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  • 1
    ISSN: 1432-0428
    Keywords: Key words: Hyaluronan ; prostaglandin ; sulphated proteoglycan ; glycosaminoglycan ; mesangial cell.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Exposure in vivo or in vitro to elevated glucose increases production of vasoactive prostaglandins by glomeruli and mesangial cells. This study aimed to determine whether this increased prostaglandin production could provide a link with later structural changes in diabetic nephropathy. Glomerular cores were prepared from control rats and streptozotocin-diabetic rats (3 weeks' duration). Over 24 h in culture hyaluronan production from diabetic glomerular cores was higher than production from control glomerular cores whether maintained in 5.6 mmol/l glucose (105.6 ± 15.5 vs 53.6 ± 8.5 ng hyaluronan per 250 glomerular cores, p 〈 0.001); in 25 mmol/l glucose (149.3 ± 34.8 vs 62.7 ± 7.8 ng hyaluronan per 250 glomerular cores, p 〈 0.01); or in 45 mmol/l glucose (176.8 ± 23.3 vs 102.0 ± 17.9 ng hyaluronan per 250 glomerular cores, p 〈 0.01). At 5.6 mmol/l glucose, exposure in vitro to prostaglandin E2 caused an increase in hyaluronan production [maximal at 10 − 9 mol/l prostaglandin E2, 237 ± 19 vs 42 ± 4, ng hyaluronan per 250 glomerular cores, p 〈 0.001 (control) and 195 ± 7 vs 103 ± 5, ng hyaluronan per 250 glomerular cores, p 〈 0.001 (diabetic) ]. In both control and diabetic glomerular cores hyaluronan production was reduced significantly by the cyclooxygenase inhibitor indomethacin (10−5 mol/l) [24.7 ± 3.33 vs 40.25 ± 4.11 ng hyaluronan per 250 glomerular cores, p 〈 0.05 (control) and 36.5 ± 6.25 vs 118.0 ± 22.6, p 〈 0.01 (diabetic) ]. A direct spectrophotometric microassay was used to determine the concentration of sulphated glycosaminoglycans derived from papain-digested glomerular core proteoglycans. Release of sulphated glycosaminoglycans from diabetic glomerular cores maintained at 5.6 mmol/l glucose was decreased [41.9 ± 1.1 vs 54.0 ± 1.0 μg of sulphated glycosaminoglycans (chondroitin sulphate) per 250 glomerular cores p 〈 0.01]. A decrease in sulphated glycosaminoglycans was also shown from control glomerular cores maintained at 25 mmol/l glucose. At this glucose concentration, addition of exogenous hyaluronan or prostaglandin E2 significantly reduced sulphated glycosaminoglycans from control and diabetic glomerular cores. It is concluded that increased prostaglandin production secondary to high glucose environment can lead to an increased glomerular hyaluronan synthesis. This can substantially affect the levels of sulphated glycosaminoglycans in the extracellular matrix. We propose that these effects provide a possible link between the initial biochemical consequences of hyperglycaemia and later structural changes seen in the glomerulus in diabetes. [Diabetologia (1995) 38: 298–305]
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0428
    Keywords: Hyaluronan ; prostaglandin ; sulphated proteoglycan ; glycosaminoglycan ; mesangial cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Exposure in vivo or in vitro to elevated glucose increases production of vasoactive prostaglandins by glomeruli and mesangial cells. This study aimed to determine whether this increased prostaglandin production could provide a link with later structural changes in diabetic nephropathy. Glomerular cores were prepared from control rats and streptozotocin-diabetic rats (3 weeks' duration). Over 24 h in culture hyaluronan production from diabetic glomerular cores was higher than production from control glomerular cores whether maintained in 5.6 mmol/l glucose (105.6±15.5 vs 53.6±8.5 ng hyaluronan per 250 glomerular cores, p〈0.001); in 25 mmol/l glucose (149.3±34.8 vs 62.7±7.8 ng hyaluronan per 250 glomerular cores, p〈0.01); or in 45 mmol/l glucose (176.8±23.3 vs 102.0±17.9 ng hyaluronan per 250 glomerular cores, p〈0.01). At 5.6 mmol/l glucose, exposure in vitro to prostaglandin E2 caused an increase in hyaluronan production [maximal at 10−9 mol/l prostaglandin E2, 237±19 vs 42±4, ng hyaluronan per 250 glomerular cores, p〈0.001 (control) and 195±7 vs 103±5, ng hyaluronan per 250 glomerular cores, p〈0.001 (diabetic)]. In both control and diabetic glomerular cores hyaluronan production was reduced significantly by the cyclooxygenase inhibitor indomethacin (10−5 mol/l) [24.7±3.33 vs 40.25±4.11 ng hyaluronan per 250 glomerular cores, p〈0.05 (control) and 36.5±6.25 vs 118.0±22.6, p〈0.01 (diabetic)]. A direct spectrophotometric microassay was used to determine the concentration of sulphated glycosaminoglycans derived from papain-digested glomerular core proteoglycans. Release of sulphated glycosaminoglycans from diabetic glomerular cores maintained at 5.6 mmol/l glucose was decreased [41.9±1.1 vs 54.0±1.0 Μg of sulphated glycosaminoglycans (chondroitin sulphate) per 250 glomerular cores p〈0.01]. A decrease in sulphated glycosaminoglycans was also shown from control glomerular cores maintained at 25 mmol/l glucose. At this glucose concentration, addition of exogenous hyaluronan or prostaglandin E2 significantly reduced sulphated glycosaminoglycans from control and diabetic glomerular cores. It is concluded that increased prostaglandin production secondary to high glucose environment can lead to an increased glomerular hyaluronan synthesis. This can substantially affect the levels of sulphated glycosaminoglycans in the extracellular matrix. We propose that these effects provide a possible link between the initial biochemical consequences of hyperglycaemia and later structural changes seen in the glomerulus in diabetes.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 214 (1967), S. 1159-1159 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Direct contact appears to be essential for the demonstration of specific reactions between tissue cells and sensitized lymphocytes2-4. The intensity of these reactions has been attributed to the proportion of immunologically competent lymphocytes5 and to the antigenic pattern of the target cell6. ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical and experimental pharmacology and physiology 11 (1984), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 1. The removal of hyaluronic acid (HA) from the blood-stream was studied in four normal human subjects after injection of high molecular weight preparations labelled with 3H in the acetyl position. The plasma half-life of the injected material ranged between 2.5 and 5.5 min.2. The daily turnover of HA in the circulation was estimated to be at least 150 mg. Its elimination was predominantly extrarenal, the upper molecular weight limit for renal excretion being 25 000.3. Evidence for rapid degradation was provided by the identification of 3H2O in urine. Calculations from the specific activity of urinary 3H2O indicated that approximately 55% of the acetyl content of the injected HA was completely oxidized within 3 h, and 85% within the first day.4. It is concluded that hyaluronic acid in the amounts currently used for therapeutic purposes should not accumulate significantly in the circulation.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 25 (1969), S. 375-376 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Zusammenfassung Es wurde gefunden, dass rohe Calcitoninpräparate die Inkorporation von14C-Glucose in die Glycosaminoglycan-(GAG)-Synthese fördern. Unter denselben Zellkulturbedingungen wurde Calcitonin mit stark spezifischer Aktivität rasch inaktiviert und zeigte keine stimulierende Wirkung; wurde aber der Serumgehalt im Milieu stark eingeschränkt, so verursachte das Calcitonin (50 Einheiten/mg) eine hundertprozentige Erhöhung der14C-GAG-Synthese.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Rheumatology international 7 (1987), S. 267-269 
    ISSN: 1437-160X
    Keywords: Collagen antibodies ; HLA antigens ; Ross River virus disease ; Epidemic polyarthritis ; Rheumatoid arthritis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Antibody activity against collagen was measured in 53 samples of serum from 48 patients with active signs of epidemic polyarthritis (EPA) following infection with Ross River virus. Activity was higher against denatured collagen than against native collagen, but was within the normal range for each. Determination of HLA phenotypes permitted a search for any relationship between HLA type and differences in collagen antibody levels within the normal range. No relationship was detected with HLA antigens predominating in EPA or with HLA antigens that are associated with high collagen-antibody levels in rheumatoid arthritis (RA), which suggests that the latter associations may represent failure to control collagen antibody levels after the onset of RA. The findings also provide evidence against a role for nonspecific enhancement of humoral immune responses in the pathogenesis of EPA, and constitute a further point of distinction between EPA and RA.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Rheumatology international 8 (1988), S. 113-117 
    ISSN: 1437-160X
    Keywords: Ross River virus ; Polyarthritis ; Immune complexes ; Complement ; Rheumatoid factors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Immune complexes were sought in serum and synovial fluid in Ross River virus disease (epidemic polyarthritis). Multiple samples from 15 patients showing varied degrees of disease activity over a 3 month period were analysed for their content of complement components C3 and C4, and for C1q solid-phase and Raji cell binding activity. Levels of C3 and C1q binding activity were normal. C4 and Raji cell binding activity were normal except for three high levels of Raji cell binding, of which two were accompanied by low levels of C4, with normal C3 and C1q binding. Synovial fluid showed anomalous Raji cell reactivity of uncertain significance. Conglutinin solid-phase binding activity and IgG rheumatoid factor were compared in the serum of 20 patients during active disease and after recovery. The results were identical and within the normal range in both phases. One patient developed IgM rheumatoid factor in a low titre late in his illness. Although these findings do not entirely exclude a role for immune complexes formed at the onset in the circulation or tissues, it is concluded from this and other evidence that circulating complexes are not commonly responsible for the persistence of syndroms in this disease.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1437-160X
    Keywords: Synovial fibroblasts ; Morphology ; Prostanoids ; Mononuclear cells ; Interleukin 1
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Supernatant media from cultured human mononuclear blood leukocytes (MCCM) induced morphological changes in normal human synovial fibroblasts in culture, including the formation of cells with a dendritic or stellate morphology and, less frequently, cells with a striking fenestrated appearance. These changes were fully reversed within 1 h of removing the MCCM. They were inhibited by indomethacin, the glucocorticoids hydrocortisone, prednisolone and dexamethasone, and by colcemid, but not by actinomycin D and only weakly by cycloheximide. The morphological responses to MCCM could be reproduced by MCCM fractions containing interleukin 1-like activity and by purified forms of human interleukin 1 (IL-1), including monocyte-derived IL-1β and recombinant IL-1α. These responses were also inhibited by indomethacin, indicating a link with prostanoid production. However, the morphological responses were not related to the stimulation of plasminogen activator activity due to MCCM, MCCM fractions, or IL-1.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1435-1528
    Keywords: Viscoelastic behaviour ; Carreau model ; dynamic properties ; hyaluronic acid ; protein ; synovial fluid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract Steady-shear and dynamic properties of a pooled sample of cattle synovial fluid have been measured using techniques developed for low viscosity fluids. The rheological properties of synovial fluid were found to exhibit typical viscoelastic behaviour and can be described by the Carreau type A rheological model. Typical model parameters for the fluid are given; these may be useful for the analysis of the complex flow problems of joint lubrication. The two major constituents, hyaluronic acid and proteins, have been successfully separated from the pooled sample of synovial fluid. The rheological properties of the hyaluronic acid and the recombined hyaluronic acid-protein solutions of both equal and half the concentration of the constituents found in the original synovial fluid have been measured. These properties, when compared to those of the original synovial fluid, show an undeniable contribution of proteins to the flow behaviour of synovial fluid in joints. The effect of protein was found to be more prominent in hyaluronic acid of half the normal concentration found in synovial fluid, thus providing a possible explanation for the differences in flow behaviour observed between synovial fluid from certain diseased joints compared to normal joint fluid.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1437-160X
    Keywords: Synovial cells ; Prostacyclin ; Mononuclear cells ; Retinoic acid ; Rheumatoid arthritis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Fibroblast-like synovial cells, isolated from intact joints of non-arthritic human donors and from explants of rheumatoid and non-rheumatoid synovial tissue, released prostacyclin (PGI2) when incubated in conditioned medium from human peripheral blood mononuclear cells (MCCM). The effect of MCCM on the rate of PGI2 synthesis (measured by radioimmunoassay as the stable product, 6-keto-PGF1 α) was clearly established within 2 h and appeared to require RNA and protein synthesis as judged by inhibition with actinomycin D and cycloheximide, respectively. Low concentrations of dexamethasone suppressed the increase in PGI2 levels. Prostaglandin E2 (PGE2) levels were also raised by the MCCM and reduced by dexamethasone. All-trans retinoic acid did not stimulate the levels of either prostanoid. These findings offer an explanation for some of the inflammatory events occurring in rheumatoid lesions.
    Type of Medium: Electronic Resource
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