels, eclosion rate and embryonic development. In our study, zebrafish were subjected to a 5-month feeding trial whereby olive (OLV), linseed (LIN), fish (FIS) or corn (CRN) oil were used to compose four isonitrogenous and isoenergetic diets. A positive correlation was found between ovary EPA and whole-body E2 concentration (P = 0.005). The developmental dynamics was affected by dietary lipids and embryos from CRN treatment females; which had higher percentage of ARA in ovary (1.48 ± 0.44%) (P = 0.015), developed faster at 8–9 h postfertilization (hpf) than the ones originated from females receiving other diets (P = 0.0069). This effect was not sustained during later observation periods, suggesting ARA may act as a modulator of developmental dynamics only during initial phases. There was no clear effect of dietary lipid source on ovary protein content (P = 0.304) and eclosion rates at 72 hpf (P = 0.0623). Dietary fatty acids play an important role in reproductive outcome; however, additional studies are necessary to elucidate the mechanisms by which HUFA affect embryonic development.

Dietary fats significantly influence the survival of penumbral neurons in a rat model of chronic ischemic by modifying lipid mediators, inflammatory biomarkers, NOS production, and redox-dependent apoptotic signals

ObjectiveBrain stroke is the third most important cause of death in developed countries. We studied the effect of different dietary lipids on the outcome of a permanent ischemic stroke rat model. MethodsWistar rats were fed diets containing 7% commercial oils (S, soybean; O, olive; C, coconut; G, grape seed) for 35 d. Stroke was induced by permanent middle cerebral artery occlusion. Coronal slices from ischemic brains and sham-operated animals were supravitally stained. Penumbra and core volumes were calculated by image digitalization after 24, 48, and 72 h poststroke. Homogenates and mitochondrial fractions were prepared from different zones and analyzed by redox status, inflammatory markers, ceramide, and arachidonate content, phospholipase A2, NOS, and proteases. ResultsSoybean (S) and G diets were mainly prooxidative and proinflammatory by increasing the liberation of arachidonate and its transformation into prostaglandins. O was protective in terms of redox homeostatic balance, minor increases in lipid and protein damage, conservation of reduced glutathione, protective activation of NOS in penumbra, and net ratio of anti-to proinflammatory cytokines. Apoptosis (caspase-3, milli- and microcalpains) was less activated by O than by any other diet. ConclusionDietary lipids modulate NOS and PLA2 activities, ceramide production, and glutathione import into the mitochondrial matrix, finally determining the activation of the two main protease systems involved in programmed cell death. Olive oil appears to be a biological source for the isolation of protective agents that block the expansion of brain core at the expense of penumbral neurons.

The effect of dietary fatty acid composition on the hepatic fatty acid content and plasma lipid profile in rats

The objective of the present study was to evaluate in a model organism the effect of different dietary lipids on plasma concentration of total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) and triacylglycerols (TAG). One hundred adult male rats (Wistar Albino) were divided into 10 groups with 10 animals each and fed for 7 weeks either basic feed mixture (control diet, C) or basic feed mixture with 5% of palm oil (P), safflower oil (SF), salmon oil (S), fish oil (F), Schizochytrium microalga oil (A), and 20% of beef tallow (T; four groups), respectively. The T-groups were fed for another 7 weeks T-, SF-, F- and A-diet, respectively. At the end of both the first and the second 7-week fattening period, plasma lipid concentration and hepatic fatty acid content was determined. Both A and F diets fed for 7 weeks decreased (P &lt; 0.05) plasma TC (0.98 mmol∙l-1) compared to control (1.19 mmol∙l-1). The highest (P &lt; 0.05) plasma TC was established in rats fed for 7 weeks the SF-diet following the previous 7-week T-treatment (2.15 mmol∙l-1). A-diet had the most positive (decreasing) effect on TAG concentrations (0.68–0.86 mmol∙l-1 compared to 1.22 and 2.88 mmol∙l-1 found in the C and T diets, respectively; P &lt; 0.05). Both plasma TC and TAG were in a negative relationship (P &lt; 0.01) with the hepatic eicosapentaenoic acid and docosahexaenoic acid (DHA) contents, respectively. It was concluded that dietary Schizochytrium microalga oil (with high DHA content) may have the potential for decreasing the risk of cardiovascular diseases.

&lt;b&gt;Dietary lipid sources affect freshwater catfish jundiá, &lt;i&gt;Rhamdia quelen&lt;/i&gt;, survival, when challenged with&lt;i&gt; Aeromonas hydrophila&lt;/i&gt;&lt;/b&gt; - doi: 10.4025/actascianimsci.v35i4.19617

The immune modulatory activity of diet long chain polyunsaturated fatty acids in fish has been previously demonstrated, although results for freshwater species are controversial. This study evaluates the effect of different dietary lipids on freshwater catfish jundia, Rhamdia quelen, survival and its non-specific response (phagocytosis) after being inoculated with the pathogen Aeromonas hydrophila. Five diets were offered to jundia fingerlings during 150 days prior to challenge: cod liver oil (FO), sunflower oil (SO), linseed oil (LO), canola oil (CO) and coconut oil (CNO). Accumulated mortality was significantly lower in fish fed FO and CNO diets and higher in fish fed LO. In spite of the highest values observed for phagocytotic activity in CNO-fed fish (50.0 + 12.7%) and in FO-fed fish (45.0 + 10.5%) when compared to those fed other diets, no significant differences in phagocytosis were reported. Results show the relevance of a balanced dietary lipid source with adequate concentrations of n-3 and n-6 series of fatty acids to prevent mortality after pathogen challenge.

Goose fat, a promising nutrient for fish feeding, activates antioxidant enzymes in rainbow trout, Oncorhynchus mykiss

The objective of this experiment was to test effects of different dietary lipids in rainbow trout feeding on the activity and expression of antioxidant enzymes, superoxide dismutase (SOD), glutathione peroxidase (GPx) and glutathione S-transferase (GST). Four iso-nitrogenous and iso-lipidic casein–gelatin based experimental diets were formulated. The sources of dietary lipids were cod liver oil (CO, rich in polyunsaturated fatty acids), goose fat (GF, rich in saturated fatty acids and monounsaturated fatty acids), soybean oil (SO, rich in linoleic acid), and a blend of CO, GF and SO. Dietary treatments had no significant effect on growth performance and survival was not affected. SOD, GPx and GST enzymes had the maximum activity in GF diet. However qPCR data showed that SOD and GPx mRNA levels were minimum in GF group. Overall data showed that rainbow trout liver enzymes were activated upon GF diet probably activating the enzyme structure itself without stimulating gene expression.

Effect of different dietary lipids on immune response of neutropenic mice infected with Listeria monocytogenes

Effect of different dietary lipids on immune response of neutropenic mice infected with <i>Listeria monocytogenes</i>

Effects of the use of soybean oil and animal fat in the diet of laying hens on production performance and egg quality

The effects of different dietary lipids on the fatty acid profiles of eggs produced by 20 and 54 wk old Dekalb laying hens were investigated. Laying hens were subjected to three defined treatments according to the source of lipid added to their diets: soybean oil, beef tallow, and a control diet (without the addition of oil). The experimental design was in a 3x2 factorial arrangement (three treatments and two different ages). The fatty acid composition of the yolks in the eggs produced by the laying hens was analyzed. The eggs produced by laying hens on the soybean oil diet had a large amount of polyunsaturated fatty acids (PUFA) omega-6 (n-6) and omega-3 (n-3) in their yolks (23.55, 2.30% respectively), whereas egg yolks from hens who were given beef tallow had higher percentages of monounsaturated fatty acids (47.53%) compared to soybean oil (47.53%) and the control diet (38.72%). The percentages of trans fats present in the egg yolks in all treatments were considered very low (0.91; 0,11; 0.05%). Young layers are more efficient at depositing n-3 fatty acids (1.40%), specially C22:6 (0.76%) with the best ratio n6:n-3 (13.97) compared to old layers (1.35; 0.72; 14.81% respectively). Based on these results, it was concluded that the amount of fatty acids present in the egg yolks can be modified by the sources of lipids included in the diet and that independent of the sources of lipid in the diet and the age of the chicken, egg yolks have insignificant amounts of trans fatty acids.

Effects of lipid sources in the diet of laying hens on the fatty acid profiles of egg yolks

The effects of different dietary lipids on the fatty acid profiles of eggs produced by 20- and 54-wk-old Dekalb laying hens were investigated. The 4 treatments were based on the lipid source added to the diet: soybean oil, sunflower oil, linseed oil, or control (no added oil). The experimental design was a simple random-sample design using a 4 × 2 factorial arrangement (4 treatments and 2 ages). The fatty acid composition of the yolks of eggs produced by the laying hens was analyzed. The fatty acid profiles found in the egg yolks were the same as those provided in each diet. Eggs laid by hens fed the diet containing soybean oil had a large amount of n-6 polyunsaturated fatty acids (PUFA), whereas eggs laid by hens fed the diet containing linseed oil had the highest percentage of n-3 PUFA. A decrease in PUFA deposition in egg yolks was observed as the laying hens got older. Eggs of hens fed the diet containing linseed oil presented an n-6:n-3 ratio of 2.01 in younger chickens and 2.17 in older ones. The trans fat percentages found in the egg yolks of all treatments were very low. It was concluded that the quantity of fatty acids present in the egg yolk may be altered according to the source of lipids in the diets; the addition of linseed oil to the ration of laying hens resulted in the production of n-3-enriched eggs and excellent n-6:n-3 ratios, and the egg yolks had insignificant amounts of trans fat, irrespective of the different lipid sources added to the diets or the age of the chickens.

Effects of dietary lipids on the fatty acid composition and lipid metabolism of the green sea urchin Strongylocentrotus droebachiensis

The effects of different dietary lipids (hydrogenated coconut oil, corn oil, linseed oil, and mixtures of corn oil, linseed oil, menhaden oil, and/or soy lecithin) on the fatty acid composition of the sea urchin Strongylocentrotus droebachiensis were investigated. Dietary lipid compositions were reflected in the fatty acid profiles of sea urchin guts, gonads and shells. The shells had the highest level of 20:4n-6 and 20:5n-3, while the highest levels of monounsaturated fatty acids were seen in the guts. Tissue levels of 20:4n-6 and 20:5n-3 were influenced by the dietary levels of 18:2n-6 and 18:3n-3. The addition of soy lecithin to the diet (CLnML) enhanced the production and incorporation of 20:4n-6 in shell and gonad. Sea urchin also synthesized and incorporated 20 and 22 carbon non-methylene-interrupted dienoic fatty acids (NMIDs) in all tissue lipids. The NMID content varied among the different tissues and was influenced by the dietary lipid source. The hydrogenated coconut oil (HCO) diet resulted in the greatest NMID content, while the lowest levels were seen in sea urchins fed diets containing a mixture of corn oil, linseed oil, menhaden oil and lecithin (CLnML). The NMID content was lowest in gut and highest in the shell. Significant levels of mead acid (20:3n-9) were detected in the shells of sea urchins fed the EFA-deficient diet (HCO). The enzymatic capabilities of sea urchins to desaturate and elongate 18:2n-6 to 20:4n-6 and 18:3n-3 to 20:5n-3, as well as the capabilities to de novo synthesize NMID were hypothesized. Possible physiological roles and mechanisms for formation of NMID are discussed.

Effects of different dietary lipids on the fatty acid composition of broiler abdominal fat

The effect of three different lipid sources (soybean oil, chicken oil or bovine fat) on the abdominal fat fatty acid composition in 50 day-old broiler chickens was evaluated. A completely randomized design was used, with 4 treatments, 8 repetitions and 40 Arbor Acres broiler chicks of each sex. The four treatments were isocaloric and isoproteic with the following characteristics: T1 Control (Soybean-corn); T2 Control + 3% soybean oil; T3 Control + 3% chicken oil; and T4 Control + 3% bovine fat. The lipids from the diets had significantly statistical effects (p<0,05) on the fatty acid composition of broiler abdominal fat. Multivariate techniques also showed differences in fatty acid composition within treatments due to sex. The studied dietary lipids affected the polyunsaturated/saturated fatty acid ratio (P/S) but had only small effects on the n-6: n-3 fatty acid ratio.

Evaluation of crude palm oil and refined palm olein as dietary lipids in pelleted feeds for a tropical bagrid catfishMystus nemurus(Cuvier &amp; Valenciennes)

The effects of different dietary lipids on the growth, feed utilization and tissue fatty acid composition of a tropical bagrid catfish Mystus nemurus (Cuvier & Valenciennes) were investigated. Eight isonitrogenous and isoenergetic semi-purified diets were fed to triplicate groups of M. nemurus fingerlings for 10 weeks. Diet lipid levels were fixed at 10%, with 1% coming from residual oil in fishmeal and the remainder from cod liver oil (CLO), corn oil (CORN), soybean oil (SBO), crude palm oil (CPO), refined, bleached and deodorized palm olein (RBDPO) or various combinations of these oils. Catfish fed diets supplemented with 9% RBDPO showed significantly (P < 0.05) higher growth rates compared with fish fed the other seven diets. No significant differences in growth performance or feed efficiency ratio were observed between M. nemurus fed 9% CLO, CORN or CPO or fish fed diets containing 4% CLO with either 5% CORN, SBO, CPO or RBDPO. Based upon these results, palm oil-based diets can be used effectively for M. nemurus without compromising growth or feed utilization efficiency. Muscle and liver fatty acid composition of M. nemurus reflected that of the dietary oils added in pelleted diets fed to the fish. Considering the lower cost and availability of palm oil (compared with imported vegetable oils and fish oils) in many tropical countries, its use in dietary formulations for M. nemurus, and possibly other catfish species, will make these fish feeds less expensive.

Effect of Dietary Fatty Acids on Ca2+-ATPase Activity of the Sarcoplasmic Reticulum of Rainbow Trout Skeletal Muscle

Effects of different dietary lipids, corn oil, cod liver oil, and beef tallow, on lipid compositions and Ca2+-ATPase activity of the rainbow trout Salmo gairdneri sarcoplasmic reticulum (SR) were examined. The levels of phosphatidylethanolamine (PE) of the muscle and the SR were lower in fish fed for 2 months on diets rich in n-6 fatty acids or deficient in polyunsaturated fatty acids (PUFA) than in those fed n-3 fatty acid rich diet. Fatty acid compositions of muscle well reflected those of the diets. On the other hand, the SRs contained higher levels of polyunsaturated fatty acids, such as 22:6n-3, than muscle. In particular, PE fractions of each SR exhibited very high contents of polyunsaturated fatty acids and feeding PUFA-deficient diet for 3 months failed to reduce markedly the level of 22:6n-3 in PEs. Fatty acid compositions of phosphatidylcholine (PC) fractions of the SRs were altered by dietary fatty acids more easily than those of PEs. n-3 Fatty acid rich diet feeding caused reduction of SR Ca2+-ATPase activities. There was hardly any difference in peptide mapping patterns of Ca2+-ATPase proteins through the experimental stages, suggesting that there was practically no change of the Ca2+-ATPase moiety itself in the primary structure. These results suggested that dietary fatty acid compositions would alter lipid class and fatty acid compositions of the rainbow trout SRs and consequently lipid conformation changes. It was concluded that such physiological changes in lipids might affect the SR Ca2+-ATPase activities.

Effects of different dietary lipids on growth and tissue fatty acid changes in fry of the carp Catla catla (Hamilton)

A study was conducted with fry of Catla catla (Hamilton) to investigate the effects of dietary lipid supplements on growth, feed conversion, tissue fatty acid composition and the intestinal lipase activity. Four treatment diets were prepared using purified ingredients incorporating sunflower oil (n-6 fatty acids), cod liver oil (n-3 fatty acid source) and a mixture (1:1) of sunflower and cod liver oil in three diets. The fourth diet was lipid-free and served as the control. The best growth and survival was recorded for fish given the diet having a mixture of n-3 and n-6 fatty acids (weight gain was 380% and survival was 93%), followed by the n-6 diet (320% and 88%), the n-3 diet (290% and 84%) and the lipid-free diet (239.9% and 82%). Feed conversion ratio (FCR) and per cent protein deposited (PPD) followed a similar trend. The intestinal lipase activity (expressed as μg α-naphthol liberated mg_1 protein hr-1) was 83.3, 74.2, 80.1 and 53.7 for n-3 and n-6, n-6, n-3 and lipid-free diet treatments respectively. The fatty acid profile of the whole body was shown to be influenced by dietary fatty acid composition. The results of this laboratory study indicated that a combination of n-3 and n-6 fatty acids is important for growth and survival of this species. The extent to which such observations will be relevant in field conditions can be stated only after results of feeding trials in ponds are available.

Influence of dietary fats and vitamin e on plasma and hepatic vitamin a and β‐carotene levels in rats fed excess β‐carotene

Effects of different dietary lipids and excess vitamin E on plasma and hepatic concentrations of beta-carotene were evaluated in rats fed diets containing a large excess (0.2%) of beta-carotene. Male weanling Wistar Kyoto rats were fed beta-carotene-supplemented diets containing various dietary lipids as follows: Group I, a saturated fat (coconut oil); Group II, a monounsaturated fat (olive oil); Group III, a polyunsaturated fat rich in omega-6 fatty acids (safflower oil); Group IV, same as Group III plus vitamin E; and Group V, a polyunsaturated fat rich in omega-3 fatty acids (menhaden oil). All diets contained 2% safflower oil to provide sufficient amounts of linoleic acid (an essential fatty acid). Rats were killed after six weeks of feeding the various diets, and the concentrations of beta-carotene and vitamin A were determined in plasma and liver. Plasma vitamin A levels were not altered by any of the dietary lipids or by an excess of vitamin E. The concentrations of beta-carotene in plasma were the lowest in rats fed the diet containing menhaden oil. The feeding of the diet containing an excess of vitamin E also resulted in a significant decrease in plasma beta-carotene concentration. Similarly, the hepatic beta-carotene concentration was also reduced to about one-half in rats fed the diet containing an excess of vitamin E. Liver beta-carotene concentration was higher in Groups II and III than in the other three dietary groups. Hepatic vitamin A concentrations were also affected by the type of dietary fat.(ABSTRACT TRUNCATED AT 250 WORDS)

Effect of different dietary lipids on the immune responses of Hartley strain guinea pigs.

A diet containing 20% by weight of fat rich in unsaturated fatty acids reduced the ability of guinea pigs to form antibody and the delayed hypersensitivity response in vivo against a single antigen. Reduced responses in vivo are manifested on first challenge only, subsequent antigenic challenges showed responses similar to those of animals fed a normal diet. However, cells from animals fed large amounts of unsaturated fats when cultured in vitro with antigen and sera of normal animals fed a low-fat diet did not show reduced delayed hypersensitivity (macrophage migration inhibition and lymphocyte transformation). The serum of animals fed high-fat diets greatly inhibited the response to mitogens and to antigen in vitro of lymphocytes from tuberculin-sensitized animals fed either low or high-fat diet. As serum from animals fed low-fat diets did not have this effect, it is postulated that the inhibitory activity is due to a lipid or lipoprotein derivative of unsaturated fatty acids. Animals fed high-fat diets remained healthy, and showed no disorder related to the fat and no susceptibility to infection.