Search results for "Trifluoperazine"

showing 10 items of 10 documents

Uptake of polyphosphate microparticles in vitro (SaOS-2 and HUVEC cells) followed by an increase of the intracellular ATP pool size

2017

Recently two approaches were reported that addressed a vitally important problem in regenerative medicine, i. e. the successful treatment of wounds even under diabetic conditions. Accordingly, these studies with diabetic rabbits [Sarojini et al. PLoS One 2017, 12(4):e0174899] and diabetic mice [Müller et al. Polymers 2017, 9, 300] identified a novel (potential) target for the acceleration of wound healing in diabetes. Both studies propose a raise of the intracellular metabolic energy status via exogenous administration either of ATP, encapsulated into lipid vesicles, or of polyphosphate (polyP) micro-/nanoparticles. Recently this physiological polymer, polyP, was found to release metabolic …

0301 basic medicineConfocal MicroscopyBioenergeticsPhysiologyPolymerslcsh:Medicine02 engineering and technologyTrifluoperazineBiochemistryAdenosine TriphosphateEndocrinologyPolyphosphatesSpectroscopy Fourier Transform InfraredMedicine and Health Scienceslcsh:ScienceStainingMicroscopySecretory PathwayMultidisciplinaryChemistryLight MicroscopyCell Staining021001 nanoscience & nanotechnologyEndocytosisMicrospheres3. Good healthCell biologyChemistryMacromoleculesCell ProcessesPhysical SciencesRabbits0210 nano-technologyIntracellularResearch Articlemedicine.drugEndocrine DisordersMaterials by StructureMaterials ScienceBioenergeticsResearch and Analysis MethodsEndocytosisCell Line03 medical and health sciencesTissue RepairDiabetes Mellitusotorhinolaryngologic diseasesmedicineAnimalsHumansCalcium metabolismWound Healinglcsh:RSpectrometry X-Ray EmissionBiology and Life SciencesCell BiologyPolymer Chemistrydigestive system diseasesIn vitroMetabolism030104 developmental biologySpecimen Preparation and TreatmentCell cultureMetabolic DisordersMicroscopy Electron ScanningCalciumlcsh:QEnergy MetabolismPhysiological ProcessesWound healingConfocal Laser MicroscopyPowder DiffractionPLOS ONE
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DIFFERENT ABILITY OF TRIFLUOPERAZINE TO INHIBIT AGONIST-INDUCED CONTRACTION OF LUNG PARENCHYMA STRIPS FROM CONTROL AND SENSITIZED GUINEA-PIGS

1988

Abstract There is increasing interest in the therapeutic potential of calcium antagonists in asthma. Among them the use of calmodulin antagonists deserves consideration. In the present work the effect of trifluoperazine on contractions generated by different mechanisms (CaCl2, KCl, acetylcholine, histamine and 5-hydroxytryptamine) in lung parenchyma strip isolated from control and actively sensitized guinea-pigs has been studied. Trifluoperazine produced both in unsensitized and sensitized lung strips, a concentration-dependent, right, downward displacement of the concentration-response curves to the agonists used, although the sensitization procedure resulted in a potentiation in the abili…

AgonistMalemedicine.medical_specialtySerotoninmedicine.drug_classGuinea PigsPharmaceutical ScienceTrifluoperazineIn Vitro TechniquesPotassium ChlorideContractilityGuinea pigchemistry.chemical_compoundCalcium ChlorideInternal medicineParenchymamedicineAnimalsLungSensitizationPharmacologyMuscle SmoothAcetylcholineTrifluoperazinemedicine.anatomical_structureEndocrinologychemistryHistamineAcetylcholinemedicine.drugHistamineMuscle Contraction
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On the activity of trifluoperazine and palmitoylcarnitine in mice: Delayed hypersensitivity models

2001

Abstract The effect of pre- and post-challenge treatments with trifluoperazine and palmitoylcarnitine, two protein kinase C (PKC) inhibitors characterised by their interaction with the phospholipid enzyme cofactor, on the inflammation caused by delayed hypersensitivity (DTH) to dinitrofluorobenzene (DNFB) and sheep red blood cells (SRBC) in mice is reported. The activity of dexamethasone and two immunosupressors, azathioprine and methotrexate, is also evaluated. The effectiveness of pre-treatment with each of the test drugs diminished when the DNFB challenge dose increased, whereas trifluoperazine and azathioprine were more active when administered after the challenge at the high DNFB dose.…

ErythrocytesAnti-Inflammatory Agentschemical and pharmacologic phenomenaInflammationTrifluoperazinePharmacologyDexamethasoneGeneral Biochemistry Genetics and Molecular BiologyMicechemistry.chemical_compoundAzathioprinemedicineAnimalsHypersensitivity DelayedEnzyme InhibitorsGeneral Pharmacology Toxicology and PharmaceuticsProtein Kinase CPalmitoylcarnitineProtein kinase CDexamethasoneSheepbusiness.industryPalmitoylcarnitineGeneral MedicineTrifluoperazineMethotrexatechemistryDelayed hypersensitivityDinitrofluorobenzeneFemaleMethotrexatemedicine.symptombusinessHaptenImmunosuppressive Agentsmedicine.drugLife Sciences
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Calcium antagonist properties of cinnarizine, trifluoperazine and verapamil in guinea-pig normal and skinned trachealis muscle.

1990

In guinea-pig trachealis, depolarized by a K(+)-rich medium, Ca2+ (0.01-10 mM) caused concentration-related spasm. Verapamil (0.5-5 microM), cinnarizine (10-100 microM) and trifluoperazine (16-160 microM) each produced concentration-dependent antagonism of Ca2+ characterized by a rightward and downward displacement of the log concentration-effect curve for Ca2+. The rank order of potencies of these antagonists, measured as the IC75 against Ca2+ (10 mM)-induced contraction of depolarized trachea, was verapamil (5.6 microM) greater than cinnarizine (59 microM) greater than trifluoperazine (91 microM). In skinned trachea, verapamil in concentrations up to 100 microM did not modify the concentr…

MaleCinnarizineContraction (grammar)StereochemistryGuinea PigsPharmaceutical Sciencechemistry.chemical_elementTrifluoperazinePharmacologyCalciumIn Vitro TechniquesCinnarizinemedicineAnimalsPharmacologyAntagonistMuscle SmoothCalcium Channel BlockersTrifluoperazineTracheaMechanism of actionchemistryVerapamilTrachealis muscleVerapamilFemalemedicine.symptommedicine.drugThe Journal of pharmacy and pharmacology
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Effects of Calcium Antagonists on Rat Normal and Skinned Fundus

1992

Abstract Calcium chloride (CaCl2) (0·1−25 Mm, in K+-depolarized tissue), KCl (10−112 Mm) and acetylcholine (1 × 10−9 m−1 Mm) produced concentration-dependent contractions of rat isolated fundus. Verapamil (0·01−100 μm), cinnarizine (1−100 μm), trifluoperazine (10−500 μm) and dantrolene (50−250 μm) each produced a concentration-related rightward and downward shift of the log concentration-effect curve for CaCl2. The rank order of potencies of these antagonists, measured as the IC50 against Ca2+ (25 Mm)-induced contraction of depolarized fundus, was verapamil (2.5 μm) > cinnarizine (8·7 μm) > trifluoperazine (85·1 μm) > dantrolene (> 250 μm). Cinnarizine (0·5 Mm) a…

MaleContraction (grammar)CinnarizineGuinea PigsPharmaceutical Sciencechemistry.chemical_elementTrifluoperazineIn Vitro TechniquesPharmacologyCalciumDantroleneDantroleneCinnarizinemedicineAnimalsGastric FundusPharmacologyChemistryMuscle SmoothRats Inbred StrainsCalcium Channel BlockersTrifluoperazineRatsVerapamilAnesthesiaVerapamilFemalemedicine.symptomAcetylcholinemedicine.drugMuscle contractionJournal of Pharmacy and Pharmacology
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COOLING-INDUCED CONTRACTION OF TRACHEA ISOLATED FROM NORMAL AND SENSITIZED GUINEA-PIGS

1991

Fast (−7°C/min) cooling of guinea-pig isolated trachea produced a rapidly developing, transient contraction followed by relaxation. Cooling-induced contraction was dependent on temperature (30, 20 or 10°C) and responses in trachea obtained from actively sensitized guinea pigs were significantly greater (20 and 10°-C) than those observed in normal trachea. Cooling to 20°C was selected for subsequent experiments. Pre-treatment with sufficient concentrations of atropine, clemastine, cromoglycate, indomethacin, or nordihydroguaiaretic acid did not depress contraction to cooling in either normal or sensitized trachea. This indicates a direct effect of cooling. The contraction. produced by coolin…

MaleContraction (grammar)Guinea PigsTrifluoperazineOuabainDrug Hypersensitivitychemistry.chemical_compoundmedicineAnimalsVanadateOuabainPharmacologyMuscle SmoothGeneral Medicinerespiratory systemMolecular biologyNordihydroguaiaretic acidCold TemperatureTracheamedicine.anatomical_structurechemistryAnesthesiaPhorbolFemalemedicine.symptomVanadatesRespiratory tractMuscle contractionmedicine.drugMuscle Contraction
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Antagonism of calcium by zinc in guinea-pig isolated taenia caeci and trachealis muscle

1989

1 In guinea-pig isolated taenia caeci and trachealis bathed in a K+-rich, Ca2+-free medium, CaCl2 (0.01-10 mM) produced a concentration-dependent contraction. Zn2+ (0.01-1 mM), Cd2+ (0.01-1 mM), verapamil (0.01-100 microM) and trifluoperazine (1-100 microM) were effective antagonists of CaCl2-induced responses. 2 Zn2+ and Cd2+ in concentrations from 0.01 to 1 mM were without effect on the tone of taenia and trachea in normal Tris solution. Conversely, Zn2+ and Cd2+, in concentrations of 1 mM, caused contraction of these tissues in a K+-rich, Ca2+-free medium. Zn2+ (1 mM)-induced contractions of taenia and trachea were completely inhibited by verapamil (10 microM). 3 In taenia and trachea sk…

Maleinorganic chemicalsmedicine.medical_specialtyContraction (grammar)Guinea Pigschemistry.chemical_elementTrifluoperazineIn Vitro TechniquesCalciumGuinea pigInternal medicinemedicineAnimalsCecumPharmacologyChemistryCell MembraneMuscle SmoothAcetylcholineTrifluoperazineTracheaZincEndocrinologyVerapamilTrachealis muscleVerapamilCalciumFemalemedicine.symptomAcetylcholineCadmiumResearch Articlemedicine.drugMuscle contraction
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Differentiation of calcium antagonists with respect to their effects in normal and skinned taenia caeci preparations

1987

Abstract In taenia preparations, depolarized by a K+-rich medium, Ca2+ caused contraction and cinnarizine (0.4–100 μM), trifluoperazine (2–100 μM) and verapamil (0.02–10 μM) caused concentration-dependent antagonism of Ca2+, displacing the Ca2+ log concentration-effect curve to the right and depressing the maximal response. Equieffective (IC75) antispasmogenic concentrations were selected. The antispasmogenic effects of verapamil were readily offset by removing the drug from the bathing fluid but those of the other drugs were not. The calcium antagonists (antispasmogenic IC75) were then tested for spasmolytic activity in tissues generating tension in response to the EC80 of Ca2+. Verapamil …

Malemedicine.medical_specialtyCinnarizineContraction (grammar)Guinea PigsPharmaceutical Sciencechemistry.chemical_elementTrifluoperazineIn Vitro TechniquesCalciumCinnarizineGuinea pigCalmodulinInternal medicinemedicineAnimalsPharmacologyDose-Response Relationship DrugbiologyParasympatholyticsCalcium Channel Blockersbiology.organism_classificationTrifluoperazineIntestinesEndocrinologyVerapamilchemistryTaeniaVerapamilCalciumFemaleIntracellularMuscle Contractionmedicine.drugJournal of Pharmacy and Pharmacology
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NADPH-diaphorase activity of nitric oxide synthase in the olfactory bulb: co-factor specificity and characterization regarding the interrelation to N…

1994

The neuronal form of the enzyme nitric oxide synthase (nNOS) synthesizes the messenger molecule nitric oxide (NO). In addition to NO formation, nNOS exhibits a so-called NADPH-diaphorase (NADPH-d) activity. This study focused on the characterization of NADPH-d activity with regard to NO formation in the rat olfactory bulb. In this area of the brain pronounced staining is localized in discrete populations of neuronal somata and in olfactory glomeruli. Diaphorase staining combined with demonstration of nNOS by polyclonal antibodies revealed that NADPH-d activity of neuron somata is associated with nNOS immunoreactivity. It is concluded that neuron somata exhibit NADPH-d activity of nNOS. NAD…

Olfactory systemMaleHistologyMiconazoleCytochrome c GroupBiologyArginineNitric OxideNitric oxideSubstrate SpecificityRats Sprague-Dawleychemistry.chemical_compoundDiaphoraseAnimalsEgtazic AcidNADPH dehydrogenaseomega-N-MethylarginineStaining and LabelingCytochrome cNADPH DehydrogenaseMolecular biologyImmunohistochemistryOlfactory BulbTrifluoperazineOlfactory bulbRatsNitric oxide synthasenervous systemBiochemistrychemistrybiology.proteinOmega-N-Methylarginine26-DichloroindophenolAmino Acid OxidoreductasesAnatomyNitric Oxide SynthaseThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society
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IDENTIFICATION OF A CALMODULIN-BINDING SITE WITHIN THE DOMAIN I OF BACILLUS THURINGIENSISCry3Aa TOXIN

2012

Bacillus thuringiensis Cry3Aa toxin is a coleopteran specific toxin highly active against Colorado Potato Beetle (CPB).We have recently shown that Cry3Aa toxin is proteolytically cleaved by CPB midgut membrane associated metalloproteases and that this cleavage is inhibited by ADAM metalloprotease inhibitors. In the present study, we investigated whether the Cry3Aa toxin is a calmodulin (CaM) binding protein, as it is the case of several different ADAM shedding substrates. In pull-down assays using agarose beads conjugated with CaM, we demonstrated that Cry3Aa toxin specifically binds to CaM in a calcium-independent manner. Furthermore, we used gel shift assays and (1)H NMR spectra to demons…

chemistry.chemical_classificationCalmodulinmedicine.diagnostic_testPhysiologyToxinBinding proteinProteolysisPeptideGeneral MedicineTrifluoperazineBiologymedicine.disease_causebiology.organism_classificationBiochemistryMolecular biologychemistryBiochemistryInsect ScienceBacillus thuringiensismedicinebiology.proteinBinding sitemedicine.drugArchives of Insect Biochemistry and Physiology
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