Significance of phenolic compounds in tropical forages for the ruminal bypass of polyunsaturated fatty acids and the appearance of biohydrogenation intermediates as examined in vitro

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.

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;


2004 ◽  
Vol 84 (2) ◽  
pp. 221-228 ◽  
Author(s):  
R. K. Selvaraj ◽  
G. Cherian

The effects of polyunsaturated fatty acids on delayed type hypersensitivity (DTH), egg yolk antibody content, immune tissue fatty acid profile and lipid oxidation products of layer birds were investigated. One hundred and twenty layer birds were fed diets containing conjugated linoleic acid (CLA) + animal fat (Diet I), sunflower oil (Diet II), canola + flax oil (Diet III) or fish oil (Diet IV). The total added lipid content of the diet was 3%. Birds fed Diets III and IV had higher content of n-3 fatty acids in lymphocyte and splenocytes. Thiobarbituric reactive substances were higher (P < 0.05) in the breast and thigh muscle of Diet IV fed birds. Serum and yolk anti-BSA antibody contents were higher (P < 0.05) in birds fed Diets III and IV. DTH was decreased (P < 0.05) in birds fed Diets IV and III. The number of lymphocyte CD4+ and CD8+ cells and spleen mononuclear cell CD4+, CD8+ and IgM+ cells did not differ (P > 0.05) between treatment groups. Feeding n-3 fatty acids increased antibody-mediated immune response, while n-6 fatty acids and CLA increased cell-mediated immune response. Key words: Conjugated linoleic acid, polyunsaturated fatty acids, delayed type hypersensitivity, immunoglobulins


1986 ◽  
Vol 106 (3) ◽  
pp. 445-448 ◽  
Author(s):  
T. Gerson ◽  
A. John ◽  
A. S. D. King

SummaryTwo experiments were carried out to test the effects of ryegrass maturity on rumen lipid metabolism. In the first experiment the effect of stage of maturity of perennial ryegrass on lipid metabolism in the rumen was studied with grazing sheep fitted with rumen cannulae. The pasture was either immature (13·8% crude protein), mature (8·1% crude protein) or senescent (5·5% crude protein).The ratesin vitroof triacyl glycerol lipolysis and linoleic acid (18: 2w6) hydrogenation were found to decrease with increasing age of the ryegrass.In the second experiment the sheep were dosed with emulsified linseed oil (30 g) via rumen cannulae while grazing immature or senescent ryegrass and the rumen digesta and blood plasma sampled at 0, 4 and 8 h after dosing.The proportions of linseed oil retained in the rumen were greater and blood plasma linoleic (18:2w6) and linolenic (18:3w3) acid concentrations higher when senescent ryegrass was fed.It was concluded that the rates of rumen lipolysis and hydrogenation decreased with the age of pasture and that after dosing with linseed oil the polyunsaturated fatty acid concentrations in blood plasma increased.


2013 ◽  
Vol 12 (6) ◽  
pp. 516-520 ◽  
Author(s):  
Julakorn Panatuk ◽  
Suthipong Uriyapongs ◽  
Chainarong Nawanukraw ◽  
Chirasak Phoemchala ◽  
Pitukpol Pornanake

1978 ◽  
Vol 174 (2) ◽  
pp. 585-593 ◽  
Author(s):  
Catherine T. Hammer ◽  
Eric D. Wills

The fatty acid compositions of the lipids and the lipid peroxide concentrations and rates of lipid peroxidation were determined in suspensions of liver endoplasmic reticulum isolated from rats fed on synthetic diets in which the fatty acid composition had been varied but the remaining constituents (protein, carbohydrate, vitamins and minerals) kept constant. Stock diet and synthetic diets containing no fat, 10% corn oil, herring oil, coconut oil or lard were used. The fatty acid composition of the liver endoplasmic reticulum lipid was markedly dependent on the fatty acid composition of the dietary lipid. Feeding a herring-oil diet caused incorporation of 8.7% eicosapentaenoic acid (C20:5) and 17% docosahexaenoic acid (C22:6), but only 5.1% linoleic acid (C18:2) and 6.4% arachidonic acid (C20:4), feeding a corn-oil diet caused incorporation of 25.1% C18:2, 17.8% C20:4 and 2.5% C22:6 fatty acids, and feeding a lard diet caused incorporation of 10.3% C18:2, 13.5% C20:4 and 4.3% C22:6 fatty acids into the liver endoplasmic-reticulum lipids. Phenobarbitone injection (100mg/kg) decreased the incorporation of C20:4 and C22:6 fatty acids into the liver endoplasmic reticulum of rats fed on a lard, corn-oil or herring-oil diet. Microsomal lipid peroxide concentrations and rates of peroxidation in the presence of ascorbate depended on the nature and quantity of the polyunsaturated fatty acids in the diet. The lipid peroxide content was 1.82±0.30nmol of malonaldehyde/mg of protein and the rate of peroxidation was 0.60±0.08nmol of malonaldehyde/min per mg of protein after feeding a fat-free diet, and the values were increased to 20.80nmol of malonaldehyde/mg of protein and 3.73nmol of malonaldehyde/min per mg of protein after feeding a 10% herring-oil diet in which polyunsaturated fatty acids formed 24% of the total fatty acids. Addition of α-tocopherol to the diets (120mg/kg of diet) caused a very large decrease in the lipid peroxide concentration and rate of lipid peroxidation in the endoplasmic reticulum, but addition of the synthetic anti-oxidant 2,6-di-t-butyl-4-methylphenol to the diet (100mg/kg of diet) was ineffective. Treatment of the animals with phenobarbitone (1mg/ml of drinking water) caused a sharp fall in the rate of lipid peroxidation. It is concluded that the polyunsaturated fatty acid composition of the diet regulates the fatty acid composition of the liver endoplasmic reticulum, and this in turn is an important factor controlling the rate and extent of lipid peroxidation in vitro and possibly in vivo.


2011 ◽  
Vol 51 (2) ◽  
pp. 95 ◽  
Author(s):  
O. Dayani ◽  
G. R. Ghorbani ◽  
A. K. Esmailizadeh

Eight multiparous Holstein cows in mid lactation (average days in milking of 160 ± 40) were used in a replicated 4 by 4 Latin square design, each experimental period lasting 3 weeks, to determine the effects of whole cottonseed (WCS) treatment and dietary crude protein (CP) concentration on the profile of milk fatty acids. Each 3-week experimental period consisted of 2 weeks for ration adaptation followed by 1 week for data collection. The experimental diets consisted of: (1) Control (without WCS), 16% CP; (2) 20% WCS, 16% CP; (3) 20% WCS, 13% CP; and (4) 20% crushed WCS, 13% CP. Minerals and vitamin supplements were the same in all experimental diets. The WCS treatment led to increased DM intake, fat-corrected milk yield, fat concentration, proportion of long-chain fatty acids, unsaturated fatty acids and ratio of unsaturated to saturated fatty acids (P < 0.05). Decreased concentration of dietary CP from 16 to 13% (diet 2 compared with diet 3) led to a decrease in both milk yield and milk composition (P < 0.05). WCS crushed in diets with 13% CP (diet 4 compared with diet 3) increased (P < 0.05) the concentration of conjugated linoleic acid in milk fat. The results demonstrated that adding WCS to the diet of lactating cows improves both milk yield and milk fatty acid profile, particularly the proportion of conjugated linoleic acid.


2009 ◽  
Vol 2009 ◽  
pp. 1-7 ◽  
Author(s):  
Ingeborg Hanbauer ◽  
Ignacio Rivero-Covelo ◽  
Ekrem Maloku ◽  
Adam Baca ◽  
Qiaoyan Hu ◽  
...  

Feeding mice, over 3 generations, an equicaloric diet in which α-linolenic acid, the dietary precursor of n-3 polyunsaturated fatty acids, was substituted by linoleic acid, the dietary precursor of n-6 polyunsaturated fatty acids, significantly increased body weight throughout life when compared with standard diet-fed mice. Adipogenesis observed in the low n-3 fatty acid mice was accompanied by a 6-fold upregulation of stearyl-coenzyme A desaturase 1 (Scd1), whose activity is correlated to plasma triglyceride levels. In total liver lipid and phospholipid extracts, the sum of n-3 fatty acids and the individual longer carbon chain acids, eicosapentaenoic acid (20:5n3), docosapentaenoic acid (22:5n3), and docosahexaenoic acid (22:6n3) were significantly decreased whereas arachidonic acid (20:4n6) was significantly increased. In addition, low n-3 fatty acid-fed mice had liver steatosis, heart, and kidney hypertrophy. Hence, reducing dietary α-linolenic acid, from 1.02 energy% to 0.16 energy% combined with raising linoleic acid intake resulted in obesity and had detrimental consequences on organ function.


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