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At least 19 recordsLinked to original sources
PubMed1981

Differential diagnosis of maldigestion and malabsorption of fat. II. Comparison of 131I-triolein with 14C-triolein in normal, pancreatic juice-deficient, short bowel and bile-deficient dogs.

To determine whether or not purified 131I-triolein produces the same behavior as 14C-triolein in the intraluminal phase, and to assess whether or not 0.10 +/- 0.02 of the Digestion-Absorption Index (DAI) obtained from clinical cases is an adequate value for differentiating maldigestion from malabsorption of fat, dogs, pancreatic juice-deficient, short bowel and bile-deficient were prepared. Both the pancreatic juice-deficient and bile-deficient groups indicated a high fecal excretion of 14C- and 131I-radioactivity, and the short bowel group indicated a moderate fecal excretion of fat. Daily fecal fat levels in each group were in parallel to the 3-day fecal excretion of radioactivity. However, the Digestive-Adsorption Index of the pancreatic juice-deficient group of 0.602 in 14C and 0.620 in 131I, and indicated that a considerable portion of the ingested triolein was excreted into the feces without hydrolysis. DAI in the short bowel group were 0.020 in 14C and 0.022 in 131I, and in the bile-deficient group, the indices were 0.031 in 14C and 0.021 in 131I. Both latter groups showed a malabsorptive defect. Additionally, the Digestion-Absorption Index of the pancreatic juice-deficient group was higher than 0.10 +/- 0.02 of the clinical borderline mentioned in the foregoing paper, and that of the other two groups was lower. Therefore, this borderline may represent adequate values for the differentiation of fat malassimilation. On the other hand, it was confirmed that 14C-triolein and 131I-triolein showed similar behavior in the intraluminal phase, and that the 131I-triolein test was adequate for clinical testing for fat digestion and absorption.

Animals↗
PubMed2003

Accumulation of organochlorinated pesticides by triolein-containing semipermeable membrane device (triolein-SPMD) and rainbow trout.

An important advance in aquatic ecotoxicology is the development and application of biomimetic sampling technology for hydrophobic contaminants. In this paper, accumulation kinetics of five organochlorinated pesticides, i.e. hexachlorobenzene, lindan, aldrin, heptachlor epoxide and 4,4'-DDT, by triolein-containing semipermeable membrane device (triolein-SPMD) and by fish (rainbow trout) were compared in a laboratory continuous flow system. Accumulation kinetics of organochlorinated pesticides by the triolein-SPMD and by rainbow trout were linear during the exposure period of 20 d, except for lindan. Approach of an asymptote could be observed for lindan at the end of the exposure for rainbow trout. When the kinetic data were used to calculate the first-order uptake rate constants, it was found that the uptake rates of the chemicals in triolein-SPMD were 1-2.5 times higher than those in the fish. The estimated bioconcentration factors of the five pesticides in rainbow trout were in the range of 1000-7000 and the device concentration factor in the range of 1500-18000. Although equilibrium was not reached for most pesticides under 21-d exposure period, correlations between C(L)/C(w) and K(ow) (R(2)=0.887) and C(f)/C(w) and K(ow) (R(2)=0.931) could be observed which was a clear indication that triolein-SPMD accumulates chlorinated pesticides in a quite similar way as fish do. Our results show that triolein-SPMD could serve as a good surrogate for rainbow trout for simulating accumulations of chlorinated pesticides and may be used as a universal surrogate for fish in natural waters.

Animals↗
PubMed1984

Mechanism of action of lipoprotein lipase on triolein particles: effect of apolipoprotein C-II.

Triolein particles stabilized by a phosphatidylcholine monolayer were used to study the lipoprotein lipase (LpL) reaction. They were prepared in two different sizes and with triolein and phosphatidylcholine in the molar ratios of 0.9-1.2 : 1 (small particles) and 8-17 : 1 (large particles). The rate of hydrolysis by LpL of phosphatidylcholine on the surface of both lipid particles was only 1/20 as much as that of triolein, even if it was activated to the maximum by apolipoprotein C-II (apoC-II). Thus, the phospholipase activity of LpL was low enough to measure the initial rate of hydrolysis of triolein without causing a gross change of the surface of the lipid particle. When the hydrolysis of triolein by LpL was monitored, fatty acid was released at a constant rate until all of the triolein molecules were hydrolyzed. The enzyme required 220 +/- 17 and 66 +/- 9 nM apoC-II for its half-maximal activity (Km (apoC-II] with small and large particles as a substrate (1.15 mM triolein for small and 2.13 mM triolein for large particles), respectively, using various concentrations of LpL. The Km(apoC-II) values for these two substrates became similar when LpL activity was analyzed with respect to the density of apoC-II on the phosphatidylcholine monolayer at the surface of the particles (bound apoC-II/phosphatidylcholine). The concentration of substrate particles did not affect the Km(apoC-II) values. The presence of an adequate amount of apoC-II increased the maximal activity of LpL (Vmax(triolein)) from 0.48 +/- 0.21 to 6.81 +/- 0.45 and from 0.32 +/- 0.04 to 7.13 +/- 0.64 mmol/h/mg with a slight decrease in the apparent Michaelis constant (Km(triolein)) for small (from 90 to 54 microM triolein) and large (from 1.00 to 0.65 mM triolein) particles, respectively. Although the apparent Km for triolein in large particles was about ten times greater than that in small particles, the values became similar when they were corrected for the concentration of phosphatidylcholine (50-100 microM phosphatidylcholine), which corresponded to the surface area of the substrate particles. It was suggested that bound apoC-II molecules were transferred relatively slowly to other lipid particles while LpL molecules moved rapidly among the lipid particles.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed2004

Purification of triolein for use in semipermeable membrane devices (SPMDs).

Analyses of triolein-containing semipermeable membrane devices (SPMDs) have sometimes been impeded by interferences caused by impurities endemic to triolein that codialyze with the analytes. Oleic acid and methyl oleate have been the most troublesome of these impurities because of their relatively high concentrations in triolein and because significant residues of both can persist even after size exclusion chromatographic (SEC) fractionation. These residues have also been blamed for false-positive signals during bioindicator testing of SPMD dialysates. To prevent these problems, a simple, cost-effective procedure was developed for purifying triolein destined for use in SPMDs: the bulk triolein is repeatedly (6x) partitioned against methanol. Tests of the procedure show that 14C-oleic acid is completely removed from the triolein. After SEC fractionation, dialysates of standard-size SPMDs made with the purified triolein contain less than 5 microg of methyl oleate as compared to sometimes more than 500 microg for dialysates (also after SEC) of SPMDs made with unpurified triolein. Gas chromatographic analyses with flame ionization and electron capture detection show that the purification treatment also greatly reduces the number and size of peaks caused by unidentified contaminants in the triolein. Microtox basic assay of dialysates of SPMDs shows that those made with the purified triolein have lower acute toxicities than dialysates of SPMDs made with unpurified triolein. Yeast estrogen screen (YES) testing of SPMDs fabricated with unpurified and purified triolein demonstrates that the purification process removes all background estrogenic activity.

Biological Assay↗
PubMed1999

Triolein-induced pulmonary embolization and increased microvascular permeability in isolated perfused rat lungs.

BACKGROUND: The pathophysiologic mechanism of the fat embolism syndrome is poorly understood. This study was designed to determine the effects of fat emboli on pulmonary vasculature. METHOD: Triolein was infused into isolated rat lungs perfused with Krebs-Henseleit buffer. Pulmonary arterial pressure and microvascular permeability (Kf) were measured at baseline and 20 minutes after the triolein infusion. RESULT: The 99% triolein produced dose-dependent increases in both pulmonary arterial pressure and Kf. The 65% triolein, containing free fatty acid, resulted in a greater increase in Kf. Pretreatment with indomethacin attenuated the increase in Kf after 65% triolein but not after 99% triolein. CONCLUSION: Pure triolein induced mainly embolization in the pulmonary vasculature, and 65% triolein caused embolization and subsequently increased vascular permeability, which are, at least in part, mediated by the action of cyclooxygenase products. Free fatty acids might induce permeability edema by means of a cyclooxygenase-dependent mechanism. We conclude that triolein-induced increases in pulmonary arterial pressure and Kf in isolated rat lungs provides a useful model of acute lung injury by fat embolism.

1-Methyl-3-isobutylxanthine↗
PubMed2005

[Preparation of triolein-embedded CA membrane and its characteristics].

Triolein is successfully embedded into cellulose acetate (CA) by phase inversion. This prepared flat membrane can effectively remove trace lipophilic organic pollutants from water. Structure of hybrid membrane is mainly observed by scanning electron microscope (SEM). Triolein dispersion by mechanical rabbling and ultrasound are investigated. Ultrasound can more effectively strengthen triolein dispersion than mechanical rabbling. Effect of casting membrane temperature (room temperature, 0 degrees C) shows low temperature can help to forming smaller triolein droplets. In addition, interaction between triolein and CA belongs to physical mixing by the observation of FT-IR, accordingly triolein structure is not changed and adsorptive capacity for persistent organic pollutants is not affected. Triolein in hexane is analyzed by fluorometric measure. The results show that triolein is completely embedded into membrane, so it is impossible that triolein leaks into water in the process of the adsorption.

Adsorption↗
PubMed1981

Solubilization and localization of triolein in phosphatidylcholine bilayers: a 13C NMR study.

Cosonicated mixtures of egg phosphatidylcholine and small amounts (less than 5% wt/wt) of triolein have been studied by 13C NMR spectroscopy. The 50.3-MHz 13C NMR spectrum of vesicles preparations containing 90% isotopically substituted [1-13C]triolein showed two carbonyl resonances at chemical shift values that indicate hydrogen bonding of H2O molecules with the carbonyl groups. The extent of hydration, estimated from the chemical shift values that indicate hydrogen bonding of H2O molecules with the chemical shift values (173.07 ppm and 172.39 is approximately 50%. The data suggest that the triolein is located in the bilayer with the three carbonyl groups at the aqueous interface. The acyl chains are extended toward the bilayer interior, with a conformation of the glyceryl region such that the primary (alpha) carbonyls are closer to the aqueous medium than is the secondary (beta) carbonyl. Thus, triolein is present in the bilayer in an orientation appropriate for enzymatic hydrolysis, with the second substrate (H2O) in close proximity to the hydrolytic site, and with a conformation that could explain, in part, enzymatic specificity for hydrolysis at the alpha position. Spectra of vesicles containing greater than or equal to 3% triolein showed two additional carbonyl peaks characteristic of pure (neat) triolein. This allowed a determination of the maximum solubility (approximately 2.8%) of surface-oriented triolein in the bilayer phase. Beyond this limit all excess triolein partitions into a separate oil phase.

Hydrogen Bonding↗
PubMed1983

Solubilization of triolein and cholesteryl oleate in egg phosphatidylcholine vesicles.

The incorporation of cholesteryl oleate and triolein into phospholipid vesicles was studied in cosonicated mixtures of 94 weight % egg phosphatidylcholine and 6 weight % neutral lipid (0-6% triolein and 6-0% cholesteryl oleate). 13C NMR spectroscopy was used to quantitate both neutral lipids in vesicles containing 90% isotopically substituted [carbonyl-13C]cholesteryl oleate and [carbonyl-13C]triolein. Vesicles were also prepared with radiolabeled cholesteryl oleate and triolein and the composition of ultracentrifugal subfractions determined by chemical and radioisotopic methods. For a given starting composition, the incorporation of neutral lipids into vesicles was similar for vesicles prepared and analyzed by the two methodologies. The maximum solubility in vesicles prepared at 55 degrees C with a single neutral lipid was 3.1 weight % triolein (2.8 mol %) and 2.3 weight % cholesteryl oleate (2.8 mol %). In sonication mixtures with both triolein and cholesteryl oleate, the incorporation of each lipid into vesicles was proportional to the starting concentration; the total incorporation of neutral lipid was less than or equal to 4.0% (weight or mole per cent). The solubility limits were intermediate between the theoretical cases of complete additivity and complete competition. The [13C]carbonyl chemical shifts showed that the carbonyl groups of the vesicle-solubilized neutral lipids were close to the vesicle surface and that excess triolein and cholesteryl oleate partitioned into an oil phase containing both triolein and cholesteryl oleate.

Cholesterol Esters↗
PubMed1990

Uptake, incorporation and metabolism of (3H)triolein in the isolated perfused rabbit heart.

The purpose of these experiments was to study the uptake and metabolism of exogenous triglyceride in the isolated perfused rabbit heart. When infused into the rabbit heart, [9,10-3H(N)]triolein was retained and incorporated into a lipid fraction that had the chromatographic mobility of authentic triolein. Incorporation of labeled triolein was not likely to be the result of a lipoprotein lipase-mediated lipolysis/resynthesis cycle, since: (i) The distribution of radioactivity following administration of [3H]oleic acid was markedly different from the distribution of radioactivity following the administration of [3H]triolein; (ii) heparin was administered to the rabbits at the time of sacrifice; and (iii) the hearts were perfused with a protein-free buffer for 20 min prior to the labelling period. When isoproterenol was administered to hearts labelled with [3H]triolein, there was an increased output of total radioactivity, composed of labelled free fatty acids, diacylglycerol and monoacylglycerol. In these same hearts, there was an increased output of glycerol in response to isoproterenol. However, following the administration of bradykinin or angiotensin II, neither the radioactivity nor the glycerol content of the perfusate was changed. These data suggest that [3H]triolein is selectively incorporated into the triglyceride pool of the isolated perfused rabbit heart. Furthermore, this [3H]triolein is available to hormonally-activated lipolytic enzymes.

Angiotensin II↗
PubMed1983

Estimation of 14C-triolein assimilation from postprandial serum radioactivity of 14C.

In an attempt to establish a test of lipid assimilation, based on the measurement of the postprandial serum radioactivity of 14C from ingested 14C-triolein, the activity of 14C was measured in serum samples, drawn 1,2,3,4,6 and 9 h after ingestion in 48 consecutive patients suspected of malassimilation. Simultaneously, faecal excretion of 14C was measured to estimate 14C-triolein assimilation (F-14C-Ass). F-14C-Ass served as reference of 14C-triolein assimilation. The sum of the 2- and 4-h serum concentration of 14C (S-(2 + 4)14C) was found to be most useful as an estimate of 14C-triolein assimilation, with regard to both the diagnostic value and applicability. At a level of 1.0% of dose/l serum, S-(2 + 4)14C correctly discriminated between normal and reduced 14C-triolein assimilation in 83% of the patients (95% confidence limits 70-93%). A significant correlation between 14C-triolein assimilation and S-(2 + 4)14C was found (r = 0.91, P less than 0.001). Since 14C-triolein assimilation correlates closely with the assimilation of dietary lipids, S-(2 + 4)14C seems to provide in a simple way sufficient information about lipid assimilation to be useful as a clinical test.

Carbon Radioisotopes↗
PubMed1991

The [14C]-triolein breath test is not valid as a test of fat absorption.

The [14C]-triolein breath test is used as a test of fat absorption. However, its validity has not been established. The aim of this study was to investigate, whether the absorption of [14C]-triolein could be estimated from the breath test, and whether the breath test could be useful as a clinical test. The [14C]-triolein absorption was estimated from faecal measurements, using 51CrCl3 as non-absorbable marker. The breath test was done according to the standard technique with hourly estimations of the 14CO2 expiration. Fifty-one patients participated. A nearly perpendicular, curvilinear relation between the 6-h cumulative 14CO2 expiration and the [14C]-triolein absorption was found, and no obvious cut-off level for normal 14CO2 expiration could be identified. Accordingly, the diagnostic sensitivity of the breath test was 80% at the expense of a specificity of 45%. In 19 patients duplicate measurements were done. A high intra- and inter-individual variation in the fraction of absorbed [14C]-triolein, expired within 6 h, was found. It is concluded that expiration of 14CO2 is influenced by factors other than the absorption of [14C]-triolein, and that the [14C]-triolein breath test is not useful as test of fat absorption.

Breath Tests↗