Differential effects of fatty acid chain length on the viability of two species of cactophilic Drosophila

• 1.1. Two columnar cacti in the Sonoran Desert, agria and organpipe, contain medium chain (C₈−C₁₂) fatty acids.
• 2.2. Necrotic tissues of these cacti serve as feeding and breeding substrates for Drosophila mojavensis but not D. nigrospiracula.
• 3.3. Results show that capric and lauric acids are the predominant fatty acids of both cacti.
• 4.4. Fatty acid chain length exhibits a differential effect on larval viability with caprylic acid (Q) having the greatest and myristic acid (C₁₄) having the least effect.
• 5.5. Drosophila mojavensis is more tolerant of free fatty acids than D. nigrospiracula, and this partly explains the ability of D. mojavensis to utilize agria and organpipe cacti.

     

Cortical and medullary lipids of normal and nephrosclerotic human kidney

• 1.1. Major lipid classes from cortical and medullary zones of normal and nephrosclerotic human kidneys have been isolated and the fatty acid composition of each determined.
• 2.2. The nephrosclerotic tissue contained two times more total lipid than the normal kidney but, irrespective of kidney pathology, phospholipids were the major cortical lipids and neutral lipids were the predominant lipids in medullary zones.
• 3.3. Human kidney contained large amounts of phosphatidylcholines, phosphatidylethanolamines and sphingomyelins and although these were slightly increased in the sclerotic kidney, anatomical differences in phospholipid content were not significant.
• 4.4. Quantitative differences between the zones of normal kidney were found with triglycerides, diglycerides. free fatty acids and cholesterol; overall, the sclerotic tissue contained more triglycerides and small amounts of cholesterol esters with less significant regional differences.
• 5.5. Palmitic, oleic and stearic acid were the major fatty acids of neutral lipids; these plus linoleic acid were prevalent in phospholipids.

     

Fatty acid profile of the digestive gland and mantle in the bivalve Macoma balthica

• 1.1. Digestive gland and mantle fatty acids were studied in spring and summer in the bivalve Macoma balthica off the southern coast of Finland. The presence of lipids was also examined histochemically in various clam tissues.
• 2.2. the neutral lipid content of the digestive gland increased ca 4.5-fold during the annual growth period.
• 3.3. Neutral lipid fatty acids of the digestive gland, of which palmitoleic, eicosapentaenoic and palmitic acids were predominant, were clearly distinguished from phospho- and glycolipid fatty acids.
• 4.4. The degree of unsaturation of phospholipid fatty acids was higher in the cold season both in the digestive gland and mantle, mainly due to the titer of eicosapentaenoic acid.

     

Influence of dietary sources of fat on lipid synthesis in mink (Mustela vison) mammary tissue

• 1.1. The fatty acid composition of the triglyceride fraction of mink milk sampled during mid-lactation (day 28 post partum) from two nursing mink was compared to that of plasma samples and to the fatty acid composition of the feed rations used.
• 2.2. Chemical analysis of the triglyceride composition of mink milk demonstrated only minute concentrations of fatty acids with a chain length below C₁₄.
• 3.3. The saturated C_16:0- and C_18:0-unit fatty acids in mink milk made up for 24–40% of the total amount of fatty acids extracted, the remainder being represented by mono and polyunsaturated long-chain (C₁₆-C₂₄) fatty acids.
• 4.4. Preliminary in vitro experiments proved the incorporation of¹⁴C-labelled glucose, acetate or palmitate into triacylglycerols in cultures of mink mammary tissue to be linear for at least 2 hr.
• 5.5. The in vitro capacity for de novo fatty acid synthesis in mink mammary tissue using 14C-labelled glucose or acetate was low, i.e. ranging from 0.096–0.109 nmol/g (fresh tissue)/min, and amounted to only about 5% of that obtained in the case of [¹⁴C]palmitic acid incubation.
• 6.6. Following ¹⁴C-labeIled acetic or palmitic acid incubation of mink mammary tissue neither desaturation nor chain elongation was observed.
• 7.7. In response to long-term feeding on rations with two different sources of animal fat (F = fish oil or L = lard) the influence of compositional changes in dietary neutral lipids on the fatty acid composition of the lipids of mink milk is discussed.

     

A further contribution to the knowledge of the blood lipid fractions from the african elephant Loxodonta africana

• 1.1. Plasma lipids from 5 African elephants were extracted and fractionated into cholesterol esters, free fatty acids, triglycerides, phosphatidylcholine, phosphatidylethanolamine, phosphatidylinositol, sphingomyelin and glycosphingolipids. The fatty acids of various individual fractions were investigated by gas-chromatography.
• 2.2. All animals, except one, had a high linoleic acid content in cholesterol esters indicating an adequate supply of linoleic acid in the diet.
• 3.3. Phosphatidyl choline had a strong saturated character originating from the presence of unusually high quantities of stearic acid.
• 4.4. Phosphatidylethanolamine was present in small quantities and was characterized by a low content of arachidonic acid.
• 5.5. Sphingomyelin did not contain any long chain saturated acids. Instead it contained 10.2–47.0% of a long chain acid which was most likely monounsaturated.
• 6.6. The presence of significant quantities of glycosphingolipids was established.

     

Lipid digestion in cod (gadus morhua)

• 1.1. Cod, 2.6–3.4 kg. were fed a mixed diet of sprat, capelin oil and wheat flour.
• 2.2. Lipids from the feed, stomach and four intestinal segments were separated into tri-, di- and monoglycerides and free fatty acids and analysed by GLC.
• 3.3. All lipolytic products were concentrated in 14:0, 16:0 and 18:0, up to 60% and extremely low in the ω-3 fatty acids.
• 4.4. Residual triglycerides contained 80% of saturated and monoenoic fatty acids.
• 5.5. Linoleic acid increased from 2% in feed TG to 10% in TG of the rectum.

     

The pathway of the biosynthesis of non-methylene-interrupted dienoic fatty acids in molluscs

• 1.1. The metabolic fate of 1-¹⁴C-acetate administered to the marine bivalve mollusc Mytilus edulis was investigated.
• 2.2. The active incorporation of the label in 20:2 non-methylene-interrupted dienoic (NMID) fatty acids was found.
• 3.3. Acetate incorporation patterns and specific radioactivity of mussel acids suggest that 22:2Δ7,13 and 22:2/gD7,15 arose by C₂ elongation of 20:2Δ5,11 and 20:2Δ5,13 respectively.
• 4.4. The proposed pathway of NMID fatty acid biosynthesis in molluscs is discussed.

     

Palmitic acid metabolism in hepatopancreas of the freshwater shrimp Macrobrachium borellii

• 1.1. The palmitic acid fate as substrate for the synthesis of either glycerides or other fatty acids was studied in vivo and in the microsomal fraction from hepatopancreas of Macrobrachium borellii.
• 2.2. Most of the palmitic acid administered in vivo circulated to the hepatopancreas, being incorporated mainly in the triacylglycerol (TG) fraction.
• 3.3. Palmitic acid transformations into palmitoleic, stearic and oleic acids were observed in the hepatopancreas.
• 4.4. The in vitro biosynthesis of TG in hepatopancreas was more active than in other tissues. In the microsomal fraction, palmitic acid was also incorporated mainly in TG, and followed the α-glycerophosphate pathway.

     

Effects of milk fat,unhydrogenated and partially hydrogenated vegetable oils on serum lipoproteins in growing pigs

• 1.1. Crossbred Yorkshire (Yorkshire × Landrace) pigs were fed butter oil, cream, low erucic acid rapeseed oil, sunflower oil and partially hydrogenated sunflower oil in amounts representing 30% of energy for periods of up to 13 weeks.
• 2.2. After 13 wk of feeding serum total cholesterol levels of pigs fed milk fat were significantly higher than of pigs fed vegetable oils.
• 3.3. The difference in cholesterol was mainly due to an increase in the density range of 1.063–1.125 g/ml containing pig LDL₂ and some HDL.
• 4.4. A shift towards smaller LDL particle size was apparent in pigs fed milk fat.
• 5.5. The effects of dietary trans fatty acids did not differ from cis polyunsaturated or monounsaturated fatty acids.

     

Spingophosphonolipids in microsomes of Diplodon delodontus. Distribution and effect on the membrane microviscosity

• 1.1. The distribution of ceramide aminoethylphosphonate (CAEP) in microsomal membranes obtained from different tissues of the bivalve mollusc Diplodon delodontus was determined.
• 2.2. The concentration of CAEP reached from 9 to 19% of the total microsomal polar lipids, depending on the kind of tissue.
• 3.3. Palmitic acid was the main fatty acid in the ceramide moiety, followed by stearic and eicosamonoenoic acids.
• 4.4. Artificial membranes were prepared with microsomal phospholipids or phospholipids plus sterols, with and without the addition of CAEP.
• 5.5. It was shown that the phosphonate confers minor mobility to the membranes. This effect is more effective when the membrane contains the natural sterols and the phospholipids are unsaturated.

     

Changes in the phospholipid composition and in fatty acids of phosphatidylcholine and phosphatidylethanolamine of various tissues of the developing tadpole of Agalychnis dacnicolor

• 1.1. Lipid changes occur in the developing tadpole of A. dacnicolor. The phosphatidylcholine content of liver and tail decrease during metamorphosis.
• 2.2. In liver, the fatty acids of phosphatidylcholine and phosphatidylethanolamine become more unsaturated.
• 3.3. In skin, phosphatidylcholine becomes more unsaturated and phosphatidylethanolamine becomes more saturated.
• 4.4. In tail, phosphatidylcholine becomes more saturated and phosphatidylethanolamine shows no change.
• 5.5. Triglycerides become more unsaturated in skin but become more saturated in tail.

     

Presence of an essential polyunsaturated fatty acid in intradigestive bacterial symbionts of a deposit-feeder echinoid (Echinodermata)

• 1.1. Fatty acids were isolated from bacteria of the family Beggiatoaceae and closely related to the genus Thiothrix. These bacteria are symbionts that live in the gut of Echinocardium cordatum.
• 2.2. Ten pronounced chromatographic peaks were observed that correspond to 14:0, 15:0, 15:0, 16:0, 16:1, 17:0, 18:0, 18:1, 18:3 and 19:0 fatty acids.
• 3.3. The fatty acid 18:3 had a retention time and mass spectrum identical to those of linolenic acid.
• 4.4. The presence of an essential fatty acid has never before been reported in a non-photosynthetic organism. This essential fatty acid in the symbiotic bacteria could be of nutritional importance for their echinoid host.
• 5.5. The presence of this essential fatty acid supports a phylogenetic affinity between Beggiatoaceae and Cyanobacteria that are the only bacteria known to synthetize linolenic polyunsaturated fatty acid (PUFA).

     

Modulation of mitochondrial ATPase sensitivity to inhibitors and stimulators by diet-induced changes in membrane lipid

• 1.1. Weanling rats were fed diets differing in fatty acid composition to determine if changes induced in cardiac mitochondrial membrane structural components alter the sensitivity of mitochondrial ATPase to inhibition by oligomycin and stimulation by 2,4-dinitrophenol.
• 2.2. Mitochondrial ATPase assayed in situ within the mitochondrial membrane isolated from animals fed diets higher in fatty acids of longer chain length, exhibited greater oligomycin sensitivity and lower 2,4-dinitrophenol-induced stimulation.
• 3.3. Concomitant diet-induced changes occur in the fatty acid, composition of phosphatidylcholine, phosphatidylethanolamine and cardiolipin, increasing overall length of fatty-acyl tails in the membrane phospholipids.
• 4.4. Diet fat mediated alterations in oligomycin sensitivity of mitochondrial ATPase and membrane fatty acid chain length suggest that _vivo changes in thickness of the lipid bilayer may alter mitochindrial ATPase functions.
• 5.5. The present study extends the concept that dietary fat affects mitochondrial membrane structure and function by demonstrating that the membrane-dependent sensitivity of mitochondrial ATPase to inhibitors and stimulators may be modulated by dietary fat.

     

The fatty acid composition of leech lipids

• 1.1. The constituent fatty acids of the neutral and phospholipids of Macrobdella ditetra, Nephelopsis obscura, Philobdella gracilis and Hirudo medicinalis have been determined.
• 2.2. Unsaturated fatty acids predominated in both neutral and phospholipid fractions of all leech species examined.
• 3.3. Arachidonic acid (20:4) was the most prevalent fatty acid in all species, accounting for as much as 36.7% of the total phospholipid fatty acids.

     

Adaptive strategies of selective fatty acid deposition in the bone marrow of desert bighorn sheep

• 1.1. The winter distribution of fatty acids in the fore and hind limb of the desert bighorn, Ovis canadensis cremnobates, increased in unsaturation distally over the length of the leg; the greatest change occurred at the level of the radius and tibia.
• 2.2. Summer fatty acid marrow composition decreased significantly in unsaturation distally when compared to winter values. The greatest changes occurred at the metacarpus (metatarsus)-phalanges.
• 3.3. The summer distribution of distally accumulated saturated fatty acids could be an adaptation to maintain the limbs as heat dissipators by insulating against conductive heat gain from a hot environment and protecting cell membranes of heterothermic tissues against thermal denaturation.

     

Lipid changes in blood serum and tissues of the Egyptian Cobra “Naja haje haje” during the hibernation cycle

• 1.Total lipids, free fatty acids, triglycerides, phospholipids and total cholesterol in blood serum, liver, brain, cardiac and skeletal muscles of Naja haje haje were determined during the different phases of the hibernation cycle.
• 2.A sharp decrease in the level of total lipids of blood serum and all tissues occurred during hibernation. Upon arousal, lipogenesis is commonly restored.
• 3.Elevated concentrations of serum free fatty acids predominated in pre-hibernation and hibernation periods, while the tissues recorded highly significant declines during hibernation.
• 4.Occurrence of marked decreases in triglycerides contents of serum and tissues except the cardiac muscles in the hibernation and arousal phases.
• 5.Sharp increases in the phospholipid contents of blood and the selected tissues were recorded during hibernation. The level declined in both liver and cardiac muscles in arousing animals.
• 6.Total cholesterol level was lowered in blood during hibernation. The cardiac muscles showed a highly significant decrease while liver, brain and skeletal muscles showed elevations in the same phase.

     

Fermentation and the production of volatile fatty acids in the alimentary tract of the rock hyrax,Procavia capensis

• 1.1. Aspects of ruminant-like metabolism were examined in the hyrax Procavia capensis.
• 2.2. High concentrations of volatile fatty acids occurred in the cardiac stomach with a predominance of acetic and lactic acids.
• 3.3. Acetic (69%), propionic (22%) and butyric (8%) acids occurred in highest concentrations in the proximal caecum, with appreciable amounts in the proximal colon, distal caecum and appendices.
• 4.4. The depot fat contained high proportions of unsaturated C₁₈ (linoleic and linolenic) acids.
• 5.5. The glucose level in the plasma was within the range established for non-ruminant herbivores.
• 6.6. The possibility of silage-like fermentation occurring in the cardiac stomach is discussed.

     

The effect of triiodothyronine on glucose utilization in adipocytes from obese rats

• 1.1. In the presence of insulin, 10⁻⁵ M 3,3',5-triiodothyronine (T₃) treatment for 1/2 hr decreased fatty acid synthesis 35% only in adipocytes from lean rats, whereas at 10⁻¹¹ M through 10⁻⁷M T₃ the obese adipocytes had nearly a 20% increase in fatty acid synthesis.
• 2.2. A 2 hr pretreatment of adipocytes with 10⁻⁹ and 10⁻⁷ M T₃ decreased insulin-stimulated fatty acid synthesis by nearly 20% in both lean and obese adipocytes.
• 3.3. In the absence of insulin, the 2 hr pretreatment with 10⁻⁹ M T₃ resulted in a 45% increase in lean adipocyte fatty acid synthesis, though the obese adipocytes required at least 10⁻⁷ M T₃ for 2 hr to increase the non-insulin-stimulated fatty acid synthesis by 50%.
• 4.4. At 10⁻⁹M T₃ concentrations non-insulin-stimulated fatty acid synthesis was increased by 200% in lean adipose tissue explants, but obese adipose expiants were not significantly affected under these conditions.
• 5.5. The addition of 10⁻⁹ M T₃ plus insulin to the explant media decreased fatty acid synthesis by 35% in both the lean and obese tissues.
• 6.6. The results also imply that the low T₃ status of the obese rat may be contributory to the elevated fatty acid synthesis observed in obese adipocytes.

     

The effects of oxalate and glucose on lipogenesis by isolated hepatocytes from normal and biotin-deficient chicks (Gallus domesticus)

• 1.1. Isolated hepatocytes synthesize fatty acids and cholesterol from lactate and acetate with lactate being the more effective substrate.
• 2.2. Biotin deficiency decreased fatty add synthesis from both substrates but stimulated cholesterogenesis.
• 3.3. Exposure of intact hepatocytes to oxalate inhibited fatty acid and cholesterol synthesis from lactate, this effect was enhanced in biotin-deficient chicks. A similar effect was not observed when acetate was the substrate.
• 4.4. Synthesis of fatty acids from lactate and acetate was stimulated by glucose, biotin deficiency increased this response. Cholesterogenesis was reduced in control but not biotin-deficient chicks.

     

Fatty acid composition of depot fats,and rumen wall of the camel (Camelus dromedarius

• 1.1. Fatty acid composition of depot fats (hump, subcutaneous, mesentry, abdomen, perinephric and peticardiac) and rumen wall of Camelus dromedarius were studied by gas-liquid chromatography.
• 2.2. All depot fats showed similar characteristics; major fatty acids found were palmitic, stearic, oleic and myristic. Small quantities of odd-numbered, palmitoleic, linoleic and linolenic acids were also present.
• 3.3. Fatty acid of rumen wall showed some differences from the general pattern.
• 4.4. Fatty acid composition of the camel is discussed in relation to that of other ruminants and monogastrics.