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 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In a study to determine the effect of saturation of fats on their ability to stimulate cholecystokinin (CCK) release six normal volunteers ate five test meals containing different fats with intervals of 1 week. Plasma CCK levels were measured by a specific radioimmunoassay and the gallbladder volume was calculated from ultrasound measurements. The sodium salt of the monounsaturated fatty acid oleic acid (3.5 g) produced a significantly greater integrated CCK response than that of the saturated fatty acid stearic acid (mean [SEM] 103 [41] vs 8[41] pmol.l-1.min). The gallbladder contracted to 42 (3)% of its initial volume after oleate but remained at 89 (8)% of its initial volume after stearate. Integrated CCK responses to dietary triglycerides (30 g) also differed significantly according to the degree of saturation--277 (58) pmol.l-1.min after corn oil (predominantly diunsaturated), 143 (14) pmol.l-1.min after olive oil (predominantly monounsaturated), and 44 (12) pmol.l-1.min after suet (predominantly saturated). The finding that unsaturated fats are stronger stimulants of CCK release than saturated fats may explain the promotion of pancreatic carcinogenesis in rats by unsaturated but not saturated fats and may support the role of CCK in this effect.
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PMID:Saturation of fat and cholecystokinin release: implications for pancreatic carcinogenesis. 257 43

Leukotoxin (9,10-epoxy-12-octadecenoate) biosynthesised from linoleate by neutrophils is highly toxic to cellular function. Its cardiovascular effects were studied in dogs together with the effects of various fatty acids. Aortic flow, left ventricular peak dP.dt-1, and aortic pressure were measured in 60 anaesthetised dogs, which were divided into 10 groups of six animals each--namely, control group (10 ml of physiological saline), three leukotoxin groups (5, 10, and 50 mg.kg-1), two linoleic acid groups (10 and 50 mg.kg-1), two oleic acid groups (10 and 50 mg.kg-1), and two stearic acid groups (10 and 50 mg.kg-1). Leukotoxin injected intravenously depressed cardiac function in a dose dependent manner. Administration of leukotoxin 5 mg.kg-1 showed no significant cardiotoxic effect. However, 10 mg.kg-1 of leukotoxin significantly decreased aortic flow from 0.74(0.04) to 0.40(0.07) litre.min-1 (mean(SEM], left ventricular peak dP.dt-1 from 2040(205) to 1140(217) mmHg.s-1, and aortic pressure from 106(7.1)/67(6.3) to 75(9.2)/48(6.5) mmHg 5 min after injection. Dogs given leukotoxin 50 mg.kg-1 showed more pronounced cardiodepressive effects; aortic flow was decreased to 0.19(0.06), left ventricular dP.dt-1 to 560(134), and aortic pressure to 72(15.1)/41(10.6) 5 min after injection. All dogs in this group were dead within 45 min. Administration of 10 mg.kg-1 of linoleic acid, oleic acid, or stearic acid caused no significant haemodynamic changes. Administration of linoleic acid 50 mg.kg-1 had cardiotoxic effects, but the effect was less than that of leukotoxin. Since leukotoxin appears to be a potent cardiodepressive agent it may be an important factor in the development of heart failure observed in patients with severe burns.
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PMID:Cardiovascular effects of leukotoxin (9, 10-epoxy-12-octadecenoate) and free fatty acids in dogs. 316 45

Intestinal absorption of ingested [1-13C]stearic, [1-13C]oleic, and [1-13C]linoleic acid was compared in six healthy men. A bolus of each [1-13C]-labeled fatty acid was ingested in random order at 72-hour intervals with the breakfast meal. Subjects consumed fixed diets during a 9-day fecal collection period. Pooled 9-day fecal samples were homogenized and total fat extracted. Fat extracts were saponified and methylated, and individual fatty acids were quantitated by gas-liquid chromatography. Preparative high-performance liquid chromatography was used to obtain fractions containing stearic, oleic, and linoleic acid for combustion to CO2 and assay of 13C enrichment over background. Prelabel period 24-hour samples were treated similarly to measure background 13C abundance. Total fatty acid and stearic, oleic, and linoleic acid excretion (+/- SEM) in the six volunteers over the 9-day period was 41.5 +/- 7.3, 10.0 +/- 1.3, 8.8 +/- 2.9, and 0.8 +/- 0.1 mg/day/kg body weight, respectively. The absorption efficiency for [1-13C]stearic, [1-13C]oleic, and [1-13C]linoleic acid was 78.0% +/- 4.5%, 97.2% +/- 1.7%, and 99.9% +/- 0.1%, respectively. The reduced absorption of [1-13C]stearic acid observed emphasizes the importance of correcting breath test oxidation data for fecal loss of 13C substrate. The potential application of our method to other areas of intermediary metabolism is discussed.
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PMID:Absorption of 13C-labeled stearic, oleic, and linoleic acids in humans: application to breath tests. 399 17

Results in epidemiological and experimental studies suggest that a diet rich in saturated fat may affect insulin sensitivity. However, no published data are available on the effect of stearic acid in this respect. Therefore, we examined the effects of a high-stearic acid diet and a high-oleic acid diet on glucose metabolism, serum lipids and lipoproteins, and blood coagulation factors in 15 healthy female subjects. Subjects followed the two experimental diets for 4 weeks according to a randomized crossover design. Both experimental diet periods were preceded by consumption of a baseline diet for 2 weeks. The diets provided 36% of energy (E%) as fat. In the experimental diets, 5 E% stearic or oleic acid was substituted for 5 E% of saturated fatty acids in the baseline diet. After the experimental diets, no differences were found in the insulin sensitivity index (mean+/-SEM, 5.4+/-1.9 v 5.2+/-1.6 x 10(-4) min(-1) x microU(-1) x mL(-1), nonsignificant [NS]), glucose effectiveness (0.026+/-0.006 v 0.026+/-0.003 min(-1), NS), or first-phase insulin reaction ([FPIR] 368+/-57 v 374+/-66 mU/L x min, NS). The concentration of serum lipids and lipoproteins and blood coagulation factors did not differ after the diet periods. In conclusion, a diet rich in stearic acid did not deteriorate glucose tolerance or insulin action in young healthy female subjects as compared with a diet rich in oleic acid.
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PMID:A high-stearic acid diet does not impair glucose tolerance and insulin sensitivity in healthy women. 959 42

The preparation and characterization of thick (9 microns), clear, mechanically robust and photocatalytically active films of nanocrystalline anatase titania are described. XRD and SEM analysis show the films comprise 13 nm particles of anatase TiO2. Thin (54 nm) films of the 'paste' TiO2, along with sol-gel titania films made by a more traditional route are also prepared and characterised. All titania films mediate the photocatalytic destruction of stearic acid with a quantum yield of 0.0016 +/- 0.0003, using either 365 nm (i.e. BLB) or 254 nm (germicidal) light. P25 TiO2 films also appear to mediate the same process with a similar formal quantum efficiency. Of all the films tested, the thick paste TiO2 films are the most ideally suited for use with near UV light, for reasons which are discussed. All the titania films tested exhibit photoinduced superhydrophilicity.
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PMID:Preparation and characterisation of novel thick sol-gel titania film photocatalysts. 1280 83

Static secondary ion mass spectrometry (SIMS) is introduced as an analytical technique for the examination of paint cross sections to obtain simultaneous information about the nature and distribution of pigments and the binding medium from a single sample. A sample taken from the virgin's blue robe in the panel painting The Descent from the Cross (Museo del Prado, Madrid) of the Early Netherlandish painter Rogier van der Weyden (1399/1400-1464) was selected for investigation. Data were compared with reference compounds and reference lead white linseed oil paint and egg tempera paint. The static SIMS technique gave position-sensitive mass spectra that were used to image the elemental distribution of pigments and the molecular signature of components of the oleaginous binding medium. SIMS ion images of sodium and aluminum superimposed with the blue pigment ultramarine and those of copper, lead, and calcium with the position of the mineral pigments of azurite, lead white, and chalk, respectively. Preserved monocarboxylic acids of palmitic and stearic acids present as fatty acids and fatty acid lead soaps pointed to the use of linseed oil as a binding medium. Images from the oleaginous binding medium fatty acids show a correlation with the three main paint layers. The observed palmitic/stearic acid ratios for the two ultramarine layers and azurite layers are 1.3, 1.4, and 1.8, respectively. Fatty acids and fatty acid soaps show highest ion yields near lead white, a mineral pigment that serves as a natural chemical drier and is proposed to act as a template for the initial grafting of the polyunsaturated triglycerides of the linseed oil. Almost no fatty acids were detected in other layers visible by light microscopy. The fatty acid lead soaps point toward a mature ionomeric oil paint system that developed over centuries. SIMS evidence for egg tempera, still used in the 15th century, is not detected in the paint cross section. SIMS images correlate well with SEM/EDX, FT-IR and light microscopic images and the SIMS spectral data additionally support the identification of pigment particles, lead soaps, and other binding medium components.
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PMID:Imaging secondary ion mass spectrometry of a paint cross section taken from an early Netherlandish painting by Rogier van der Weyden. 1498 95

Adsorption equilibrium of stearic acid onto natural bentonite with Turkish origin was studied at the temperatures of 298, 308 and 318 K. SEM and XRD analysis show that the bentonite used as adsorbent is composed of microcrystal and porous structure. The specific surface area was determined by BET method as 38.6 m(2)/g. The adsorption of stearic acid onto bentonite was conformed to the Langmiur and Freundlich isotherms. The equilibrium parameter, R(L) revealed that the bentonite is a good adsorbent for stearic acid. The sorption capacity of bentonite studied decreases with increasing temperature. However, it is concluded that the adsorption capacity of bentonite for the stearic acid under the same experimental conditions is in comparable level in terms of that of the rice husk ash given in literature. Thermodynamic parameters, DeltaG(ads) degrees , was calculated to be between -21.8 and -22.8 kJ mol(-1). DeltaH(ads) degrees and DeltaS(ads) degrees were found to be -9.2 kJ mol(-1) and 42.4 J mol(-1)K(-1), respectively. These parameters obtained as a function of temperature indicate that the adsorption of stearic acid onto bentonite was a spontaneous and an exothermic process. An FT-IR study on the adsorbed material was used to verify the interaction of the stearic molecule with bentonite after adsorption process.
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PMID:Adsorption thermodynamics of stearic acid onto bentonite. 1638 45

Stearic acid and triethanolamine (TEA) in a molar ratio of 2:1 were mixed in aqueous solution at 80 degrees C and subsequently cooled to ambient temperature. The structural evolution of the resultant sample during storage was characterized by using light microscopy, Cryo-SEM, differential scanning calorimetery, pH, infrared spectroscopy, elemental analysis, and simultaneous small and wide-angle X-ray diffraction. It was found that a lamellar liquid crystalline phase was formed when stearic acid and TEA solution were mixed at 80 degrees C and multilamellar spheres of a few microns diameter were formed initially after cooling. A hydrolysis reaction (i.e., the reverse reaction of neutralization between stearic acid and TEA) occurred thereafter that caused the breakdown of the lamellar gel phase and the formation of platelet stearic acid crystals. Three polymorphs of stearic acid (defined following previous work as the A, C, and E forms) were formed as the result of hydrolysis reaction, which gave rise to a strong optically pearlescent appearance.
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PMID:Interaction of the acid soap of triethanolamine stearate and stearic acid with water. 1726 56

The Langmuir monolayer is widely regarded as a model for investigating biomineralization on biological membranes, but so far the crystallization process has been elusive. In this work, we study the crystallization process of CaCO(3) on a stearic acid monolayer at the air-water interface by in situ Brewster angle microscopy and ex situ electron microscopy. It is shown that the final CaCO(3) crystals are transformed from a particle precursor rather than directly from the solvated ions under the compressed stearic acid monolayer. SEM and TEM images reveal that the precursors are uniform spherical particles of amorphous calcium carbonate (ACC) with sizes smaller than 100 nm. The amorphous particles are produced in an early stage of mineralization and can be stabilized for at least 0.5 h. Subsequently, the ACC particles tend to aggregate with increasing population and are eventually transformed into the crystalline calcite phase with the elapse of time. This work is the first to clarify the crystallization process of calcium carbonate under the monolayer at the air-water interface by a direct observation of the ACC and therefore establish the roles of stearic acid in the process.
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PMID:Observation of an amorphous calcium carbonate precursor on a stearic acid monolayer formed during the biomimetic mineralization of CaCO(3). 1909 53

Perovskite-type LaMnO(3) and La(0.8)Sr(0.2)MnO(3) with high specific surface areas were prepared by stearic acid gel combustion method. The obtained powders were characterized by XRD, FT-IR, SEM and XPS techniques. Their catalytic activities were investigated on thermal decomposition of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) by TG-DSC techniques. The experimental results show that LaMnO(3) is a more effective catalyst than La(0.8)Sr(0.2)MnO(3) for the sublimation and melting process of RDX because of its higher concentration ratio of surface-adsorbed species. And the catalytic activity of La(0.8)Sr(0.2)MnO(3) is higher than that of LaMnO(3) for thermal decomposition of liquid RDX. This could be attributed to its higher concentration ratios of surface oxygen and Mn(4+)/Mn(3+). In conclusion, the concentration ratios of surface oxygen and Mn(4+)/Mn(3+) could play key roles for RDX thermal decomposition. This study points out a potential way to develop new and more active perovskite-type catalysts for the RDX thermal decomposition.
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PMID:Combustion synthesis and effect of LaMnO3 and La0.8Sr0.2MnO3 on RDX thermal decomposition. 2006 Feb 10


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