Search results for "Muscarinic"

showing 10 items of 263 documents

Evaluation by reverse phase HPLC of [3H]acetylcholine release evoked from the myenteric plexus of the rat.

1990

Myenteric plexus-longitudinal muscle strips isolated from the small intestine of rats were incubated with [3H]choline to measure the synthesis and the release of [3H]acetylcholine. To separate different radioactive compounds (acetylcholine, choline, phosphorylcholine) from both the tissue and the overflow a new method, the reverse phase HPLC, was used. The radiochromatogram following the injection of a [3H]choline-standard and a [14C]acetylcholine-standard onto the HPLC showed a clear separation of both isotopes with a recovery rate of roughly 100%. Incubation of the muscle strips with [3H]choline caused the synthesis of [3H]acetylcholine (30,000 dpm/preparation) that increased 2-fold, when…

Malemedicine.medical_specialtyPhosphorylcholineGuinea PigsScopolaminechemistry.chemical_elementMyenteric PlexusTetrodotoxinCalciumIn Vitro TechniquesCholinechemistry.chemical_compoundInternal medicineMuscarinic acetylcholine receptormedicineExtracellularOxotremorineCholineAnimalsMyenteric plexusChromatography High Pressure LiquidPharmacologyChromatographyOxotremorineGeneral MedicineReceptors MuscarinicAcetylcholineElectric StimulationRatsEndocrinologychemistryTetrodotoxinFemaleAcetylcholinemedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Presynaptic effects of scopolamine, oxotremorine, noradrenaline and morphine on [3H] acetylcholine release from the myenteric plexus at different sti…

1987

The inhibition by three modulators (oxotremorine, noradrenaline, morphine) of acetylcholine release from the myenteric plexus preincubated with [3H]choline was investigated at different stimulation frequencies and calcium concentrations. Moreover, [3H]acetylcholine release evoked by a low (0.1 Hz) or a high (10 Hz) stimulation rate was investigated at different calcium concentrations either in the absence or presence of scopolamine. A reduced calcium concentration (0.6 mmol/l) inhibited acetylcholine release more at 0.1 Hz (74% +/- 3%) than at 10 Hz (44% +/- 8%). Scopolamine enhanced the stimulated acetylcholine release at a calcium concentration of 1.8 mmol/l. At calcium concentrations hig…

Malemedicine.medical_specialtyPhysostigmineGuinea PigsScopolamineMyenteric Plexuschemistry.chemical_elementAdrenergicStimulationIn Vitro TechniquesNeurotransmissionCalciumNorepinephrineIleumInternal medicinemedicineOxotremorineAnimalsMyenteric plexusPharmacologyMorphineOxotremorineGeneral MedicineReceptors Adrenergic alphaReceptors MuscarinicAcetylcholineElectric StimulationEndocrinologychemistryAutoreceptorCalciumFemaleAcetylcholinemedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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The effect of physostigmine on the vagally induced muscarinic inhibition of noradrenaline release from the isolated perfused rabbit atria.

1982

1. Presynaptic cholinergic-adrenergic interactions were studied on isolated perfused rabbit atria with the extrinsic right vagus and sympathetic innervation intact. The transmitter stores were labelled with 14C-choline and 3H-noradrenaline. The radioactive compounds were separated on columns and determined by scintillation spectrometry. The stimulation-evoked overflow of both transmitters was calcium-dependent and abolished by tetrodotoxin. 2. Methacholine caused a concentration-dependent decrease of atrial tension development and 3H-noradrenaline overflow evoked by 3 Hz sympathetic stimulation. Vagus nerve stimulation (1–20Hz), although nearly abolishing tension development at 20Hz, decrea…

Malemedicine.medical_specialtyPhysostigmineSympathetic Nervous Systemmedicine.medical_treatmentPhysostigmineIn Vitro TechniquesCholinechemistry.chemical_compoundNorepinephrineInternal medicineMuscarinic acetylcholine receptormedicineAnimalsCholinesterasesMethacholine CompoundsReceptors CholinergicAxonCholinesterasePharmacologybiologyChemistryMyocardiumVagus NerveGeneral MedicineReceptors MuscarinicElectric StimulationEndocrinologymedicine.anatomical_structurenervous systemcardiovascular systembiology.proteinTetrodotoxinMethacholineFemaleRabbitsVagus nerve stimulationAcetylcholinemedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Some pharmacological properties of the false cholinergic transmitter acetylpyrrolidinecholine and its precursor pyrrolidinecholine

1976

The acetylchline analogue acetylpyrrolidinecholine as well as the choline analogue pyrrolidinecholine were synthesized and the cholinergic properties of both substances were investigated on the guinea-pig ileum, rat blood pressure and frog rectus abdominis muscle. Acetylpyrrolidinecholine was 3-5 times less potent than acetylcholine on the three preparations tested. The dose-response curves to acetylpyrrolidinecholine were shifted to the right in a parallel manner by atropine and (+)-tubocurarine. The dissociation constants for atropine and (+)-tubocurarine obtained with acetylpyrrolidinecholine as agonist were not different from those obtained with acetylcholine. This indicates that acetyl…

Malemedicine.medical_specialtyPyrrolidinesGuinea PigsRana temporariaNeuromuscular JunctionNeuromuscular transmissionBlood PressureReceptors NicotinicSynaptic TransmissionCholinechemistry.chemical_compoundInternal medicineMuscarinic acetylcholine receptormedicineAnimalsAcetylcholine receptorPharmacologyMuscarineMuscarinic acetylcholine receptor M3Muscle SmoothGeneral MedicineReceptors MuscarinicAcetylcholineRatsNicotinic agonistEndocrinologyParasympathomimeticschemistryCholinergicAcetylcholineMuscle Contractionmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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Does concomitant diabetes affect treatment responses in overactive bladder patients?

2013

Summary Aims To compare the efficacy and tolerability of a muscarinic receptor antagonist, darifenacin, in the treatment of overactive bladder (OAB) patients with concomitant diabetes as compared with those without comorbidities. Methods Post hoc exploratory analysis of a published, large, non-interventional study in OAB patients treated with darifenacin including 532 diabetics and 1315 controls. Associations of diabetes with treatment responses were evaluated by multiple regression models. Results Diabetics (largely type 2 patients) and controls differed in baseline age, body weight, duration of OAB symptoms and presence of comedications. However, they exhibited similar OAB symptom episode…

Malemedicine.medical_specialtyPyrrolidinesMuscarinic Antagonistsurologic and male genital diseasesAffect (psychology)Diabetes ComplicationsDiabetes mellitusInternal medicineMuscarinic acetylcholine receptorDarifenacinMedicineHumansBenzofuransDose-Response Relationship Drugbusiness.industryUrinary Bladder OveractiveAntagonistUrinary Bladder DiseasesGeneral MedicineMiddle Agedmedicine.diseasefemale genital diseases and pregnancy complicationsEndocrinologyTreatment OutcomeUrinary IncontinenceTolerabilityOveractive bladderConcomitantRegression AnalysisFemaleNocturiabusinessmedicine.drugInternational journal of clinical practice
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Cholinergic modulation of the release of 5-hydroxytryptamine from the guinea pig ileum.

1987

Isolated segments of the guinea pig ileum were vascularly perfused and the release of 5-HT and its metabolite 5-HIAA into the portal venous effluent determined by HPLC with electrochemical detection. Test substances were applied via the arterial perfusion medium. Oxotremorine inhibited concentration-dependently the release of 5-HT and 5-HIAA (by 47% at 1 mumol/l). Scopolamine (0.1 mumol/l) did not affect the release of 5-HT and 5-HIAA, but antagonized the effect of oxotremorine. In the presence of TTX (1 mumol/l), oxotremorine (1 mumol/l) increased the release of 5-HT by 150% and that of 5-HIAA by 220%. This increase was completely blocked by scopolamine. Hexamethonium (100 mumol/l) and TTX…

Malemedicine.medical_specialtySerotoninMetaboliteGuinea PigsScopolamineHexamethonium CompoundsBiologyIn Vitro TechniquesReceptors NicotinicHexamethoniumGuinea pigchemistry.chemical_compoundIleumInternal medicineMuscarinic acetylcholine receptorOxotremorinemedicineEnterochromaffin CellsAnimalsReceptors CholinergicIntestinal MucosaPharmacologyMuscarineOxotremorineGeneral MedicineEndocrinologynervous systemchemistryEnterochromaffin cellHexamethoniumSerotoninmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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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
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Expression of nicotinic acetylcholine receptors in the rat superior cervical ganglion on mRNA and protein level.

1994

The expression of nicotinic acetylcholine receptors (nAChR) in the rat superior cervical ganglion was investigated by Western blotting, immunohistochemistry and non-radioactive in situ hybridization applying probes for the alpha 4-1 and beta 2 subunit mRNA. Immunoblot analysis of homogenized ganglia using the anti-nAChRs antibody WF6 revealed a labeled protein band of apparent molecular weight of 40 kDa which is typical for the alpha subunit of nAChRs. Applying double-labeling immunofluorescence with antibodies against tyrosine hydroxylase, nAChR-like molecules were identified in most postganglionic neurons and in a subpopulation of small intensely fluorescent (SIF) cells. alpha 4-1 and bet…

Malemedicine.medical_specialtySuperior cervical ganglionBlotting WesternFluorescent Antibody TechniqueGene ExpressionNerve Tissue ProteinsSuperior Cervical GanglionBiologyReceptors NicotinicRats Sprague-DawleyCellular and Molecular NeuroscienceGanglion type nicotinic receptorInternal medicineMuscarinic acetylcholine receptormedicineAnimalsRNA MessengerMolecular BiologyIn Situ HybridizationG alpha subunitAcetylcholine receptorNeuronsMolecular biologyRatsEndocrinologyNicotinic agonistnervous systemSmall intensely fluorescent cellFemalesense organsAcetylcholinemedicine.drugBrain research. Molecular brain research
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The effects of methacholine and calcium deprivation on the release of the false transmitter, ?-methyladrenaline, from the isolated rabbit heart

1976

1. Anaesthetized rabbits were infused for 20 min with 85 μg · kg−1 · min−1 (±)-α-methyladrenaline. The hearts dissected 15 min after the infusion contained 1.49 μg/g α-methyladrenaline; the endogenous noradrenaline content was correspondingly decreased. 2. Hearts from α-methyladrenaline-infused animals were isolated with the right sympathetic nerves intact and perfused. Ventricular rate, right atrial and right ventricular tensions were recorded using the transverse method. 3. Electrical stimulation (10 Hz, 1 ms, 1 min) of sympathetic nerves, perfusion with the nicotinic drug, p-aminophenethyltrimethylammonium (PAPETA) or perfusion with 54 mM KCl (high K+) solution evoked an output of both α…

Malemedicine.medical_specialtySympathetic Nervous SystemEpinephrineTyraminechemistry.chemical_elementStimulationCalciumPotassium ChlorideNorepinephrinechemistry.chemical_compoundInternal medicineMuscarinic acetylcholine receptormedicineAnimalsMethacholine CompoundsPharmacologyAniline CompoundsChemistryMyocardiumHeartGeneral MedicineTyramineGanglionic StimulantsElectric StimulationQuaternary Ammonium CompoundsAtropineEndocrinologySympatholyticsLiberationCalciumFemaleMethacholineRabbitsPerfusionmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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Sympathetic Nerve Stimulation on the perfused rat heart. Affinities of N-methylatropine and pirenzepine at pre- and postsynaptic muscarine receptors.

1982

Rat isolated hearts with the sympathetic nerves attached were perfused with (-)-3H-noradrenaline in order to label the storage vesicles of the adrenergic nerves. Release was induced either by electrical stimulation of the nerves (3 Hz, 1 min) or by perfusion with high K+ solution (54 mM). The overflow of 3H-noradrenaline and its metabolites was determined by liquid scintillation counting after separation of the compounds by column chromatography. The experimental conditions ensured a minor contribution of 3H-metabolites to the evoked total tritium overflow. The release of 3H-noradrenaline evoked by nerve stimulation or high K+ solution was decreased in the presence of the muscarinic agonist…

Malemedicine.medical_specialtySympathetic Nervous SystemStimulationIn Vitro TechniquesPiperazineschemistry.chemical_compoundNorepinephrineColumn chromatographyPostsynaptic potentialInternal medicinemedicineAnimalsMethacholine CompoundsReceptors CholinergicAtropine DerivativesReceptorBiotransformationPharmacologyBenzodiazepinonesMuscarineMyocardiumHeartRats Inbred StrainsGeneral MedicinePirenzepinePirenzepineReceptors MuscarinicElectric StimulationRatsEndocrinologychemistryMethacholineFemalePerfusionmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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