Search results for "Thioperamide"

showing 4 items of 4 documents

Histamine inhibits 5-hydroxytryptamine release from the porcine small intestine: Involvement of H3 receptors

1992

Abstract Strips of the porcine small intestine were incubated in vitro, and the release of 5-hydroxytryptamine (5-HT) was determined by high-pressure liquid chromatography with electrochemical detection. Removal of the mucosa resulted in a large reduction (95%) of tissue 5-HT, suggesting that enterochromaffin cells are the main source of 5-HT. The release of 5-HT was reduced by 70% after omission of calcium. Tetrodotoxin and hexamethonium reduced the release of 5-HT by 30%–40% in a nonadditive manner, indicating a spontaneous neuronal (nicotinic) excitatory input to the enterochromaffin cells. Histamine inhibited the release of 5-HT by about 50%. This effect was not affected by mepyramine o…

MaleAgonistSerotoninmedicine.medical_specialtySwinemedicine.drug_classMepyramineIn Vitro TechniquesBiology03 medical and health scienceschemistry.chemical_compound0302 clinical medicineInternal medicineIntestine SmallmedicineAnimalsReceptor030304 developmental biologyPyrilamine0303 health sciencesThioperamideHepatologyMethylhistaminesGastroenterologyHydroxyindoleacetic AcidEndocrinologychemistryEnterochromaffin cellTetrodotoxinReceptors HistamineFemaleHexamethonium030217 neurology & neurosurgeryHistamineHistaminemedicine.drugGastroenterology
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The effects of histamine on the isolated mouse uterus

2000

1. A study is made of the contractile and relaxant effects, and mechanism of action, of histamine on isolated uterus from mice treated with diethylstilboestrol, employing acetylcholine and adrenaline as contractile and relaxant standard agents. 2. Concentration-response curves for histamine agonists were obtained in the absence and presence of selective histaminergic blocking drugs (clemizole, ranitidine and thioperamide) and indomethacin. A number of experiments were carried out in uterus from reserpinised mice. Concentration-response curves for acetylcholine and adrenaline were also obtained in the absence and presence of their selective antagonist (atropine and propranolol). 3. In isolat…

Atropinemedicine.medical_specialtyVasodilator AgentsHistamine AntagonistsHistamine agonistHistamine AgonistsRanitidineMiceUterine Contractionchemistry.chemical_compoundInternal medicinemedicineAnimalsDrug InteractionsDiethylstilbestrolPharmacologyThioperamideDose-Response Relationship DrugChemistryGeneral NeuroscienceUterusHistaminergicParasympatholyticsAcetylcholineClemizoleAtropineEndocrinologyFemaleAcetylcholineHistamineHistaminemedicine.drugJournal of Autonomic Pharmacology
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Histamine and serotonin released from the rat perfused heart by compound 48/80 or by allergen challenge influence noradrenaline or acetylcholine exoc…

1994

Terminal nerve fibres of the autonomic nervous system closely approach mast cells in peripheral organs, and mutual influences between release of neurotransmitters or mast cell mediators may cause neuro-immunological interactions. We have studied the influence of mast cell degranulation on the release of endogenous noradrenaline and newly incorporated acetylcholine (such as 14C-choline/acetylcholine overflow) evoked by stimulation of extrinsic postganglionic sympathetic or preganglionic vagal nerves in the rat Langendorff heart perfused with Tyrode solution. Compound 48/80 perfused in normal hearts, or ovalbumin infused into hearts from rats sensitized to ovalbumin, enhanced the overflow of …

MaleSerotoninmedicine.medical_specialtyLangendorff heartSerotonergicHistamine ReleaseExocytosisNorepinephrinechemistry.chemical_compoundInternal medicinemedicineAnimalsp-Methoxy-N-methylphenethylaminePharmacology (medical)Mast CellsRats WistarNeurotransmitterPharmacologyThioperamideChemistryMyocardiumAllergensCompound 48/80AcetylcholineRatsPerfusionEndocrinologyHistamine H3 receptorAcetylcholineHistaminemedicine.drugFundamental & Clinical Pharmacology
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Theoretical study of selective H3 receptor antagonists of histamine

1993

Abstract The conformations and charge distributions of three selective H3 receptor antagonists of histamine were determined using the MNDO approach. The results suggest that the conformational flexibilities of betahistine, N α-(2-phenylacetyl)histamine and thioperamide are different; however, the low-energy conformations of these compounds show closely related spatial orderings. The MNDO calculations predict a significant population of the N1H form in the imidazole systems of N α-(2-phenylacetyl)histamine and thioperamide. Our results indicate that the conformational behaviour of H3 antagonists is closely similar to that reported for H2 antagonists of histamine. These results emphasize the …

education.field_of_studyThioperamideStereochemistryChemistryPopulationAntagonistMNDOCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundComputational chemistrymedicineImidazoleBetahistinePhysical and Theoretical ChemistryHistamine H3 receptoreducationHistaminemedicine.drugJournal of Molecular Structure: THEOCHEM
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