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Predicting duodenal flows and absorption of fatty acids from dietary characteristics in ovine and bovine species: a meta-analysis approach

Published online by Cambridge University Press:  14 August 2018

L. A. Prado
Affiliation:
Université Clermont Auvergne, INRA, VetAgro Sup, UMR Herbivores, F-63122 Saint-Genès-Champanelle, France
A. Ferlay
Affiliation:
Université Clermont Auvergne, INRA, VetAgro Sup, UMR Herbivores, F-63122 Saint-Genès-Champanelle, France
P. Nozière
Affiliation:
Université Clermont Auvergne, INRA, VetAgro Sup, UMR Herbivores, F-63122 Saint-Genès-Champanelle, France
P. Schmidely*
Affiliation:
AgroParisTech, INRA, UMR0791 Mosar, 16 rue Claude Bernard, F-75231 Paris, France
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Abstract

Dietary and ruminal factors modify the ruminal biohydrogenation (RBH) of polyunsaturated fatty acids (FA), with duodenal FA flows being quantitatively and qualitatively different from FA intake. Using a meta-analysis approach from a database on duodenal flows of FA in ruminants, this study aimed to determine predictive equations for duodenal and absorbed flows of saturated FA, C18:1, C18:2 and C18:3 isomers, odd- and branched-chain FA (OBCFA), C20:5n-3, C22:5n-3 and C22:6n-3 and to quantify the effects of dietary and digestive factors on those equations. The database was divided into four subsets: forage, seed, vegetable oils or animal fats (oil/fat), and fish products (fish) subsets. Models of duodenal and absorbed FA flows were obtained through variance–covariance analysis. Effects of potential interfering factors (conservation mode and botanical families of forages, lipid source, technological processing of lipid supplements, diet composition and animal characteristics) were analysed. We obtained 83 models for duodenal FA flows as a function of FA intake for saturated FA (C14:0, C16:0 and C18:0), C18:1, C18:2 and C18:3 isomers and seven other models for OBCFA. For the seed/oil/fat subset, intakes of total C18:3, C18:2 and starch content increased the duodenal t11-C18:1 flow with 0.08, 0.16 and 0.005 g/kg of dry matter intake (DMI), respectively, whereas intake level [(DMI×100)/BW] decreased it. The c9c12c15-C18:3 RBH was higher for oil/fat than seed (96.7% v. 94.8%) and a protective effect of Leguminosae v. Gramineae against RBH for that FA appeared in the forage subset. The duodenal C17:0 flow increased with starch content and decreased with ruminal pH, respectively, whereas duodenal iso-C16:0 flow decreased with dietary NDF content for the seed/oil/fat subset. The duodenal C20:5n-3, C22:5n-3 and C22:6n-3 flows depended on their respective intake and the inhibitory effect of C22:6n-3 on duodenal C18:0 flow was quantified. Thirteen models of absorbed FA flows were performed depending on their respective duodenal flows. This study determined the effects of different qualitative and quantitative dietary and digestive factors, allowing for improved predictions of duodenal and absorbed FA flows.

Type
Research Article
Copyright
© The Animal Consortium 2018 

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References

Aldai, N, Delmonte, P, Alves, SP, Bessa, RJB and Kramer, JKG 2018. Evidence for the initial steps of DHA biohydrogenation by mixed ruminal microorganisms from sheep involves formation of conjugated fatty acids. Journal of Agricultural Food and Chemistry 66, 842855.Google Scholar
Baumont, R, Dulphy, JP, Sauvant, D, Tran, G, Meschy, F, Aufrère, J, Peyraud, JL and Champciaux, P 2007. Les tables de la valeur des aliments. In Alimentation des bovins, ovins et caprins - Besoins des animaux - Valeurs des aliments – Tables INRA 2007, pp. 181–275. Editions Quae, Versailles, France.Google Scholar
Belanche, A, Doreau, M, Edwards, JE, Moorby, JM, Pinloche, E and Newbold, CJ 2012. Shifts in the rumen microbiota due to the type of carbohydrate and level of protein ingested by dairy cattle are associated with changes in rumen fermentation. Journal of Nutrition 142, 16841692.Google Scholar
Bibby, J and Toutenburg, H 1977. Prediction and improved estimation in linear models. John Wiley & Sons, Berlin, Germany. p. 201.Google Scholar
Chapoutot, P, Martin, O, Nozière, P and Sauvant, D 2015. Systool Web, a new one-line application for the French INRA « systali » project. In Proceedings of the 66th Annual Meeting of the European Society of Animal Science, 31 August to 4 September, Wageningen Academic Publishers, Warsaw, Poland, p. 265.Google Scholar
Chilliard, Y, Glasser, F, Ferlay, A, Bernard, L, Rouel, J and Doreau, M 2007. Diet, rumen biohydrogenation and nutritional quality of cow and goat milk fat. European Journal of Lipid Science and Technology 109, 828855.Google Scholar
Chilliard, Y, Martin, C, Rouel, J and Doreau, M 2009. Milk fatty acids in dairy cows fed whole crude linseed, extruded linseed, or linseed oil, and their relationship with methane output. Journal of Dairy Science 92, 51995211.Google Scholar
Christie, WW and Han, X 2010. Lipid extraction, storage and sample handling. In Lipid analysis, isolation, separation, identification and lipidomic analysis (Chapter 3, ed. PJ Barnesand Associates), 4th edition pp. 5566. The Oily Press, Bridgwater, UK.Google Scholar
Devillard, E, McIntosh, FM, Newbold, CJ and Wallace, RJ 2006. Rumen ciliate protozoa contain high concentrations of conjugated linoleic acids and vaccenic acid, yet do not hydrogenate linoleic acid or desaturate stearic acid. British Journal of Nutrition 96, 697704.Google Scholar
Doreau, M, Lee, MRF, Ueda, K and Scollan, ND 2005. Métabolisme ruminal et digestibilité des acides gras des fourrages. In Proceedings of the 12th Rencontres Recherches Ruminants, 7 and 8 December, Paris, France, pp. 101–104.Google Scholar
Ferlay, A, Bernard, L, Meynadier, A and Malpuech-Brugère, C 2017. Production of trans and conjugated fatty acids in dairy ruminants and their putative effects on human health: a review. Biochimie 141, 107120.Google Scholar
Fievez, V, Colman, E, Castro-Montoya, JM, Stefanov, I and Vlaeminck, B 2012. Milk odd- and branched-chain fatty acids as biomarkers of rumen function - an update. Animal Feed Science and Technology 172, 5165.Google Scholar
Glasser, F, Schmidely, P, Sauvant, D and Doreau, M 2008. Digestion of fatty acids in ruminants: a meta-analysis of flows and variation factors: 2. C18 fatty acids. Animal 2, 691704.Google Scholar
Halmemies-Beauchet-Filleau, A, Vanhatalo, A, Toivonen, V, Heikkilä, T, Lee, MRF and Shingfield, KJ 2013. Effect of replacing grass silage with red clover silage on ruminal lipid metabolism in lactating cows fed diets containing a 60:40 forage-to-concentrate ratio. Journal of Dairy Science 96, 58825900.Google Scholar
Harfoot, CG and Hazlewood, GP 1997. Lipid metabolism in the rumen. In The rumen microbial ecosystem (ed. PN Hobson and CS Stewart), pp. 382426. Chapman and Hall, London, UK.Google Scholar
INRA 2010. Alimentation des bovins, ovins et caprins - Besoins des animaux - Valeurs des aliments -Tables INRA 2007 - mise à jour 2010. Editions Quae, Paris, France.Google Scholar
Kairenius, P, Toivonen, V and Shingfield, KJ 2011. Identification and ruminal outflow of long-chain fatty acid biohydrogenation intermediates in cows fed diets containing fish oil. Lipids 46, 587606.Google Scholar
Kim, YJ, Liu, RH, Rychlik, JL and Russell, JB 2002. The enrichment of a ruminal bacterium (Megasphaera elsdenii YJ-4) that produces the trans-10, cis-12 isomer of conjugated linoleic acid. Journal of Applied Microbiology 92, 976982.Google Scholar
Kucuk O, Hess BW and Rule DC 2004. Soybean oil supplementation of a high-concentrate diet does not affect site and extent of organic matter, starch, neutral detergent fiber, or nitrogen digestion, but influences both ruminal metabolism and intestinal flow of fatty acids in limit-fed lambs. Journal of Animal Science 82, 2985–2994. Google Scholar
Laverroux, S, Glasser, F, Gillet, M, Joly, C and Doreau, M 2011. Isomerization of vaccenic acid to cis and trans C18:1 isomers during biohydrogenation by rumen microbes. Lipids 46, 843850.Google Scholar
Lourenço, M, Ramos-Morales, E and Wallace, RJ 2010. The role of microbes in rumen lipolysis and biohydrogenation and their manipulation. Animal 4, 10081023.Google Scholar
Maxin, G, Glasser, F, Doreau, M and Baumont, R 2013. Prévision de la teneur en matières grasses et de la composition en acides gras des fourrages. In Proceedings of the 20th Rencontres Recherches Ruminants, 4 and 5 December, Paris, France, pp. 49–52.Google Scholar
Moher, D, Liberati, A, Tetzlaff, J and Altman, DG 2009. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Public Library of Science Medicine 6, 264269.Google Scholar
Sauvant, D and Nozière, P 2013. Integrative model of the digestive tract including the interactions involved in energy and protein digestion in ruminants. In Energy and protein metabolism and nutrition in sustainable animal production (ed. JW Oltjen, E Kebreab and H Lapierre), pp. 317318. Wageningen Academic Publishers, Wageningen, The Netherlands.Google Scholar
Sauvant, D, Schmidely, P, Daudin, JJ and St-Pierre, NR 2008. Meta-analyses of experimental data in animal nutrition. Animal 2, 12031214.Google Scholar
Schmidely, P, Glasser, F, Doreau, M and Sauvant, D 2008. Digestion of fatty acids in ruminants: a meta-analysis of flows and variation factors. 1. Total fatty acids . Animal 2, 677690.Google Scholar
Shingfield, KJ, Bernard, L, Leroux, C and Chilliard, Y 2010a. Role of trans fatty acids in the nutritional regulation of mammary lipogenesis in ruminants. Animal 4, 11401166.Google Scholar
Shingfield, KJ, Lee, MRF, Humphries, DJ, Scollan, ND, Toivonen, V, Reynolds, CK and Beever, DE 2010b. Effect of incremental amounts of fish oil in the diet on ruminal lipid metabolism in growing steers. British Journal of Nutrition 104, 5666.Google Scholar
Van Ranst, G, MRF, L and Fievez, V 2011. Red clover polyphenol oxidase and lipid metabolism. Animal 5, 512521.Google Scholar
Vlaeminck, B, Fievez, V, Cabrita, ARJ, Fonseca, AJM and Dewhurst, RJ 2006. Factors affecting odd- and branched-chain fatty acids in milk: a review. Animal Feed Science and Technology 13, 389417.Google Scholar
Vlaeminck, B, Gervais, R, Rahman, MM, Gadeyne, F, Gorniak, M, Doreau, M and Fievez, V 2015. Postruminal synthesis modifies the odd- and branched-chain fatty acid profile from the duodenum to milk. Journal of Dairy Science 98, 48294840.Google Scholar
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