Effect of Dietary Vegetable Oil Supplementation on C18 Fatty Acids and Conjugated Linoleic Acid Production; An In vitro Fermentation Study

2013 ◽  
Vol 12 (6) ◽  
pp. 516-520 ◽  
Author(s):  
Julakorn Panatuk ◽  
Suthipong Uriyapongs ◽  
Chainarong Nawanukraw ◽  
Chirasak Phoemchala ◽  
Pitukpol Pornanake
2006 ◽  
Vol 95 (4) ◽  
pp. 688-695 ◽  
Author(s):  
Renaville Bénédicte ◽  
Anne Mullen ◽  
Fiona Moloney ◽  
Yvan Larondelle ◽  
Yves-Jacques Schneider ◽  
...  

Stearoyl-CoA desaturase (SCD) is a key enzyme that determines the composition and metabolic fate of ingested fatty acids, in particular the conversion of trans-vaccenic acid (TVA) to conjugated linoleic acid (CLA). The present study addressed the hypothesis that intestinal TVA absorption and biotransformation into CLA can be modulated by EPA and 3,10-dithia stearic acid (DSA) via altered SCD mRNA levels and desaturation indices (cis-9, trans-11-CLA:TVA and oleic acid:stearic acid ratios) in Caco-2 and T84 cells, two well-established in vitro models of the human intestinal epithelium. The study determined the effect of acute (3h with 0·3mm-EPA or 0·3mm-DSA) and acute-on-chronic (1 week with 0·03mm-EPA or -DSA, followed by respectively, 0·3mm-EPA or -DSA for 3h) treatments. In both cell lines, acute EPA treatment did not alter SCD desaturation indices, whereas the acute-on-chronic treatment affected these surrogate markers of SCD activity. This was associated with reduced sterol regulatory-element binding protein-1c and SCD mRNA levels. In contrast, acute and acute-on-chronic DSA treatments significantly reduced SCD desaturation indices without affecting SCD mRNA levels in Caco-2 cells. The present study on intestinal cells shows that the conversion rate of TVA to c9, t11-CLA is affected by other fatty acids present in the diet such as EPA, confirming previous observations in hepatic and mammary cell models.


2013 ◽  
Vol 58 (No. 7) ◽  
pp. 328-341 ◽  
Author(s):  
M. Czauderna ◽  
J. Kowalczyk ◽  
M. Marounek

The influence of selenite (Se<sup>IV</sup>) or selenate (Se<sup>VI</sup>) added to ovine ruminal fluid containing linseed oil (LO) on the profile of fatty acids (FA), particularly conjugated linoleic acid (CLA) isomers, was investigated. The ruminal fluid was incubated in vitro at 39&deg;C under CO<sub>2</sub> either alone (the control fluid) or with LO (3.3 mg/ml) or with a combination of LO with either a low (0.167 &mu;g/ml) or high (1.67 &mu;g/ml) level of Se as Se<sup>IV</sup> or Se<sup>VI</sup>. LO added to ruminal fluids also provides an extra source of energy. The tubes with the examined fluids were removed after 0, 6, 12, 18, or 24 h of in vitro incubation and then analyzed to determine the FA levels. The lower and higher concentration of Se<sup>IV </sup>in the fluids with the LO revealed negligible effect on the concentration of the sum of the CLA isomers (&sum;CLA) in the fluid compared with the fluid with LO alone. The addition of a higher amount of Se<sup>IV</sup> to the fluid containing LO usually decreased the concentration of &sum;CLA compared with the fluid containing the lower concentration of Se<sup>IV</sup> and LO. The concentration of c9t11c15C18:3 (cLNA) in the fluids with LO, irrespective of the presence of extra Se, increased throughout the incubations, although the addition of Se<sup>IV </sup>or Se<sup>VI</sup> to the fluids containing LO numerically reduced the increase of the concentration of cLNA compared with the fluid with LO alone. The concentration sum of the C18:1 isomers (&Sigma;C18:1) in the control fluid numerically decreased throughout the incubations, while LO added to the fluid increased the concentration of &Sigma;C18:1 throughout the incubations. LO added to the fluid, irrespective of the presence of Se<sup>IV</sup> or Se<sup>VI</sup>, significantly increased the concentration of &Sigma;C18:1 compared with the control fluid and the fluids with Se<sup>IV </sup>or Se<sup>VI</sup>. The concentrations of C16:0 and C18:0 in the control fluid and the fluids containing Se<sup>IV</sup> or Se<sup>VI </sup>numerically increased throughout the incubations and were usually lower than in the fluids containing LO without or with Se<sup>IV </sup>or Se<sup>VI</sup>. The concentration of C18:3n-3 decreased throughout the incubation of the fluids containing LO, irrespective of the presence of Se<sup>IV </sup>or Se<sup>VI</sup>. LO added to the fluids, irrespective of the presence of Se<sup>IV</sup> or Se<sup>VI</sup>, increased the concentration of C18:2n-6 compared with the control fluid and the fluids with Se<sup>IV </sup>or Se<sup>VI</sup>. The higher concentration of Se<sup>IV</sup> or Se<sup>VI</sup> in the fluid with LO most efficiently increased the concentration of c5c8c11c14c17C20:5 compared with the control fluid or the fluids containing LO, irrespective of the presence of the lower concentration of Se<sup>IV</sup> or Se<sup>VI</sup>. LO added to the fluid, irrespective of the presence of Se<sup>IV </sup>or Se<sup>VI</sup>, increased the concentration of polyunsaturated FA compared with the control fluid or the fluids containing Se<sup>IV </sup>or Se<sup>VI</sup>. &nbsp; &nbsp;


2020 ◽  
Vol 50 (7) ◽  
Author(s):  
Rayudika Aprilia Patindra Purba ◽  
Chalermpon Yuangklang ◽  
Pramote Paengkoum

ABSTRACT: Piper betle L. is edible plant richer in polyphenols that might improve feed utilization in rumen diet. The objective of the present study was to investigate the effect of various Piper betle L. powder (PL) doses on in vitro rumen microorganisms, ruminal biogas and fermentation end-product production, and biohydrogenation including lipolysis-isomerization. The completely randomized design used five levels of PL supplementation (0, 25, 50, 75 and 100 mg DM) incubated with 400 mg of a basal substrate of Pangola hay and concentrate (50:50). The matrix compounds (g/kg DM) of 0.27 catechin, 0.11 rutin, 3.48 quercetin, 0.41 apigenin, 0.04 myricetin, 0.27 kaempferol, 0.76 eugenol and 0.22 caryophyllene derived from PL altered the fermentation pattern, with an increase in degradable nutrients and total volatile fatty acids and acetogenesis without shifting pH during fermentation. These values promoted in vitro gas production, with higher carbon dioxide and lower methane production. Although, hydrogen recovery from lipolysis-isomerization in biohydrogenation was limited, PL successfully promoted stearic acid (C18:0) accumulation by changing the biohydrogenation pathway of fatty acids, causing more C18:1 trans-11 rather than C18:2 trans-11, cis-15. Consequently, this resulted in more conjugated linoleic acid (CLA) cis-9, trans-11, CLA trans-10, cis-12 and CLA trans-11, cis-13. Enhanced PL supply increased total bacteria and fungal zoospores due to a reduction in rumen protozoa. In conclusion, our results demonstrated that PL is a feed additive with potential for ruminants, promising improved ruminal fermentation and biohydrogenation, while reducing methane production.


2009 ◽  
Vol 19 (10) ◽  
pp. 574-581 ◽  
Author(s):  
Rachel Gervais ◽  
Fleur Gagnon ◽  
Ehab E. Kheadr ◽  
Marie-Rose Van Calsteren ◽  
Edward R. Farnworth ◽  
...  

2011 ◽  
Vol 51 (12) ◽  
pp. 1127 ◽  
Author(s):  
Anuraga Jayanegara ◽  
Michael Kreuzer ◽  
Elizabeth Wina ◽  
Florian Leiber

The purpose of the present study was to assess the influence of phenol-rich tropical ruminant feeds on the extent of ruminal biohydrogenation (BH) of polyunsaturated fatty acids (PUFA). Samples of 27 tropical forages (mainly tree and shrub leaves), characterised by different phenolic profiles, were incubated in vitro (n = 4 replicates) with buffered rumen fluid for 24 h using the Hohenheim gas test method. Linseed oil was added as a rich source of PUFA. In the plants, total extractable phenols (TEP), non-tannin phenols, condensed tannins, and fatty acids were determined. After terminating incubation, the fatty acid profile present in fermentation fluid (total syringe content) was analysed by gas chromatography. The relationship between TEP and the disappearance of α-linolenic acid from the incubation fluid was negative (R2 = 0.48, P < 0.001), indicating that TEP reduced the ruminal BH of this PUFA. Similarly, TEP were negatively related with the disappearances of linoleic acid (R2 = 0.52, P < 0.001) and oleic acid (R2 = 0.58, P < 0.001). The appearance of rumenic acid, an important conjugated linoleic acid isomer, was positively correlated with TEP (R2 = 0.30, P < 0.01), while the opposite result was seen with stearic acid (R2 = 0.22, P < 0.05). Leaves of avocado (Persea americana) were particularly interesting, because they changed the BH pattern at a moderate TEP content of 73 g/kg DM. It is concluded that, in the tropical feedstuffs investigated, TEP have an impact on ruminal fatty acid BH and are associated with an increased bypass of PUFA and the generation of conjugated linoleic acid.


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