Fatty Acid Composition of Cod Liver Oil Determined by Urea Fractionation and Modified Programmed Temperature Gas Chromatography

1970 ◽  
Vol 53 (5) ◽  
pp. 1074-1079
Author(s):  
John L Iverson
Keyword(s):  
Fatty Acids ◽  
Fatty Acid ◽  
Long Chain Fatty Acids ◽  
Cod Liver Oil ◽  
Marine Oils ◽  
Urea Fractionation ◽  
Fractionation Procedure ◽  
Before And After ◽  
Ppm Level ◽  
Acid Structure

Abstract Esters of fatty acids in marine oils, with similar GLC retention times, are concentrated in separate fractions by this proposed urea fractionation procedure. Esters which are present at the ppm level and are normally hidden under major peaks can then be detected. By modified programmed temperature gas chromatographic techniques, it is possible to detect trace amounts of the short and long chain fatty acids. Accurate identifications are assured by the correlation of fatty acid structure with the preferential order in which they form complexes and retention times before and after hydrogenation. Cod liver oil was found to contain 130 fatty acids. Most of the esters present in trace amounts are predominately C20 to C34 acids which have not been previously reported.

Fatty Acid Composition of Cocoa Butter Oil by Urea Fractionation and Programmed Temperature Gas Chromatography

1969 ◽  
Vol 52 (4) ◽  
pp. 685-688
Author(s):  
John L Iverson ◽  
P G Harrill ◽  
Robert W Weik
Keyword(s):  
Fatty Acids ◽  
Gas Chromatography ◽  
Fatty Acid Composition ◽  
Fatty Acid ◽  
Cocoa Butter ◽  
Chain Length ◽  
Butter Oil ◽  
Urea Fractionation ◽  
Fractionation Procedure ◽  
Long Chain

Abstract This proposed urea fractionation procedure concentrates esters with similar GLC retention times in separate fractions. GLC peaks of esters present in cocoa butter oil in trace amounts (0.001–0.1%), which are normally hidden under major peaks, can then be detected. By modified programmed temperature GLC techniques, it is possible to detect the short and long chain length fatty acids present in cocoa butter oil. The odd and even chain length saturated acids from C10 to C28, mono-unsaturates C16 to C24, branched acids C16 to C24, and linoleic and linolenic acids were detected.

scholarly journals Differential Effects of Fatty Acid Saturation and Chain Length on NASH in Juvenile Iberian Pigs

2020 ◽  
Vol 4 (Supplement_2) ◽  
pp. 682-682 ◽  
Author(s):  
Kayla Dillard ◽  
Morgan Coffin ◽  
Gabriella Hernandez ◽  
Victoria Smith ◽  
Catherine Johnson ◽  
...  
Keyword(s):  
Fatty Acids ◽  
Body Weight ◽  
Fatty Acid ◽  
Liver Injury ◽  
Olive Oil ◽  
Coconut Oil ◽  
Long Chain Fatty Acids ◽  
Medium Chain ◽  
Long Chain ◽  
Chain Fatty Acids

Abstract Objectives Non-alcoholic fatty liver disease (NAFLD) represents the major cause of pediatric chronic liver pathology in the United States. The objective of this study was to compare the relative effect of inclusion of isocaloric amounts of saturated medium-chain fatty acids (hydrogenated coconut oil), saturated long-chain fatty acids (lard) and unsaturated long-chain fatty acids (olive oil) on endpoints of NAFLD and insulin resistance. Methods Thirty-eight 15-d-old Iberian pigs were fed 1 of 4 diets containing (g/kg body weight × d) 1) control (CON; n = 8): 0 g fructose, 10.5 g fat, and 187 kcal metabolizable energy (ME), 2) lard (LAR; n = 10): 21.6 g fructose, 17.1 g fat (100% lard) and 299 kcal ME, 3) hydrogenated coconut oil (COCO; n = 10): 21.6 g fructose, 16.9 g fat (42.5% lard and 57.5% coconut oil) and 299 kcal ME, and 4) olive oil (OLV, n = 10): 21.6 g fructose, 17.1 g fat (43.5% lard and 56.5% olive oil) and 299 kcal ME, for 9 consecutive weeks. Body weight was recorded every 3 d. Serum markers of liver injury and dyslipidemia were measured on d 60 at 2 h post feeding, with all other serum measures assessed on d 70. Liver tissue was collected on d 70 for histology, triacylglyceride (TG) quantification, and metabolomics analysis. Results Tissue histology indicated the presence of steatosis in LAR, COCO and OLV compared with CON (P ≤ 0.001), with a further increase in in non-alcoholic steatohepatitis (NASH) in OLV and COCO compared with LAR (P ≤ 0.01). Alanine and aspartate aminotransferases were higher in COCO and OLV (P ≤ 0.01) than CON. All treatment groups had lower liver concentrations of methyl donor's choline and betaine versus CON, while bile acids were differentially changed (P ≤ 0.05). COCO had higher levels of TGs with less carbons (Total carbons < 52) than all other groups (P ≤ 0.05). Several long-chain acylcarnitines involved in fat oxidation were higher in OLV versus all other groups (P ≤ 0.05). Conclusions Inclusion of fats enriched in medium-chain saturated and long-chain unsaturated fatty acids in a high-fructose high-fat diet increased liver injury, compared with fats with a long-chain saturated fatty acid profile. Further research is required to investigate the mechanisms causing this difference in physiological response to these dietary fat sources. Funding Sources ARI, AcornSeekers.

Effects of cold acclimation on lipid metabolism in adipose tissue

1961 ◽  
Vol 200 (4) ◽  
pp. 847-850 ◽  
Author(s):  
Judith K. Patkin ◽  
E. J. Masoro
Keyword(s):  
Fatty Acids ◽  
Adipose Tissue ◽  
Fatty Acid ◽  
Lipid Metabolism ◽  
Cold Acclimation ◽  
Long Chain Fatty Acids ◽  
Synthetic Capacity ◽  
And Control ◽  
Long Chain ◽  
Chain Fatty Acids

Cold acclimation is known to alter hepatic lipid metabolism. Liver slices from cold-acclimated rats have a greatly depressed capacity to synthesize long-chain fatty acids from acctate-1-C14. Since adipose tissue is the major site of lipogenic activity in the intact animal, its fatty acid synthetic capacity was studied. In contrast to the liver, it was found that adipose tissue from the cold-acclimated rat synthesized three to six times as much long-chain fatty acids per milligram of tissue protein as the adipose tissue from the control rat living at 25°C. Evidence is presented indicating that adipose tissue from cold-acclimated and control rats esterify long-chain fatty acids at the same rate. The ability of adipose tissue to oxidize palmitic acid to CO2 was found to be unaltered by cold acclimation. The fate of the large amount of fatty acid synthesized in the adipose tissue of cold-acclimated rats is discussed.

Caprenin 1. Digestion, Absorption, and Rearrangement in Thoracic Duct-Cannulated Rats

1991 ◽  
Vol 10 (3) ◽  
pp. 325-340 ◽  
Author(s):  
D. R. Webb ◽  
R. A. Sanders
Keyword(s):  
Fatty Acids ◽  
Fatty Acid ◽  
Female Rats ◽  
Acid Uptake ◽  
Long Chain Fatty Acids ◽  
Male And Female ◽  
Medium Chain ◽  
Male And Female Rats ◽  
Long Chain ◽  
Chain Fatty Acids

Caprenin (CAP) is a triglyceride that primarily contains caprylic (C8:0), capric (C10:0), and behenic (C22:0) acids. This study was undertaken to determine whether or not CAP is qualitatively digested, absorbed, and rearranged like other dietary fats and oils that contain these medium-chain and very long-chain fatty acids. In vitro results showed that neat CAP, coconut oil (CO) and peanut oil (PO) were hydrolyzed by porcine pancreatic lipase. All of the neat triglycerides also were digested in vivo by both male and female rats. This was shown by the recovery of significantly more extractable lymphatic fat than with fat-free control animals and by the recovery of orally administered triglyceride-derived fatty acids in lymph triglycerides. However, substantially more PO (74%) and CO (51%) were recovered in lymph relative to CAP (10%). These quantitative differences are consistent with the fatty acid composition of each triglyceride and primary routes of fatty acid uptake. The 24-h lymphatic recovery of CAP-derived C8:0, C10:0, and C22:0 averaged 3.9%, 17.8%, and 11.2%, respectively, for male and female rats. The C8:0 and C10:0 results approximated those obtained with CO (2.0% and 16.3%, respectively). In contrast, the 24-h absorbability of C22:0 in CAP was significantly less than that seen in PO (55.4%). Finally, there was no evidence of significant rearrangement of the positions of fatty acids on glycerol during digestion and absorption. Those fatty acids recovered in lymphatic fat tended to occupy the same glyceride positions that they did in the neat administered oils. However, the lymph fats recovered from all animals dosed with fat emulsions were enriched with endogenous lymph fatty acids. It is concluded that CAP is qualitatively digested, absorbed, and processed like any dietary fat or oil that contains medium-chain and very long-chain fatty acids.

scholarly journals Up-regulation of the expression of the gene for liver fatty acid-binding protein by long-chain fatty acids

1996 ◽  
Vol 319 (2) ◽  
pp. 483-487 ◽  
Author(s):  
Claire MEUNIER-DURMORT ◽  
Hélène POIRIER ◽  
Isabelle NIOT ◽  
Claude FOREST ◽  
Philippe BESNARD
Keyword(s):  
Fatty Acids ◽  
Fatty Acid ◽  
Fatty Acid Binding Protein ◽  
Fold Increase ◽  
Long Chain Fatty Acids ◽  
Liver Fatty Acid ◽  
Fatty Acid Binding ◽  
Acid Binding Protein ◽  
Fabp Gene ◽  
Long Chain

The role of fatty acids in the expression of the gene for liver fatty acid-binding protein (L-FABP) was investigated in the well-differentiated FAO rat hepatoma cell line. Cells were maintained in serum-free medium containing 40 µM BSA/320 µM oleate. Western blot analysis showed that oleate triggered an approx. 4-fold increase in the cytosolic L-FABP level in 16 h. Oleate specifically stimulated L-FABP mRNA in time-dependent and dose-dependent manners with a maximum 7-fold increase at 16 h in FAO cells. Preincubation of FAO cells with cycloheximide prevented the oleate-mediated induction of L-FABP mRNA, showing that protein synthesis was required for the action of fatty acids. Run-on transcription assays demonstrated that the control of L-FABP gene expression by oleate was, at least in part, transcriptional. Palmitic acid, oleic acid, linoleic acid, linolenic acid and arachidonic acid were similarly potent whereas octanoic acid was inefficient. This regulation was also found in normal hepatocytes. Therefore long-chain fatty acids are strong inducers of L-FABP gene expression. FAO cells constitute a useful tool for studying the underlying mechanism of fatty acid action.

scholarly journals Milk urea nitrogen and milk fatty acid compositions in dairy cows with subacute ruminal acidosis

2020 ◽  
Vol 65 (No. 8) ◽  
pp. 336-345 ◽  
Author(s):  
K Kara
Keyword(s):  
Fatty Acids ◽  
Fatty Acid ◽  
Dairy Cows ◽  
Ph Value ◽  
Milk Fatty Acid ◽  
Long Chain Fatty Acids ◽  
Subacute Ruminal Acidosis ◽  
Urea Nitrogen ◽  
Ruminal Acidosis ◽  
Long Chain

The present study was aimed at comparing the milk urea nitrogen (MUN) and milk fatty acid (MFA) compositions in Holstein cows with subacute ruminal acidosis (SARA) to those values of Holstein cows that did not have SARA. Also, the correlations among rumen pH value and the compositions of MUN and MFA in milk were determined. Dairy cows (n = 16) with subacute ruminal acidosis (SARA) (pH value 5.60 ± 0.02) and control dairy cows (n = 16) (control) (pH value 6.20 ± 0.04) were studied. The MUN concentrations (578 µg/l) of the dairy cows with SARA was lower than those (1 315 µg/l) of the control dairy cows (P < 0.001). In the milk of the dairy cows with SARA, the unsaturated fatty acids (UFA), thrombogenic index (TI), and hypocholesterolemic fatty acid index (hcFA) decreased; but the saturated fatty acids (SFA), atherogenic (AI) and hypercholesterolemic fatty acid (HcFA) indexes (P < 0.01) increased. The rumen pH value and the concentration of the MUN were positively correlated with the proportions of the monounsaturated fatty acids (MUFA), polyunsaturated fatty acids (PUFA), omega-3 fatty acids (n-3), omega-6 fatty acids (n-6), omega-9 fatty acids (n-9), long-chain fatty acids (LCFA) and very-long-chain fatty acids (VLCFA) and the n-3/n-6 ratio of the milk samples (P < 0.05). Consequently, the dairy cow with SARA that are in early-lactation can affect the carbohydrate fermentation, fatty acid hydrogenation and protein degradation. The MUN concentration in the dairy cows with SARA seriously decreased. The SARA changes the milk fatty acid composition and decreases the MUFA, PUFA, n-3, oleic acid and hypocholesterolemic fatty acids and the hypocholesterolemic/hypercholesterolemic ratio (h/H) values of milk. Therefore, the nutritional and functional quality for human nutrition decreases in the milk of dairy cows with SARA.

scholarly journals Ankyrin-bound fatty acid turns over rapidly at the erythrocyte plasma membrane.

1987 ◽  
Vol 7 (8) ◽  
pp. 2981-2984 ◽  
Author(s):  
M Staufenbiel
Keyword(s):  
Fatty Acids ◽  
Plasma Membrane ◽  
Fatty Acid ◽  
Long Chain Fatty Acids ◽  
Acid Modification ◽  
Skeletal Protein ◽  
Erythrocyte Plasma Membrane ◽  
Polypeptide Backbone ◽  
Long Chain ◽  
Regulatory Significance

The membrane skeletal protein ankyrin was shown to be continuously acylated and deacylated with long-chain fatty acids in mature erythrocytes. At least a fraction of the lipid bound to ankyrin turned over rapidly (half-life, approximately 50 min) compared with the polypeptide backbone, which was stable throughout the erythrocyte life. This indicates a regulatory significance of the fatty acid modification for the function of ankyrin.

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