Einfluß gestaffelter Rapssaatanteile im Legehennenfutter auf das Fettsäurenmuster des Eifettes unter besonderer Berücksichtigung der polyungesättigten Fettsäuren

Influence of Graded Levels of Rape Seed in Laying Hen Diets on the Fatty Acid Composition of the Yolk Fat with Special Consideration of the Polyunsaturated Fatty Acids Technical treated rape seed was evaluated as feed ingredient for laying hens and the influence of rape oil on the fatty acid composition of the egg yolks was also investigated. Rape seed levels of 7.5%, 15% and 22.5% were fed both to brown and white laying hens (Lohmann Brown, LB, and Lohmann Selected Leghorn, LSL, resp.). A depression in performance was recorded only with the highest rape inclusion level for the parameters feed conversion (LB-hens) and daily egg production (LSL-hens). The fatty acid composition of the egg yolk was influenced in a dose-response related manner. The percentage of the saturated fatty acids decreased with increasing levels of rape seed whereas the mono-unsaturated fatty acids and the n-6 polyunsaturated fatty acids were hardly influenced. The level of the polyunsaturated n-3 fatty acids was characterized by a strong dose-dependent increase. In addition, long chained polyunsaturated fatty acids of the n-3 family - not present in rape oil - were detected in the yolks.     

Lysophosphatidic Acid Produced by Hen Egg White Lysophospholipase D Induces Vascular Development on Extraembryonic Membranes

Lysophosphatidic acid (lysoPtdOH), a lysophospholipid mediator, exerts diverse physiological effects, including angiogenesis, through its specific G‐protein‐coupled receptors. Previously, we showed that unfertilized hen egg white contains polyunsaturated fatty acid‐rich lysoPtdOH and lysophospholipase D (lysoPLD). Here, we examined whether lysoPtdOH was produced by lysoPLD in the presence and absence of a hen fertilized ovum and what the physiological role of lysoPtdOH in hen egg white is. Mass spectrometry showed that fertilized hen egg white contained about 8 μM lysoPtdOH before incubation with an ovum, mainly comprised of 18:1‐ (12.6 %), 18:2‐ (37.8 %) and 20:4‐molecular species (41.5 %). In an early gestation period, the lysoPtdOH was increased up to 9.6 μM, concomitant with a decrease in the level of polyunsaturated lysophosphatidylcholine (lysoPtdCho). Moreover, lysoPtdOH‐degrading activities were found in egg white and the vitelline membrane, showing that these enzymes control lysoPtdOH levels in egg white. In an egg yolk angiogenesis assay, two lysoPtdOH receptor antagonists, Ki16425 and N‐palmitoyl serine phosphoric acid (NASP), inhibited blood vessel formation induced by exogenously added 18:1‐lysoPtdOH and its precursor lysoPtdCho on the hen yolk sac. Ki16425 and NASP also inhibited blood vessel formation in the chorioallantoic membrane (CAM). Furthermore, the relatively higher levels of LPA₁, LPA₂, LPA₄ and LPA₆ mRNA were present in the yolk sac and CAM. These results suggest that lysoPtdOH produced from lysoPtdCho by the action of lysoPLD in hen egg white is involved in the formation of blood vessel networks through several lysoPtdOH receptors on various extraembryonic membranes, including the yolk sac membrane and CAM.     

Incorporation of dietary linoleic and conjugated linoleic acids and related effects on eggs of laying hens

In the present study, laying hens received 29 g per kg diet of a preparation containing either 70% linoleic acid (LA) or approximately the same amount of conjugated linoleic acid (CLA) in the control and experimental treatments, respectively. The CLA preparation consisted predominantly of cis-9,trans-11 and trans-10,cis-12 fatty acid isomers as free fatty acids in a ratio of 1∶1. The diets were fed for 8 wk to determine the effect of dietary CLA on quality characteristics of eggs. In addition, the fatty acid composition of liver and heart was analyzed. Performance parameters (egg weight, feed efficiency) were not significantly affected by feeding the diets supplemented with CLA. The overall amount of CLA that was incorporated into yolk was 7.95 g CLA/100 g total fatty acids, or approximately 400 mg CLA/egg. The transfer efficiency of the cis-9,trans-11 isomer was higher than that of the trans-10,cis-12 isomer; however, the transfer rate of CLA isomers into yolk and tissues was significantly lower than that of linoleic acid. Dietary CLA increased the concentration of saturated fatty acids in yolk and tissues at the expense of monounsaturated fatty acids. The proportions of myristic, palmitic, and stearic acids in yolk lipids were also changed by dietary CLA. Additionally, long-chain polyunsaturated fatty acids (arachidonic acid and docosahexaenoic acid) were decreased without changing the balance of the n−6/n−3 ratio in egg yolk. The inclusion of CLA in layer diets altered the shape of the yolk and various egg parameters (albumen height, foam index, and yolk index). The results of this study indicate that CLA induces various changes in lipid and fatty acid metabolism of laying hens and affects quality characteristics of eggs.     

Examination of acetolysis products of phosphatidylcholine by gas chromatography-mass spectrometry

A comparison of monoacetyldiglycerides obtained from authentic phosphatidylcholines by acetolysis with those obtained by phospholipase C-acetylation was made to examine the intermolecular acyl migration, the intramolecular acyl migration between C-1 and C-2, and the formation of 1,3-isomer in the acetolysis reaction. Egg yolk phosphatidylcholine also was used. It was revealed that is acetolysis, the intermolecular acyl migration and selective degradation of polyunsaturated fatty acids did not take place at all. The intramolecular acyl migration, including the formation of 1,3-isomer, occurred to a small extent. Appreciable difference was not found in comparison of molecular species compositions of monoacetyldiglycerides derived by both methods from egg yolk phosphatidylcholine, except small differences found in the contents of two kinds of molecular species.     

Omega‐3 long‐chain polyunsaturated fatty acid enriched eggs by microalgal supplementation

The health promoting effects of omega‐3 polyunsaturated fatty acids (n‐3 PUFA) are mainly ascribed to the n‐3 long chain (LC)‐PUFA, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). However, their intake is mostly below the recommended daily intake. A possible way to raise their average intake is to enrich food products with n‐3 LC‐PUFA. Addition of autotrophic microalgae to the diet of the laying hens can increase the level of these fatty acids in the egg yolk. Moreover, depending on the microalgal species, other nutritionally interesting algal carotenoids can also be transferred to the egg yolk. As a consequence egg yolk colour changes may occur. A survey conducted among 511 people showed that they will buy n‐3 PUFA enriched products, such as enriched eggs, and are even prepared to pay more for these products. However, the change of the yolk colour must be taken into account, since consumer' acceptability decreases when a deeply red yolk colour is obtained.     

Validation of Two Methods for Fatty Acids Analysis in Eggs

A comparative study between two methods (lipid extraction followed by saponification and methylation, and direct methylation) to determine the fatty acids in egg yolk was evaluated. Direct methylation of the samples resulted in lower fatty acid content and greater variation in the results than the lipid extraction followed by saponification and methylation. The low repeatability observed for the direct HCl methylation method was probably due to a less efficient extraction and conversion of the fatty acids into their methyl esters as compared to the same procedure starting with the lipid extract. As the lipid extraction followed by esterification method was shown to be more precise it was validated using powdered egg certified as reference material (RM 8415, NIST) and applied to samples of egg, egg enriched with polyunsaturated omega-3 fatty acids (n-3 PUFA), and commercial spray-dried whole egg powder.     

Isovaleroyl triglycerides from the blubber and melon oils of the beluga whale (Delphinapterus leucas)

The fatty acid compositions of the blubber and melon oils from the beluga whale (Delphinapterus leucas) have been determined by gas liquid chromatography (GLC). The melon oil contains a high level (60.1 mole %) of isovaleric acid, substantial amounts of long chain branched acids (16.9%), and very little polyunsaturated material (0.5%). The blubber oil contains less isovaleric (13.2%), fewer long chain branched acids (2.7%), and appreciable amounts (10.9%) of the polyunsaturated acids typical of marine oils. The blubber and melon oils were also examined for lipid class composition by thin layer chromatography on silicic acid, direct GLC of the hydrogenated oil, and gel permeation chromatography. Both oils are composed almost entirely of triglycerides, which can be separated chromatographically into molecules containing 0, 1 and 2 isovaleric acid moieties. No triisovalerin could be detected. The blubber oil contains 68.9 mole % normal triacyl-, 24.2% diacyl-monoisovaleroyl-, and 7.0% monoacyl-diisovaleroyl-triglycerides (acyl=long chain acid). Monoacyl-diisovalerin constitutes 86.7 mole % of the melon oil. This unusual compound may play a role in the echolocation system of the beluga whale.     

Encapsulation of Long-Chain n-3 Polyunsaturated Fatty Acids Using Egg Yolk

Egg yolk is well known for its excellent emulsifying property. In this article, egg yolk was used as the encapsulating matrix to prevent the oxidation of n-3 long-chain polyunsaturated fatty acids from fish oil. A 2 × 2 × 5 complete block design with three replications was used. Two levels of fish oil (1% and 5%) and two levels of esterification type (triglycerides or ethyl esters) of eicosapentaenoic/docosahexaenoic fatty acids were used. Time was considered a fixed factor with five levels. Emulsions were prepared by homogenization and stored for up to 4 weeks at 4–6 °C, with weekly sampling. Emulsions were analyzed for particle size and distribution, encapsulation efficiency, and surface oil. The oxidative stability of the emulsions was evaluated before and after cooking at 150–170 °C for 75 s. The addition of triglycerides resulted in a larger average particle size (234 ± 12.4 nm). All emulsions achieved 100% encapsulation efficiency and showed no significant change in the surface oil concentration during storage. After 4 weeks of storage, the concentration of eicosapentaenoic + docosahexaenoic fatty acids in nonencapsulated fish oil triglycerides and ethyl esters decreased by 20.32% and 14.74%, respectively, while the emulsions showed no significant differences. In addition, no peroxide or propanal formation was detected in raw emulsions over the storage period. Propanal formation was negligible in cooked samples, and the peroxide value showed no differences between the egg yolk control and the emulsions. Therefore, egg yolk was observed to be an efficient encapsulating food matrix that protects n-3 polyunsaturated fatty acids against oxidation and degradation.     

Abnormal serum lysophospholipids in multiple myeloma patients

Lysophosphatidylcholine (LPC) and lysophosphatidic acid (LPA) mediate various kinds of biological activities and play an important role in cellular signal transduction. We analyzed serum phospholipids obtained from 16 multiple myeloma (MM) patients and observed that serum LPA level was significantly higher in MM patients (5.3±0.5 nmol/mL) than in normal controls (1.7±0.3 nmol/mL). LPC level was also higher than that in normal controls, and it correlated significantly with the concentration of LPA (r=0.678, P<0.01). In MM patients, palmitic acid/linoleic acid ratios in phosphatidylcholine and LPC were higher than those in normal controls. In the 12-mon follow-up study of two patients with the immune globulin G type, we recognized that the increase of LPC, LPA, and arachidonic acid/linoleic acid ratio in phosphatidylinositol corresponded with a decline in the serum albumin level and choline esterase activity.     

Dietary High‐Oleic Acid Soybean Oil Dose Dependently Attenuates Egg Yolk Content of n‐3 Polyunsaturated Fatty Acids in Laying Hens Fed Supplemental Flaxseed Oil

Chickens can hepatically synthesize eicosapentaenoic acid (20:5 n‐3) and docosahexaenoic acid (22:6 n‐3) from α‐linolenic acid (ALA; 18:3 n‐3); however, the process is inefficient and competitively inhibited by dietary linoleic acid (LNA; 18:2 n‐6). In the present study, the influence of dietary high‐oleic acid (OLA; 18:1 n‐9) soybean oil (HOSO) on egg and tissue deposition of ALA and n‐3 polyunsaturated fatty acids (PUFA) synthesized from dietary ALA was investigated in laying hens fed a reduced‐LNA base diet supplemented with high‐ALA flaxseed oil (FLAX). We hypothesized that reducing the dietary level of LNA would promote greater hepatic conversion of ALA to very long‐chain (VLC; >20C) n‐3 PUFA, while supplemental dietary HOSO would simultaneously further enrich eggs with OLA without influencing egg n‐3 PUFA contents. Nine 51‐week‐old hens each were fed 0, 10, 20, or 40 g HOSO/kg diet for 12 weeks. Within each group, supplemental dietary FLAX was increased every 3 weeks from 0 to 10 to 20 to 40 g/kg diet. Compared to controls, dietary FLAX maximally enriched the total n‐3 and VLC n‐3 PUFA contents in egg yolk by 9.4‐fold and 2.2‐fold, respectively, while feeding hens 40 g HOSO/kg diet maximally attenuated the yolk deposition of ALA, VLC n‐3 PUFA, and total n‐3 PUFA by 37, 15, and 32%, respectively. These results suggest that dietary OLA is not neutral with regard to the overall process by which dietary ALA is absorbed, metabolized, and deposited into egg yolk, either intact or in the form of longer‐chain/more unsaturated n‐3 PUFA derivatives.     

Über trans-Lipoide: Die Lipoide des Hühnerei-Dotters

Trans Lipids: The Egg Yolk Lipids of the Hen The feeding of hens with a trans-containing edible fat resulted in an increase in the trans fatty acids of the egg yolk lipids to the extent of 10%, which completely disappeared within 14 days after stopping the trans-containing feed. The fatty acids in the triglyceride fractions contained in each case more trans unsaturated fatty acids than those in the corresponding phosphatide fractions. The gas chromatographic analysis of the fatty acid methyl esters showed that the triglycerides contained more oleic acid than the phosphatide fatty acids whereas stearic as well as polyunsaturated components were concentrated predominently in the phosphatides. The analysis of the fatty acid methyl esters from triglyceride and phosphatide fractions after feeding of trans-containing fat showed distinct changes in both the groups, thus for example a reduction of oleic acid in the neutral fat analogous to that in the total lipids as against its increase in phosphatides. The amount of linoleic acid in the phosphatide fatty acids increased while it remained constant in triglyceride fatty acids.     

Einfluß von Futterfetten auf die Qualität tierischer Veredlungsprodukte

Effects of Feed Fats on Quality of Animal Product At the same level of energy supply intake of fats/oils do not lead to a higher fat deposition in the carcass. Additionally, fats are carrier of fat soluble vitamins A, D, E, K and improve their absorption from the intestinal tract. The fatty acid profile of fat deposited in the organism, as for example in egg yolk is influenced by the intake of fatty acids provided by feed. This especially concerns linoleic- and linolenic acid as well as lauric- and myristic acid, High contents of polyunsaturated fatty acids negatively influence oxidative stability as well as consistency of body fat and therefore quality of animal products. An improved oxidation protection can be carried out by supplementation of antioxidants. Medium-chain, saturated fatty acids reveal positive effects on both criteria.     

The influence of dietary fat on the lipogenic activity and fatty acid composition of rat white adipose tissue

The in vivo fatty acid synthesis rate, selected enzyme activities and fatty acid composition of rat white adipose tissue from animals fed semisynthetic diets of differing fat type and content were studied. All animals were starved for 48 hr and then refed a fat-free (FF) diet for 48 hr. They were then divided into three groups. One group was continued on the FF diet for 48 hr. Another group was fed a diet containing 44% of calories from corn oil (CO). The final group was fed a diet containing 44% of calories from completely hydrogenated soybean oil (HSO). The animals on the FF diet had a marked increase in adipose tissue fatty acid synthesis during the 96-hr feeding peroid (as measured by³H incorporation into adipose fatty acids). Addition of either CO or HSO to the diets did not significantly inhibit fatty acid synthesis in dorsal or epididymal adipose tissue. The activities of the enzymes' fatty acid synthetase, ATP-citrate lyase and glucose-6-phosphate dehydrogenase increased on the FF diet and generally were not inhibited significantly by the addition of either fat to the diets. Linoleic acid was the major polyunsaturated fatty acid (ca. 22%) in adipose tissue. Monounsaturated fatty acids (palmitoleic, oleic,cis-vaccenic) made up ca 38% of the total adipose fatty acids, while saturated fatty acids accounted for about 32% (myristic, palmitic and stearic). White adipose tissue in mature male rats was a major depot for n−3 fatty acids. There were differences in the fatty acid composition of epididymal and dorsal adipose tissue, particularly in their content of long chain, polyunsaturated fatty acids with epididymal tissue containing more of these compounds than dorsal fat. The fatty acid composition of the white adipose tissue did not change significantly during fasting or 96 hr of refeeding the FF diets. The addition of HSO to the diet for 48 hr had little influence on the adipose tissue fatty acid composition, but the addition of CO to the diet caused a 7% increase in the dorsal adipose tissue linoleate content (as percentage of total dorsal adipose tissue fatty acids) within 48 hr compared to animals fed the stock diet and those starved for 48 hr. The fatty acid synthesis data indicated that adipose tissue in the rat can continue to be a source of de novo fatty acid synthesis in animals consuming high-fat diets.     

Composition of phospholipids of white muscle of six tuna species

A comparative study of the phospholipids of white muscle of six of the comercially utilized tuna species, including quantitative analyses of phospholipid classes and studies of the acyl composition of the major components. Plasmalogen compounds also were identified and quantified. Choline and ethanolamine glycerophospholipids were the most abundant classes in all the samples, as well as the only molecules containing plasmalogens (16∶0, 18∶0, and 18∶1 alkenyl ether chains). The patterns of fatty acid distribution within each of the phospholipid classes showed general similarities in the species analyzed. However, ratios between certain saturated and polyunsaturated fatty acids in different phospholipid classes showed remarkable diffences. The high content of n−3 polyunsaturated fatty acids in the principal phospholipids, such as the plasmalogens, and taking into account the fatty acids possible importance in human nutrition, indicates that the white muscle of tuna species may be a potentially important dietary item.     

Synthesis of phosphatidylcholine with (n−3) fatty acids by phospholipase A 2 in microemulsion

Phosphatidylcholine containing a long chain polyunsaturated acyl group at the 2-position has been prepared by phospholipase A 2 catalyzed esterification of lysophosphatidylcholine with polyunsaturated fatty acids EPA (C20∶5) or DHA (C22∶6). Preliminary studies showed that the other fatty acids, such as lauric acid (C12), palmitic acid (C16), stearic acid (C18) and linoleic acid (C18∶2), were also incorporated. To our knowledge, phospholipase A 2 catalyzed condensation reactions have not been reported in the literature before. The reactions were performed in sodiumbis(2-ethylhexyl)-sulfosuccinate-based microemulsions containing small amounts of water. Synthesis of the same phospholipid by transesterification of phosphatidylcholine with the polyunsaturated acids in microemulsion failed; however, enzymatic hydrolysis to lysophosphatidylcholine was facile, quantitative conversion from phosphatidylcholine being attained after 16 hr reaction time. An additional observation was that, unlike enzymatic hydrolysis of phospholipids, the condensation reaction catalyzed by phospholipase A 2 was totally independent of the presence of calcium.     

An enzymatic method for the synthesis of mixed-acid phosphatidylcholine

The enzymatic synthesis of PC with decanoic acid in the sn-1 and hexanoic acid in the sn-2 position is described. The procedure comprises the following enzymatic steps: (i) treatment of egg yolk with phospholipase A₂ (PLA₂) to hydrolyze egg yolk PC to 1-acyl lysophosphatidylcholine (LPC); (ii) esterification of 1-acyl LPC with hexanoic acid catalyzed by PLA₂ to yield PC with hexanoic acid in the sn-2 position; (iii) removal of the FA in the sn-1 position by lipase-catalyzed ethanolysis to yield 2-hexanoyl LPC; and finally (iv) introduction of decanoic acid in this position by lipase-catalyzed esterification of 2-hexanoyl LPC to yield 1-decanoyl-2-hexanoyl-PC. Two egg yolks with a weight of 16 g were required to obtain 160 mg of the desired product. The chemical purity of the PC product and the positional purity of the FA were around 99%. The method is applicable for the synthesis of other mixed-acid PC species as well.     

Parenteral Lipid Emulsions in Guinea Pigs Differentially Influence Plasma and Tissue Levels of Fatty Acids,Squalene, Cholesterol,and Phytosterols

Lipid emulsions are made by mixing vegetable and/or fish oils with egg yolk and contain different types and amounts of fatty acids and sterols. This study assessed the effects of oral diet, soybean oil (SO)-, fish oil (FO)-, a mixture of olive and soybean oil (OOSO)-, and a mixture of fish, olive, coconut, and soybean oil (FOCS)-based emulsions on plasma triacylglycerols and plasma and tissue fatty acid and sterol content following acute and chronic intravenous administration in the guinea pig. Upon acute administration, peak triacylglycerols were highest with SO and lowest with OOSO. Upon chronic administration, the plasma triglyceride levels did not increase in any group over that of the controls. Fatty acid levels varied greatly between organs of animals on the control diets and organs of animals following acute or chronic lipid administration. Squalene levels increased in plasma following acute administration of OOSO, but plasma squalene levels were similar to control in all emulsion groups following chronic administration. Total plasma phytosterol levels were increased in the SO, OOSO, and FOCS groups following both acute and chronic infusions, whereas phytosterols were not increased following FO infusion. Total phytosterol levels were higher in liver, lung, kidney and adipose tissue following SO and OOSO. Levels were not increased in tissues after FO and FOCS infusion. These results indicate that fatty acid and sterol contents vary greatly among organs and that no one tissue reflects the fatty acid or sterol composition of other tissues, suggesting that different organs regulate these compounds differently.     

Dietary modifications of animal fats: status and future perspectives

The purpose of modifying animal fats is to produce high quality products, which meet the dietary recommendations for a reduced intake of fat in the human diet, notably that of certain saturated fatty acids and cholesterol, and an increased intake of mono- (MUFA) and polyunsaturated fatty acids (PUFA) in order to minimize the risk for obesity, cancer, cardiovascular, and other life-style diseases. The body fat of farm animals is partly synthesized from dietary carbohydrates, partly from dietary fatty acids. In monogastric animals, preruminants and poultry PUFAs are readily absorbed and deposited in the edible parts of the body and incorporated into egg yolk lipids. In ruminants, however, PUFAs are hydrogenated to mainly saturated fatty acids by the rumen microorganisms with some formation of MUFAs, trans-, odd-, branched chain, and conjugated fatty acids. The latter fatty acids are absorbed, deposited in adipose and muscle tissue and incorporated into milk lipids, unless dietary PUFAs are protected against hydrogenation. Thus, it is relatively easy to change the fatty acid composition of pork, poultry meat, lamb, and veal, whereas beef and milk can only be enriched significantly with PUFAs by manipulation. Products enriched with PUFAs are, however, prone to oxidation, and enrichment with antioxidants, notably with dietary vitamin E, is necessary in order to prevent the risk of oxidative damage.     

Isolation of egg‐yolk phospholipids and enzymatic modification of their acyl chains

Phospholipids (PLs) have many biological and technological functions. Among the main sources of PLs egg yolk is the most attractive because of the high content of phosphatidylcholine (PC). The nutritional value of PLs can be increased by different methods, including enzymatic enrichment with polyunsaturated fatty acids (PUFA). Depending on the enzymes and reaction systems used, a‐linolenic acid (ALA) was introduced into the sn‐1 or sn‐2 position. Useful methods of PL isolation and positional analysis were elaborated.     

Dietary effect on ω3 fatty acid contents in hybrid striped bass

Hybrid striped bass, a cross of female striped bass and male white bass, were divided into two groups. One group was fed 38% protein trout feed (TF), and the other group was fed 30% protein catfish feed (CF). The dietary effect on polyunsaturated fatty acid contents in the bass was studied. The body weight of bass fed TF and CF averaged 727.46 and 379.92 g, respectively. The crude fat content in the TF group was 11.75 g, and it was 6.00 g in the CF group. Gas-liquid chromatographic analysis indicated that the bass fed TF contained higher amounts of eicosapentaenoic acid and docosahexaenoic acid than the bass fed CF. This study confirmed that fish diets greatly influence the fatty acid composition in fish tissue.