Search results for "Potassium Chloride"

showing 10 items of 87 documents

Effect of divalent cations on KCl- and noradrenaline-induced contractile responses in rat aorta after nifedipine treatment.

1999

Abstract Nifedipine (1 μM) relaxed the sustained contractile responses induced by 1 μM noradrenaline or 60 mM KCl in rat aortic strips. After washing, a second addition of the spasmogens gave smaller tonic contractions than the first one. Even more, a third addition of KCl also gave a smaller contraction than the first one, but a complete recovery of the contractile response to noradrenaline was obtained by a third addition of this agonist. Application of cumulative amounts of Ca2+ or Ba2+ (2.4–24 mM) on the residual contraction in response to these agents after nifedipine treatment, but in the absence of the blocker, restored the magnitude of the contractile responses. Addition of cumulati…

AgonistMalemedicine.medical_specialtyContraction (grammar)Nifedipinemedicine.drug_classCations DivalentVasodilator AgentsAorta ThoracicIn Vitro TechniquesTonic (physiology)DivalentPotassium ChlorideNorepinephrineNifedipineInternal medicinemedicine.arterymedicineAnimalsVasoconstrictor AgentsRats WistarPharmacologychemistry.chemical_classificationAortaChemistryCardiovascular AgentsRatsEndocrinologyVasoconstrictionCalciummedicine.symptomIsotonic SolutionsVasoconstrictionMuscle contractionmedicine.drugGeneral pharmacology
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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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Influence of hormonal treatment on the response of the rat isolated uterus to histamine and histamine receptor agonists.

1992

The response of the isolated uterus to histamine and histamine agonists was investigated in progesterone- and oestrogen-treated rats. The uterine inhibitory responses to histamine and 4-methylhistamine (a histamine H2 receptor agonist) were similar in KCl-contracted uteri from progesterone- and oestrogen-treated rats. The histamine H1 receptor agonist, 2-pyridyl-ethylamine, produced a relaxant response only in progesterone dominant uterus. This was inhibited by the histamine H1 receptor antagonist. In the rat isolated uterus which was not preconstricted by KCl, neither histamine, 4-methylhistamine, nor 2-pyridyl-ethylamine produced any effect in the presence or absence of ranitidine. Raniti…

Agonistmedicine.medical_specialtymedicine.drug_classPyridinesHistamine H1 receptorBiologyRanitidineHistamine agonistPotassium ChlorideRanitidinechemistry.chemical_compoundHistamine receptorUterine ContractionHistamine H2 receptorInternal medicinemedicineAnimalsDrug InteractionsHistamine H4 receptorProgesteronePharmacologyMethylhistaminesUterusEstrogensRats Inbred StrainsRatsEndocrinologychemistryReceptors HistamineFemaleHistaminemedicine.drugHistamineEuropean journal of pharmacology
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Antispasmodic effect of 4'-methylepigallocatechin on guinea pig ileum.

2012

AbstractThe antispasmodic effect of 4′-methylepigallocatechin (MEC), which was isolated from Maytenus rigida Mart (Celestraceae), was investigated in vitro in guinea pig intestinal segments. In the isolated ileum, MEC (1 nM–100μM) did not modify the ileal spontaneous tonus or the electrically elicited contractions. MEC (8μM) significantly (p<0.01) reduced the submaximal contractions induced by histamine (2μM), carbachol (100μM) and BaCl2 (0.03M). An additive relaxing action (p<0.001) was observed by co-incubation of verapamil (10 nM) and MEC (8μM). Although MEC (1nM–100μM) did not modify the contractions elicited by 60mM KCl, it significantly reduced the CaCl2 contractile response without c…

AntispasmodicBarium CompoundsGuinea Pigs4′-MethylepigallocatechinIleumPharmacologyCatechinPotassium ChlorideGuinea pigCalcium ChlorideChloridesIleum4'-methylepigallocatechinDrug DiscoverymedicineAnimalsGuinea pig ileumPharmacologyChemistryPlant ExtractsGuinea pig ileumParasympatholyticsMuscle SmoothGeneral MedicineMaytenusSymptomatic reliefIn vitromedicine.anatomical_structureVerapamilAnesthesiaAntispasmodicAntispasmodic EffectCarbacholmedicine.drugHistamineMuscle ContractionFitoterapia
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Absence of muscarinic modulation of vasopressin release from the isolated rat neurohypophysis

1975

1. Isolated rat neurohypophyses were incubated in Locke solution at 37°C and the vasopressin output into the medium determined by bioassay. 2. Potassium chloride 60 mM caused a 9-fold increase in the rate of vasopressin release that was abolished when calcium chloride was omitted from the Locke solution. 3. Acetylcholine 5.5×10−4 M neither alone nor in the presence of atropine 2.9×10−6 M changed the “resting” release of vasopressin. 4. Neither acetylcholine 5.5×10−4 M nor oxotremorine 10−4 and 3×10−4 M altered the vasopressin release evoked by potassium chloride 60 mM. 5. In contrast to the peripheral adrenergic nerve fibres, the secretory terminal fibres of the neurohypophysis do not appea…

Atropinemedicine.medical_specialtyVasopressinVasopressinschemistry.chemical_elementIn Vitro TechniquesCalciumInhibitory postsynaptic potentialPotassium ChloridePituitary Gland PosteriorInternal medicineMuscarinic acetylcholine receptormedicineOxotremorineAnimalsPharmacologyNeurosecretionChemistryOxotremorineGeneral MedicineAcetylcholineRatsAtropineEndocrinologyNicotinic agonistParasympathomimeticsCalciumFemaleAcetylcholinemedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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MitoKATP-channel opener protects against neuronal death in rat venous ischemia.

2005

OBJECTIVE: Mitochondrial adenosine triphosphate-dependent potassium (mitoK ATP ) channels are present in the brain, and several reports have shown their neuroprotective, preconditioning effect against an ischemic insult. The role of mitoK ATP channels in the penumbra area has not been studied thoroughly. In a model of venous ischemia, widespread penumbra-like low flow areas are created, which are susceptible to cortical spreading depression. Thus, we studied effects of mitoK ATP channels on infarct size in this model. METHODS: Male Wistar rats were subjected to two-vein occlusion by photochemical thrombosis of two adjacent cortical veins combined with KCI-induced cortical spreading depressi…

Brain InfarctionMalemedicine.medical_specialtyPotassium ChannelsPhotochemistryIschemiaBrain EdemaPotassium ChlorideIschemiaInternal medicinemedicineDiazoxideLaser-Doppler FlowmetryAnimalsChannel blockerDrug InteractionsRats WistarNeuronsAnalysis of VarianceCell Deathbusiness.industryPenumbraCortical Spreading DepressionDiazoxidemedicine.diseaseCerebral VeinsPotassium channelRatsTolerance inductionDisease Models AnimalNeuroprotective AgentsCerebral blood flowRegional Blood FlowAnesthesiaCortical spreading depressionCardiologySurgeryNeurology (clinical)businessHydroxy AcidsAnti-Arrhythmia AgentsDecanoic Acidsmedicine.drugNeurosurgery
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The presence of KCl in the exposure medium strongly influences the mutagenicity of metabolites of polycyclic aromatic hydrocarbons in Escherichia col…

1994

Abstract Previous studies demonstrated that the ion composition of the exposure medium may strongly influence the mutagenicity of many compounds in the liquid preincubation modification of the reversion assay with his − Salmonella typhimurium strains. Similar influences were now observed in the reversion assay with trp − Escherichia coli strain WP2 uvrA . The exposure medium was 8 mM sodium phosphate buffer (pH 7.4), containing no other ions or 125 mM KCl. Omission of KCl resulted in an about 10-fold enhancement of the mutagenic activity of 7-methylbenz[ a ]anthracene 5,6-oxide, but in a strong decrease in the mutagenicity of 1-hydroxymethylpyrene sulphate, close to the limit of detection. …

Cell Membrane PermeabilityReversionMutagenSulfuric Acid Estersmedicine.disease_causePotassium Chloridechemistry.chemical_compoundSuppression GeneticmedicineBenz(a)AnthracenesEscherichia coliEscherichia coliDetection limitAnthraceneChromatographyPyrenesStrain (chemistry)biologyDose-Response Relationship DrugMutagenicity TestsGeneral Medicinebiology.organism_classificationEnterobacteriaceaeCulture MediachemistryBiochemistryMutagenesisBacteriaMutagensMutation research
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Contralateral potentials in the suprasylvian gyrus evoked by pulvinar stimulation.

1974

AbstractIn encephale isole cats the transmission of the bioelectrical activity in the suprasylvian gyrus, evoked by contralateral pulvinar stimulation was explored. Through the excitability increase and decrease of the pulvinar (by strychnine or KCl, respectively), the surgical removal of the ipsilateral suprasylvian gyrus and the electrocoagulation of the posterior commissure it appeared that the transmission of the activity in the suprasylvian gyrus evoked by contralateral pulvinar stimulation occurs through both the callosal and the interthalamic pathway.

Cerebral CortexCATSPhysiologybusiness.industryBrainStimulationStrychnineStrychnineBiochemistryElectric StimulationCorpus CallosumPotassium Chloridechemistry.chemical_compoundmedicine.anatomical_structurePosterior commissureGyruschemistryThalamusSurgical removalmedicineCatsAnimalsbusinessNeuroscienceEvoked PotentialsArchives internationales de physiologie et de biochimie
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Study on the histamine-like activity of guanfacine

1990

Abstract The effects of guanfacine have been studied on guinea-pig isolated atria and diethylstilboestrol-treated rat isolated uterus to determine whether it possesses histamine-like activity. Guanfacine produced a concentration-dependent negative chronotropic effect which was not modified by ranitidine (0.1 μM). In rat isolated uterus contracted by KCl, clonidine (5–5000 μM) produced concentration-dependent relaxation which was blocked by ranitidine (0.1 μM), but guanfacine only produced relaxation at high concentrations (100–1000 μM), and this was not affected by ranitidine (0.1 μM). It is concluded that guanfacine, unlike clonidine, does not produce effects due to activation of H2-recept…

Chronotropicmedicine.medical_specialtyGuinea PigsUterusPharmaceutical SciencePharmacologyClonidinePotassium ChlorideGuinea pigRanitidineUterine Contractionchemistry.chemical_compoundInternal medicinemedicineAnimalsHeart AtriaDiethylstilbestrolPharmacologyDose-Response Relationship Drugbusiness.industryRats Inbred StrainsMyocardial ContractionGuanfacineRatsGuanfacineClonidineEndocrinologymedicine.anatomical_structureMechanism of actionchemistryFemalemedicine.symptombusinessAdrenergic alpha-AgonistsHistaminemedicine.drugJournal of Pharmacy and Pharmacology
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Effects of phorbol 12,13-diacetate on human isolated bronchus

2000

Protein kinase C appears to be involved in the regulation of airway contractility. Phorbol 12,13-diacetate (PDA; 0.01-10 microM), a protein kinase C activator, produced a transient relaxation followed by a sustained contraction of human isolated bronchus. Different protein kinase C inhibitors (calphostin C, staurosporine and 1-(5-isoquinolinesulfonyl)-2-methylpiperazine) (H-7), nifedipine (NIF; 1 microM) or incubation with Ca(2+)-free medium, inhibited the spasmogenic response to phorbol, while ouabain (10 microM) suppressed only the initial relaxation. These results indicate that the initial relaxation, in response to PDA, is related to the activation of Na(+)/K(+)-ATPase, while the ensuin…

Cromakalimmedicine.medical_specialtyBronchiIn Vitro TechniquesOuabainPotassium ChlorideContractilityCalcium Chloridechemistry.chemical_compoundTheophyllineInternal medicinePhorbol EstersmedicineExtracellularHumansStaurosporineOuabainEgtazic AcidProtein Kinase CProtein kinase CPharmacologyDose-Response Relationship DrugChemistryEndocrinologyCalphostin CPhorbolBiophysicsmedicine.symptommedicine.drugMuscle contractionEuropean Journal of Pharmacology
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