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      Corn germ meal as substitute for corn in the diet of confined Santa Inês sheep: chemical and lipid meat composition Translated title: Gérmen do milho como substituto ao milho na dieta de ovinos Santa Inês confinados: composição química e lipídica da carne

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          Abstract

          The per capita consumption of sheep meat in Brazil is still small compared to meat originating from other animal species, the lipid profile of meat named as responsible for reduced consumption. Despite the influence of sex, breed, weight at slaughter and environment, diet is seen as a major factor influencing the lipid composition of sheep meat. This study evaluated the effect of replacing corn by corn germ meal (0, 25, 50, 75 and 100%) in the diet of Santa Inês sheep on the meat's chemical and lipid composition. Forty non-emasculated animals were distributed in a randomized block experimental design, with five treatments and eight replications, and slaughtered after 70 days of confinement. There was no influence of the substitution on the meat's chemical composition. No effects on the total saturated fatty acids (SFA) were observed, but there was a decreasing linear effect on the total monounsaturated fatty acids (MFA) and an increasing linear effect on the total polyunsaturated fatty acids (PFA). The PFA:SFA and ω-6:ω-3 ratios increased with the substitution level. Corn germ meal had no effect on the meat's chemical composition, but improved the nutritional quality of the lipid fraction, enriching it with compounds beneficial for human health.

          Translated abstract

          O consumo per capta de carne ovina no Brasil ainda é pequeno quando comparado às carnes oriundas de outras espécies animais, sendo o perfil lipídico da carne apontado como responsável pelo consumo reduzido. Apesar de sofrer influência de sexo, raça, peso ao abate e ambiente, a dieta é tida como principal fator que influencia a composição lipídica da carne ovina. Avaliou-se o efeito da substituição do milho pelo gérmen integral de milho na dieta de ovinos da raça Santa Inês sobre a composição química e lipídica da carne. Quarenta animais não castrados da raça Santa Inês foram distribuídos em delineamento inteiramente casualizado, com cinco tratamentos e oito repetições, e abatidos após 70 dias de confinamento. Não houve influência sobre a composição química da carne. Não houve efeito sobre o total de ácidos graxos saturados (AGS), mas verificou-se efeito linear decrescente para o total de ácidos graxos monoinsaturados e crescente para o total de ácidos graxos poli-insaturados (AGP). As relações AGP:AGS e ω-6:ω-3 elevaram-se com a substituição. O gérmen integral de milho não influencia a composição química da carne, mas melhora a qualidade nutricional da fração lipídica, enriquecendo-a com compostos benéficos à saúde humana.

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          Most cited references45

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          Manipulation of the n-3 polyunsaturated fatty acid content of muscle and adipose tissue in lambs.

          Fifty Suffolk-crossbred wether lambs, with an initial live weight of 29 +/- 2.1 kg, were allocated to one of five concentrate-based diets formulated to have a similar fatty acid content (60 g/kg DM), but containing either linseed oil (high in 18:3n-3); fish oil (high in 20:5n-3 and 22:6n-3); protected linseed and soybean (PLS; high in 18:2n-6 and 18:3n-3); fish oil and marine algae (fish/algae; high in 20:5n-3 and 22:6n-3); or PLS and algae (PLS/algae; high in 18:3n-3 and 22:6n-3). Lambs were slaughtered when they reached 40 kg. Growth performance and intake were similar (P > 0.35) among treatments. By contrast, gain:feed was higher (P 0.87) but was least (P < 0.05) in the phospholipid fraction in lambs fed the linseed oil diet. Lambs fed either diet containing marine algae contained the highest (P < 0.05) percentage of 22:6n-3 in the phospholipid (mean of 5.2%), 2.8-fold higher than in sheep fed the fish oil diet. In lambs fed the fish/algae diet, the percentage of 20:5n-3 was highest (P < 0.05), contributing some 8.7, 0.8, and 0.5% of the total fatty acids in the muscle phospholipid, neutral lipids, and adipose tissue, respectively. The percentage of 18:3n-3 in the phospholipid fraction of the LM was highest (P < 0.05) in lambs fed the linseed oil diet (6.9%), a value double that of sheep fed the PLS diet. By contrast, lambs fed the PLS diet had twice the percentage of 18:3n-3 in the muscle neutral lipids (3.8%) than those offered the linseed oil diet, and 5.5-fold greater than lambs fed the fish/algae treatment (P < 0.05), an effect that was similar in the adipose tissue. The percentage of 18:2n-6 was highest (P < 0.05) in lambs fed the PLS diet, where it contributed 33.7, 10.1, and 11.2% in the muscle phospholipid, neutral lipids, and adipose tissue, respectively. The highest (P < 0.05) muscle PUFA-to-saturated fatty acid (P:S) ratio was obtained in lambs fed the PLS diet (0.57), followed by the PLS/algae diet (0.46), and those fed the fish oil or linseed oil diets had the lowest ratios (0.19 and 0.26, respectively). The favorable P:S ratio of lambs fed the PLS/algae diet, in conjunction with the increased levels of 20:5n-3 and 22:6n-3, enhanced the nutritional qualities of lamb to more closely resemble what is recommended for the human diet.
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            Effects of amount and source of fat on the rates of lipolysis and biohydrogenation of fatty acids in ruminal contents.

            Because the percentage loss of unsaturated fatty acids across the rumen has varied considerably in previous in vivo studies, we conducted five experiments to identify potential factors that might affect the in vitro rates of lipid lipolysis and biohydrogenation in ruminal contents. The factors examined included the amount of fat added to the substrate, the source of added fat, the diet fed to the donor fistulated cow, and the time of collection of inoculum from the donor cow. Lipolysis and biohydrogenation were expressed as the rates of disappearance of neutral lipid and unsaturated fatty acids, respectively, from the culture contents over time using a first-order model. The rate of lipolysis of soybean oil declined from 44%/h to less than 30%/h as the percentage of soybean oil in the culture substrate increased from 2 to 10%. The overall rate of biohydrogenation of C18:2 was 14.3%/h, but declined 1.2%/h for each percentage unit increase in C18:2 added to the substrate. Compared with C18:2, the rates of biohydrogenation of C18:1 were generally lower (averaged 3.6 %/h) for all fat sources. The rate of biohydrogenation of C18:2 in soybean oil was not affected by the amount of grain or fat fed to the donor cow, or the time after feeding that ruminal inoculum was collected. Based on these findings, high linoleic acid concentrations in the diet would possibly reduce biohydrogenation and increase the postruminal flow of this unsaturated fatty acid. Also, lipolysis may vary considerably due to amount and source of lipid added to the diet, but this has little influence on the initial disappearance rates of linoleic or oleic acids from ruminal contents.
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              Effect of level of linseed on fatty acid composition of muscles and adipose tissues of lambs with emphasis on trans fatty acids.

              The effects of linseed content in concentrates on the fatty acid (FA) composition of adipose tissues and muscles of lambs were studied in a 2×4 design: males (M) vs. females (F) and linseed content (0%, L0, 3%, L3, 6%, L6, 9%, L9). FA proportions were determined both on a DB-wax and on a CP-Sil column in perirenal (PR), dorsal subcutaneous (SC) adipose tissue and in longissusmus dorsi muscle (IM). No effects of linseed contents in the diet on growth performances either in male or female lambs were observed. Linseed supplementation tended to decrease the fatness score. The proportion of linolenic acid increased linearly with the linseed content in the diet, from: 0.6, 0.5, and 0.5% for L0 to 1.9, 1.6, and 1.3% for L9, in PR, SC and IM, respectively. The increase in n-3 PUFA and in total PUFA was similar to that of linolenic acid. The n-6:n-3 ratio decreased from 5.7, 5.3 and 5.8 for L0 to 1.8, 1.7 and 2.7 for L9, in PR, SC and IM, respectively. There was no change in the proportion of docosahexaenoic acid with linseed supplementation. The proportions of C18:1trans-10 and C18:1trans-11 did not vary in PR, SC and IM with linseed supplementation. The total proportion of trans-octadecenoic acid was high in each tissue type and group of lambs. C18:1trans-10 represented about half of the total trans-octadecenoic isomers. With an increase in linolenic acid, most cis- and trans-octadecenoic isomers also increased, but trans-10 and trans-11 isomers did not and cis-9 and cis-11 isomers decreased. With linseed supplementation there was a decrease in the Δ9 desaturase indices in SC.
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                Author and article information

                Contributors
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Role: ND
                Journal
                cagro
                Ciência e Agrotecnologia
                Ciênc. agrotec.
                Editora da Universidade Federal de Lavras (Lavras )
                1981-1829
                December 2014
                : 38
                : 6
                : 581-588
                Affiliations
                [1 ] Universidade Federal Rural de Pernambuco Brazil
                [2 ] Universidade Federal da Paraíba Brazil
                [3 ] Universidade Federal da Paraíba Brazil
                Article
                S1413-70542014000600007
                10.1590/S1413-70542014000600007
                2be7f6f5-78a5-4b7e-9900-b193acdbac78

                http://creativecommons.org/licenses/by/4.0/

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                Product

                SciELO Brazil

                Self URI (journal page): http://www.scielo.br/scielo.php?script=sci_serial&pid=1413-7054&lng=en
                Categories
                AGRICULTURE, MULTIDISCIPLINARY

                General agriculture
                CLA,co-products,lipid profile,co-produtos,perfil lipídico
                General agriculture
                CLA, co-products, lipid profile, co-produtos, perfil lipídico

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