Search results for " acetylcholine"

showing 10 items of 239 documents

Antagonist discrimination between subtypes of tachykinin receptors in the guinea-pig ileum.

1986

1. The effects of substance P and eledoisin on spontaneous and electrically-evoked release of [3H]acetylcholine, and on smooth muscle were studied in the guineapig myenteric plexus-longitudinal muscle preparation preloaded with [3H]choline. Substance P and eledoisin caused transient increases in spontaneous release of [3H]acetylcholine and in longitudinal muscle tone. Both tachykinins were equipotent in contracting the muscle, but eledoisin was more potent than substance P in eliciting [3H]acetylcholine release. The release caused by substance P was enhanced in the presence of naloxone and scopolamine which suggests that the release is modulated through opioid and muscarinic receptors. 2. S…

Malemedicine.medical_specialtyEledoisinGuinea PigsScopolamineSubstance P(+)-NaloxoneSubstance Pcomplex mixtureschemistry.chemical_compoundEledoisinIleumInternal medicineMuscarinic acetylcholine receptormedicineAnimalsNeurotransmitterReceptorReceptors TachykininPharmacologyNaloxoneGeneral MedicineAcetylcholineReceptors NeurotransmitterEndocrinologychemistryFemaleTachykinin receptorAcetylcholinemedicine.drugMuscle ContractionNaunyn-Schmiedeberg's archives of pharmacology
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A muscarinic receptor different from the M1, M2, M3 and M4 subtypes mediates the contraction of the rabbit iris sphincter

1992

In order to analyse the subtype of muscarinic receptors involved in the methacholine-induced contraction of the rabbit iris sphincter we have determined equilibrium dissociation constants (KB) of various antagonists in the sphincter muscle. The values were compared with those observed at M1 (rabbit vas deferens), M2 (heteroreceptors in rat iris) and M3 receptors (guinea-pig ileum), or at the muscarinic receptors in the guinea-pig uterus. The methacholine-induced contraction of the uterus from immature guinea-pigs was competitively antagonized by pirenzepine (6.64, -log KB), 4-DAMP (8.39), hexahydrodifenidol (HHD; 7.00 for the (R)- and 5.40 for the (S)-enantiomer), p-fluoro-hexahydrosiladife…

Malemedicine.medical_specialtyGuinea PigsIrisBiologyInternal medicineMuscarinic acetylcholine receptormedicineAnimalsReceptorEvoked PotentialsMethacholine ChloridePharmacologyVas deferensMuscarinic acetylcholine receptor M3Muscle SmoothMuscarinic acetylcholine receptor M2General MedicineReceptors MuscarinicPirenzepineDissociation constantmedicine.anatomical_structureEndocrinologyFemaleRabbitsmedicine.symptomMuscle ContractionMuscle contractionmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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Enhancement of guinea-pig intestinal peristalsis by blockade of muscarinic M1-receptors

1988

1. The effects of pirenzepine and hyoscine on the peristaltic reflex were investigated in the guinea-pig isolated small intestine. Peristalsis was induced by raising the intraluminal pressure and the volume of fluid propelled was taken as a measure of the efficiency of peristaltic activity. 2. Low concentrations of pirenzepine (0.1-1 nM) and of hyoscine (0.01 nM) significantly enhanced peristalsis, whereas larger concentrations of both drugs caused inhibition. Pirenzepine was about 6 times less potent than hyoscine in increasing peristalsis, but was about 100 times less potent in inhibiting it. 3. Neither tolazoline (1 microM) nor naloxone (0.3 microM) affected the stimulatory action of pir…

Malemedicine.medical_specialtyGuinea PigsScopolamineIn Vitro TechniquesBiologyGuinea pigInternal medicineIntestine SmallMuscarinic acetylcholine receptormedicineAnimalsTolazolinegamma-Aminobutyric AcidPeristalsisPharmacologyDrug SynergismPirenzepineBicucullineReceptors MuscarinicPirenzepineEndocrinologyReflexGABAergicGastrointestinal MotilityResearch Articlemedicine.drugBritish Journal of Pharmacology
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Muscarinic inhibition of acetylcholine release from a novel in vitro preparation of the guinea-pig trachea

1990

An isolated preparation of the guinea-pig trachea is described which allows the simultaneous measurement of acetylcholine release and smooth muscle contraction. Incubation of the epithelium-free preparation with [3H]choline resulted in the formation of [3H]acetylcholine. Electrical stimulation caused the release of [3H]acetylcholine and a contractile response. Tetrodotoxin and omission of calcium from the medium abolished both the evoked release and contractions. The muscarinic agonists oxotremorine, carbachol and pilocarpine concentration-dependently inhibited the electrically evoked acetylcholine release and contracted the tracheal smooth muscle. Pre- and postsynaptic EC50 values for a gi…

Malemedicine.medical_specialtyGuinea Pigschemistry.chemical_elementStimulationTetrodotoxinIn Vitro TechniquesCalciumEpitheliumCholineGuinea pigchemistry.chemical_compoundInternal medicineMuscarinic acetylcholine receptormedicineAnimalsPharmacologyOxotremorineMuscle SmoothGeneral MedicineSmooth muscle contractionReceptors MuscarinicAcetylcholineElectric StimulationTracheaEndocrinologychemistryTetrodotoxinBiophysicsCalciummedicine.symptomAcetylcholinemedicine.drugMuscle contractionNaunyn-Schmiedeberg's Archives of Pharmacology
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A useful muscarinic parameter and the differential recording of atrial and ventricular tension in the perfused rabbit heart

1971

1. A simple method of recording right atrial tension from the Langendorff perfused rabbit has been described; it is based on the “transverse” method of recording cardiac contractions described by Beckett (1970). 2. Right atrial and ventricular tensions were recorded by transducers attached to threads stitched into the right atrium and right ventricle, the heart being retained and prevented from rotating by two threads stitched into the intraventricular septum as described by Beckett. 3. Right ventricular diastolic tension was adjusted to 7.5 g. Interference with the atrial record by ventricular systole was overcome by adjustment of diastolic right atrial tension to its optimal value between…

Malemedicine.medical_specialtyHeart VentriclesTransducersDiastoleBlood PressureHeart RateInternal medicineMuscarinic acetylcholine receptormedicineAnimalsVentricular FunctionHeart Atriacardiovascular diseasesSympathomimeticsPharmacologyCardiac cyclebusiness.industryP waveHeartVagus NerveGeneral MedicineAtrial FunctionStimulation ChemicalCardiovascular physiologyGanglionPerfusionmedicine.anatomical_structureParasympathomimeticsVentricleMuscle TonusAnesthesiacardiovascular systemCardiologyFemaleRabbitsbusinessPerfusionMuscle ContractionNaunyn-Schmiedebergs Archiv f�r Pharmakologie
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α4-1 Subunit mRNA of the nicotinic acetylcholine receptor in the rat olfactory bulb: cellular expression in adult, pre- and postnatal stages

1996

In addition to their role in signal transduction, nicotinic acetylcholine receptors have been shown in vi-tro to be involved in neuronal growth cone regulation during development. This idea is supported by recent histochemical findings showing that iso- and archicortical nicotinic alpha4-1 receptor mRNA expression precedes cholinergic fiber ingrowth. To test whether this also holds true for rhinencephalic parts of the telencephalon, we have studied the olfactory bulb by digoxigenin-mediated in situ hybridization, using an alpha4-1 isoform-specific riboprobe and an alkaline-phosphatase-based detection system. Development is characterized by early intense alpha4-1 mRNA expression (embryonic d…

Malemedicine.medical_specialtyHistologyIn situ hybridizationReceptors NicotinicBiologyPathology and Forensic MedicinePregnancyInternal medicinemedicineAnimalsRNA MessengerRats WistarIn Situ HybridizationAcetylcholine receptorCerebrumRNA ProbesCell BiologyOlfactory BulbRatsOlfactory bulbNicotinic acetylcholine receptormedicine.anatomical_structureNicotinic agonistEndocrinologyCholinergicFemaleSignal transductionDigoxigeninCell and Tissue Research
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Muscarinic inhibition of endogenous noradrenaline release from rabbit isolated trachea: receptor subtype and receptor reserve.

1994

The aim of the present study was to characterize putative muscarine receptors on sympathetic nerve terminals in the rabbit trachea. Release of endogenous noradrenaline from in vitro incubated rabbit trachea was evoked by electrical field stimulation (3 Hz, 540 pulses) and quantified by high performance liquid chromatography with electrochemical detection. The muscarine receptor agonist oxotremorine inhibited the evoked release of noradrenaline completely at 1 mumol/l (EC50: 64 nmol/l). The concentration response curve was very steep (Hill coefficient of 2.3). Scopolamine shifted the concentration response curve of oxotremorine to the right (-log KB 8.48) demonstrating specific, inhibitory m…

Malemedicine.medical_specialtyIndomethacinCholinergic AgentsEndogenyMuscarinic AntagonistsIn Vitro TechniquesMuscarinic AgonistsHigh-performance liquid chromatographyReceptor subtypechemistry.chemical_compoundNorepinephrineAdrenergic AgentsInternal medicineMuscarinic acetylcholine receptormedicineAnimalsReceptorPharmacologyMuscarineBinding SitesPhenoxybenzamineChemistryRabbit (nuclear engineering)General Medicinerespiratory systemReceptors MuscarinicIn vitroElectric StimulationTracheaEndocrinologyFemaleRabbitsNaunyn-Schmiedeberg's archives of pharmacology
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Muscarinic receptors, leukotriene B4 production and neutrophilic inflammation in COPD patients.

2005

Background:  Acetylcholine (ACh) plays an important role in smooth muscle contraction and in the development of airway narrowing; preliminary evidences led us to hypothesize that ACh might also play a role in the development of airways inflammation in chronic obstructive pulmonary disease (COPD). Methods:  We evaluated the concentrations of leukotriene B4 (LTB4) in induced sputum, and the expression of Ach M1, M2, and M3 receptors in sputum cells (SC) obtained from 16 patients with COPD, 11 smokers, and 14 control subjects. The SC were also treated with ACh and the production of LTB4 assessed in the presence or absence of a muscarinic antagonist (oxitropium). In blood monocytes, we evaluate…

Malemedicine.medical_specialtyLeukotriene B4NeutrophilsImmunologyProtozoan ProteinsLeukotriene B4chemistry.chemical_compoundPulmonary Disease Chronic ObstructiveInternal medicineMuscarinic acetylcholine receptorImmunology and AllergyMedicineHumansReceptorCells CulturedAgedFlavonoidsCOPDMitogen-Activated Protein Kinase 3business.industryCalcium-Binding ProteinsSputumMuscarinic acetylcholine receptor M3Muscarinic antagonistSmooth muscle contractionMiddle Agedmedicine.diseaseImmunohistochemistryReceptors MuscarinicAcetylcholinerespiratory tract diseasesChemotaxis LeukocyteEndocrinologychemistryLeukocytes MononuclearFemalebusinessAcetylcholinemedicine.drugAllergy
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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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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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