Glycerolipid biosynthesis in rat adipose tissue: VIII. Effect of obesity and cell size on [14C]acetate incorporation into lipids

[¹⁴C]Acetate incorporation into different lipid fractions was measured as a function of adipocyte size by using the larger and smaller adipocytes derived from Sprague-Dawley rats. In both the larger and smaller adipocytes, [¹⁴C]acetate was incorporated into phospholipid, diacylglycerol, free fatty acid and triacylglycerol fractions. Although the rates of lipid formation were significantly higher in the larger adipocytes compared to the smaller ones, the proportions of the various lipids formed from [¹⁴C]acetate did not change significantly as a function of cell size. In some experiments, isolated adipocytes derived from obese Zucker rats were fractionated further to isolate an adipocyte preparation which was similar in size to those obtained from lean animals. The matching adipocytes derived from lean and obese animals did not differ significantly with respect to lipid formation from [¹⁴C]-acetate. These studies suggest that the larger adipocytes are more active in lipogenesis from [¹⁴C]-acetate than the smaller ones and that the increased capacity of lipogenesis in obese adipose tissue noted proviously (Biochem. J., 170, 153–160, 1978) is not an intrinsic property of all the obese adipocytes, but is limited mainly to the larger adipocytes.     

Studies on cell proliferation in inguinal adipose tissue during early development in the rat

[2-¹⁴C] Thymidine was injected into rats aged 3, 5 and 10 days, and incorporation of the precursor into deoxyribonucleic acid (DNA) of the inguinal fat tissue was measured for short time periods. Using chromatographic procedures to measure the distribution of thymidine and its metabolites in the soluble fraction of the tissue, degradation of the precursor was found to be similar at all ages. The data indicate that thymidine was more rapidly utilized for DNA synthesis in 3-day-old rats than in older animals. When¹⁴C-thymidine was injected in vivo and adipocytes and stromal cells were then separated from the inguinal tissue of 3-and 5-day-old rats, the incorporation into DNA was significant in both types of cells already 30 min after pulse labeling. Stromal cells took up twice as much of label as the adipocytes. Furthermore, real incorporation into DNA was found in the adipocytes when incubated in vitro in a culture medium supplemented with¹⁴C-thymidine. The possibility is discussed that early in postnatal life adipocytes might synthesize DNA for further cell division.     

Effect of lactation on lipolysis in rat adipose tissue

The concentrations of nonesterified fatty acids and glycerol in rat parametrial adipose tissue increased at peak lactation. Adipose tissue from lactating rats showed higher rates of release of nonesterified fatty acids and glycerol when incubated in vitro than did tissue from nonlactating rats, but there was a substantial increase in the esterification of fatty acids during involution. These results support earlier evidence that fat reserves were mobilized during lactation.     

Effects of parathion on lipolysis in isolated rat adipose tissue cells

The effects of the pesticide, Parathion (0,0-diethyl 0-p-nitrophenyl thiophosphate) and various lipolytic and antilipolytic agents on lipolysis in adipose tissue were studied with isolated fat cells from rat epididymal fat pads. Lipolysis was measured as the release of free fatty acids into an albumin-bicarbonate medium. Parathion depressed lipolysis in a linear manner at concentrations ranging from 10⁻⁹ to 10⁻³M. At a concentration of 10⁻⁵M, Parathion depressed the lipolytic response to epinephrine (0.15 μg/ml) and slightly to cyclic 3′,5′-adenosine monophosphate (10⁻³ M) and enhanced the antilipolytic response to nicotinic acid (33 μM). It is possible that Parathion may interfere with adenyl cyclase activity. Scientific Contribution No. 400. Agricultural Experiment Station, University of Connecticut, Storrs, Conn. 06268.     

Effect of cancer cachexia on triacylglycerol/fatty acid substrate cycling in white adipose tissue

The effect of cancer cachexia on the TAG/FA substrate cycle in white adipose tissue was determined in vivo using the MAC16 murine model of cachexia. When compared with non-tumor-bearing animals, the rate of TAG-glycerol production was found to be increased almost threefold in animals bearing the MAC13 tumor, which does not induce cachexia, but was not further elevated in animals bearing the MAC16 tumor. In both cases TAG-glycerol production and de novo synthesis of TAG-FA were also increased above non-tumor-bearing animals. In animals bearing the MAC16 tumor, the TAG-FA rates were significantly higher than in animals bearing the MAC13 tumor. This suggests that the presence of the tumor alone is sufficient to cause an increase in cycling rate, and in the absence of an elevated energy intake (MAC16) this may contribute to the depletion of adipose tissue.     

Influence of particle size on densification and abnormal expansion of LTCC multilayer substrate

Abstract

Two series of LTCC (low temperature cofired ceramic) multilayer substrates were fabricated using glass powders with different particle sizes. The series with finer particle size always showed better densification properties. Abnormal expansion was found in the experimental samples as a result of the emergence and growth of a second crystalline phase, Al₃Si₂O₁₃.     

Lipids of cultured hepatoma cells: VI. Glycerolipid and monoenoic fatty acid biosynthesis in minimal deviation hepatoma 7288C

1-14C-Acetic, 1-14C-palmitic, or 1-14C-stearic acid was incubated with minimal deviation hepatoma 7288C cells grown in culture to assess: de novo fatty acid synthesis, oxidation, desaturation, and elongation of saturated fatty acids, as well as the ability of media fatty acids to serve as precursors of cellular glycerolipids. Distribution of radioactivity in the individual lipid classes and the various fatty acids of triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine was determined. The radioactivity among the monoenoic acid isomers derived from triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine was analyzed by reductive ozonolysis. Only small amounts of the labeled substrates were oxidized to carbon dioxide. Except for labeled stearic acid, which also was incorporated heavily into phosphatidyl inositol and phosphatidyl serine, most radioactivity was recovered in triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine. Synthesis of cholesterol and long chain fatty acids from labeled acetic acid demonstrated that these cells can perform de novo synthesis of fatty acids and cholesterol. Both labeled palmitic and stearic acids were desaturated to the corresponding delta9 monoenes, and palmitic and palmitoleic acids were elongated. The nexadecenoic acid fraction isolated from triglyceride, phosphatidyl choline, and phosphatidyl ethanolamine, when acetic or palmitic acid was the labeled substrate, showed that greater than 70 percent of the labeled acids were the delta9 isomer. Radioactivity of the octadecenoic acid fraction derived from labeled acetic or palmitic acids was nearly equally divided between the delta9 isomer, oleic acid, and the delta11 isomer, vaccenic acid. Desaturation of labeled stearic acid produced only oleic acid. These data demonstrate that the biosynthesis of vaccenic acid in these cultured neoplastic cells proceeds via the elongation of palmitoleic acid. The relatively high level of vaccenic acid synthesis in these cells suggests that the reported elevation of "oleic acid" in many neoplasms may result from increased concentration of vaccenic acid.     

Specific distribution of fatty acids in the triglycerides of rainbow trout adipose tissue. Influence of temperature

In the trout, the unsaturated fatty acids are preferentially located in the β-position and the saturated fatty acids in the α-position of triglycerides. This fatty acid distribution is retained even with diets containing lard. The fish are, therefore, able to modify completely the fatty acid distribution of dietary triglycerides. There is no retention of the β-monoglyceride structure during the biosynthetic processes. However, the modification of the dietary fatty acid distribution by the trout seems to be more difficult at 18 C than at 10C. Presented in part at the 13th World Congress of the International Society for Fat Research, Marseille, France, 1976.     

In vivo incorporation of lauric acid into rat adipose tissue triacylglycerols

An in vivo approach was taken to examine fatty acid esterification in adipose tissue using a coconut oilenriched diet. Rats were fed a diet containing cocounut oil (50% lauric acid) for six weeks. Triacylglycerols from perirenal adipose tissue were fractionated by silver nitrate-thin layer chromatography and, then, preparative gas chromatography. The distribution of 169 triacylglycerol types accounting for 97% of total triacylglycerols was determined. There was evidence for a very high content of mixed triacylglycerols composed of intermediate (12∶0 and 14∶0) and long acyl moieties. No significant differences were observed between the experimental distribution of triacylglycerol types and the random distribution, calculated from the total fatty acid composition. This indicated that most long chain triacylglycerols stored before coconut oil feeding would have been rearranged after the six weeks of coconut oil feeding. The experimental proportion of trilauroylglycerol reached 2%, as expected from its random proportion, and the proportions of dilauroylacylglycerols were slightly higher than the random values. Present results were compared with those previously obtained from triacylglycerols of adipose tissue of rats fed a low-fat standard diet (1,2). From our results and those of other authors, it is suggested that lauric acid is a good substrate forsn-glycero-3-phosphate acyltransferase and diacylglycerol acyltransferase in rat adipose tissue.     

Influence of age and body size on alarm responses in a freshwater snail Pomacea canaliculata

A hypothesis that size selection of prey by predators elicits size-specific responses from prey was examined. Freshwater snails, Pomacea canaliculata, ages 1, 3, 7, 15, 30, or 60 days, were given an extract of 3-day-old snails, and 3-day-old snails were given extracts of snails of the other ages or eggs. Snails 15 days or younger crawled out of the water in response to the 3-day-old snail extract, but older ones did not. The 3-day-old snails responded to the extracts of snails of all examined ages, but not to the extract of eggs. Snails of four size classes, 3-days-old, small (shell lengths 8–12 mm), medium (13–20 mm), and large (>28 mm) were given extracts of snails of each of these four classes. The 3-day-old snails crawled out of the water in response to the extract of 3-day-old snails, but showed a lower or no response to other extracts. Larger snails buried themselves in the soil in response to the extract of snails of similar sizes. These responses are discussed in the context of the evolution of the snail's avoidance behavior in response to the size-dependent prey choice by the predator.     

Autoxidation of tissue lipids. I. Incorporation of dietary fatty acids and formation of monocarbonyl compounds in adipose tissue lipids of the vitamin E-deficient rat

Male weanling rats were fed vitamin E-deficient and vitamin E-supplemented diets containing 5% corn oil or cod-liver oil for 16 weeks, after which their adipose tissue lipids were extracted and analyzed in a nitrogen atmosphere for carbonyl compounds and fatty acids. The vitamin E-deficient cod-liver oil-fed rats, exhibiting incisor depigmentation and darkened adipose tissue, yielded lipids which had a lower iodine value, contained less polyunsaturated fatty acids, and contained more carbonyl compounds, particularly alkanals and alk-2-enals, than the lipids from the animals fed the vitamin E-supplemented cod-liver oil diet. The tissues of the vitamin E-deficient corn oil-fed rats contained less linoleate and more monocarbonyl compounds than those of the vitamin E-supplemented corn oil-fed animals. The results indicate that vitamin E protection is necessary for the incorporation of C₂₀ and C₂₂ fatty acids into the tissues from the diet and that in the deficiency of vitamin E, a low level of autoxidation occurs in the tissues.     

Dietary diacylglycerol prevents high-fat diet-induced lipid accumulation in rat liver and abdominal adipose tissue

The inhibitory effects of 1,3-diacylglycerol (DAG) on diet-induced lipid accumulation in liver and abdominal adipose tissue of rats were investigated in the present study. Male Sprague-Dawley rats were given free access to diets containing 7 wt% TAG (low TAG), 20 wt% TAG (high TAG), or 20 wt% DAG (high DAG), respectively, for 8 wk. The body weight of rats in the 20% high-TAG group increased significantly, and the weights of their abdominal adipose tissue and liver also showed a significant increase compared with rats in the low-TAG group. However, the high-DAG diet resulted in both a significant reduction in body weight gain (with a decrease of 70.5%) and an increase in the ratio of abdominal fat to body weight (by 127%) compared with the high-TAG diet. As well, the liver TAG and serum TAG levels of the high-DAG group were significantly lower than those of the high-IAG group. These effects were associated with up-regulation of acyl-CoA carnitine acyltransferase (ACAT) and down-regulation of acyl-CoA DAG acyltransferase (DGAT) in the liver. However, no significant difference was observed in the activities of alanine aminotransferase and aspartate aminotransferase among the groups (P>0.05). The present results indicate that dietary DAG reduced fat accumulation in viscera and body, and these effects may be involved with up-regulation of ACAT and down-regulation of DGAT in the liver.     

Animal endogenous triglycerides: III. Swine,rat and chicken liver: Comparison with adipose tissue

The endogenous triglycerides of swine, rat and chicken livers were fractionated by silver ion thin layer chromatography and the resulting fractions were analyzed for their fatty acid composition and distribution. Whereas the endogenous triglycerides of swine adipose tissue differ markedly from those of rat and chicken adipose tissue in the location of the major fatty acids, the liver triglycerides of the three species are quite similar. They also resemble rat and chicken adipose triglycerides.     

Consumption of resistant starch decreases postprandial lipogenesis in white adipose tissue of the rat

Chronic consumption of diets high in resistant starch (RS) leads to reduced fat cell size compared to diets high in digestible starch (DS) in rats and increases total and meal fat oxidation in humans. The aim of the present study was to examine the rate of lipogenesis in key lipogenic organs following a high RS or DS meal. Following an overnight fast, male Wistar rats ingested a meal with an RS content of 2% or 30% of total carbohydrate and were then administered an i.p bolus of 50 μCi ³H₂O either immediately or 1 hour post-meal. One hour following tracer administration, rats were sacrificed, a blood sample collected, and the liver, white adipose tissue (WAT), and gastrocnemius muscle excised and frozen until assayed for total ³H-lipid and ³H-glycogen content. Plasma triglyceride and NEFA concentrations and ³H-glycogen content did not differ between groups. In all tissues, except the liver, there was a trend for the rate of lipogenesis to be higher in the DS group than the RS group which reached significance only in WAT at 1 h (p < 0.01). On a whole body level, this attenuation of fat deposition in WAT in response to a RS diet could be significant for the prevention of weight gain in the long-term.     

Steroids in bovine muscle and adipose tissue

Thin layer and gas liquid chromatography, (GLC) were employed as complementary techniques to investigate naturally-occurring steroids in the unsaponifiable matter of bovine muscle and adipose tissue. Three GLC liquid phases, differing in selective partition properties, were used to effectively identify unknown steroids. The results indicate that cholesterol and minor amounts of desmosterol, Δ⁷-cholestenol, lanosterol, dihydrolanosterol, dehydromethostenol, Δ⁸-methostenol, Δ⁷-methostenol, cholestanol and possibly ergosterol were present in the bovine tissues. The minor steroids, with the exception of cholestanol and ergosterol, are steroid precursors in cholesterol biosynthesis. Common hormonal steroids were not found in the unsaponifiables of the tissues.     

Effect of dietary linoleic acid content on the distribution of triacylglycerol molecular species in rat adipose tissue

The present study examined the effect of varying dietary linoleate intake (0.01, 0.24, 2.4, 24, 80 or 160 g/kg diet) for 24 weeks on the distribution of triacylglycerol (TG) molecular species in rat epididymal adipose tissue. Adipose TG fractions were purified by thin-layer chromatography and separated into different molecular species by reversephase high-performance liquid chromatography. The identification of TG species was based on fatty acid composition, retention time and the theoretical carbon number. When the dietary 18∶2n−6 content was equal to or less than 24 g/kg, no significant amounts of n−6 fatty acids (mainly 18∶2n−6) were observed in adipose tissue TG despite the fact that the levels of 20∶4n−6 in liver phospholipids increased significantly. There were 12 major molecular species in adipose tissue when the dietary 18∶2n−6 content was less than 2.4 g/kg. When the diteary 18∶2n−6 content reached 24 g/kg, an additional six TG species containing one, two or three molecules of 18∶2n−6 were observed. The levels of TG molecules containign two or three 18∶2n−6 residues were further increased when the diet contained very large amounts of linoleic acid (160 g/kg). Conversely, those TG species containing only one 18∶2n−6 residue became less abundant. It is suggested that the accumulation of these linoleate-rich TG molecular species in adipose tissue, particularly di- and trilinoleoyl containing TG, is the result of an adequate or an excessive intake of linoleic acid.     

Mass transfer and substrate utilization in biofilm reactors

Mass transfer within microbial films is described using Monod-type biological kinetics in terms of properties of packing material and the feed solution. For this purpose, computer techniques have been developed for the numerical evaluation of the normalized biofilm mathematical model. A second-order partial differential equation, describing the mechanisms of dispersion phenomena inside the liquid layer, was then solved to determine the mass transfer coefficient. The application of the theory to earlier experimental data has also been demonstrated.     

The distribution of labeled palmitic acid into the diglycerides and triglycerides of rat adipose tissue

After in vitro incubation of rat epididymal fat pads with radioactive palmitic acid, the distribution of the label in the different lipid classes and in different triglycerides was determined by silica gel and silver nitrate-silica gel thin-layer chromatography (TLC). The radioactivity of the diglycerides was approximately half of the triglycerides. This ratio did not change with alteration in the time of incubation. It remained unaltered even after a subsequent 10-min incubation in a nonradioactive medium. When the fat pads were incubated, first with¹⁴C-, then with³H-labeled palmitic acid, the³H/¹⁴C ratio was slightly lower in diglycerides than in triglycerides. The fully saturated molecules contained 38% of the radioactivity of triglycerides. Addition of oleic acid or norepinephrine to the labeled palmitic acid-containing medium decreased this value. Subsequent incubation with these compounds did not alter the distribution of radioactivity.     

Incorporation ofcis-octadecenoic acids into the rat liver mitochondrial membrane phospholipids and adipose tissue triglycerides

The incorporation of the dietarycis 18∶1 (n−12) andcis 18∶1 (n−10) into liver mitochondrial membrane phospholipids and adipose tissue trigly cerides was studied in 4 groups of rats fed diets containing 10 weight percent (wt%) of fat with the following contents of octadecenoic acids: 50%cis 18∶1(n−12) +9%cis 18∶1 (n−9); 25%cis 18∶1 (n−12)+32%cis 18∶1 (n−9); 50%cis 18∶1 (n−10)+10%cis 18∶1 (n−9); or 54%cis 18∶1 (n−9). Dietary linoleic acid was 3 wt% in all 4 groups. In the mitochondrial membranes, the isomeric octadecenoic acids were primarily incorporated into the 1-position of phosphatidylcholines and phosphatidylethanolamines at the expense of saturated fatty acids. The maximal incorporations observed in the 1-position of phosphatidylethanolamines were 4.8% 18∶1 (n−12) and 8.9% 18∶1 (n−10). No effects on the contents of polyunsaturated fatty acids in the phospholipids were seen. In the adipose tissue, the isomeric octadecenoic acids were incorporated at a level of 13%cis 18∶1 (n−12) or 23%cis 18∶1 (n−10), paralleled by a reduction in the content of oleic acid. Presented in part at the 9th Scandinavian Symposium on Lipids, Visby, Sweden, June 1977.