Abstract

Groups of rats bearing Morris minimal deviation hepatoma 7288CTC were fed a fat-free diet supplemented with either 0.5% safflower oil (diet A), 15% safflower oil or free acids (diets Band C), or 15% safflower oil or free safflower fatty acids (diet D) for 4 weeks. A group of normal rats was also fed diet D. Triglycerides, cholesteryl esters, phosphatidylcholines, and phosphatidylethanolamines isolated from livers and hepatomas of animals on each diet were analyzed quantitatively for positional isomers in the cis- and trans-octadecenoate fractions. When sufficient samples could be obtained, the cis- and trans-hexadecenoate fractions were also analyzed. Plasma from normal rats on diet D was analyzed in the same manner. The octadecenoate fractions of all hepatoma and liver lipid classes from animals fed diets A, B, and C were greater than 95% the cis isomers. Trans isomers accounted for approximately 15, 30, 50, and 70% of the octadecenoate fractions isolated from liver triglycerides, cholesteryl esters, phosphatidylcholines, and phosphatidylethanolamines, respectively, of animals fed diet D. In contrast, all hepatoma lipid classes from animals on diet D contained the same approximate percentage of trans isomers (15 to 20%). Oleic and vaccenic acids were the major positional cis-octadecenoate isomers of all liver and hepatoma lipid classes from animals fed diets A, B, and C. The ratios of oleic to vaccenic, unaffected by diets A, B, and C, differed for each lipid class in liver, but the ratios were similar for the two hepatoma neutral lipid classes and for the two phospholipid classes. The cis-octadecenoate fractions from all liver and hepatoma lipid classes of animals fed diet D consisted predominantly of the delta9, delta11, and delta12 isomers. The cis delta10 isomer, which was a major isomer of the diet, was almost excluded from liver, hepatoma, and plasma lipids. The positional isomers of the trans-octadecenoate fractions from liver and hepatoma triglycerides and cholesteryl esters exhibited the same approximate distribution as the trans fatty acids of diet D. In contrast, the 10-trans-octadecenoate, like 10-cis-octadecenoate, was almost excluded from the phospholipids of liver and plasma. Unlike liver, the hepatoma phospholipids contained 10-trans-octadecenoate at approximately half the percentage of neutral lipids. Because diet D contained no hexadecenoic fatty acids, the occurrence of trans-hexadecenoate isomers in liver and plasma lipids indicated a chain shortening process. Predominance of the 8-trans-hexadecenoate isomer indicated a preference of the 10-trans-octadecenoate isomer for chain shortening.

Highlights

  • From the Division of Gastroenterology, Departments of Medicine and Biochemistry, University of Missouri School of Medicine and Harry S

  • Triglycerides, cholesteryl esters, phosphatidylcholines, and phosphatidylethanolamines isolated from livers and hepatomas of animals on each diet were analyzed quantitatively for positional isomers in the cis- and trans-octadecenoate fractions

  • 15, 30, 50, and 70% of the octadecenoate fractions isolated from liver triglycerides, cholesteryl esters, phosphatidylcholines, and phosphatidylethanolamines, respectively, of animals fed diet D

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Summary

AND METHODS

Weanling male Buffalo strain rats weighing 175 to 200 g were placed on one of four diets consisting of a fat-free diet An additional group of normal animals without hepatomas was maintained on diet D. After 4 weeks, the animals were killed and normal rat livers, livers of rate bearing hepatomas (denoted hereafter as host liver), and. Pooled host livers and pooled hepatomas from each diet and individual normal livers were weighed, lyophilized, and reweighed. The neutral lipid classes were separated by thin layer chromatography on absorbent layers of Silica Gel G developed in a solvent system of hexane/diethyl ether/acetic acid Phospholipid classes were resolved by thin layer chromatography on absorbent layers of Silica Gel HR developed in a solvent system of chloroform/methanol/acetic acid/0.9% saline Dutton of the Northern Regional Research Laboratory, Peoria, Ill., was used The nature of this catalyst and its selectivity toward polyunsaturated fatty acids have been described [29, 30]. Other chemicals and reagents used were reagent grade or better

RESULTS AND DISCUSSION
Diet D
Geometrical Isomers of Individual
Positional isomer percentages”
Positional isomer percentagea
Triglycerides trans
Additions and Corrections
The first
Full Text
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