51 research outputs found

    THE MICROSCOPIC DETECTION OF ANIMAL PROTEINS IN FEEDS

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    Životinjske bjelančevine, dobiveni od termički obrađenih životinjskih nusproizvoda podrijetlom od kopnenih sisavaca, peradi ili riba, zbog svoje hranjive vrijednosti, često se koriste kao dodatak krmnim smjesama. Sitne strukture nekih organa vidljive su mikroskopski pod različitim povećanjima. Mikroskopski u krmivima možemo identificirati dijelove kosti, mišića, hrskavice, dlake, perje, ljuske od jaja, riblje ljuske i ligamente. Dijelove mekih tkiva i kože najčešće ne možemo identificirati zbog termičke obrade u kafilerijama. Uvođenje mikroskopske metode u rutinsku laboratorijsku pretragu za identifikaciju životinjskih tkiva u krmivima, nužna je zbog bolesti goveđe spongiformne encefalopatije (GSE) i njene povezanosti s uporabom i hranidbom životinja životinjskim bjelančevinama.Additional animal proteins in feeds because of their edibility, is by adding ground slaughter by-products originating either from ruminants, poultry or fish. This means that fine structures are visible after microscopic inspection at different magnification. The principal particles of animal origin that might be present in feeds are bones, muscle fibres, cartilage, hairs, feather filaments, egg shells, fish scales and ligaments. Parts from organs, skin and other soft tissues are generally absent, because of their denaturation after sterilisation. The need of this identification is based on the prohibition on adding animal proteins to feeds intended for farm animals therefore a connection between appearance of Bovine spongiform encephalopathy (BSE) and feeding animals with animal proteins

    THE MICROSCOPIC DETECTION OF ANIMAL PROTEINS IN FEEDS

    Get PDF
    Životinjske bjelančevine, dobiveni od termički obrađenih životinjskih nusproizvoda podrijetlom od kopnenih sisavaca, peradi ili riba, zbog svoje hranjive vrijednosti, često se koriste kao dodatak krmnim smjesama. Sitne strukture nekih organa vidljive su mikroskopski pod različitim povećanjima. Mikroskopski u krmivima možemo identificirati dijelove kosti, mišića, hrskavice, dlake, perje, ljuske od jaja, riblje ljuske i ligamente. Dijelove mekih tkiva i kože najčešće ne možemo identificirati zbog termičke obrade u kafilerijama. Uvođenje mikroskopske metode u rutinsku laboratorijsku pretragu za identifikaciju životinjskih tkiva u krmivima, nužna je zbog bolesti goveđe spongiformne encefalopatije (GSE) i njene povezanosti s uporabom i hranidbom životinja životinjskim bjelančevinama.Additional animal proteins in feeds because of their edibility, is by adding ground slaughter by-products originating either from ruminants, poultry or fish. This means that fine structures are visible after microscopic inspection at different magnification. The principal particles of animal origin that might be present in feeds are bones, muscle fibres, cartilage, hairs, feather filaments, egg shells, fish scales and ligaments. Parts from organs, skin and other soft tissues are generally absent, because of their denaturation after sterilisation. The need of this identification is based on the prohibition on adding animal proteins to feeds intended for farm animals therefore a connection between appearance of Bovine spongiform encephalopathy (BSE) and feeding animals with animal proteins

    Correlates of sexual initiation among European adolescents.

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    BACKGROUND: Sexuality is a physiological component of adolescent development, though early initiation is associated with reproductive health risk. This study aimed at identifying correlates and predictors of sexual initiation in a large multinational cohort of European adolescents. METHODS: A questionnaire addressing socio-demographics, behaviours, mental health and sexual activity, was delivered to 11,110 adolescents recruited from 168 randomly selected schools in 10 European countries between 2009 and 2011. A follow-up questionnaire was delivered after 12 months. The longitudinal association of baseline risk behaviors, psychological attributes and contextual vulnerabilities, with sexual initiation during follow-up was evaluated through simple and multivariable age/sex stratified logistic regression. Multinomial logistic regression measured the association between predictors and sexual initiation with or without coexisting reproductive risk factors, such as multiple partners or infrequent condom use. RESULTS: Baseline sexual experience was reported by 19.2% of 10,757 respondents (median age 15; IQR 14-15; females 59.6%). This was significantly more frequent among pupils older than 15 (41%) and males (20.8%). Of 7,111 pupils without previous experience who were available at follow-up (response rate 81.8%), 17% reported sexual initiation, without differences between females and males. Baseline smoking (age/sex adjusted odds ratio [aOR] 3.63), alcohol use (aOR 2.95), illegal drugs use (aOR 2.72), and poor sleep (aOR 1.71) predicted sexual initiation. Stratified analyses showed a particularly strong association in case of younger and female pupils, and, among girls, when initiation was reported together with multiple partners and/or infrequent condom use. Externalizing (i.e. conduct and hyperactivity) symptoms independently predicted sexual initiation. Internalizing difficulties (i.e. emotional and peer problems) were negatively associated with early and risky sexual initiation among boys. Significant predictors included also being bullied, fighting, truancy, and low parental involvement. CONCLUSIONS: Adolescent sexual behaviours are related to non-sexual risk behaviours, psychological difficulties and contextual vulnerabilities. While gateway effects explain some associations, a comprehensive model is needed to understand adolescent sexual behaviours, their physical, mental, and social health outcomes, and their potential positive effects on wellbeing. Tailored interventions may need to consider younger girls as a particularly vulnerable group in view of a strong association between non-sexual and sexual behaviors

    Elongase Reactions as Control Points in Long-Chain Polyunsaturated Fatty Acid Synthesis

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    Extent: 9p.Background: Δ6-Desaturase (Fads2) is widely regarded as rate-limiting in the conversion of dietary α-linolenic acid (18:3n-3; ALA) to the long-chain omega-3 polyunsaturated fatty acid docosahexaenoic acid (22:6n-3; DHA). However, increasing dietary ALA or the direct Fads2 product, stearidonic acid (18:4n-3; SDA), increases tissue levels of eicosapentaenoic acid (20:5n-3; EPA) and docosapentaenoic acid (22:5n-3; DPA), but not DHA. These observations suggest that one or more control points must exist beyond ALA metabolism by Fads2. One possible control point is a second reaction involving Fads2 itself, since this enzyme catalyses desaturation of 24:5n-3 to 24:6n-3, as well as ALA to SDA. However, metabolism of EPA and DPA both require elongation reactions. This study examined the activities of two elongase enzymes as well as the second reaction of Fads2 in order to concentrate on the metabolism of EPA to DHA. Methodology/Principal Findings: The substrate selectivities, competitive substrate interactions and dose response curves of the rat elongases, Elovl2 and Elovl5 were determined after expression of the enzymes in yeast. The competitive substrate interactions for rat Fads2 were also examined. Rat Elovl2 was active with C20 and C22 polyunsaturated fatty acids and this single enzyme catalysed the sequential elongation reactions of EPA→DPA→24:5n-3. The second reaction DPA→24:5n-3 appeared to be saturated at substrate concentrations not saturating for the first reaction EPA→DPA. ALA dose-dependently inhibited Fads2 conversion of 24:5n-3 to 24:6n-3. Conclusions: The competition between ALA and 24:5n-3 for Fads2 may explain the decrease in DHA levels observed after certain intakes of dietary ALA have been exceeded. In addition, the apparent saturation of the second Elovl2 reaction, DPA→24:5n-3, provides further explanations for the accumulation of DPA when ALA, SDA or EPA is provided in the diet. This study suggests that Elovl2 will be critical in understanding if DHA synthesis can be increased by dietary means.Melissa K. Gregory, Robert A. Gibson, Rebecca J. Cook-Johnson, Leslie G. Cleland and Michael J. Jame

    Elongation of very long-chain (>C24) fatty acids in Clarias gariepinus: Cloning, functional characterization and tissue expression of elovl4 elongases

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    Elongation of very long-chain fatty acid 4 (Elovl4) proteins participate in the biosynthesis of very long-chain (>C24) saturated and polyunsaturated fatty acids (FA). Previous studies have shown that fish possess two different forms of Elovl4, termed Elovl4a and Elovl4b. The present study aimed to characterize both molecularly and functionally two elovl4 cDNA from the African catfish Clarias gariepinus. The results confirmed that C. gariepinus possessed two elovl4-like elongases with high homology to two previously characterized Elovl4 from Danio rerio, and thus they were termed accordingly as Elovl4a and Elovl4b. The C. gariepinus Elovl4a and Elovl4b have open reading frames (ORF) of 945 and 915 base pairs, respectively, encoding putative proteins of 314 and 304 amino acids, respectively. Functional characterization in yeast showed both Elovl4 enzymes have activity towards all the PUFA substrates assayed (18:4n-3, 18:3n-6, 20:5n-3, 20:4n-6, 22:5n-3, 22:4n-6 and 22:6n-3), producing elongated products of up to C36. Moreover, the C. gariepinus Elovl4a and Elovl4b were able to elongate very long-chain saturated FA (VLC-SFA) as denoted by increased levels of 28:0 and longer FA in yeast transformed with elovl4 ORF compared to control yeast. These results confirmed that C. gariepinus Elovl4 play important roles in the biosynthesis of very long-chain FA. Tissue distribution analysis of elovl4 mRNAs showed both genes were widely expressed in all tissues analyzed, with high expression of elovl4a in pituitary and brain, whereas female gonad and pituitary had the highest expression levels for elovl4b

    Late cardiac events after childhood cancer: Methodological aspects of the pan-european study pancaresurfup

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    Background and Aim Childhood cancer survivors are at high risk of long-Termadverse effects of cancer and its treatment, including cardiac events. The pan-European PanCareSurFup study determined the incidence and risk factors for cardiac events among childhood cancer survivors. The aim of this article is to describe the methodology of the cardiac cohort and nested case-control study within PanCareSurFup. Methods Eight data providers in Europe participating in PanCareSurFup identified and validated symptomatic cardiac events in their cohorts of childhood cancer survivors. Data onsymptomatic heart failure, ischemia, pericarditis, valvular disease and arrhythmia were collected and graded according to the Criteria for Adverse Events. Detailed treatment data, data on potential confounders, lifestyle related risk factors and general health problems were collected. Results The PanCareSurFup cardiac cohort consisted of 59,915 5-year childhood cancer survivors with malignancies diagnosed between 1940 and 2009 and classified according to the International Classification of Childhood Cancer 3. Different strategies were used to identify cardiac events such as record linkage to population/ hospital or regional based databases, and patient-And general practitioner-based questionnaires. Conclusion The cardiac study of the European collaborative research project PanCareSurFup will provide the largest cohort of 5-year childhood cancer survivors with systematically ascertained and validated data on symptomatic cardiac events. The result of this study can provide information to minimize the burden of cardiac events in childhood cancer survivors by tailoring the follow-up of childhood cancer survivors at high risk of cardiac adverse events, transferring this knowledge into evidence-based clinical practice guidelines and providing a platformfor future research studies in childhood cancer patients. © 2016 Feijen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
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