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1.
Iwona Komaniecka Katarzyna Susniak Adam Choma Holger Heine Otto Holst 《International journal of molecular sciences》2021,22(1)
The structure of lipid A from lipopolysaccharide (LPS) of Rhodomicrobium vannielii ATCC 17100 (Rv) a phototrophic, budding bacterium was re-investigated using high-resolution mass spectrometry, NMR, and chemical degradation protocols. It was found that the (GlcpN)-disaccharide lipid A backbone was substituted by a GalpA residue that was connected to C-1 of proximal GlcpN. Some of this GalpA residue was β-eliminated by alkaline de-acylation, which indicated the possibility of the presence of another so far unidentified substituent at C-4 in non-stoichiometric amounts. One Manp residue substituted C-4′ of distal GlcpN. The lipid A backbone was acylated by 16:0(3-OH) at C-2 of proximal GlcpN, and by 16:0(3-OH), i17:0(3-OH), or 18:0(3-OH) at C-2′ of distal GlcpN. Two acyloxy-acyl moieties that were mainly formed by 14:0(3-O-14:0) and 16:0(3-O-22:1) occupied the distal GlcpN of lipid A. Genes that were possibly involved in the modification of Rv lipid A were compared with bacterial genes of known function. The biological activity was tested at the model of human mononuclear cells (MNC), showing that Rv lipid A alone does not significantly stimulate MNC. At low concentrations of toxic Escherichia coli O111:B4 LPS, pre-incubation with Rv lipid A resulted in a substantial reduction of activity, but, when higher concentrations of E. coli LPS were used, the stimulatory effect was increased. 相似文献
2.
An unusual polar lipid component was found in some mushrooms and was isolated fromBoletus edulis. It has been identified as diacylglycero-4′-O-(N,N,N-trimethyl)-homoserine (DGTS) by its thin-layer chromatography (TLC) mobilities and staining behavior as well as by means
of infrared (IR) and nuclear magnetic resonance (1H NMR) spectroscopy and mass spectrometry. Identification of this lipid in mushrooms indicated that DGTS is widely distributed
among a diverse group of lower plants and may have chemotaxonomic significance for fungi. It is interesting that DGTS is a
component of some edible mushrooms commonly consumed in food. 相似文献
3.
Five cerebrosides (1–5), including three new ones named cortenuamide A (1), cortenuamide B (2), and cortenuamide C (3), were isolated from the fruiting bodies of the basid-iomycete Cortinarius tenuipes. The structures of those compounds were elucidated as (4E,8E)-N-d-2′-hydroxytetracosanoyl-1-O-β-d-glycopyranosyl-9-methyl-4,8-sphingadienine (1), (4E,8E)-N-d-2′-hydroxytricosanoyl-1-O-β-d-glycopyranosyl-9-methyl-4,8 sphingadienine (2), (4E, 8E)-N-d-2′-hydroxydocosanoyl-1-O-β-d-glycopyranosyl-9-methyl-4,8-sphingadienine (3), (4E, 8E)-N-d-2′-hydroxyoctadecanoyl-1-O-β-d-glycopyranosyl-9-methyl-4,8-sphingadienine (4), and (4E, 8E)-N-d-2′-hydroxypalmitoyl-1-O-β-d-glycopyranosyl-9-methyl-4,8-sphingadienine (5) by spectral and chemical methods. 相似文献
4.
Asperamides A (1) and B (2), a sphingolipid and their corresponding glycosphingolipid possessing a hitherto unreported 9-methyl-C20-sphingosine moiety, were characterized from the culture extract of Aspergillus niger EN-13, an endophytic fungus isolated from marine brown alga Colpomenia sinuosa. The structures were elucidated by spectroscopic and chemical methods as (2S,2′R,3R,3′E,4E,8E)-N-(2′-hydroxy-3′-hexadecenoyl)-9-methyl-4,8-icosadien-1,3-diol (1) and 1-O-β-d-glucopyranosyl-(2S,2′R,3R,3′E,4E,8E)-N-(2′-hydroxy-3′-hexadecenoyl)-9-methyl-4,8-icosadien-1,3-diol (2). In the antifungal assay, asperamide A (1) displayed moderate activity against Candida albicans. 相似文献
5.
Artur Muszyski Kol A. Zarember Christian Heiss Joseph Shiloach Lars J. Berg John Audley Arina Kozyr David E. Greenberg Steven M. Holland Harry L. Malech Parastoo Azadi Russell W. Carlson John I. Gallin 《International journal of molecular sciences》2021,22(7)
Granulibacter bethesdensis can infect patients with chronic granulomatous disease, an immunodeficiency caused by reduced phagocyte NADPH oxidase function. Intact G. bethesdensis (Gb) is hypostimulatory compared to Escherichia coli, i.e., cytokine production in human blood requires 10–100 times more G. bethesdensis CFU/mL than E. coli. To better understand the pathogenicity of G. bethesdensis, we isolated its lipopolysaccharide (GbLPS) and characterized its lipid A. Unlike with typical Enterobacteriaceae, the release of presumptive Gb lipid A from its LPS required a strong acid. NMR and mass spectrometry demonstrated that the carbohydrate portion of the isolated glycolipid consists of α-Manp-(1→4)-β-GlcpN3N-(1→6)-α-GlcpN-(1⇿1)-α-GlcpA tetra-saccharide substituted with five acyl chains: the amide-linked N-3′ 14:0(3-OH), N-2′ 16:0(3-O16:0), and N-2 18:0(3-OH) and the ester-linked O-3 14:0(3-OH) and 16:0. The identification of glycero-d-talo-oct-2-ulosonic acid (Ko) as the first constituent of the core region of the LPS that is covalently attached to GlcpN3N of the lipid backbone may account for the acid resistance of GbLPS. In addition, the presence of Ko and only five acyl chains may explain the >10-fold lower proinflammatory potency of GbKo–lipidA compared to E. coli lipid A, as measured by cytokine induction in human blood. These unusual structural properties of the G.bethesdensis Ko–lipid A glycolipid likely contribute to immune evasion during pathogenesis and resistance to antimicrobial peptides. 相似文献
6.
Kazimiera A. Wilk Ludwik Syper Bogdan Burczyk Adam Sokoŀowski Beata W. Domagalska 《Journal of surfactants and detergents》2000,3(2):185-192
A new group of nonionic dicephalic saccharide amides, N-dodecyl-N,N-bis[(3-d-gluconylamido)propyl]-amine, N-dodecyl-N,N-bis[(3-d-glucoheptonylamido)propyl]-amine, and N-alkyl-N,N-bis[(3-lactobionylamido)propyl]amines (alkyl: n-C12H25′
n-C16H33′, n-C18H37) were synthesized and characterized. Their structure and purity were confirmed by means of 1H and 13C nuclear magnetic resonance analysis and electrospray ionization mass spectrometry. Carbon spectra were verified using a
DEPT experiment. The surface and interfacial properties such as critical micelle concentration (CMC), standard free energy
of micellization, ΔG
CMC, surface excess concentration, ΓCMC, and surface area demand per molecule, A
CMC, were determined. The tertiary nitrogen atom seems to have a surprising effect on surfactnat packing at the interface. 相似文献
7.
Two antibacterial and xanthine oxidase inhibitory cerebrosides, one of which is chemically new, were characterized from the
chloroform-methanol (1∶1) extract of Fusarium sp. IFB-121, an endophytic fungus in Quercus variabilis. By means of chemical and spectral methods [IR, electrospray ionization MS (ESI-MS), tandem ESI-MS, 1H and 13C NMR, distortionless enhancement by polarization transfer, COSY, heteronuclear multiple-quantum coherence, heteronuclear
multiple-bond correlation, and 2-D nuclear Overhauser effect correlation spectroscopy], the structure of the new metabolite
named fusaruside was established as (2S,2′R,3R,3′E,4E,8E,10E)-1-O-β-d-glucopyranosyl-2-N-(2′-hydroxy-3′-octadecenoyl)-3-hydroxy-9-methyl-4,8,10-sphingatrienine, and the structure of the other was identified as
(2S,2′R,3R,3′E,4E,8E)-1-O-β-d-glucopyranosyl-2-N-(2′-hydroxy-3′-octadecenoyl)-3-hydroxy-9-methyl-4,8-sphingadienine. Both new and known cerebrosides, although inactive to
Trichophyton rubrum and Candida albicans, showed strong antibacterial activities against Bacillus subtilis, Escherichia coli, and Pseudomonas fluorescens, with their minimum inhibitory concentrations being 3.9, 3.9, and 1.9 μg/mL, and 7.8, 3.9, and 7.8 μg/mL, respectively. Furthermore,
both metabolites were inhibitory to xanthine oxidase, with the IC50 value of fusaruside being 43.8±3.6 μM and the known cerebroside being 55.5±1.8 μM. 相似文献
8.
New glycosphingolipid containing an unusual sphingoid base from the basidiomycete Polyporus ellisii 总被引:1,自引:0,他引:1
A new 9-methyl-sphinga-4,8-dienine-containing glucocerebroside (1), together with two additional known analogs, cerebrosides B and D, was isolated from the chloroform-soluble lipid fraction
of the ethanol and chloroform/methanol extract of the fruiting bodies of the basidiomycete Polyporus ellisli Berk. and characterized. The structure and relative stereochemistry of the new compound were identified as (2S,3R,4E,8E)-1-(β-d-glucopyranosyl)-3-hydroxy-2-[(R)-2′-hydroxyheptadecanoyl]amino-9-methyl-4,8-octadecadiene by means of spectroscopic (1H, 13C, and two-dimensional nuclear magnetic resonance; mass spectrometry) and chemical methods. 相似文献
9.
The phospholipid composition was determined for the amebocyte of the primitive arthropod Limulus polyphemus. The total fatty acid composition of the cells' lipids was analyzed by gas chromatography/mass spectrometry (GC/MS) of fatty
acid methyl esters (FAME). The FAME analysis revealed high levels of 20-carbon polyunsaturated fatty acids (PUFA), especially
arachidonic (20∶4n-6) and eicosapentaenoic (20∶5n-3) acids. Almost 20% of the total lipid profile was comprised of dimethyl
acetals of 16- to 20-carbon chain lengths, indicative of plasmalogens in the phospholipid pool. Phospholipids, analyzed by
high-pressure liquid chromatography, included phosphatidylethanolamine (PE), phosphatidylcholine (PC), phosphatidylserine
(PS), phosphatidylinositol (PI), sphingomyelin (SPH), and cardiolipin (CL). PE and PC levels predominated at 42.2 and 36.3%,
respectively. Smaller amounts of PS (9.0%) and PI (6.2%) were present, as well as low levels of SPH (4.6%), CL (1.6%), and
trace amounts of lysophosphatidylcholine. The major phospholipid species, PE, PC, PS and PI, were collected and their molecular
species were examined by electrospray-ionization mass spectrometry. The molecular species within the phospholipid classes
reflected the high levels of PUFA seen in the total lipid profile. PI was mainly composed of 18∶0a/20∶4. Over half of the PS consisted of 18∶0a/18∶1 and 18∶0a/20∶4. The major PE species were 20∶1p/20∶5, 20∶1p/20∶4, 18∶0p/20∶5, and 18∶0p/20∶4. PC had the largest distribution of molecular species, and its most abundant species were 16∶0e/20∶5, 16∶0e/20∶4, and 16∶0p/20∶4. The presence of 16∶0e/20∶4 is the first documentation of a specific precursor to platelet-activating factor in an invertebrate hemocyte. Note:
at the sn-1 position: [a=1=O-acyl, e=1-O-alkylether, and p=1-O-alk-1′-enyl (plasmalogen)]. 相似文献
10.
3-(3′,4′-Dihydroxyphenyl)-l-alanine (l-DOPA), which is synthesized in velvet bean (Mucuna pruriens), inhibits plant growth. The concentration of l-DOPA in soil is reduced by adsorption and transformation reactions, which can result in the reduction of its plant-growth-inhibitory
activity. To determine which part of the l-DOPA structure is involved in the adsorption and soil transformation reactions, we compared the kinetics of l-DOPA disappearance in a volcanic ash soil with that of l-phenylalanine (3-phenyl-l-alanine) and l-tyrosine (3-(4′-hydroxyphenyl)-l-alanine), compounds that are similar in structure to l-DOPA but do not have a catechol (o-dihydroxybenzene) moiety. l-Phenylalanine and l-tyrosine were not adsorbed and transformed in the soil at equilibrium pH values between 4 and 7. These results suggest that
the adsorption and transformation reactions of l-DOPA in the soil involve the catechol moiety and not the amino and carboxylic acid groups, which are common to all three
compounds. Like l-DOPA, (+)-catechin, another allelochemical that contains a catechol moiety, underwent adsorption and soil transformation
reactions. Thus, we concluded that the concentrations of allelochemicals bearing a catechol moiety in soils will decrease
rapidly owing to adsorption and transformation reactions, and this decrease will be faster in soils with a high pH value or
high adsorption ability. Owing to this decrease in concentration, allelopathic phenomena may not occur. 相似文献
11.
Akihiko Sugai Rie Sakuma Ikuko Fukuda Norio Kurosawa Yuko H. Itoh Kazuo Kon Susumu Ando Toshihiro Itoh 《Lipids》1995,30(4):339-344
The major ether-type lipid structures ofSulfolobus acidocaldarius (ATCC33909) were composed of caldarchaeol and calditoglycerocaldarchaeol. However, the characterization by nuclear magnetic
resonance spectroscopy and mass spectrometry showed that the structure of calditol in calditoglycerocaldarchaeol is not nonitol,
2-(1′,2′,3′-trihydroxypropyl)1,2,3,4,5,6-hexahydroxyhexane, but 2-hydroxymethyl-1-(2,3-dihydroxypropoxy),2,3,4,5-cyclopentanetetraol
with an ether linkage in the molecule. Such an intermolecular ether linkage was resistant, to BCl3 treatment, but nonresistant to 57% HI degradation treatment conducted at 100°C for 60 h, producting 2-hydroxymethyl-1,2,3,4,5-cyclopentanepentaol
from calditol as reaction product. Further, it was confirmed that the structure of calditol is essentially a derivative of
glycerol, and hydrocarbon chains were conjugated to the glycerol-like site in the structure. The calditol with an ether linkage
in the molecule suggested an important role regarding the properties of heat-resistance and acid-resistance observed inSulfolobales.
Presented at the international workshop on “Molecular Biology and Biotechnology of Extremophiles and Archaebacteria,” Wako,
Japan, August 1993. 相似文献
12.
The acceptance of Solanum surattenses as a host plant for the larvae of Manduca sexta was explained by the presence of feeding stimulants in foliage. Bioassay-guided fractionation of plant extracts resulted in the isolation of a highly active compound (1), which was identified as a furostan derivative {26-O-β-d-glucopyranosyl-(25R)-furosta-5-ene-3-β-yl-O-α-l-rhamnopyranosyl-(1″-2′)-O-α-l-rhamnopyranosyl-(1′″-3″)-O-β-d-glucopyranoside}. This compound has the same steroidal core substructure as that in a stimulant (indioside D) previously identified from potato foliage. However, the sugar substituents attached to the core are different. 相似文献
13.
Ling-Ling Yu 《Journal of Inorganic and Organometallic Polymers and Materials》2012,22(1):278-282
Two new metal–organic coordination polymers containing Mn(II) and Cd(II) with oxo-bridged and N-donor ligands, [Mn(oba)(2,2′-bipy)]
n
(1) and {[Cd(oba)(bib)]·H2O}
n
(2) [2,3′-H2oba = 2-(3-carboxyphenoxy)benzoic acid, 2,2′-bipy = 2,2′-bipyridine, and bib = 4,4′-bis(2-methylimidazole-1-ylmethyl)biphenyl],
have been prepared and characterized by elemental analysis, Fourier infrared spectroscopy, and X-ray diffraction. Complex
1 has a 3D supramolecular network constructed from 1D zigzag chain via π–π stacking interactions. Complex 2 features 1D ladder-like chain which consists of 1D helical arrays and bib pillars. Moreover,
photoluminescence properties of the bib ligand and the Cd(II) complex were investigated. 相似文献
14.
Recently, we have reported that anthocyanins show strong antioxidative activity, but no attention has been paid to anthocyanins
from the viewpoint of the reaction mechanism of alkylperoxyl radicals; therefore, we investigated the reaction products of
antioxidative anthocyanins (cyanidin 3-O-β-d-glucoside). Cyanidin 3-O-β-d-glucoside was reacted with 2,2′-azobis(2,4-dimet hylvaleronitrile) to generate the alkylperoxyl radicals, and the reaction
products were isolated by high-performance liquid chromatography. The products were identified as 4,6-dihydroxy-2-O-β-d-glucosyl-3-oxo-2,3-dihydrobenzofuran and protocatechuic acid. Based on reaction products, the antioxidative mechanism of
cyanidin 3-O-β-d-glucoside may be different from that of α-tocopherol; cyanidin 3-O-β-d-glucoside would produce another radical scavenger, as it would break down the structure and scavenge the radicals. 相似文献
15.
Dietary cyanidin 3-O-β-d-glucoside increases ex vivo oxidation resistance of serum in rats 总被引:1,自引:0,他引:1
The effect of dietary cyanidin 3-O-β-d-glucoside (C3G), a typical anthocyanin pigment, on the generation of thiobarbituric acid reactive substances (TBARS) during
serum formation ex vivo and susceptibility of serum to further lipid peroxidation was studied in rats. Rats were fed a diet containing C3G (2 g/kg)
for 14 d. Feeding C3G resulted in a significant decrease in generation of TBARS during serum formation. The serum from the
C3G-fed group showed a significantly lower susceptibility to further lipid peroxidation provoked by 2,2′-azobis (2-amidinopropane)hydrochloride
or Cu2+ than that of the control group. No significant differences were observed in serum phospholipid, triglyceride, esterified
cholesterol, and free fatty acid concentrations between the control and the C3G-fed groups. Concentrations of endogenous antioxidants
remaining in the serum after blood coagulation were not affected by the C3G feeding. These results demonstrate that feeding
C3G increases the ex vivo oxidation resistance of the serum without affecting serum endogeneous antioxidant levels, and reduces the TBARS generated
during serum formation without changing the concentrations of serum lipids. 相似文献
16.
Racemic heavy isotope analogs of 1-O-alkyl-sn-glycero-3-phosphocholine (lysoPAF) and 1-O-alkyl-2-O-acetyl-sn-glycero-3-phosphocholine (PAF) were prepared for use as internal standards to facilitate quantitative studies based on mass
spectrometry. Starting from pentadencane-1,15-diol andrac-glycerol-1,2-acetonide, a convergent synthesis of 1-O-[16′-2H3]hexadecyl and 1-O-[18′-2H3]octadecylrac-glycero-3-phosphocholine and their acetyl derivatives is described. Three deuterium atoms were introduced at the terminal
position of the 1-O-alkyl group by displacement of thep-toluensulfonyl group from 1-O-alkyl-15′-p-toluensulfonate and 1-O-alkyl-17′-p-toluensulfonate with [2H3]-methylmagnesium iodide. The 1-O-alkyl-17′-p-toluensulfonate was obtained by reaction of the 1-O-alkyl-15′-p-toluensulfonate with allylmagnesium bromide, followed by reductive ozonolysis and treatment withp-toluenesulfonyl chloride. The hydroxyl group at C-2 was protected by a benzyl group and removed at a late stage in the synthesis.
This provided the corresponding lysoderivatives or allowed preparation of racemic PAF by subsequent acetylation of the free
hydroxy group. The phosphocholine moiety was introduced at glycerol C-3 by reaction with bromoethyldichlorophosphate and trimethylamine.
The synthetic compounds were analyzed by FAB/MS and GC/NICIMS. They were shown to contain less than 0.6% protium impurity. 相似文献
17.
Two unusual lipid classes were detected by thin-layer chromatography in the neutral lipids derived from goat cauda-epididymal
sperm plasma membrane. The lipids were identified as wax esters and 1-O-alkyl-2,3-diacylglycerols based on chromatographic properties, identity of their hydrolysis products, and infrared/1H nuclear magnetic resonance spectral evidence. The membrane containedca. 3 and 5 μg/mg protein of wax esters and alkyldiacylglycerols, respectively. The relative proportions of wax esters and alkyldiacylglycerols
in the total neutral lipids were 1.5% and 2.4%, respectively. The lipids contained fatty acids with chain lengths of C14 to C22. The major fatty acids of the wax esters were 14∶0, 16∶0, 16∶1ω7, 18∶0 and 18∶1ω9. The fatty acids in alkyldiacylglycerol
were 16∶0, 18∶0, 22∶5ω3 and 22∶6ω3. Alkyldiacylglycerol was particularly rich in docosahexaenoic acid 22∶6ω3) representing
30% of the total fatty acids. The alcohols of wax ester were all saturated with C20–C29 carbon chains. The deacylated products derived from alkyldiacylglycerols were identified as hexadecyl, octadecyl and octadec-9′-enyl
glycerol ethers. 相似文献
18.
Seeds of oat (Avena sativa L.) were recently shown to contain significant quantities of a new hydroxy acid, (15R)-hydroxy-(9Z)-(12Z)-octadecadienoic acid (trivial name, avenoleic acid). In the present work, avenoleate was found to be mainly (63%) localized
in the glycolipid fraction of oat seed lipids. Fractionation of the glycolipids by thin-layer chromatography and reversed-phase
high-performance liquid chromatography revealed the presence of a main molecular species which accounted for 20% of the total
avenoleate content of oat seeds. Structural studies by chemical methods and mass spectrometry demonstrated that the avenoleate-containing
glycolipid was a galactolipid assembled of one molecule of avenoleic acid, two molecules of linoleic acid, two molecules of
D-galactose, and one molecule of glycerol. Degradation of the new galactolipid by chemical and enzymatic methods demonstrated
the localization of acyl chains, i.e., linoleate at sn-1 and linoleoylavenoleate at sn-2. Nuclear magnetic resonance spectroscopy gave independent support for this structure and also demonstrated that the two
galactoses formed an α-d-galactopyranosyl-1-6-β-d-galactopyranosyl moiety which was bound to the sn-3 position. Based on these experiments, the new galactolipid could be formulated as 1-[(9′Z),(12′Z)-octadecadienoyl]-2-[(15″R)-{9″'Z), (12″'Z)-octadecadienoyloxy}-(9″Z),(12″Z)-octadecadienoyl]-3-(α-d-galactopyranosyl-1-6-β-d-galactopyranosyl)-glycerol. Quantitatively, the amount of the avenoleate-containing galactolipid was of the same order of
magnitude as those of individual molecular species of digalactosyldiacylglycerol containing nonoxygenated acyl chains. The
content of the new galactolipid in oat seeds was 0.5–0.6 mg per g of seed. 相似文献
19.
Urszula Laska A. Wilk Irena Maliszewska Ludwik Syper 《Journal of surfactants and detergents》2006,9(2):115-124
In the search for environmentally safe surfactants made from inexpensive and renewable sources, the interest has mainly been
focused on new saccharide derivatives. This report describes the synthesis of newly designed nonionic gemini compounds comprising
two reduced sugar headgroups, two alkyl tails, and a 1,1′-ethylenebisurea entity as the spacer linking two amphiphilic glucose-derived
moieties. Thus, the series of N,N′-bis[(3-alkyl-3-deoxy-d-glucitol)ureido]ethylenediamines (bis(CnGT), with Cn=n-C9H9, n-C6-H13, n-C8H17, n-C10H21, or n-C12H25), were prepared using a convenient procedure starting from easily accessible reagents such as d-glucose, n-alkylamines, urea, and ethylenediamine. Their structure and purity were confirmed by means of elemental analysis, electrospray
ionization mass spectrometry, and 1H and 13C nuclear magnetic resonance spectroscopy. Additionally, the present contribution introduces selected properties of these
surfactants, including their thermotropic behavior and biological properties. The presence of two phase transition points,
determined using the differential scanning calorimetry method, indicates liquid-crystalline mesophase formation upon heating.
Furthermore, using the closed-bottle test (OECD Guideline 301D) as well as the biological oxygen demand test for insoluble
substances for biodegradability measurements, it has been concluded that the tested glucose-derived gemini structures achieve
more than 60% biodegradation after 64–75 test days. All tested surfactants were practically nontoxic to bacteria, yeast, and
molds. Owing to their fitting aggregation ability as well as their nontoxicity, they constitute an interesting group of surfactants
for various applications. 相似文献
20.
Indirect evidence has suggested that lipid peroxidation is associated with iron overload in vivo. As a measure of lipid peroxidation,
pentane expired in the breath of rats loaded with an accumulated dose of either 100 mg or 186–200 mg of iron injected intraperitoneally
as iron dextran was measured over a 7 to 8 week period, and the effect on pentane production of feeding antioxidant-supplemented
diets was determined. By the seventh week of feeding the diets, rats fed 0.3% L-ascorbic acid produced 17% less (P=0.03) pentane
than did rats fed the basal antioxidant-deficient diet, whereas rats fed 0.004% dl-α-tocopherol acetate produced 92% less
(P<0.001). After being fed the basal diet for 7 weeks, iron-loaded rats produced 76±9 pmol pentane/100 g body wt/min. When
synthetic antioxidants were added to the diet at a concentration of 0.25%, the order of effectiveness in decreasing pentane
production after 1 week was: N,N′-diphenyl-p-phenylenediamine > ethoxyquin > butylated hydroxyanisole > butylated hydroxytoluene > propyl gallate ∼ no antioxidant. After
removal of either ethoxyquin or N,N′-diphenyl-p-phenylenediamine from the diets for 1 week, pentane production increased to a high level. The total amount of lipid soluble
fluorophores in individual spleens of rats fed N,N′-diphenyl-p-phenylenediamine, ethoxyquin, dl-α-tocopherol acetate, ascorbic acid and no antioxidant were correlated significantly with
the corresponding total integrated amount of pentane produced by the individual rats over the 7 to 8 week period. This study
has provided some of the most direct evidence to date that lipid peroxidation is associated with iron overload in vivo. 相似文献