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* Laboratory for Animal Production and Animal Product Quality, Department of Animal Production, Ghent University, Proefhoevestraat 10, 9090 Melle, Belgium
Animal Nutrition, Management, and Welfare Research Group, Department de Ciència Animal i dels Aliments, Universitat Autònoma de Barcelona, Universitat Autònoma de Barcelona, 08193 Bellaterra, Spain
Abstract
Four different plant secondary metabolites were screened for their effect on rumen biohydrogenation of forage long chain fatty acids, using dual-flow continuous culture fermenters. Treatments were: control (no additive), positive control (12 mg/L of monensin), and plant extracts (500 and 1,000 mg/L triterpene saponin; 250 and 500 mg/L quercetin; 250 mg/L eugenol; 500 mg/L cinnamaldehyde). Monensin increased propionate, decreased acetate and butyrate proportions, and inhibited the complete biohydrogenation of fatty acids resulting in the accumulation of intermediates of the biohydrogenation process (C18:2 trans-11, cis-15 rather than C18:1 trans-11). Cinnamaldehyde reduced total VFA concentration and proportions of odd and branched chain fatty acids in total fat effluent. Apparent biohydrogenation of C18:2n-6 and C18:3n-3 was also lower, and a shift from the major known biohydrogenation pathway to a secondary pathway of C18:2n-6 was observed, as evidenced by an accumulation of C18:1 trans-10 and trans-10, cis-12 CLA. Quercetin (500 mg/L) increased total VFA concentration, but no shifts in the pathways or extent of biohydrogenation were observed. Eugenol resulted in the accumulation of C18:1 trans-15 and C18:1 cis-15, end products of an alternative biohydrogenation pathway of C18:3n-3. Triterpene saponins did not affect the fermentation pattern, the biohydrogenation pathways, or the extent of biohydrogenation. At the doses tested in this study, we could only show a direct relation between changes in the rumen fatty acid metabolism and the presence of cinnamaldehyde, but not for eugenol, quercetin, or triterpene saponins.
Key Words: biohydrogenation cinnamaldehyde eugenol flavonoids in vitro saponins
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