Search results for "LIPOPOLYSACCHARIDE"

showing 10 items of 382 documents

Expression of membrane C1q in human monocyte-derived macrophages is developmentally regulated and enhanced by interferon-γ

2001

The present study investigated when during "in vitro" maturation macrophages (MPhi) express membrane C1q (mC1q), and whether cell activation affects expression and function of mC1q. Although C1q mRNA was repeatedly detected in freshly isolated monocytes using reverse transcriptase-polymerase chain reaction, C1q protein was observed only in developing MPhi from day 1 to 4 on using immunodetection and flow cytometry. However, the quantity of mC1q and other MPhi membrane proteins differed strikingly in cells from different donors. We report here for the first time that CD14(+) and CD14(-) mC1q-bearing MPhi can develop, and that interferon-gamma increases mC1q display at the cell surface, and m…

PhagocytosisCD14CellLipopolysaccharide ReceptorsBiophysicsMonocyte/macrophageComplementEnzyme-Linked Immunosorbent AssayBiologyLymphocyte ActivationBiochemistryFlow cytometryInterferon-gammaPhagocytosisStructural BiologyGeneticsmedicineHumansMolecular BiologyCells CulturedC1qMessenger RNAmedicine.diagnostic_testComplement C1qMacrophagesCell DifferentiationCell BiologyFlow CytometryPrecipitin TestsMolecular biologyIn vitromedicine.anatomical_structureGene Expression RegulationMembrane proteinDifferentiationCell activationFEBS Letters
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Inhibition of nitric oxide synthase abrogates lipopolysaccharides-induced up-regulation of L-arginine uptake in rat alveolar macrophages

2001

It was tested whether the inducible nitric oxide synthase (iNOS) pathway might be involved in lipopolysaccharides-(LPS)-induced up-regulation of L-arginine transport in rat alveolar macrophages (AM). AM were cultured in absence or presence of LPS. Nitrite accumulation was determined in culture media and cells were used to study [3H]-L-arginine uptake or to isolate RNA for RT - PCR. Culture in presence of LPS (1 microg ml(-1), 20 h) caused 11 fold increase of nitrite accumulation and 2.5 fold increase of [3H]-L-arginine uptake. The inducible NO synthase (iNOS) inhibitor 2-amino-5,6-dihydro-6-methyl-4H-1,3-thiazine (AMT) present alone during culture had only marginal effects on [3H]-L-arginin…

PharmacologyCellular immunityArginineLipopolysaccharideBiological activityBiologyMolecular biologyNitric oxide synthasechemistry.chemical_compoundBiochemistrychemistryEnzyme inhibitorbiology.proteinAmino acid transporterNitriteBritish Journal of Pharmacology
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Effect of partially modified retro-inverso analogues derived from C-reactive protein on the induction of nitric oxide synthesis in peritoneal macroph…

1997

The ability of three modified tetrapeptides, representing fragments of the C-reactive protein (CRP) sequence and stabilized in the first peptide bond by retro-inverso modification, to affect the secretion of nitric oxide (NO) was studied in macrophages of BALB/c mice. These tetrapeptides, resembling the aminoacid sequence of tuftsin (CRP I, H-gThr-(R,S)mLys-Pro-Leu-OH, ITF 1192; CRP II, H-gGly-(R, S)mLys-Pro-Arg-OH, ITF 1127; CRP III, H-gThr-(R,S)mLys-Pro-Gln-OH, ITF 1193), were able to induce NO synthesis by peritoneal macrophages in a dose-dependent manner; the most stimulating dose was 1000 ng ml−1 for CRP II and 100 ng ml−1 for CRP I and CRP III. NO synthesis was not strictly dependent …

PharmacologyCellular immunityLipopolysaccharideTuftsinBiologyMolecular biologyNitric oxideNitric oxide synthasechemistry.chemical_compoundchemistryBiochemistryPyrrolidine dithiocarbamatebiology.proteinOmega-N-MethylarginineTumor necrosis factor alphaBritish Journal of Pharmacology
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Ganodermycin, a novel inhibitor of CXCL10 expression from Ganoderma applanatum

2011

CXCL10 (inducible protein-10) is a highly inducible chemoattractant, which contributes to the recruitment of inflammatory cells, such as macrophages and T-lymphocytes, and thereby has important roles in chronic inflammatory conditions. In a search for new inhibitors of CXCL10 expression in MonoMac6 cells, a novel compound, designated as Ganodermycin, was isolated from fermentations of the basidiomycete Ganoderma applanatum. The structure was determined by a combination of spectroscopic techniques. Ganodermycin inhibited the lipopolysaccharide (LPS)/interferon (IFN)-γ-induced CXCL10 promoter activity in transiently transfected MonoMac6 cells in a dose-dependent manner with IC(50) values of 1…

PharmacologyLipopolysaccharidebiologyGanodermaChemotaxisTransfectionPharmacologybiology.organism_classificationMolecular biologychemistry.chemical_compoundGanoderma applanatumchemistryInterferonDrug DiscoveryProtein biosynthesismedicineCXCL10medicine.drugThe Journal of Antibiotics
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Influence of fructose 1,6-diphosphate on the lung antioxidant defenses of mice with endotoxemia.

1990

PharmacologyLipopolysaccharidesAntioxidantLungFructose 1 6 diphosphateFree RadicalsChemistrymedicine.medical_treatmentMice Inbred StrainsShock SepticAntioxidantsMicemedicine.anatomical_structureBiochemistrySalmonella enteritidismedicineFructosediphosphatesAnimalsFemaleLungPharmacological research
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Inhibition of arginase in rat and rabbit alveolar macrophages by Nω-hydroxy-D,L-indospicine, effects onL-arginine utilization by nitric oxide synthase

1997

1. Alveolar macrophages (AM phi) exhibit arginase activity and may, in addition, express an inducible form of nitric oxide (NO) synthase (iNOS). Both pathways may compete for the substrate. L-arginine. The present study tested whether two recently described potent inhibitors of liver arginase (N omega-hydroxy-D,L-indospicine and 4-hydroxyamidino-D,L-phenylalanine) might also inhibit arginase in AM phi and whether inhibition of arginase might affect L-arginine utilization by iNOS. 2. AM phi obtained by broncho-alveolar lavage of rat and rabbit isolated lungs were disseminated (2.5 or 3 x 10(6) cells per well) and allowed to adhere for 2 h. Thereafter, they were either used to study [3H]-L-ar…

PharmacologybiologyArginineLipopolysaccharideOrnithineMolecular biologyNitric oxideNitric oxide synthaseArginasechemistry.chemical_compoundmedicine.anatomical_structurechemistryBiochemistryEnzyme inhibitorbiology.proteinmedicinePulmonary alveolusBritish Journal of Pharmacology
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Effects of Kaempferol and Myricetin on Inducible Nitric Oxide Synthase Expression and Nitric Oxide Production in Rats

2010

Abstract:  When administered as drugs or consumed as food components, polyphenolic compounds synthesized in plants interfere with intracellular signal transduction pathways, including pathways of nitric oxide synthase expression. However, effects of these compounds in vivo do not always correlate with nitric oxide synthase-inhibiting activities revealed in experiments with cultured cells. The initial goal of this work was to compare effects of flavonoids kaempferol and myricetin on inducible nitric oxide synthase mRNA and protein expression monitored by real-time RT-PCR and immunohistochemistry and to evaluate the impact of these effects on nitric oxide production in rat organs measured by …

Pharmacologychemistry.chemical_classificationLipopolysaccharidebiologyGeneral MedicineToxicologyNitric oxideIntracellular signal transductionNitric oxide synthasechemistry.chemical_compoundEnzymechemistryBiochemistrybiology.proteinMyricetinSignal transductionKaempferolBasic & Clinical Pharmacology & Toxicology
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Enhanced expression of haem oxygenase-1 by nitric oxide and antiinflammatory drugs in NIH 3T3 fibroblasts

2000

Haem oxygenase-1 (HO-1) can exert protective effects against oxidative stress and inflammation. Fibroblasts participate in inflammatory responses where they produce high levels of prostaglandins (PGs) and nitric oxide (NO). However, little is known of the presence of HO-1 in these cells and the possible interactions among these pathways. Incubation of cells with NO donors, spermine nonoate (SPNO) and S-nitroso-N-acetylpenicillamine (SNAP), induced a dose- and time-dependent expression of HO-1 protein. NO donors increased basal PGE2 release although they reduced PGE2 accumulated in the medium and cyclo-oxygenase (COX) activity when cells were stimulated with lipopolysaccharide (LPS). COX-2 p…

Pharmacologychemistry.chemical_classificationReactive oxygen speciesbiologyLipopolysaccharideEndogenyInflammationPharmacologymedicine.disease_causeNitric oxidechemistry.chemical_compoundMechanism of actionBiochemistrychemistrymedicinebiology.proteinmedicine.symptomEnzyme inducerOxidative stressBritish Journal of Pharmacology
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Erythromycin exertsin vivoanti-inflammatory activity downregulating cell adhesion molecule expression

2005

1. Macrolides have long been used as anti-bacterial agents; however, there is some evidence that may exert anti-inflammatory activity. Therefore, erythromycin was used to characterize the mechanisms involved in their in vivo anti-inflammatory activity. 2. Erythromycin pretreatment (30 mg kg(-1) day(-1) for 1 week) reduced the lipopolysaccharide (LPS; intratracheal, 0.4 mg kg(-1))-induced increase in neutrophil count and elastase activity in the bronchoalveolar lavage fluid (BALF) and lung tissue myeloperoxidase activity, but failed to decrease tumor necrosis factor-alpha and macrophage-inflammatory protein-2 augmented levels in BALF. Erythromycin pretreatment also prevented lung P-selectin,…

Pharmacologymedicine.diagnostic_testLipopolysaccharideCell adhesion moleculeErythromycinPharmacologyBiologychemistry.chemical_compoundBronchoalveolar lavagechemistryIn vivoImmunologymedicineTumor necrosis factor alphaCell adhesionmedicine.drugAntibacterial agentBritish Journal of Pharmacology
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Effects of γ-Butyrobetaine and Mildronate on Nitric Oxide Production in Lipopolysaccharide-Treated Rats

2008

Production of nitric oxide was measured in lipopolysaccharide-treated rats (10 mg/kg, 4 hr) using the electron paramagnetic resonance method. As compared to the control animals, the nitric oxide level in liver of lipopolysaccharide-treated rats increased from 27.6+/-4.7 to 1485+/-129 ng/g tissue, in heart from 4.8+/-0.7 to 271+/-26 ng/g tissue, in blood from 33.6+/-12.4 to 638+/-136 ng/g tissue, in kidney from 3.3+/-0.5 to 356+/-31 ng/g tissue, in brain cortex from 46.0+/-3.4 to 227+/-27 ng/g tissue, in cerebellum from 27.7+/-2.6 to 218+/-30 ng/g tissue, and in testes from 13.8+/-1.1 to 86+/-8 ng/g tissue. Administration of the antiischaemic drug, mildronate (120 mg/kg) caused a significant…

Pharmacologymedicine.medical_specialtyKidneyCerebellumLipopolysaccharidebiologyGeneral MedicineToxicologyIn vitroNitric oxideNitric oxide synthasechemistry.chemical_compoundEndocrinologymedicine.anatomical_structurechemistryAnesthesiaInternal medicineCirculatory systemmedicinebiology.proteinCarnitinemedicine.drugBasic & Clinical Pharmacology & Toxicology
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