Search results for "Acellular"

showing 10 items of 1986 documents

Docosahexaenoic acid and other fatty acids induce a decrease in pHiin Jurkat T-cells

2003

Docosahexaenoic acid (DHA) induced rapid (t1/2=33 s) and dose-dependent decreases in pHi in BCECF-loaded human (Jurkat) T-cells. Addition of 5-(N,N-dimethyl)-amiloride, an inhibitor of Na+/H+ exchanger, prolonged DHA-induced acidification as a function of time, indicating that the exchanger is implicated in pHi recovery. Other fatty acids like oleic acid, arachidonic acid, eicosapentaenoic acid, but not palmitic acid, also induced a fall in pHi in these cells. To assess the role of calcium in the DHA-induced acidification, we conducted experiments in Ca2+-free (0% Ca2+) and Ca2+-containing (100% Ca2+) buffer. We observed that there was no difference in the degree of DHA-induced transient ac…

Pharmacologychemistry.chemical_classificationmedicine.medical_specialtyIntracellular pHfood and beveragesFatty acidEicosapentaenoic acidchemistry.chemical_compoundEndocrinologychemistryBiochemistryBAPTADocosahexaenoic acidInternal medicinemedicinelipids (amino acids peptides and proteins)Arachidonic acidUnsaturated fatty acidPolyunsaturated fatty acidBritish Journal of Pharmacology
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Effect of two phenanthrene alkaloids on angiotensin II-induced leukocyte-endothelial cell interactionsin vivo

2003

The present study has evaluated the effect of two phenanthrene alkaloids, uvariopsine and stephenanthrine, on angiotensin II (Ang-II)-induced leukocyte–endothelial cell interactions in vivo and the mechanisms involved in their activity. Intravital microscopy within the rat mesenteric microcirculation was used. A 60 min superfusion with 1 nM Ang-II induced a significant increase in the leukocyte–endothelial cell interactions that were completely inhibited by 1 μM uvariopsine cosuperfusion. A lower dose of 0.1 μM significantly reduced Ang-II-induced leukocyte adhesion by 75%. When Ang-II was cosuperfused with 1 and 0.1 μM stephenanthrine, Ang-II-induced leukocyte responses were significantly …

Pharmacologychemistry.chemical_classificationmedicine.medical_specialtyReactive oxygen speciesPlatelet-activating factorSuperoxideLeukocyte RollingPharmacologyN-Formylmethionine leucyl-phenylalanineAngiotensin IIEndothelial stem cellchemistry.chemical_compoundEndocrinologychemistryInternal medicinemedicineIntracellularBritish Journal of Pharmacology
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Erythrocytäre Anionenkonzentrationen bei renaler Insuffizienz

1966

In chronic renal insufficiency, concentrations of chloride and inorganic phosphate in human red blood cells are elevated. There is no correlation between serum non-protein nitrogen and the anionic concentrations of red blood cells. Positive correlations exist between corresponding cellular and extracellular anionic concentrations.

Pharmacologymedicine.medical_specialtyChemistryCell BiologyChlorideCellular and Molecular NeuroscienceEndocrinologyInorganic phosphateBiochemistryInternal medicinemedicineExtracellularMolecular MedicineChronic renal insufficiencyMolecular Biologymedicine.drugExperientia
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pH-dependent hydrolysis of acetylcholine: Consequences for non-neuronal acetylcholine

2015

Acetylcholine is inactivated by acetylcholinesterase and butyrylcholinesterase and thereby its cellular signalling is stopped. One distinguishing difference between the neuronal and non-neuronal cholinergic system is the high expression level of the esterase activity within the former and a considerably lower level within the latter system. Thus, any situation which limits the activity of both esterases will affect the non-neuronal cholinergic system to a much greater extent than the neuronal one. Both esterases are pH-dependent with an optimum at pH above 7, whereas at pH values below 6 particularly the specific acetylcholinesterase is more or less inactive. Thus, acetylcholine is prevente…

Pharmacologymedicine.medical_specialtyHydrolysisImmunologyMetabolic acidosisHydrogen-Ion Concentrationmedicine.diseaseAcetylcholinesteraseEsteraseAcetylcholinechemistry.chemical_compoundEndocrinologychemistryButyrylcholinesteraseInternal medicineAcetylcholinesterasemedicineExtracellularHumansImmunology and AllergyCholinergicAcetylcholineButyrylcholinesterasemedicine.drugCalcium signalingInternational Immunopharmacology
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Formation of N-methylnicotinamide in the brain from a dihydropyridine-type prodrug

1999

The enhancement of brain choline levels is a possible therapeutic option in neurodegenerative diseases; however, brain choline levels are held within narrow limits by homeostatic mechanisms including the rapid clearance of excess choline from the brain. The present study tests whether N-methylnicotinamide (NMN), an inhibitor of the outward transport of choline from the brain, can elevate brain choline levels in vivo. As NMN does not cross the blood-brain barrier, we synthesized and administered the brain-permeable prodrug, 1,4-dihydro-N-methyl-nicotinamide (DNMN), and tested its effect on the levels of NMN and choline in brain extracellular fluid, using the microdialysis procedure. Administ…

Pharmacologymedicine.medical_specialtyMicrodialysisProdrugBlood–brain barrierBiochemistrychemistry.chemical_compoundmedicine.anatomical_structureCerebrospinal fluidEndocrinologychemistryBiochemistryInternal medicineExtracellular fluidBlood plasmamedicineExtracellularCholineBiochemical Pharmacology
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Effects of nitric oxide donors on cardiac contractility in wild-type and myoglobin-deficient mice

2002

1. The effects of the nitric oxide (NO) donors S-nitroso-N-acetylpenicillamine (SNAP), sodium(Z)-1-(N,N-diethylamino)diazen-1-ium-1,2-diolate (DEA-NONOate), and (Z)-1-[N-(2-Aminoethyl)-N-(2-ammonioethyl)amino]diazen-1-ium-1,2-diolate (DETA-NONOate) on force of contraction (F(c)) were studied in atrial and ventricular muscle strips obtained from wild-type (WT) and myoglobin-deficient (myo(-/-)) mice. 2. SNAP slightly reduced F(c) in preparations from WT mice at concentrations above 100 microM; this effect was more pronounced in myo(-/-) mice. 3. DEA-NONOate reduced F(c) in preparations from myo(-/-) mice to a larger extent than those from WT mice. 4. DETA-NONOate reduced F(c) in preparations…

Pharmacologymedicine.medical_specialtyWild typeSnapNitric oxideContractilitychemistry.chemical_compoundEndocrinologychemistryMyoglobinInternal medicinemedicineSoluble guanylyl cyclaseReceptorIntracellularBritish Journal of Pharmacology
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Control of oxidative metabolism in volume-overloaded rat hearts: effects of different lipid substrates.

1994

The relationship between intracellular energy parameters and myocardial O2 consumption (VO2) was studied in control and volume-overloaded hearts perfused with different lipid substrates and over a range of left ventricular work loads. In control hearts, a unique linear relationship between log of cytosolic [ATP]/[ADPf].[Pi] (where [ADPf] is concentration of free ADP) and myocardial VO2 was observed between low and high work loads for both fatty acids studied. In volume-overloaded hearts perfused in the presence of exogenous palmitate, the slope of the relationship between log [ATP]/[ADPf].[Pi] and myocardial VO2 was considerably depressed. It would seem that, under these conditions, much o…

PhosphocreatinePhysiologyRespiratory chainPalmitic AcidCardiomegalyPalmitic AcidsIn Vitro TechniquesVentricular Function LeftPhosphatesAdenosine TriphosphateOxygen ConsumptionPhysiology (medical)RespirationPiAnimalsRespiratory systemRats WistarATP synthasebiologyMyocardiumSubstrate (chemistry)HeartCreatineNADRatsAdenosine DiphosphateCytosolBiochemistrybiology.proteinCaprylatesCardiology and Cardiovascular MedicineEnergy MetabolismIntracellularThe American journal of physiology
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PRK1 phosphorylates MARCKS at the PKC sites: serine 152, serine 156 and serine 163

1996

AbstractThe 80kDa Myristolated Alanine-Rich C-Kinase Substrate (MARCKS) in a major in vivo substrate of protein kinase C (PKC). Here we report that MARCKS is a major substrate for the lipid-activated PKC-related kinase (PRK1) in cell extracts. Furthermore, PRK1 is shown to phosphorylate MARCKS on the same sites as PKC in vitro. Thus, control of MARCKS phosphorylation on these previously identified ‘PKC’ sites may be regulated under certain circumstances by PRK as well as PKC mediated signalling pathways. The implications for MARCKS as a marker of PKC activation and as a point of signal convergence are discussed.

PhosphopeptidesMARCKSPRKRecombinant Fusion ProteinsMolecular Sequence DataBiophysicsKidneyBiochemistryCell-free systemCell LineSerineStructural BiologyProtein kinase CGeneticsAnimalsAmino Acid SequenceBinding siteMARCKSPKCPhosphorylationMyristoylated Alanine-Rich C Kinase SubstrateMolecular BiologyProtein kinase CGlutathione TransferaseBinding SitesCell-Free SystemKinaseChemistryIntracellular Signaling Peptides and ProteinsMembrane ProteinsProteinsCell BiologyHaplorhiniPeptide FragmentsBiochemistryPhosphorylationElectrophoresis Polyacrylamide GelSignal transductionSequence AnalysisSignal TransductionFEBS Letters
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A comparison of spreading and motility behaviour of 8701-BC breast carcinoma cells on type I, I-trimer and type V collagen substrata. Evidence for a …

1991

Ductal infiltrating carcinoma (d.i.c.) of human breast is a highly invasive neoplasm characterized by enhanced deposition of collagen. Paradoxically, enhanced collagen deposition is not correlated with inhibition of the migration of tumour cells into the host tissue. d.i.c. is characterized by the reappearance of ‘embryonic’ type I-trimer collagen and an increase in type V collagen content in the matrix. The effects of these two collagen types were compared with type I collagen as culture substrata on the spreading pattern, cytoskeletal organization and motile behaviour of 8701-BC breast carcinoma cells using rhodamine-phalloidin staining, a DNAase I-competition assay, scanning electron mic…

PhotomicrographyStromal cellVideotape RecordingMotilityBreast NeoplasmsTrimerCell BiologyMatrix (biology)BiologyActinsCulture MediaExtracellular MatrixCell biologyCollagen type I alpha 1Carcinoma Intraductal NoninfiltratingCell MovementCell cultureImmunologyTumor Cells CulturedHumansCollagenNeoplasm MetastasisCytoskeletonType I collagenJournal of Cell Science
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Studying endocytosis in space and time by means of temporal Boolean models

2006

Endocytosis is a process by which cells carry traffic from the extracellular space into various intracellular compartments. Visualization of fluorescently tagged clathrin proteins (mediators of endocytosis) allows us to image endocytosis in real time. When imaging the plasma membrane, areas of fluorescence generated by different endocytic processes overlap spatially and temporally, forming random clumps. Here, a sequence of segmented clathrin spots is considered a realization of a non-isotropic 3D Boolean model. Estimates of the intensity, the mean perimeter and the density function of the durations of endocytic events are obtained.

PhysicsSpacetimebiologyBoolean modelEndocytic cycleEndocytosisClathrinArtificial IntelligenceSignal ProcessingExtracellularbiology.proteinBiophysicsComputer Vision and Pattern RecognitionSoftwareIntracellularPattern Recognition
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