Search results for "choline"

showing 10 items of 1138 documents

Acute effects of low doses of methyl parathion on human EEG.

2005

Abstract Biological monitoring of workers exposed to organophosphates consists mainly of measuring serum or erythrocyte cholinesterase activity. However, animal experiments and a field study suggest that quantitative analysis of EEG may be more sensitive. In a parallel group design, 25 farmers were investigated, spraying methyl parathion or water for 50 min. EEG was recorded before and after spraying. Serum and erythrocyte cholinesterase activity was compared with intraindividual pre-exposure values. Plasma methyl parathion concentrations ranged up to 12.1 μg/l, methyl paraoxon was not detectable. Based on plasma concentrations, two exposed subgroups were defined. In EEG recorded with close…

PharmacologyAcute effectsmedicine.medical_specialtyParaoxonbiologymedicine.diagnostic_testHealth Toxicology and MutagenesisLow doseGeneral MedicineElectroencephalographyToxicologychemistry.chemical_compoundEndocrinologychemistryAnesthesiaInternal medicineClosed eyesmedicineParathion methylbiology.proteinQuantitative analysis (chemistry)medicine.drugCholinesteraseEnvironmental toxicology and pharmacology
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Prostanoid receptors of the EP3 subtype mediate inhibition of evoked [3 H]acetylcholine release from isolated human bronchi

1998

1 The release of neuronal [3H]acetylcholine (ACh) from isolated human bronchi after labelling with [3H]choline was measured to investigate the effects of prostanoids. 2 A first period of electrical field stimulation (S1) caused a [3H]ACh release of 320±70 and 200±40 Becquerel (Bq) g−1 in epithelium-denuded and epithelium-containing bronchi respectively (P>0.05). Subsequent periods of electrical stimulation (Sn, n=2, 3, and 4) released less [3H]ACh, i.e. decreasing Sn/S1 values were obtained (0.76±0.09, 0.68±0.07 and 0.40±0.04, respectively). 3 Cumulative concentrations (1–1000 nM) of EP-receptor agonists like prostaglandin E2, nocloprost, and sulprostone (EP1 and EP3 selective) inhibited ev…

PharmacologyAgonistmedicine.medical_specialtybiologyChemistrymedicine.drug_classProstanoidStimulationchemistry.chemical_compoundEndocrinologyInternal medicinebiology.proteinmedicinelipids (amino acids peptides and proteins)CyclooxygenaseProstaglandin E2ReceptorNeurotransmitterAcetylcholinemedicine.drugBritish Journal of Pharmacology
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A new class of organic nitrates: investigations on bioactivation, tolerance and cross-tolerance phenomena

2009

Background and purpose:  The chronic use of organic nitrates is limited by serious side effects including oxidative stress, nitrate tolerance and/or endothelial dysfunction. The side effects and potency of nitroglycerine depend on mitochondrial aldehyde dehydrogenase (ALDH-2). We sought to determine whether this concept can be extended to a new class of organic nitrates with amino moieties (aminoalkyl nitrates). Experimental approach:  Vasodilator potency of the organic nitrates, in vitro tolerance and in vivo tolerance (after continuous infusion for 3 days) were assessed in wild-type and ALDH-2 knockout mice by isometric tension studies. Mitochondrial oxidative stress was analysed by L-012…

PharmacologyChemistryMetabolismMitochondrionPharmacologymedicine.disease_causeNitric oxideCross-tolerancechemistry.chemical_compoundBiochemistryIn vivomedicinePotencyAcetylcholineOxidative stressmedicine.drugBritish Journal of Pharmacology
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�ber die Wirkung von Acetylcholin auf die mechanischen und elektrischen Eigenschaften des denervierten Rattenzwerchfells unter dem Einflu� verschiede…

1959

PharmacologyChemistryPharmacology toxicologymedicineRat DiaphragmGeneral MedicinePharmacologyAcetylcholinemedicine.drugNaunyn-Schmiedeberg's Archiv f�r Experimentelle Pathologie und Pharmakologie
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Effects of (+)-tubocurarine on [3H]acetylcholine release from the rat phrenic nerve at different stimulation frequencies and train lengths

1987

The effect of (+)-tubocurarine (TC) on the release of [3H]acetylcholine from the rat phrenic nerve-hemidiaphragm preincubated with [3H]choline was investigated at different stimulation frequencies and train lengths. At 0.5 Hz (100 pulses) TC failed to modulate the evoked acetylcholine release. A slight (30%) inhibition was observed at 1 Hz (100 pulses). Release of acetylcholine evoked at 5, 25 and 50 Hz (100 pulses) or 100 Hz (200 pulses) was markedly reduced by TC. The degree of inhibition (60%) was similar between 5 Hz and 100 Hz. A concentration of 1 mumol/l TC was a maximal effective concentration at 5 Hz whilst at all higher stimulation frequencies a 10-fold higher concentration was ne…

PharmacologyChemistryTubocurarineMotor nerveRats Inbred StrainsStimulationGeneral MedicineIn Vitro TechniquesReceptors NicotinicNeurotransmissionAcetylcholineElectric StimulationRatsPhrenic NerveNicotineElectrophysiologyNicotinic agonistAnesthesiamedicineBiophysicsAnimalsAcetylcholinemedicine.drugPhrenic nerveNaunyn-Schmiedeberg's Archives of Pharmacology
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Die Wirkung von Acetylcholin, Dekamethonium und d-Tubocurarin am isolierten Rattenzwerchfell in Abh�ngigkeit von der Denervationsdauer

1955

An 41 isolierten Zwerchfellpraparaten der Ratte wurde zu verschiedenen Zeitpunkten nach Exharese des N. phrenicus die Wirkung von Acetylcholin (Ach), Decamethonium (C 10) und d-Tubocurarin (dTc) untersucht. Die Reaktionen des Muskels zeigten eine charakteristische Abhangigkeit von der Denervationsdauer. Ach verursachte eine Verminderung der Hubhohe elektrisch ausgeloster Einzelzuckungen, Kontraktur und Kontraktur-Ruckstand. Die Wirkung von C 10 ahnelte der von Ach weitgehend. Dagegen fuhrte Gabe von dTc zu einer Senkung der „Grundlinie“ und zur Verminderung der Hubhohe der Einzelzuckungen.

PharmacologyDenervationD-TubocurarineDecamethoniumChemistryPharmacology toxicologymedicineRat DiaphragmGeneral MedicinePharmacologyAcetylcholinemedicine.drugNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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Über den Einfluss von Acetylcholin auf das Membranpotential denervierter Rattenzwerchfelle

1957

The membran potential of isolated rat-diaphragms has been measured by means of intracellular micro-electrodes, in order to study changes of the resting potential and of the depolarizing action of acetylcholine after section of the phrenic nerve. Within 80 days after denervation, the membrane potential was found to fall exponentially from 87 mV to 66 mV. The action of acetylcholine, on the other hand, was found to be independent of the duration of denervation: between the 4th and the 80th day of denervation: 10−5g/ml acetylcholine always caused the membrane potential to fall by an average of the 9 mV.

PharmacologyDenervationMembrane potentialmedicine.medical_specialtyChemistryDepolarizationCell BiologyResting potentialCellular and Molecular NeuroscienceEndocrinologyInternal medicinemedicineMolecular MedicineRat DiaphragmMolecular BiologyIntracellularAcetylcholinemedicine.drugPhrenic nerveExperientia
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In vitro studies of methanol and dichloromethanol extracts ofJuniperus oxycedrus L.

1997

The present study evaluated the effect of methanol and dichloromethanol extracts obtained from the leaves and stems of Juniperus oxycedrus against neurotransmitter-induced contraction in different isolated tissues of rats and guinea-pigs. Diverse concentrations of these extracts inhibit the concentration curve response to histamine, serotonin and acetylcholine. These results contribute to explaining the use of this plant in folk medicine. © 1997 John Wiley & Sons, Ltd.

PharmacologyFolk medicineTraditional medicineBiological activityBiologyPharmacognosybiology.organism_classificationIn vitrochemistry.chemical_compoundchemistryBotanymedicineMethanolJuniperus oxycedrusHistamineAcetylcholinemedicine.drugPhytotherapy Research
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Muscarinic acetylcholine receptor trafficking in streptolysin O-permeabilized MDCK cells.

1996

We investigated the validity of streptolysin O (SLO)-permeabilized Madin-Darbin canine kidney (MDCK) cells which express muscarinic acetylcholine receptors (mAChRs) coupled to pertussis toxin-sensitive guanine nucleotide-binding proteins (G proteins) for the study of the molecular machinery that regulated mAChR internalization and recycling. Exposure of SLO-permeabilized cells to carbachol-reduced cell surface receptor number by up to 40% without changing total receptor number. The kinetics and maximal extent of receptor internalization as well as the potency of carbachol to induce receptor internalization were almost identical in SLO-permeabilized and non-permeabilized cells. Using this se…

PharmacologyG protein-coupled receptor kinasemedia_common.quotation_subjectB-cell receptorMuscarinic acetylcholine receptor M3General MedicineMuscarinic acetylcholine receptor M1BiologyKidneyReceptors MuscarinicPermeabilityCell biologyAdenosine TriphosphateDogsBacterial ProteinsCell surface receptorGTP-Binding ProteinsGuanosine 5'-O-(3-Thiotriphosphate)Muscarinic acetylcholine receptor M5StreptolysinsEnzyme-linked receptorAnimalsInternalizationCells Culturedmedia_commonNaunyn-Schmiedeberg's archives of pharmacology
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Murine embryonic stem cell line CGR8 expresses all subtypes of muscarinic receptors and multiple nicotinic receptor subunits: Down-regulation of α4- …

2015

Non-neuronal acetylcholine mediates its cellular effects via stimulation of the G-protein-coupled muscarinic receptors and the ligand-gated ion channel nicotinic receptors. The murine embryonic stem cell line CGR8 synthesizes and releases non-neuronal acetylcholine. In the present study a systematic investigation of the expression of nicotinic receptor subunits and muscarinic receptors was performed, when the stem cells were grown in the presence or absence of LIF, as the latter condition induces early differentiation. CGR8 cells expressed multiple nicotinic receptor subtypes (α3, α4, α7, α9, α10, β1, β2, β3, β4, γ, δ, e) and muscarinic receptors (M1, M3, M4, M5); M2 was detected only in 2 …

PharmacologyImmunologyMuscarinic acetylcholine receptor M3Down-RegulationMuscarinic acetylcholine receptor M2Cell DifferentiationMuscarinic acetylcholine receptor M1BiologyReceptors NicotinicReceptors MuscarinicCell biologyCell LineMiceProtein SubunitsNicotinic agonistGanglion type nicotinic receptorGene Expression RegulationMuscarinic acetylcholine receptor M5Muscarinic acetylcholine receptorImmunology and AllergyAnimalsAlpha-4 beta-2 nicotinic receptorEmbryonic Stem CellsInternational immunopharmacology
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