Search results for "choline"

showing 10 items of 1138 documents

Vibrio cholerae cytolysin: assembly and membrane insertion of the oligomeric pore are tightly linked and are not detectably restricted by membrane fl…

2000

AbstractHemolytic strains of Vibrio cholerae secrete a cytolysin that, upon binding as a monomer, forms pentameric pores in animal cell membranes. Pore formation is inhibited at low temperature and in the absence of cholesterol. We here posed the following questions: firstly, can oligomerization be observed in the absence of pore formation? Secondly, is membrane fluidity responsible for the effect of temperature or of cholesterol upon pore formation? The first issue was approached by chemical cross-linking, by electrophoretic heteromer analysis, and by electron microscopy. None of these methods yielded any evidence of a non-lytic pre-pore oligomer. The second question was addressed by the u…

DiphenylhexatrieneCell Membrane PermeabilityMembrane permeabilityMembrane FluidityBacterial ToxinsBiophysicsPorinsFluorescence PolarizationBiologymedicine.disease_causePore forming toxinBiochemistrychemistry.chemical_compoundProtein oligomerizationBacterial ProteinsBacteriocinsmedicineMembrane fluidityProtein oligomerizationVibrio choleraePhospholipidsFluorescent DyesLiposomeCytotoxinsCell MembraneCell BiologyFluoresceinsCholesterolMembranechemistryBiochemistryVibrio choleraeLiposomesPhosphatidylcholinesCytolysinDiphenylhexatrieneBiochimica et Biophysica Acta (BBA) - Biomembranes
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Time-resolved fluorescence and fourier transform infrared spectroscopic investigations of lateral packing defects and superlattice domains in composi…

2003

Time-resolved fluorescence and Fourier transform infrared spectroscopies were used to investigate the lateral organization of lipids in compositionally uniform and fully equilibrated 1-palmitoyl-2-oleoyl-phosphatidylcholine/cholesterol (POPC/CHOL) liposomes prepared by a recently devised low-temperature trapping method. Independent fluorescence decay lifetime and rotational dynamics parameters of diphenylhexatriene (DPH) chain-labeled phosphatidylcholine (DPH-PC) in these liposomes were recovered from the time-resolved fluorescence measurements as a function of cholesterol molar fraction (X(CHOL)) at 23 degrees C. The results indicate significantly greater lifetime heterogeneity, shorter av…

DiphenylhexatrieneModels MolecularMacromolecular SubstancesMembrane FluidityLipid BilayersBiophysicsAnalytical chemistry010402 general chemistryMole fraction01 natural sciences03 medical and health scienceschemistry.chemical_compoundPhosphatidylcholineSpectroscopy Fourier Transform InfraredMembrane fluiditypolycyclic compoundsComputer SimulationLipid bilayerPOPCRotational correlation time030304 developmental biology0303 health sciencesLiposomeMembranestechnology industry and agricultureSignal Processing Computer-Assisted0104 chemical sciencesCrystallographyCholesterolSpectrometry FluorescencechemistryLiposomesPhosphatidylcholinesAnisotropylipids (amino acids peptides and proteins)AlgorithmsBiophysical journal
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A New Dosimeter Methacholine Challenge Protocol Based On A Single Methacholine Concentration

2010

Dosimeterbusiness.industryAnesthesiaMedicineMethacholinebusinessmedicine.drugMethacholine challengeB18. WE'RE GETTING THERE! NON-INVASIVE ASSESSMENT OF AIRWAY FUNCTION
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On the Electrostatic Component of the Adhesional Interaction between Solid Substrates and Langmuir Monolayers

1991

The work of adhesion between Langmuir monolayers and solid surfaces in a hydrophilic Langmuir-Blodgett configuration has been measured as function of the surface charge densities σ of the contacting surfaces. It was derived from the equilibrium meniscus height which was measured with the transfer fluorescence microscope. The surface charge density of the contacting surfaces was varied by changing the subphase pH. With both surfaces negatively charged (dimyristoylphosphatidylethanolamine onto SiO2-substrates) and low charge densities (σ < 1 e−/100 A2)) we observe a decrease of the adhesion with increasing charge density. At high charge densities (dimyristoylphosphatidic acid onto SiO2-substr…

Double layer (biology)Langmuirchemistry.chemical_compoundChemistryGeneral Chemical EngineeringDipalmitoylphosphatidylcholineMonolayerAnalytical chemistryCharge densityAdhesionSurface chargeDouble layer forcesBerichte der Bunsengesellschaft für physikalische Chemie
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Pharmacokinetics of oligodeoxynucleotides encapsulated in liposomes: effect of lipid composition and preparation method

2000

1. The effect of the method employed to prepare liposomes and their lipid composition were evaluated in terms of the encapsulation efficiency and pharmacokinetic features of two oligodeoxynucleotides of a 21 mer: the normal (N-Odn) and the phosphorothioate (S-Odn) oligodeoxynucleotide. 2. Liposomes were prepared by the classical method of multilamellar vesicles (MV) and by the dehydration-rehydration method (DR). Two lipid mixtures were used to prepare liposomes--the predominant lipid being phosphatidylcholine (PC) and sphingomyelin (SM) respectively. 3. The DR method for liposome preparation provided the highest encapsulation efficiency, regardless of liposome lipid composition and the typ…

Drug CompoundingHealth Toxicology and MutagenesisLipid compositionMultilamellar vesiclesToxicologyBiochemistryPreparation methodMicechemistry.chemical_compoundPharmacokineticsPhosphatidylcholineAnimalsPharmacologyPlasma clearanceLiposomeChromatographyChemistryhemic and immune systemsGeneral MedicineThionucleotidesrespiratory systemLipidsOligodeoxyribonucleotidesBiochemistryInjections IntravenousLiposomesSphingomyelinXenobiotica
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Acute renal failure and liver dysfunction after subcutaneous injection of 3-sn-phosphatidylcholine (Lipostabil®)-case report.

2011

INTRODUCTION Drug-induced tubulointerstitial nephritis and acute tubular necrosis are common, and are often caused by drugs especially antibiotics or non-steroidal anti-inflammatory drugs. Drug-induced liver dysfunction and renal failure after subcutaneous injection of phosphatidylcholine was not reported so far. 3-sn-Phosphatidylcholine has been described as a cell lysis reaction-inducing drug. Its in vitro data indicated a relevant toxicity potential. In particular human cell types such as fibroblast-like preadipocytes, vascular and skeletal muscle cells, or renal epithelial cells react more sensitive than other human cell types. CASE REPORT We present a 28-year-old woman who received 3.5…

DrugAdultmedicine.medical_specialtymedicine.drug_classNauseamedia_common.quotation_subjectInjections SubcutaneousAntibioticsUrologyRenal functionSubcutaneous injectionmedicineHumansFat embolismAcute tubular necrosismedia_commonNephritisbusiness.industryGastroenterologyAcute Kidney Injurymedicine.diseaseSurgeryToxicityPhosphatidylcholinesFemalemedicine.symptombusinessZeitschrift fur Gastroenterologie
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Rapamycin-Loaded Polymeric Nanoparticles as an Advanced Formulation for Macrophage Targeting in Atherosclerosis

2021

Recently, rapamycin (Rapa) represents a potential drug treatment to induce regression of atherosclerotic plaques

DrugBiodistributionmedia_common.quotation_subjectPharmaceutical ScienceExcipientNanoparticlelcsh:RS1-44102 engineering and technologyPharmaceutical formulationArticlelcsh:Pharmacy and materia medica03 medical and health scienceschemistry.chemical_compoundPhosphatidylcholinemedicine030304 developmental biologymedia_commonKOdia-PC0303 health sciencesrapamycin (Rapa)technology industry and agriculture021001 nanoscience & nanotechnologyIn vitromacrophage targetingpolymeric nanoparticleschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPolycaprolactoneBiophysicsatherosclerosis0210 nano-technologymedicine.drugPharmaceutics
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Effects of Some Directly-Acting Smooth Muscle Relaxant Drugs on Isolated Human Preparations of the Upper Urinary Tract

1985

It is generally assumed that drugs which induce relaxation of smooth muscles may be of clinical importance in some urological disorders; such drugs are indeed widely used, for example in the therapy of unstable bladders or to facilitate the passage of ureteral stones. Antispasmodic action may be classified in neurotropic and musculo-tropic action; the former acting on the autonomic nervous system and the latter directly on smooth muscle cells. Examples for the first type of action are anticholinergic drugs or alpha-adrenoceptor-antagonists, whereas papaverine is a classic drug with the second type of action.

DrugPapaverinebusiness.industrymedia_common.quotation_subjectPharmacologyAutonomic nervous systemSmooth musclemedicineUrological DisordersAntispasmodicbusinessAnticholinergic Drugsmedicine.drugmedia_commonUpper urinary tract
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Pharmacokinetic rationale for switching from donepezil to galantamine.

2001

Galantamine, the most recently approved acetylcholinesterase inhibitor (AChEI) for use in the United States, has allosteric modulating activity at nicotinic receptors and inhibits acetylcholinesterase. This dual mechanism of action may make galantamine an attractive option for patients with Alzheimer's disease who have not benefited from their current therapy; thus, methods for switching patients from donepezil or rivastigmine to galantamine are needed. Protocols for switching patients from one AChEI to another must consider both the time required for washout of the first drug and the rate of dose escalation of the second drug. Both issues depend on the pharmacodynamics, pharmacokinetics, a…

Drugmedicine.drug_classmedia_common.quotation_subjectPharmacologyModels Biologicalchemistry.chemical_compoundPharmacokineticsPiperidinesAlzheimer DiseaseGalantamineMedicineHumansPharmacology (medical)DonepezilDonepezilmedia_commonAgedPharmacologyRivastigminebusiness.industryGalantamineAcetylcholinesterasechemistryAcetylcholinesterase inhibitorPharmacodynamicsIndansCholinesterase Inhibitorsbusinessmedicine.drugClinical therapeutics
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The non-neuronal cholinergic system

2012

EXPRESSIONBasic scienceAutoimmunityBiologyPharmacologyReceptors NicotinicLYMPHOCYTESGeneral Biochemistry Genetics and Molecular BiologyANTIGEN-SPECIFIC IGG(1)LUNG-CANCERNICOTINENeoplasmsSECRETE ACETYLCHOLINEAnimalsHumansAcetylcholine metabolismGeneral Pharmacology Toxicology and PharmaceuticsCANCER CELLSACETYLCHOLINE-RECEPTORSGeneral MedicineReceptors MuscarinicAcetylcholineACETYLTRANSFERASECholinergic systemNeuroscienceKNOCKOUT MICELife Sciences
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