Search results for "SMOOTH"

showing 10 items of 710 documents

Multiple actions of glaucine on cyclic nucleotide phosphodiesterases, α1-adrenoceptor and benzothiazepine binding site at the calcium channel

1992

1. In the present study, the properties of glaucine (an aporphine structurally related to papaverine) were compared with those of papaverine, diltiazem, nifedipine and prazosin. The work includes functional studies on rat isolated aorta contracted with noradrenaline, caffeine or KCl, and a determination of the affinity of glaucine at calcium channel binding sites of alpha-adrenoceptors, by use of [3H]-(+)-cis-diltiazem, [3H]-nitrendipine and [3H]-prazosin binding to cerebral cortical membranes. The effects of glaucine on the different molecular forms of cyclic nucleotide phosphodiesterases (PDE) isolated from bovine aorta were also determined. 2. Contraction evoked by noradrenaline (1 micro…

MaleReceptor complexAporphinesPhosphodiesterase InhibitorsStereochemistryAorta ThoracicIn Vitro TechniquesPharmacologyBinding CompetitiveMuscle Smooth VascularNorepinephrineRadioligand Assaychemistry.chemical_compoundPrazosinmedicineAnimalsRats WistarPharmacologyPapaverineVoltage-dependent calcium channelChemistryCalcium channelDihydropyridinePhosphodiesterasePrazosinReceptors Adrenergic alphaGlaucineRats3'5'-Cyclic-AMP Phosphodiesterasescardiovascular systemCattleCalcium ChannelsResearch ArticleMuscle Contractionmedicine.drugBritish Journal of Pharmacology
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Investigations of the dual contractile/relaxant properties showed by antioquine in rat aorta.

1993

1. In the present study we assessed the activity of antioquine, a bisbenzyltetrahydroisoquinoline alkaloid isolated from Pseudoxandra sclerocarpa, by examining its effects on the contractile activity of rat isolated aorta, specific binding of [3H]-(+)-cis-diltiazem, [3H]-nitrendipine and [3H]-prazosin to cerebral cortical membranes and the different molecular forms of cyclic nucleotide phosphodiesterases (PDE) isolated from bovine aorta. 2. Contractions in rat aorta induced by high concentrations of KCl (80 mM) and noradrenaline (1 microM) were inhibited by antioquine in a concentration-dependent manner (0.1 microM- 300 microM). The alkaloid appeared more potent against KCl-induced contract…

MaleReceptor complexmedicine.medical_specialtyPhosphodiesterase InhibitorsMuscle RelaxationReceptors Drugchemistry.chemical_elementAorta ThoracicCalciumIn Vitro TechniquesBenzylisoquinolinesCalcium in biologyMuscle Smooth VascularNorepinephrineRadioligand AssayAlkaloidsCytosolInternal medicineCaffeinemedicinePrazosinExtracellularAnimalsRats WistarPharmacologyCyclic nucleotide phosphodiesteraseChemistryPhosphoric Diester HydrolasesCalcium channelDihydropyridineCalcium Channel BlockersPyrrolidinonesRatsKineticsEndocrinologyBiophysicsCalciumCattleRoliprammedicine.drugMuscle ContractionResearch ArticleBritish journal of pharmacology
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Anti-atherogenic Effects of 17β-Estradiol

2013

Estrogens are secreted primarily by the ovaries and placenta, by the testes in men and also produced by peripheral steroidogenic conversion. The 3 major naturally occurring estrogens are: 17β-estradiol (E2), estrone and estriol, of which E2 is the predominant and most active. The actions of E2 are mediated by at least 3 different receptors - the classical ERs (ERα and ERβ) and G-protein coupled receptor 30 (GPR30). E2 signaling in cardiomyocytes involves ERα- and ERβ-independent pathways, and treatment with the E2 receptor antagonists (Selective Estrogen Receptor Modulators- SERMs), which are agonists of GPR30, inhibits cardiac cell growth. Effects of E2 in preventing endothelial dysfunctio…

MaleSelective Estrogen Receptor Modulatorsmedicine.medical_specialtyVascular smooth muscleEndotheliummedicine.drug_classEndocrinology Diabetes and MetabolismOvariectomyClinical BiochemistryInflammation030204 cardiovascular system & hematologyBiologyBiochemistry03 medical and health sciencesestrogen 17β-estradiol atherogenic factors atherosclerosis0302 clinical medicineEndocrinologyRisk FactorsInternal medicinemedicineAnimalsHumansEndothelial dysfunctionReceptorEstradiolBiochemistry (medical)Estrogen Replacement TherapyGeneral Medicinemedicine.diseaseAtherosclerosis3. Good healthmedicine.anatomical_structureEndocrinologySelective estrogen receptor modulatorEstrogen030220 oncology & carcinogenesisDiet AtherogenicFemalemedicine.symptomGPER
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Effects of 5-HT4 receptor stimulation on basal and electrically evoked release of acetylcholine from guinea-pig myenteric plexus

1992

The effects of 5-methoxytryptamine and 5-hydroxytryptamine (5-HT) on both basal and electrically evoked outflow of tritium were studied in guinea-pig myenteric plexus preparations preincubated with [3H]-choline. Basal outflow. 5-Methoxytryptamine caused a transient and calcium-dependent increase in basal outflow of [3H]acetylcholine that was abolished by tetrodotoxin. Ondansetron (1 μmol/1) did not affect the stimulatory response of 5-methoxytryptamine but ICS 205-930 (1 and 3 μmol/1) produced parallel rightward displacements of the concentration-response curve to 5-methoxytryptamine. The PKB value for ICS 205-930 was 6.6 suggesting an involvement of 5-HT4 receptors. 5-HT caused an increase…

MaleSerotoninmedicine.medical_specialtyGuinea PigsNeuromuscular JunctionMyenteric Plexus5-HT4 receptorStimulationIn Vitro TechniquesBiologyTritium5-HT3 receptorCholine5-Methoxytryptaminechemistry.chemical_compoundIleumInternal medicinemedicineAnimalsReceptorMyenteric plexusPharmacologyMuscle SmoothGeneral MedicineSmooth muscle contractionAcetylcholineElectric StimulationStimulation ChemicalEndocrinologychemistryReceptors SerotoninMetitepinebiology.proteinFemaleCholinesterase InhibitorsAcetylcholinemedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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Participation of Intracellular Calcium Stores in Serotonin-Induced Contractions in Rat Aorta

1993

Serotonin 1 mumol/l induces a contractile response in the isolated rat aorta in both the presence or absence of extracellular Ca. The present study analyzes the influence of temperature and caffeine on subsequent serotonin-induced contractions. In Ca-free medium, the contraction elicited by serotonin was higher at 25 degrees C than at 37 degrees C. In addition, the existence of two independent intracellular Ca pools releasable by serotonin, one of them also sensitive to caffeine, is postulated. The results also showed that addition of serotonin decreases the contractile response to this agonist in Ca-free medium.

MaleSerotoninmedicine.medical_specialtychemistry.chemical_elementAorta ThoracicCalciumBiologyMuscle Smooth VascularCalcium in biologychemistry.chemical_compoundCaffeinemedicine.arteryInternal medicinemedicineExtracellularAnimalsRats WistarPharmacologyAortaTemperatureGeneral MedicineAnatomyCulture MediaRatsEndocrinologychemistryVasoconstrictionCalciumSerotoninmedicine.symptomCaffeineIntracellularMuscle contractionPharmacology
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Amplifying effect of serotonin on contractile responses in rat aorta and depletion of intracellular Ca-stores

1993

1. Serotonin, 1 microM, induces a contractile response in isolated rat aorta in the presence or absence of extracellular Ca. 2. In Ca-free media, the fast phasic contraction is lower in magnitude and further addition of serotonin evokes no response. 3. Recovery of the contractile response in Ca-free medium is obtained by a 40 min incubation in Ca-containing solution. 4. In Ca, Mg-free medium, the response to serotonin is significantly higher than that obtained in the presence of Mg. 5. An amplifying effect of serotonin on the contractile responses induced by serotonin itself or by noradrenaline was observed in Ca-containing but not in Ca-free solution.

MaleSerotoninmedicine.medical_specialtychemistry.chemical_elementAorta ThoracicIn Vitro TechniquesCalciumBiologyMuscle Smooth VascularNorepinephrine (medication)NorepinephrineInternal medicinemedicine.arterymedicineExtracellularAnimalsMagnesiumRats WistarPharmacologyCalcium metabolismAortaAcetylcholineRatsEndocrinologychemistryCatecholamineCalciumSerotoninmedicine.symptomMuscle Contractionmedicine.drugMuscle contractionGeneral Pharmacology: The Vascular System
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A flexible approach to the crossing hazards problem

2010

We propose a simple and flexible framework for the crossing hazards problem. The method is not confined to two-sample problems, but may also work with continuous exposure variables whose effect changes its sign at some time-point of the observed follow-up time. Penalized partial likelihood estimation relies upon the assumption of a smooth hazard ratio via low-rank basis splines with a conventional difference penalty to ensure smoothness, and additional ad hoc penalties to obtain restricted estimates useful in the context of crossing hazards. The framework naturally also leads to a statistical test that has good power for revealing a global effect under several alternatives, including crossi…

MaleStatistics and ProbabilityMathematical optimizationBiometryEpidemiologyContext (language use)Time-varying effectSimple (abstract algebra)P-splineHumansCrossing pointProportional Hazards ModelsMathematicsStatistical hypothesis testingLikelihood FunctionsSmoothnessBasis (linear algebra)Work (physics)Survival AnalysisCrossing hazardPower (physics)FemaleRestricted estimationSettore SECS-S/01 - StatisticaAlgorithmsSign (mathematics)
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The effects of racemic bethanechol and its (R)- and (S)-enantiomers on pre- and postjunctional muscarine receptors in the guinea-pig ileum

1985

The effect of racemic bethanechol and its (R)- and (S)-enantiomers on smooth muscle contraction and outflow of [3H]-acetylcholine were studied in the guinea-pig myenteric plexus-longitudinal muscle preparation that had been preincubated with [3H]-choline. (S)-, racemic, and (R)-bethanechol caused concentration-dependent contractions of the longitudinal muscle. The potency ratio of the strong isomer (S) to the weak one (R) was 915. Racemic and (S)-bethanechol concentration-dependently inhibited the evoked outflow of [3H]-acetylcholine. Racemic bethanechol was more potent than (S)-bethanechol. (R)-bethanechol up to a concentration of 1 mM did no affect the evoked outflow of [3H]-acetylcholine…

MaleStereochemistryGuinea PigsMyenteric PlexusBethanecholchemistry.chemical_compoundBethanechol CompoundsIleumMuscarinic acetylcholine receptormedicineAnimalsPharmacologyMuscarineChemistryMuscle SmoothStereoisomerismGeneral MedicineSmooth muscle contractionBethanecholReceptors MuscarinicRacemic mixtureFemaleCholinesterase InhibitorsEnantiomermedicine.symptomAcetylcholineMuscle Contractionmedicine.drugMuscle contractionNaunyn-Schmiedeberg's Archives of Pharmacology
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The new radioligand [H-3]-L 748,337 differentially labels human and rat beta(3)-adrenoceptors

2013

As no suitable radioligand exists for the detection of β3-adrenoceptors, we have explored the radioligand binding properties of a tritiated version of the selective β3-adrenoceptor antagonist L 748,337. Kinetic and equilibrium saturation and competition binding experiments were performed with [(3)H]-L 748,337 on membrane fractions of HEK and CHO cells stably transfected with human and rat β-adrenoceptor subtypes. Based on both association/dissociation kinetic and equilibrium saturation binding studies in transfected HEK cells, [(3)H]-L 748,337 exhibited an affinity of approximately 2 nM for human β3-adrenoceptors. Competition studies with agonists and subtype-selective antagonists validated…

MaleStereochemistryUrinary BladderCHO CellsIn Vitro TechniquesAminophenolsBinding CompetitiveRats Sprague-Dawley03 medical and health sciencesRadioligand Assay0302 clinical medicineCricetulusRadioligandAnimalsHumans030304 developmental biologyPharmacology0303 health sciencesSulfonamidesbiologyChemistryChinese hamster ovary cellHEK 293 cellsAntagonistMuscle SmoothTransfectionbiology.organism_classificationMolecular biologyRadioligand AssayRatsMembraneHEK293 CellsReceptors Adrenergic beta-3CricetulusAdrenergic beta-3 Receptor Antagonists030217 neurology & neurosurgeryEuropean Journal of Pharmacology
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Distribution of origin of nitric oxide synthase-immunoreactive nerve fibers in the rat epididymis.

1996

Abstract Distribution of neuronal nitric oxide synthase-immunoreactive (nNOS-IR) nerve fibers and somata in the rat epididymis and major pelvic ganglia was studied by immunohistochemical methods. In the epididymis, the supply of nNOS-IR fibers was highest in the cauda and became progressively fewer toward the caput. In the cauda and corpus, nNOS-IR fibers were distributed throughout the subepithelial tissues and around the epithelium. The pattern of distribution of vasoactive intestinal polypeptide (VIP)- and tyrosine hydroxylase (TH)-immunoreactive fibers in the epididymis was similar but the latter was generally more numerous in a given region as compared to that of nNOS-IR fibers. A popu…

MaleStilbamidinesTyrosine 3-MonooxygenaseVasoactive intestinal peptidePopulationBiologyRats Sprague-DawleyNerve FibersDorsal root ganglionGanglia SpinalmedicineAnimalseducationMolecular Biologyreproductive and urinary physiologyFluorescent DyesEpididymisNeuronseducation.field_of_studyNeurotransmitter AgentsHypogastric PlexusGeneral NeuroscienceVas deferensSmooth muscle contractionAnatomyEpididymisCholine acetyltransferaseImmunohistochemistryEpitheliumRatsbody regionsmedicine.anatomical_structurePhenotypenervous systemNeurology (clinical)Nitric Oxide SynthaseDevelopmental BiologyVasoactive Intestinal PeptideBrain research
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