Search results for " potential"

showing 10 items of 2713 documents

The cortical representation of pain.

1999

Anatomical and physiological studies in animals, as well as functional imaging studies in humans have shown that multiple cortical areas are activated by painful stimuli. The view that pain is perceived only as a result of thalamic processing has, therefore, been abandoned, and has been replaced by the question of what functions can be assigned to individual cortical areas. The following cortical areas have been shown to be involved in the processing of painful stimuli: primary somatosensory cortex, secondary somatosensory cortex and its vicinity in the parietal operculum, insula, anterior cingulate cortex and prefrontal cortex. These areas probably process different aspects of pain in para…

Cerebral CortexSecondary somatosensory cortexPainFunctional imagingAnesthesiology and Pain Medicinemedicine.anatomical_structureStimulus modalityNeurologySomatosensory evoked potentialCerebral cortexNeural PathwaysmedicineAnimalsHumansNeurology (clinical)PsychologyPrefrontal cortexInsulaNeuroscienceAnterior cingulate cortexPain
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Synthesis and inhibitory activity of dimethylamino-chalcone derivatives on the induction of nitric oxide synthase.

2002

A series of nine dimethylamino-chalcone derivatives (1,3-diaryl-propenones) was synthesized and screened as potential inhibitors of NO and PGE(2) production in the RAW 264.7 macrophage cell line. 4-Dimethylamino-2',5'-dimethoxychalcone (6) was found to be the most potent and dual inhibitor (IC(50s) in the submicromolar range) of NO and PGE(2) production. 2',6'-Dimethoxylation appeared to be an effective requirement for selective and potent inhibition of nitric oxide synthase induction as it was confirmed by Western blot analysis. Chalcone (6) at 25 mg kg(-1) by oral route, inhibited significantly the formation of oedema in the carrageenan-induced model of inflammation in mice.

ChalconeAnti-Inflammatory AgentsDrug Evaluation PreclinicalAdministration OralNitric Oxide Synthase Type IIInflammationInhibitory postsynaptic potentialChemical synthesisDinoprostoneNitric oxideCell Linechemistry.chemical_compoundMiceStructure-Activity RelationshipChalconeWestern blotDrug DiscoverymedicineOral routeAnimalsEdemaPharmacologychemistry.chemical_classificationmedicine.diagnostic_testbiologyMacrophagesOrganic ChemistryDual inhibitorMacrophage cellGeneral MedicineMolecular biologyNitric oxide synthaseEnzymeBiochemistrychemistryEnzyme inhibitorCell cultureEnzyme Inductionbiology.proteinmedicine.symptomNitric Oxide SynthaseDimethylaminesEuropean journal of medicinal chemistry
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Cytotoxicity of two naturally occurring flavonoids (dorsmanin F and poinsettifolin B) towards multi-factorial drug-resistant cancer cells.

2015

Abstract Introduction The expression of diverse resistance mechanisms in cancer cells is one of the major barriers to successful cancer chemotherapy. Methods In the present study, we assessed the cytotoxicity of two naturally occurring flavonoids dorsmanin F ( 1 , a flavanone) and poinsettifolin B ( 2 , a chalcone) against 9 drug-sensitive and multidrug-resistant (MDR) cancer cell lines. The resazurin reduction assay was used to evaluate the cytotoxicity of these compounds, whilst caspase-Glo assay was used to detect caspase activation. Cell cycle, mitochondrial membrane potential (MMP) and levels of reactive oxygen species (ROS) were all analysed via flow cytometry. Results Compounds 1 and…

ChalconePharmaceutical ScienceApoptosisPharmacologyBiologychemistry.chemical_compoundInhibitory Concentration 50ChalconesCell Line TumorDrug DiscoverymedicineCytotoxic T cellHumansDoxorubicinCytotoxicityPharmacologyFlavonoidsMembrane Potential MitochondrialMolecular StructureCell CycleCell cycleMolecular biologyAntineoplastic Agents PhytogenicDrug Resistance MultipleComplementary and alternative medicinechemistryApoptosisDrug Resistance NeoplasmCaspasesCancer cellMolecular MedicineReactive Oxygen SpeciesFlavanonemedicine.drugPhytomedicine : international journal of phytotherapy and phytopharmacology
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Cytotoxicity and modes of action of 4'-hydroxy-2',6'-dimethoxychalcone and other flavonoids toward drug-sensitive and multidrug-resistant cancer cell…

2014

Abstract Introduction Resistance of cancer to chemotherapy is a main cause in treatment failure. Naturally occurring chalcones possess a wide range of biological activities including anti-cancer effects. In this work, we evaluated the antiproliferative activity of three chalcones [4′-hydroxy-2′,6′-dimethoxychalcone ( 1 ), cardamomin ( 2 ), 2′,4′-dihydroxy-3′,6′-dimethoxychalcone ( 3 )], and four flavanones [( S )-(–)-pinostrobin ( 4 ), ( S )-(–)-onysilin ( 5 ) and alpinetin ( 6 )] toward nine cancer cell lines amongst which were multidrug resistant (MDR) types. Methods The resazurin reduction assay was used to detect the antiproliferative activity of the studied samples whilst flow cytometr…

ChalconePharmaceutical ScienceApoptosisPharmacologyBiologychemistry.chemical_compoundInhibitory Concentration 50ChalconesCell Line TumorDrug DiscoverymedicineHumansCytotoxicityPharmacologyFlavonoidsMembrane Potential MitochondrialMolecular StructurePlant ExtractsCancerHep G2 CellsCell cyclemedicine.diseaseMolecular biologyAntineoplastic Agents PhytogenicDrug Resistance MultipleMultiple drug resistanceLeukemiaComplementary and alternative medicinechemistryApoptosisCell cultureDrug Resistance NeoplasmMolecular MedicinePolygonumReactive Oxygen SpeciesPhytomedicine : international journal of phytotherapy and phytopharmacology
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Cytotoxicity of three naturally occurring flavonoid derived compounds (artocarpesin, cycloartocarpesin and isobavachalcone) towards multi-factorial d…

2015

Abstract Introduction Cancer remains an aggressive deadly disease, if drug resistance develops. This problem is aggravated by the fact that multiple rather than single mechanisms are involved in resistance and that multidrug resistance (MDR) phenomena cause inefficacy of many clinical established anticancer drugs. We are seeking for novel cytotoxic phytochemicals to combat drug-resistant tumour cells. Methods In the present study, we investigated the cytotoxicity of three naturally occurring flavonoids including two flavones artocarpesin (1) and cycloartocarpesin (2) and one chalcone, isobavachalcone (3) against 9 drug-sensitive and MDR cancer cell lines. The resazurin reduction assay was u…

ChalconePharmaceutical SciencePharmacologyBiologyFlavoneschemistry.chemical_compoundInhibitory Concentration 50ChalconesCell Line TumorDrug DiscoverymedicineCytotoxic T cellHumansCytotoxicityPharmacologychemistry.chemical_classificationMembrane Potential MitochondrialMolecular StructureCell CycleCell cyclemedicine.diseaseFlavonesAntineoplastic Agents PhytogenicDrug Resistance MultipleMultiple drug resistanceLeukemiaComplementary and alternative medicinechemistryDrug Resistance NeoplasmCaspasesCancer cellMolecular MedicineReactive Oxygen SpeciesPhytomedicine : international journal of phytotherapy and phytopharmacology
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Penetration enhancer containing vesicles as carriers for dermal delivery of tretinoin.

2011

The ability of a recently developed novel class of liposomes to promote dermal delivery of tretinoin (TRA) was evaluated. New penetration enhancer-containing vesicles (PEVs) were prepared adding to conventional phosphatidylcholine vesicles (control liposomes) different hydrophilic penetration enhancers: Oramix® NS10 (OrNS10), Labrasol® (Lab), Transcutol® P (Trc), and propylene glycol (PG). Vesicles were characterized by morphology, size distribution, zeta potential, incorporation efficiency, stability, rheological behaviour, and deformability. Small, negatively charged, non-deformable, multilamellar vesicles were obtained. Rheological studies showed that PEVs had fluidity higher than conven…

Chemical PhenomenaStereochemistryDrug CompoundingSus scrofaPharmaceutical ScienceTretinoinAdministration CutaneousPermeabilityGlyceridesDiffusionchemistry.chemical_compoundGlucosidesPhosphatidylcholineZeta potentialAnimalsMicroparticleOrganic ChemicalsTransdermalSkinLiposomeDrug CarriersViscosityVesiclefungiPenetration (firestop)PermeationchemistryAnimals NewbornLiposomesBiophysicsEthylene GlycolsPharmaceutical VehiclesRheologyDialysisHydrophobic and Hydrophilic InteractionsInternational journal of pharmaceutics
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Observable Electric Potential and Electrostatic Potential in Electrochemical Systems

1999

The role of the electric potential in the description of transport processes in electrochemical systems is critically analyzed. Since the electrostatic potential drop between two parts of a system ...

Chemical physicsChemistryComputational chemistryElectric potential energyMaterials ChemistryObservableElectric potentialPhysical and Theoretical ChemistryElectrochemistryVoltage dropSurfaces Coatings and FilmsElectrochemical potentialThe Journal of Physical Chemistry B
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Modelling the Reverse ElectroDialysis process with seawater and concentrated brines

2012

Technologies for the exploitation of renewable energies have been dramatically increasing in number, complexity and type of source adopted. Among the others, the use of saline gradient power is one of the latest emerging possibilities, related to the use of the osmotic/chemical potential energy of concentrated saline solutions. Nowadays, the fate of this renewable energy source is intrinsically linked to the development of the pressure retarded osmosis and reverse electrodialysis technologies. In the latter, the different concentrations of two saline solutions is used as a driving force for the direct production of electricity within a stack very similar to the conventional electrodialysis …

Chemical potentialSettore ING-IND/26 - Teoria Dello Sviluppo Dei Processi ChimiciSettore ING-IND/25 - Impianti Chimici020209 energyOcean Engineering02 engineering and technology7. Clean energyModellingSaline gradient powerSaline gradient power; Reverse electrodialysis; Modelling; Multi-scale; gPROMSStack (abstract data type)Reversed electrodialysisReverse electrodialysi0202 electrical engineering electronic engineering information engineeringOsmotic powergPROMSMulti-scaleWater Science and Technologybusiness.industryChemistryPressure-retarded osmosisEnvironmental engineeringElectrodialysis021001 nanoscience & nanotechnologyPollution6. Clean waterRenewable energySeawater0210 nano-technologybusinessDesalination and Water Treatment
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Cationized albumin-biocoatings for the immobilization of lipid vesicles

2010

Tethered lipid membranes or immobilized lipid vesicles are frequently used as biomimetic systems. In this article, the authors presented a suitable method for efficient immobilization of lipid vesicles onto a broad range of surfaces, enabling analysis by quantitative methods even under rigid, mechanical conditions-bare surfaces such as hydrophilic glass surfaces as well as hydrophobic polymer slides or metal surfaces such as gold. The immobilization of vesicles was based on the electrostatic interaction of zwitterionic or negatively charged lipid vesicles with two types of cationic chemically modified bovine serum albumin (cBSA) blood plasma proteins (cBSA-113 and cBSA-147). Quantitative an…

Chemistry(all)Surface PropertiesAnalytical chemistryGeneral Physics and AstronomyPhysics and Astronomy(all)Microscopy Atomic ForceGeneral Biochemistry Genetics and Molecular BiologyBiomaterialsCoated Materials BiocompatibleMaterials Science(all)CationsZeta potentialGeneral Materials ScienceBovine serum albuminSurface plasmon resonanceLiposomebiologyChemistryBiochemistry Genetics and Molecular Biology(all)VesicleSerum Albumin BovineGeneral ChemistryAdhesionMembraneLiposomesBiophysicsbiology.proteinAdsorptionProtein adsorptionProtein BindingBiointerphases
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Geometric Structure and Torsional Potential of Biisothianaphthene. A Comparative DFT and ab Initio Study

1997

We present a study of the torsional potential of biisothianaphthene and compare it to that of bithiophene. The calculations are performed at the ab initio and semiempirical Hartree−Fock (HF), ab initio post-Hartree−Fock, and density functional theory (DFT) levels. Our study has two major aims:  (i) on the physico-chemical side, to asses the optimal conformation of biisothianaphthene and evaluate the rotational barriers toward coplanar structures and (ii) on the methodological side, to asses the usefulness of DFT approaches. In contrast to previous estimates, the torsional potential of biisothianaphthene is found to differ markedly from that of bithiophene. For biisothianaphthene, strongly r…

ChemistryAb initioStructure (category theory)General ChemistryBiochemistryMolecular physicsCatalysisCrystalColloid and Surface ChemistryComputational chemistryPhysics::Atomic and Molecular ClustersDensity functional theoryTorsional potentialConformational isomerismJournal of the American Chemical Society
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