Search results for "JUNCTION"

showing 10 items of 862 documents

Uptake and metabolism of [3H]choline by the rat phrenic nerve-hemidiaphragm preparation

1987

A whole nerve-muscle preparation (about 160 mg) or an end-plate preparation (about 25 mg) of the rat phrenic nerve-hemidiaphragm were incubated with [3H]choline, to investigate choline uptake and choline metabolism. Choline uptake was measured from the disappearance of choline from the incubation medium during the loading period and from the retention of tritium in the tissue after the loading and washout period. Based on the results obtained with both methods the end-plate preparation takes up three times as much choline than the whole nerve-muscle preparation or a small muscle strip that was cut outside the end-plate region and had a similar size as the end-plate preparation. Choline upta…

Malemedicine.medical_specialtyMetaboliteDiaphragmNeuromuscular JunctionPhospholipidIn Vitro TechniquesBiologyMotor EndplateNeuromuscular junctionCholinechemistry.chemical_compoundPhosphatidylcholineInternal medicinemedicineAnimalsCholinePhrenic nervePharmacologyRats Inbred StrainsHemicholinium 3General MedicineMetabolismMuscle DenervationRatsPhrenic NerveLysophosphatidylcholinemedicine.anatomical_structureEndocrinologychemistryNaunyn-Schmiedeberg's Archives of Pharmacology
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Presynaptic nicotine receptors mediating a positive feed-back on transmitter release from the rat phrenic nerve.

1986

The effects of 1,1-dimethyl-4-phenylpiperazinium (DMPP) and of nicotine receptor antagonists on [3H]acetylcholine release from the rat phrenic nerve preincubated with [3H]choline were investigated in the absence and presence of cholinesterase inhibitors (presynaptic effects). Additionally, the effects of hexamethonium and tubocurarine on the muscle contraction of the indirectly stimulated diaphragm were examined (postsynaptic effects). DMPP (1-30 microM) increased (76-92%), whereas hexamethonium (0.001-1 mM) and tubocurarine (1-10 microM) decreased (52-60%) the release of [3H]acetylcholine following a train of 100 pulses at 5 Hz. The release caused by a longer train (750 pulses at 5 Hz) was…

Malemedicine.medical_specialtyMotor nerveTubocurarineHexamethonium CompoundsIn Vitro TechniquesReceptors NicotinicNeuromuscular junctionFeedbackchemistry.chemical_compoundPostsynaptic potentialInternal medicinemedicineAnimalsCholinesterasePhrenic nervePharmacologyNeurotransmitter AgentsbiologyRats Inbred StrainsGeneral Medicinemusculoskeletal systemElectric StimulationRatsPhrenic NerveEndocrinologymedicine.anatomical_structurechemistrybiology.proteinHexamethoniummedicine.symptomDimethylphenylpiperazinium IodideAcetylcholineMuscle contractionmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Myasthenia-like syndrome induced by cardiovascular agents. Report of a case

1987

The case of a myasthenia-like syndrome induced by cardiovascular drugs is reported. The clinical and electrophysiological features of the case are discussed. © 1987 Masson Italia Periodici S.r.l.

Malemedicine.medical_specialtyNeurologyNeuromuscular JunctionCoronary DiseaseDermatologyPeruvosideMyasthenia-like syndromeSynaptic TransmissionPropafenoneimmune system diseasesMyasthenia GravisHumansMedicineperuvosideEtafenone hydrochlorideAgedNeuroradiologyOphthalmoplegiaNeuroscience (all)business.industryGeneral NeuroscienceGeneral Medicinenervous system diseasesCardenolidesPsychiatry and Mental healthAnesthesiaCardiovascular agentetafenone hydrochlorideDrug Therapy CombinationSettore MED/26 - NeurologiaNeurosurgeryNeurology (clinical)businessmedicine.drug
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Impaired neuromuscular transmission during partial inhibition of acetycholinest-erase: The of stimulus-induced antiromic backfiring in the generation…

1992

Neuromuscular transmission was studied in the rat phrenic nerve-hemidiaphragm preparation with acetylcholinesterase (AChE) partially inactivated. Enzyme inhibition resulted in (1) increased single-twitch tension of the diaphragm; (2) compound muscle action potential (CMAP) containing repetitive discharges; (3) stimulus-induced antidromic backfiring (SIAB) seen in the phrenic nerve; and (4) repetitive nerve stimulation (RNS) eliciting a decrement-increment (D-I) phenomenon (i.e., amplitude reduction maximal with the second CMAP). Using a high-calcium and low-magnesium solution, SIAB and the decrement of the second CMAP during RNS were intensified, whereas closely spaced trains and (+)-tubocu…

Malemedicine.medical_specialtyPhysiologyDiaphragmNeuromuscular JunctionNeuromuscular transmissionAction PotentialsReceptors NicotinicSynaptic TransmissionRats Sprague-DawleyCellular and Molecular NeurosciencePostsynaptic potentialPhysiology (medical)Internal medicinemedicineAnimalsRepetitive nerve stimulationEvoked PotentialsPhrenic nerveChemistrymusculoskeletal systemElectric StimulationNeostigmineRatsAntidromicCompound muscle action potentialPhrenic NerveEndocrinologymedicine.anatomical_structurePeripheral nervous systemAcetylcholinesteraseNeurology (clinical)NeuroscienceAcetylcholinemedicine.drugMuscle & Nerve
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Suppression by cholinesterase inhibition of a Ca(2+)-independent efflux of [3H]acetylcholine from the neuromuscular junction of the isolated rat diap…

1992

Abstract Endplate preparations of the left rat hemidiaphragm were incubated with [ 3 H]choline to label neuronal acetylcholine stores. Elevation of the concentration (13.5–135 mmol/l) of extracellular potassium chloride (KC1) stimulated the release of [ 3 H]acetylcholine in a concentration-dependent manner. KC1 (27 mmol/l) still caused a significant efflux of [ 3 H]acetylcholine in a Ca 2+ -free medium. Inhibitors of cholinesterase (physostigmine, diisopropylfluorophosphate) suppressed by 80% this Ca 2+ -independent efflux of [ 3 H]acetylcholine. Vesamicol (10 μmol/l), the blocker of the vesicular acetylcholine carrier, also suppressed the stimulated, Ca 2+ -independent efflux of [ 3 H]acet…

Malemedicine.medical_specialtyPhysostigmineVesamicolPhysostigmineDiaphragmNeuromuscular JunctionIn Vitro TechniquesTritiumNeuromuscular junctionCholinePotassium ChlorideRats Sprague-Dawleychemistry.chemical_compoundPiperidinesInternal medicinemedicineCholineAnimalsCholinesterasePharmacologyMuscarinebiologyAcetylcholineRatsEndocrinologymedicine.anatomical_structurechemistrybiology.proteinCalciumFemaleCholinesterase Inhibitorsmedicine.symptomAcetylcholinemedicine.drugMuscle contractionEuropean journal 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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Antiabsence effects of carbenoxolone in two genetic animal models of absence epilepsy (WAG/Rij rats and lh/lh mice).

2005

Carbenoxolone (CBX), the succinyl ester of glycyrrhetinic acid, is an inhibitor of gap junctional intercellular communication. We have tested its possible effects upon two genetic animal models of epilepsy (WAG/Rij rats and lethargic (lh/lh) mice). Systemic administration of CBX was unable to significantly affect the occurrence of absence seizures in WAG/Rij rats. In particular, intravenous (5-40 mg/kg) or intraperitoneal (i.p.; 10-80 mg/kg) administration of CBX was unable to significantly modify the number and duration of spike-wave discharges (SWDs) in WAG/Rij rats, whereas the bilateral microinjection (0.05, 0.1, 0.5 and 1 microg/0.5 microl) of CBX into nucleus reticularis thalami (NRT)…

Malemedicine.medical_specialtyTime FactorsCarbenoxoloneConnexinConnexinsCellular and Molecular Neurosciencechemistry.chemical_compoundEpilepsyMiceMice Neurologic MutantsInternal medicinemedicineAnimalsGlycyrrhizinMicroinjectionGap junctionsPharmacologyDose-Response Relationship DrugGap junctionElectroencephalographyRats Inbred StrainsEpilepsy Carbenoxolone WAG/Rij rat Lethargic mouse Gap junction Connexin Absence seizuresmedicine.diseaseRatsDisease Models AnimalEndocrinologymedicine.anatomical_structurechemistryEpilepsy AbsenceGene Expression RegulationThalamic NucleiSystemic administrationCarbenoxoloneepilepsyAutoradiographyNucleusmedicine.drugGap junctions; Carbenoxolone ; epilepsyNeuropharmacology
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Increased Cx43 and Angiogenesis in Exercised Mouse Hearts

2007

Several studies focused on the macroscopic architecture of increased cardiac wall induced by exercise training. Our goal was to evaluate myocardiocyte, interstitial and vascular component, and connexin-43 expression in endurance-trained mouse hearts. Sixty-three 10-week-old male Swiss mice were divided into four sedentary groups (C0, C15, C30 and C45) and three groups exercised respectively for 15 (T15-D; running intensity [RI]: 3.18 m/min; running duration [RD]: 75 min/first week and 150 min/second week), 30 (T30-D; RI: 3.96 m/min; RD: 150 min/third week and 225 min/fourth week) and 45 days (T45-D; RI: 3.96 m/min and 4.8 m/min, respectively for the fifth and sixth week; RD: 300 min) on a t…

Malemedicine.medical_specialtyconnexin-43Neovascularization PhysiologicConnective tissueCardiomegalyPhysical Therapy Sports Therapy and RehabilitationheartMuscle hypertrophyNeovascularizationMiceangiogenesisendurance trainingEndurance trainingInternal medicinemedicineAnimalsOrthopedics and Sports MedicineInterventricular septumTreadmillSettore M-EDF/02 - Metodi E Didattiche Delle Attivita' Sportivebusiness.industryGap Junctionsmedicine.anatomical_structureEndocrinologyConnective TissueVentricleConnexin 43Circulatory systemPhysical Endurancemedicine.symptomhypertrophybusinessInternational Journal of Sports Medicine
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Brain and behavioral alterations in subjects with social anxiety dominated by empathic embarrassment

2020

Significance People are increasingly affected by social anxiety that includes emotional hypersensitivity and inaccurate interpretation of social encounters, and varies markedly in its subjective manifestations. We searched for insights into the underlying neurocognitive mechanisms of Taijin-kyofusho (TKS), a specific subtype of social-anxiety disorder common in East Asia and dominated by empathic or other-oriented embarrassment. We found TKS to be characterized by enhanced affective and reduced cognitive empathy. Moreover, analysis of functional MRI data—collected while subjects viewed videos of badly singing people—revealed disruption of the cognitive–empathy network, possibly obstructing …

Malesosiaalisten tilanteiden pelkoBrain activity and meditationmedia_common.quotation_subjectEmotionsSOCIAL ANXIETYintersubject correlationTemporoparietal junctionEMPATHYInferior frontal gyrusEmbarrassmentEmpathy050105 experimental psychologyINTERSUBJECT CORRELATIONYoung Adult03 medical and health sciencesCognitiontoiminnallinen magneettikuvaus0302 clinical medicineempatiamedicineHumans0501 psychology and cognitive sciencesFUNCTIONAL MAGNETIC RESONANCE IMAGINGembarrassmentempathymedia_commonBrain MappingMultidisciplinary05 social sciencesSocial anxietyCognitive flexibilityBrainPhobia SocialBiological SciencesMagnetic Resonance Imagingfunctional magnetic resonance imagingembarrasmentmedicine.anatomical_structurePosterior cingulateFemalesocial anxietyPsychologyEMBARRASSMENT030217 neurology & neurosurgeryNeuroscienceClinical psychologyProceedings of the National Academy of Sciences
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Expression of Cx36 in mammalian neurons

2000

Cx36 is the first mammalian member of a novel subgroup of the connexin family, characterized by a long cytoplasmic loop, a peculiar gene structure and a preferential expression in cell types of neural origin. In the present review we summarize the evidence in favour of its predominant expression in neuronal cells in the mammalian central nervous system, such as results from experiments with specific neurotoxins and co-localization of Cx36 mRNA and a neuronal marker. We also report a detailed description of Cx36 mRNA distribution in the rat and human central nervous system by in situ hybridization and, for each brain region, we correlate the novel findings with previous morphological or func…

MammalsMessenger RNAGeneral NeuroscienceCentral nervous systemGap JunctionsGene ExpressionConnexinCell CommunicationMolecular neuroscienceIn situ hybridizationBiologyCell junctionConnexinsmedicine.anatomical_structureSynapsesGene expressionmedicineAnimalsHumanssense organsNeurology (clinical)NeuronEye ProteinsNeuroscienceBrain Research Reviews
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