Search results for "Calcium antagonist"

showing 4 items of 4 documents

Synthesis and studies of calcium channel blocking and antioxidant activities of novel 4-pyridinium and/or N-propargyl substituted 1,4-dihydropyridine…

2014

The novel 1,4-dihydropyridine derivatives containing the cationic pyridine moiety at the position 4, and the N-propargyl group as a substituent at position 1 of the 1,4-DHP cycle were designed, synthesised, and assessed in biological tests. Among all the novel compounds, the 4-(N-dodecyl) pyridinium group-containing compounds 11 (without the N-propargyl group) and 12 (with the N-propargyl group) demonstrated the highest calcium antagonistic properties against neuroblastoma SH-SY5Y (IC50 about 5–14 mM) and the vascular smooth muscle A7r5 cell (IC50 – 0.6–0.7 mM) lines, indicating that they predominantly target the L-type calcium channels. These compounds showed a slight total antioxidant act…

AntioxidantVoltage-dependent calcium channelChemistryStereochemistryGeneral Chemical EngineeringCalcium channelmedicine.medical_treatmentSubstituentCationic polymerizationchemistry.chemical_elementGeneral ChemistryCalciumN-Dodecyl pyridiniumMitochondrial processesStructure–activity relationshipschemistry.chemical_compound14-DihydropyridinesAntioxidant activityPropargylmedicineCalcium antagonistsPyridiniumPropargyl substituentComptes Rendus Chimie
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Prolonged Cerebral Circulation Time Is the Best Parameter for Predicting Vasospasm during Initial CT Perfusion in Subarachnoid Hemorrhagic Patients

2016

Purpose We sought to imitate angiographic cerebral circulation time (CCT) and create a similar index from baseline CT perfusion (CTP) to better predict vasospasm in patients with subarachnoid hemorrhage (SAH). Methods Forty-one SAH patients with available DSA and CTP were retrospectively included. The vasospasm group was comprised of patients with deterioration in conscious functioning and newly developed luminal narrowing; remaining cases were classified as the control group. The angiography CCT (XA-CCT) was defined as the difference in TTP (time to peak) between the selected arterial ROIs and the superior sagittal sinus (SSS). Four arterial ROIs were selected to generate four correspondin…

MalePhysiologyCerebral arterieslcsh:MedicinePerfusion scanningCardiovascular MedicineDiagnostic Radiology030218 nuclear medicine & medical imagingCerebral circulation0302 clinical medicineBlood FlowMedicine and Health SciencesVasospasm IntracranialCardiovascular Imaginglcsh:ScienceRoutes of AdministrationCerebral IschemiaMultidisciplinarymedicine.diagnostic_testPharmaceuticsRadiology and ImagingAngiographyVasospasmArteriesHematologyMiddle AgedBody FluidsBloodNeurologyCerebrovascular CirculationCardiologyCalcium Antagonist TherapyFemaleRadiologyAnatomyResearch ArticleSuperior sagittal sinusmedicine.medical_specialtySubarachnoid hemorrhageImaging TechniquesPerfusion ImagingResearch and Analysis Methods03 medical and health sciencesDrug TherapyDiagnostic MedicineIntravenous InjectionsInternal medicinemedicineHumansPharmacologybusiness.industrylcsh:RHemodynamicsBiology and Life SciencesAngiography Digital SubtractionCerebral ArteriesSubarachnoid Hemorrhagemedicine.diseasenervous system diseasesHealth CareSSS*AngiographyCardiovascular AnatomyBlood Vesselslcsh:QTomography X-Ray ComputedbusinessReceptor Antagonist Therapy030217 neurology & neurosurgeryPLOS ONE
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Gastric relaxation induced by apigenin and quercetin: Analysis of the mechanism of action

2009

Abstract Aims Recently, flavonoids have been shown to cause murine gastric relaxation. In the present study we examined the mechanism of action underlying gastric relaxation induced by apigenin and quercetin in isolated mouse stomach. Main methods The mechanical activity from the whole stomach was detected as changes in the endoluminal pressure and the response to increasing concentrations of both flavonoids were tested before and after different pharmacological treatments. Key findings Apigenin and quercetin-induced a concentration-dependent gastric relaxation, apigenin being more potent than quercetin. The responses were unaffected by 2′5′dideoxyadenosine, an inhibitor of adenylate cyclas…

Malemedicine.medical_specialtyCarbacholNifedipineMuscle Relaxationchemistry.chemical_elementCalcium antagonistIn Vitro TechniquesMuscarinic AgonistsCalciumPharmacologySettore BIO/09 - FisiologiaGeneral Biochemistry Genetics and Molecular BiologyPotassium ChlorideMicechemistry.chemical_compoundSmooth muscleInternal medicineCyclic AMPmedicineAnimalsheterocyclic compoundsApigeninGeneral Pharmacology Toxicology and PharmaceuticsCyclic GMPCyclic nucleotide phosphodiesteraseChemistryRyanodine receptorStomachMuscle SmoothGeneral MedicineCalcium Channel BlockersMice Inbred C57BLEndocrinologyMechanism of actionGastric toneApigeninFlavonoidCalciumCarbacholQuercetinmedicine.symptomQuercetinIntracellularMuscle Contractionmedicine.drugLife Sciences
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Differential antiepileptic effects of the organic calcium antagonists verapamil and flunarizine in neurons of organotypic neocortical explants from n…

1988

Effects of the organic calcium antagonists verapamil and flunarizine on pentylenetetrazol induced paroxysmal depolarizations were tested in organotypic neocortical explants taken from neonatal rats. In these in vitro experiments the papaverin derivative verapamil depressed, and finally abolished, epileptic discharges in all cases. The piperazine derivative flunarizine, however, which is known to suppress epileptic discharges in hippocampal CA3 neurons (Bingmann and Speckmann 1986), showed no significant antiepileptic effects in the explanted neocortical neurons. Thus, the present findings may indicate that the suppressive action of flunarizine on the generation of paroxysmal depolarizations…

chemistry.chemical_elementNeocortexCalciumPharmacologyHippocampal formationMembrane PotentialsOrgan Culture TechniquesSeizuresMedicineAnimalsPentylenetetrazolFlunarizineMembrane potentialCerebral CortexNeuronsEpilepsyNeocortexbusiness.industryGeneral NeuroscienceNewbornRatsmedicine.anatomical_structurechemistryAnimals NewbornVerapamilCerebral cortexCalcium antagonistsVerapamilPentylenetetrazolebusinessNeuroscienceFlunarizinemedicine.drugExperimental Brain Research
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