Acid Composition Of Muscle Phospholipids Research Articles

Fish oil reverses the altered glucose transporter, phosphorylation, insulin receptor substrate-1 protein level and lipid contents in the skeletal muscle of sucrose-rich diet fed rats

The role and underlying mechanisms by which n−3 polyunsaturated fatty acids (PUFA) prevent/reverse SRD-induced insulin resistance (IR) in the muscle are not completely understood. Therefore, we examined: triglyceride, diacylglycerol, PKCθ, Glut-4, enzymatic hexokinase activity, IRS-1 protein mass level, and fatty acid composition of muscle phospholipids. Rats were fed a SRD during 6 months. Thereafter, half the animals continued with SRD up to 8 months; the other half was fed a SRD in which CO (8%wt/wt) was replaced by FO (7%+1% CO) for 2 months. Results were compared with those obtained in rats fed a control diet (CD). In SRD-fed rats, FO oil normalized/improved lipid storage and PKCθ protein mass level. Effects of insulin were comparable with those of CD-fed rats. FO reversed impaired glucose phosphorylation, IRS-1, and, under insulin stimulation, Glut-4 protein mass level. FO normalized insulin resistance and increased n−3 PUFAs in muscle phospholipids.

Dietary fatty acids modify insulin secretion of rat pancreatic islet cells in vitro.

The type of dietary fat affects the action of insulin by changes induced in the fatty acid composition of cell membranes. Little is known, however, about the effects of dietary fatty acids on insulin secretion or the possible relation between the fatty acid composition of the membrane phospholipids and insulin secretion. We therefore studied the effects of dietary fatty acids on insulin secretion stimulated by glucose, forskolin and arginine, and on the insulin content of isolated pancreatic islets, as well as on the fatty acid composition of muscle phospholipids, which were used as markers of the diet-induced modifications in the cell membranes. Five groups of rats were fed for one month with diets varying only in their fat composition: olive oil, sunflower oil, soybean oil, fish oil and palmitic acid (16:0) + soybean oil (SAT). The SAT group had higher insulin secretion, independently of the secretagogue used. No significant differences were found in insulin content between the groups. The dietary fatty acids modified the fatty acid composition of the muscle phospholipids, both in endogenously synthesized fatty acids and in those which were unable to be synthesized by the organism. No statistically significant relation was found between insulin secretion and the content of certain fatty acids in the muscle phospholipids.

Heterosis, sex and breed differences in the fatty acid composition of muscle phospholipids in beef cattle

SummaryLongissimus dorsi muscle tissue was biopsied between the 12th and 13th ribs of 96 purebred Jersey, purebred Limousin and Jersey × Limousin crossbred calves at the age of 9–10 months. Fatty acids of the phospholipid fraction were extracted and analysed for sex and breed differences. Heterosis, additive and maternal variances were estimated. All calves grazed pasture in a single management group and were biopsied from the same anatomical site. Steer calves had significantly higher proportions of the 14 : 0, 14 : 1, 18 : 2, 20 : 3 fatty acids and less of the 16‐di‐methyl‐acetal than heifer calves. Significant breed differences were observed: Limousin calves had the highest proportions of 16 : 0, 24 : 0 and saturated fatty acids (SFA), whereas Jersey×Limousin calves had the most 18 : 0 and elongation index. Dominant effects were evident in the proportions of 16 : 0, 18 : 0, SFA and elongation index. Additive genetic effects were significant in the proportions of 16 : 0, 18 : 0, 18 : 1n‐9, total SFA and desaturation and elongation indices. Combined maternal and additive effects were significant for long chain polyunsaturated fatty acids 18 : 2, 20 : 3 and 20 : 4.

Influence of swine genotype on fatty acid composition of phospholipids in longissimus muscle.

Our objective for this study was to determine whether there is a difference in the fatty acid composition of phospholipids in longissimus muscle from pigs of different genotypes. In Exp. 1, 15 Hampshire x Yorkshire-Landrace (YL), 15 Duroc x YL, and 15 Danbred x YL were used. Animals were of similar age and were fed identical diets. In Exp. 2, longissimus muscle samples from pigs of seven genetically different lines were analyzed. In both experiments, saturated fatty acids (SFA, 16:0 and 18:0) constituted approximately 31.5% of the total fatty acids. Monounsaturated fatty acid (MUFA, 18:1 and 20:1) levels ranged from 12.3 to 16.9%, and PUFA (mainly 18:2 and 20:4) accounted for 50.8 to 57.0% of the total fatty acids. Fatty acid composition of muscle phospholipids from Duroc and Hampshire x YL pigs was identical. Muscle phospholipids from Danbred x YL pigs contained more PUFA (approximately 3%, P < .05) and less SFA (approximately 2%, P < .05) than phospholipids from the two other genotypes. Differences in SFA and PUFA of muscle from the seven lines were of the same order of magnitude. Differences in MUFA content were not significant.

Fatty acid composition of muscle and adipose tissue from crossbred bulls and steers.

Fatty acid composition of total lipid extracts of muscle and adipose samples from crossbred bulls (N = 34) and steers (N = 35) was determined by gas-liquid chromatography. Samples of semitendinosus, triceps brachii and longissimus muscle and of subcutaneous and perinephric adipose tissue were excised from the right side of each carcass. In addition, thin-layer chromatography was utilized to obtain phospholipid and triacylglycerol fractions from total lipid extracts of semitendinosus and longissimus muscle and subcutaneous adipose tissue from 10 bull and steer cohorts (N = 20). The most prominent sex condition effect was in percentage of total poly-unsaturated fatty acids (PUFA). Bull tissues contained higher (P less than .01) percentages of PUFA than those of steers at all sampling sites. This reflected higher percentages of linoleate (C18:2), linolenate (C18:3) and arachidonate (C20:4) in bull tissues. Most of the PUFA were present as phospholipids in muscle samples. The fatty acid composition of muscle phospholipids was similar regardless of sex condition or muscle sampled. Total lipid extracts of semitendinosus and triceps brachii muscles of both bulls and steers contained from 6 to 10% more unsaturated fatty acids (UFA) compared with M. longissimus. Muscle triacylglycerols contained relatively high percentages of saturated fatty acids (SFA). Semitendinosus and longissimus samples from steers contained higher (P less than .05 and P less than .01, respectively) percentages of total SFA than those from bulls. Steer samples contained slightly higher percentages of palmitic acid (C16:0) compared with bulls at all sampling sites, and this difference was significant for M. longissimus. The fat:lean ratio of muscle tissue is the major factor that determines fatty acid composition.

Effects of ethanol on fatty acid composition of muscle phospholipids of rats fed nutritionally complete liquid diets

Although the effects of ethanol on phospholipid fatty acid composition have been examined in single cell organisms and in rodents given ethanol as a vapor or in solution as sole drinking fluid, there are no reports of analogous experiments with nutritionally adequate liquid diets as the source of ethanol. In this experiment, young, 88 ± 5 g, male Sprague-Dawley rats given a nutritionally adequate liquid diet containing ethanol voluntarily consumed 12–18 g ethanol per kg body weight per day after 23 days. In 27 days with food intakes 64% of control, weight gains of ethanol-fed animals (group 2) were 50% of ad lib.-fed control animals (group 1) but 88% of isoenergetically pair-fed animals (group 3). Thus, energy in the ethanol diet was utilized for growth 88% as efficiently as isoenergetic diets containing dextrin. Liver and gastrocnemius muscle weights of group 2 were significantly lower than group 3 but brain weights were not similarly affected. Blood ethanol levels determined on days 14 and 24 were above 200 mg/dl at 10:00 p.m. and 7:00 a.m. but decreased to 50 mg/dl at 4:00 p.m. on a feeding schedule that began at 5:00 p.m. Dependence was confirmed by withdrawal symptomology. Compared to group 1, phospholipids isolated from gastrocnemius muscles of group 2 exhibited significant modifications in fatty acid composition. In ethanol-fed animals, 18:0 and 20:4 were lower, and 18:1 and 18:2 were higher, than ad lib.-fed controls. However, when group 2 was compared to group 3, the pair-fed control, there was no significant difference in fatty acid composition. The observed changes in fatty acid composition appear to have been due to the reduced food consumption that accompanied the model rather than to ethanol per se. These findings underline the importance of appropriate controls in liquid diet animal models of alcoholism.