Search results for "guinea"

showing 10 items of 412 documents

Effect of vasoactive intestinal polypeptide on the release of serotonin from the in vitro vascularly perfused small intestine of guinea pig.

1989

Isolated segments of the guinea pig small intestine were vascularly perfused and the release of endogenous serotonin (5-HT) and its metabolite 5-hydroxyindoleacetic acid (5-HIAA) into the portal vein was measured. All test substances were intraarterially perfused. Vasoactive intestinal polypeptide (VIP, 1 pmol/l-100 nmol/l) inhibited the spontaneous release of 5-HT and 5-HIAA. The maximal inhibitory effect (about 60%) was seen at 100 pmol/l. The effect of VIP on the spontaneous release of 5-HT and 5-HIAA was not changed in the presence of 1 mumol/l tetrodotoxin (TTX). Raising intraluminal pressure by 500 Pa for 5 min increased the release of 5-HT and 5-HIAA by about 25%. Raising the intralu…

Malemedicine.medical_specialtySerotoninMetaboliteVasoactive intestinal peptideGuinea PigsTetrodotoxinBiologyIn Vitro TechniquesGuinea pigchemistry.chemical_compoundInternal medicineIntestine SmallmedicineAnimalsPharmacologyMuscle SmoothGeneral MedicineHydroxyindoleacetic AcidSmall intestineEndocrinologymedicine.anatomical_structurenervous systemGastrointestinal hormonechemistryEnterochromaffin cellTetrodotoxinSerotoninhormones hormone substitutes and hormone antagonistsMuscle ContractionVasoactive Intestinal PeptideNaunyn-Schmiedeberg's archives of pharmacology
researchProduct

Characterization of the muscarine receptors involved in the modulation of serotonin release from the vascularly perfused small intestine of guinea pi…

1989

Isolated small intestinal segments of the guinea pig were arterially perfused and the release of 5-hydroxytryptamine (5-HT) and its metabolite 5-hydroxyindoleacetic acid (5-HIAA) into the portal venous effluent measured by HPLC with electrochemical detection. Test substances were applied via the arterial perfusion medium. McN-A-343, pilocarpine and oxotremorine inhibited concentration-dependently the outflow of 5-HT and 5-HIAA. Pirenzepine (0.03-0.1 mumol/l) which can discriminate between M1 and M2-receptor subtypes antagonized completely this inhibitory effect. In the presence of 1 mumol/l tetrodotoxin (TTx), all three muscarine receptor agonists increased the outflow of 5-HT and 5-HIAA. O…

Malemedicine.medical_specialtySerotoninPopulationGuinea PigsIndomethacinTetrodotoxinIn Vitro Techniqueschemistry.chemical_compoundInternal medicineMuscarinic acetylcholine receptorIntestine SmallmedicineOxotremorineAnimalsReceptoreducationNeurotransmitterPharmacologyeducation.field_of_studyMuscarineOxotremorine(4-(m-Chlorophenylcarbamoyloxy)-2-butynyl)trimethylammonium ChlorideGeneral MedicinePirenzepineHydroxyindoleacetic AcidPirenzepineReceptors MuscarinicPerfusionEndocrinologychemistryFemaleSerotoninmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
researchProduct

AF-DX 116 differentiates between prejunctional muscarine receptors located on noradrenergic and cholinergic nerves.

1989

Prejunctional affinity constants of the cardioselective muscarine receptor antagonist AF-DX 116 (11-[(2-[(diethyl-amino)methyl]-1-piperidinyl)acetyl]-5,11-dihydro-6 H-pyrido [2,3-b] [1,4] benzodiazepine-6-one) were determined for muscarine autoreceptors on cholinergic nerves of the guinea-pig ileum and for heteroreceptors on noradrenergic nerves of the rat heart and guinea-pig iris. AF-DX 116 antagonized with low affinity the muscarinic inhibition induced by arecaidine propargyl ester of the stimulation-evoked [3H]acetylcholine overflow (pA2 6.74) from the guinea-pig ileum. In contrast, AF-DX 116 was more potent in antagonizing the methacholine-induced inhibition of the stimulation-evoked […

Malemedicine.medical_specialtySympathetic Nervous Systemmedicine.drug_classGuinea PigsIrisBiologyIn Vitro TechniquesParasympathetic nervous systemchemistry.chemical_compoundNorepinephrineNorepinephrineIleumParasympathetic Nervous SystemInternal medicineMuscarinic acetylcholine receptormedicineAnimalsCholinergic neuronPharmacologyMuscarineMyocardiumHeartMuscle SmoothRats Inbred StrainsGeneral MedicinePirenzepineReceptor antagonistPirenzepineReceptors MuscarinicAcetylcholineRatsEndocrinologymedicine.anatomical_structurechemistryAcetylcholinemedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
researchProduct

Effectiveness of theophylline to increase cyclic AMP levels and force of contraction in electrically paced guinea-pig auricles. Comparison with isopr…

1977

The effects of theophylline (3×10−5 M–5×10−3 M), isoprenaline (10−6 M), excess calcium (7.2 mM) and ouabain (3×10−7 M) on force of contraction and c-AMP content were studied in electrically driven (frequency 3 Hz) left auricles isolated from guinea pigs pretreated with reserpine.

Malemedicine.medical_specialtyTime FactorsContraction (grammar)Guinea Pigschemistry.chemical_elementIn Vitro TechniquesCalciumOuabainGuinea pigTheophyllineInternal medicineIsoprenalineCyclic AMPmedicineAnimalsTheophyllineOuabainPharmacologyChemistryMyocardiumCardiac Pacing ArtificialIsoproterenolGeneral MedicineReserpineMyocardial ContractionPropranololC++ AMPEndocrinologyCalciumFemalemedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
researchProduct

Action of the racemate and the isomers of the platelet-activating factor antagonist bepafant (WEB 2170) after oral administration to guinea-pigs and …

1991

The aim of the present study was to clarify whether there is a difference in terms of potency and pharmacodynamic half time between the isomers and the racemate of the platelet-activating factor antagonist WEB 2170 (bepafant) after oral administration to guineapigs or rats. The following experiments were performed in the guinea-pig. Infusion of platelet-activating factor at 30 ng/ (kg × min) for 30 min to anaesthetized guinea-pigs induced a decrease of respiratory flow and mean arterial blood pressure. Oral pretreatment with WEB 2170 or isomers, respectively, 60 min before infusion of plateletactivating factor inhibited these changes in a dose-dependent manner. The ED50S for inhibition of r…

Malemedicine.medical_specialtyTime FactorsGuinea PigsAdministration OralBlood PressureGuinea pigStructure-Activity Relationshipchemistry.chemical_compoundOral administrationInternal medicinemedicineAnimalsPotencyPlatelet Activating FactorED50PharmacologyDose-Response Relationship DrugPlatelet-activating factorChemistryAntagonistRats Inbred StrainsStereoisomerismAzepinesGeneral MedicineTriazolesRatsEndocrinologyPharmacodynamicsPulmonary VentilationHalf timeNaunyn-Schmiedeberg's Archives of Pharmacology
researchProduct

Effect of different treatments in calcium-free medium on basal tone and contractile responses of guinea pig tracheae.

1995

Acetylcholine (ACh; 0.1 mmol/l) and KCl (80 mmol/l) induce a biphasic contractile response in isolated guinea pig tracheae maintained at 37 degrees C either in the presence or absence of extracellular Ca2+. Exposure of the tissue to Ca(2+)-free solution evokes a significant decrease in basal tone and the sources of Ca2+ appear to be decreased by prolonged agonist stimulation, and even more by successive agonist stimulation. After an incubation period of 20 min in Ca(2+)-containing solution, the response is restored. Mg(2+)-depletion in Ca(2+)-free medium increased the contractile response to ACh, but not to KCl, and delayed the tonic component of the next contraction elicited in Ca(2+)-cont…

Malemedicine.medical_specialtyTime FactorsGuinea Pigschemistry.chemical_elementCalciumPotassium ChlorideGuinea pigBasal (phylogenetics)Tone (musical instrument)Organ Culture TechniquesInternal medicinemedicineExtracellularAnimalsMagnesiumPharmacologyIon TransportContractile responseMuscle SmoothGeneral MedicineFree mediumAcetylcholineTracheaCalcium Channel AgonistsEndocrinologychemistryCalciumAcetylcholinemedicine.drugMuscle ContractionPharmacology
researchProduct

Papaverine decreases the efflux of42K in guinea-pig atrial heart muscle

1980

The effects of papaverine on resting potential and efflux of42K were investigated in guinea-pig left atria. Papaverine significantly reduced the potassium efflux in beating preparations. In resting preparations, the efflux of potassium was only slightly affected. However, the resting potential was significantly reduced by papaverine by about 5 mV.

Malemedicine.medical_specialtyTime FactorsPotassiumGuinea PigsPharmacology toxicologyPotassium RadioisotopesAction Potentialschemistry.chemical_elementIn Vitro TechniquesGuinea pigPapaverineInternal medicinemedicineAnimalsPharmacologyPapaverineChemistryMyocardiumGeneral MedicineMyocardial ContractionResting potentialEndocrinologyPotassiumFemaleEffluxmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
researchProduct

Nothodissotis (Melastomataceae), a new genus from Atlantic Central Africa, including the new species N. alenensis from Equatorial Guinea

2019

Based on morphological and phylogenetic evidence, a new genus of Melastomataceae (Melastomateae), Nothodissotis Veranso-Libalah & G.Kadereit, gen. nov., is described from Atlantic Central Africa. Nothodissotis is distinguished from other African Melastomateae genera by its calyx-lobes that are notched at apex and asymmetrical (vs. entire and symmetrical). Nothodissotis includes two species: the type species N.barteri (Hook.f.) Veranso-Libalah & G.Kadereit, comb. nov. (syn. Dissotisbarteri Hook.f.), and the new species N.alenensis Veranso-Libalah & O. Lachenaud, sp. nov., described and illustrated here. Both species are restricted to open vegetation on rock outcrops w…

MelastomataceaeBiodiversity & ConservationZoologyPlant ScienceBiologyphylogenyHypanthiumFloristics & DistributionMagnoliopsidaAtlantic Ocean IslandsGenuslcsh:BotanymorphologyIUCN Red ListVulnerable speciesPlantaeEcology Evolution Behavior and SystematicsMolecular systematicsTaxonomynew speciesAppendagevulnerable speciesCentral AfricaNomenclatureMyrtalesDissotisplant conservationbiology.organism_classificationlcsh:QK1-989TracheophytaType speciesMelastomataceaeAfricaEquatorial GuineaConservation statusNothodissotisResearch ArticleIdentification keyPhytoKeys
researchProduct

Bacterial Cytolysin Perturbs Round Window Membrane Permeability Barrier In Vivo: Possible Cause of Sensorineural Hearing Loss in Acute Otitis Media

1998

ABSTRACT The passage of radioiodinated streptolysin-O (SLO) and albumin through the round window membrane (RWM) was studied in vivo. When applied to the middle ear, SLO became quantitatively entrapped in this compartment and no passage to the cochlea occurred. However, flux of radioiodinated albumin through the toxin-damaged RWM was observed. We propose that the passage of noxious macromolecules, such as proteases, from a purulent middle-ear effusion may be facilitated by pore-forming toxins, resulting in cochlear damage and sensorineural hearing loss.

Membrane permeabilityHearing lossHearing Loss SensorineuralImmunologyGuinea PigsBiologyIn Vitro TechniquesMicrobiologyPermeabilityBacterial ProteinsIn vivoAlbuminsmedicineotorhinolaryngologic diseasesAnimalsCochleaRound windowMembranesOtitis Media with EffusionAnatomyBacterial Infectionsmedicine.diseaseCochleaInfectious Diseasesmedicine.anatomical_structureRound Window EarStreptolysinsBiophysicsMiddle earParasitologySensorineural hearing lossCytolysinsense organsmedicine.symptom
researchProduct

Specific suppression of pentylenetetrazol-induced epileptiform discharges in CA3 neurons (hippocampal slice, guinea pig) by the organic calcium antag…

1989

Antiepileptic actions of the organic calcium antagonists flunarizine (cinnarizine derivate) and verapamil (papaverin derivat) on pentylenetetrazol-induced epileptic bioelectric activity were tested in CA3 neurones of hippocampal slices. In all experiments both calcium antagonists reduced the amplitudes and/or durations of paroxysmal depolarizations as well as their rate of occurrence, when the bath concentrations of flunarizine or verapamil exceeded 20 mumol/l. When they were added to the bath solution before pentylenetetrazol application, recordings of the resting membrane potential, of the membrane resistance, of action potentials and of spontaneous as well as of evoked excitatory and inh…

Membrane potentialmedicine.medical_specialtyGeneral NeuroscienceGuinea Pigschemistry.chemical_elementIn Vitro TechniquesCalciumInhibitory postsynaptic potentialHippocampusEndocrinologyVerapamilchemistrySeizuresPostsynaptic potentialInternal medicinemedicineExcitatory postsynaptic potentialAnimalsPentylenetetrazoleVerapamilPentylenetetrazolFlunarizineFlunarizinemedicine.drugExperimental Brain Research
researchProduct