Search results for "muscle relaxation"

showing 10 items of 94 documents

Effect of explosive type strength training on isometric force- and relaxation-time, electromyographic and muscle fibre characteristics of leg extenso…

1985

Eleven male subjects (20-32 years) accustomed to strength training went through progressive, high-load strength training for 24 weeks with intensities ranging variably between 70 and 120% during each month. This training was also followed by a 12-week detraining period. An increase of 26.8% (P less than 0.001) in maximal isometric strength took place during the training. The increase in strength correlated (P less than 0.05) with significant (P less than 0.05-0.01) increases in the neural activation (IEMG) of the leg extensor muscles during the most intensive training months. During the lower-intensity training, maximum IEMG decreased (P less than 0.05). Enlargements of muscle-fibre areas, …

AdultMalemedicine.medical_specialtyTime FactorsWeight LiftingPhysiologyStrength trainingMuscle RelaxationeducationNeuromuscular JunctionIsometric exerciseElectromyographyMuscle hypertrophyPhysical medicine and rehabilitationInternal medicineIsometric ContractionmedicineHumansMuscle fibreLegPhysical Education and Trainingmedicine.diagnostic_testbusiness.industryElectromyographyMusclesSkeletal muscleMuscle relaxationmedicine.anatomical_structureCardiologymedicine.symptombusinessMuscle contractionMuscle ContractionActa physiologica Scandinavica
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Repeated sugammadex reversal of muscle relaxation during lumbar spine surgery with intraoperative neurophysiological multimodal monitoring

2016

Intraoperative neurophysiological monitoring during spine surgery is usually acomplished avoiding muscle relaxants. A case of intraoperative sugammadex partial reversal of the neuromuscular blockade allowing adequate monitoring during spine surgery is presented. A 38 year-old man was scheduled for discectomy and vertebral arthrodesis throughout anterior and posterior approaches. Anesthesia consisted of total intravenous anesthesia plus rocuronium. Intraoperatively monitoring was needed, and the muscle relaxant reverted twice with low dose sugammadex in order to obtain adequate responses. The doses of sugammadex used were conservatively selected (0.1 mg/kg boluses increases, total dose neede…

AdultMalemedicine.medical_specialtymedicine.drug_classMuscle RelaxationContext (language use)Critical Care and Intensive Care MedicineSugammadexSugammadexAnestesia03 medical and health sciencesSpine surgery0302 clinical medicine030202 anesthesiologyIntraoperative neurophysiological monitoringHumansMedicineAnesthesiaAndrostanolsNeuromuscular blocking drugsRocuroniumMonitorizacion neurofisiologica intraoperatoriaNeuromuscular BlockadeLumbar Vertebraebusiness.industryMuscle relaxantCirugia de raquisFarmacos bloqueantes neuromuscularesNeuromuscular Nondepolarizing AgentsSurgeryAnesthesiology and Pain MedicineMuscle relaxationRocuronioAnesthesiaNeuromuscular BlockadeRocuroniumbusiness030217 neurology & neurosurgeryNeuromuscular Nondepolarizing Agentsgamma-Cyclodextrinsmedicine.drugIntraoperative neurophysiological monitoringRevista Española de Anestesiología y Reanimación
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Relationship between electrical and mechanical properties of motor units.

1990

In six healthy volunteers, the size of the motor unit action potential (MUAP) was related to its contractile behaviour. Electrical activity was determined by measuring amplitude and area of the potential, using the macro electromyography (EMG) technique. The mechanical response was characterised by contraction time, twitch force and relaxation time, recorded with the spike triggered averaging technique. With increasing tension of the whole muscle corresponding to an increasing threshold, the force of single units enlarged exponentially compared to their EMG. There was only a weak relationship between contraction time and electrical activity and none between EMG and relaxation time.

AdultMaterials scienceMuscle RelaxationAction PotentialsElectromyographymedicineHumansMotor Neuronsmedicine.diagnostic_testTension (physics)ElectromyographyMusclesBiomechanicsAnatomyMiddle AgedBiomechanical PhenomenaMotor unitPsychiatry and Mental healthElectrophysiologyAmplitudeMuscle relaxationSurgeryNeurology (clinical)medicine.symptomMuscle contractionBiomedical engineeringMuscle ContractionResearch ArticleJournal of neurology, neurosurgery, and psychiatry
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Lumbopelvic flexibility modulates neuromuscular responses during trunk flexion–extension

2016

Various stimuli such as the flexibility of lumbopelvic structures influence the neuromuscular responses of the trunk musculature, leading to different load sharing strategies and reflex muscle responses from the afferents of lumbopelvic mechanoreceptors. This link between flexibility and neuromuscular response has been poorly studied. The aim of this study was to investigate the relationship between lumbopelvic flexibility and neuromuscular responses of the erector spinae, hamstring and abdominal muscles during trunk flexion-extension. Lumbopelvic movement patterns were measured in 29 healthy women, who were separated into two groups according to their flexibility during trunk flexion-exten…

AdultReflex Stretchmedicine.medical_specialtyFlexibility (anatomy)Muscle RelaxationBiophysicsNeuroscience (miscellaneous)ElectromyographyBicepsPelvis03 medical and health sciences0302 clinical medicineLumbarAbdomenmedicineHumansRange of Motion ArticularMuscle SkeletalPelvisLeg030222 orthopedicsmedicine.diagnostic_testbusiness.industryTrunkBiomechanical PhenomenaMuscle relaxationmedicine.anatomical_structurePhysical therapyFemaleNeurology (clinical)business030217 neurology & neurosurgeryHamstringMuscle ContractionJournal of Electromyography and Kinesiology
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Relaxation of human isolated mesenteric arteries by vasopressin and desmopressin.

1994

1. The effects of vasopressin and deamino-8-D-arginine vasopressin (DDAVP, desmopressin) were studied in artery rings (0.8-1 mm in external diameter) obtained from portions of human omentum during the course of abdominal operations (27 patients). 2. In arterial rings under resting tension, vasopressin produced concentration-dependent, endothelium-independent contractions with an EC50 of 0.59 +/- 0.12 nM. The V1 antagonist d(CH2)5Tyr(Me)AVP (1 microM) and the mixed V1-V2 antagonist desGly-d(CH2)5D-Tyr(Et)ValAVP (0.01 microM) displaced the control curve to vasopressin to the right in a parallel manner without differences in the maximal responses. In the presence of indomethacin (1 microM) the…

AgonistAdultMaleVasopressinmedicine.medical_specialtymedicine.drug_classVasopressinsMuscle RelaxationIndomethacinVasodilationIn Vitro TechniquesArginineNitric OxideMuscle Smooth VascularInternal medicineArginine vasopressin receptor 2medicineHumansDeamino Arginine VasopressinMesenteric arteriesVasopressin receptorPharmacologyChemistryAntagonistMiddle AgedReceptor antagonistMesenteric ArteriesArginine VasopressinEndocrinologymedicine.anatomical_structureNG-Nitroarginine Methyl EsterFemaleEndothelium Vascularhormones hormone substitutes and hormone antagonistsResearch ArticleMuscle Contraction
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Involvement of cholinergic nicotinic receptors in the menthol-induced gastric relaxation.

2014

We have previously demonstrated that menthol reduces murine gastric tone in part through a neural mechanism, involving adrenergic pathways and reduction of ongoing release of acetylcholine from enteric nerves. In the present study we aimed to verify whether the gastric relaxation to menthol may be triggered by interaction with neural receptors or ionic channels proteins, such as transient receptor potential (TRP)-melastatin8 (TRPM8), TRP-ankyrin 1 (TRPA1), 5-hydroxytriptamine 3 (5-HT3) receptor or cholinergic nicotinic receptors. Spontaneous mechanical activity was detected in vitro as changes in intraluminal pressure from isolated mouse stomach. Menthol (0.3-30 mM) induced gastric relaxati…

AgonistMalemedicine.medical_specialtySerotoninmedicine.drug_classDimethylphenylpiperaziniumMuscle RelaxationTRPM Cation ChannelsPharmacologyReceptors NicotinicSettore BIO/09 - Fisiologiachemistry.chemical_compoundMiceGanglion type nicotinic receptorTransient Receptor Potential ChannelsIsothiocyanatesInternal medicinemedicineTRPM8AnimalsSerotonin 5-HT3 Receptor AntagonistsRNA MessengerTRPA1 Cation ChannelPharmacologyStomachmenthol gastric relaxation TRPM8 TRPA1 nicotinic receptorsReceptor antagonistOndansetronMice Inbred C57BLMentholEndocrinologyNicotinic agonistchemistryPurinesHexamethoniumAcetanilidesAlpha-4 beta-2 nicotinic receptorGastrointestinal Motilitymedicine.drugEuropean journal of pharmacology
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Evidence for the presence of P2y and P2x receptors with different functions in mouse stomach.

2005

To clarify the function of P2 receptor subtypes in mouse stomach, the motor responses to ATP, alpha,beta-methyleneATP (alpha,beta-MeATP), P2X receptor agonist, 2-methylthioATP (2-MeSATP), P2Y receptor agonist, and the effects of the desensitisation of P2X receptors with alpha,beta-MeATP and of P2Y receptors with ADPbetaS were analysed recording the endoluminal pressure from whole-organ. ATP-induced relaxation was antagonised by suramin, non-selective P2 receptor antagonist, by desensitisation of P2Y receptors with ADPbetaS, and increased by desensitisation of P2X receptors with alpha,beta-MeATP. alpha,beta-MeATP produced biphasic responses: relaxation, reduced by P2X- or P2Y desensitisation…

Agonistmedicine.medical_specialtyP2Y receptorRelaxationContraction (grammar)medicine.drug_classSuraminMuscle RelaxationTetrodotoxinP2 receptorBiologyIn Vitro TechniquesSettore BIO/09 - Fisiologiachemistry.chemical_compoundMiceAdenosine TriphosphateInternal medicinemedicineAnimalsReceptorPharmacologyContractionDose-Response Relationship DrugReceptors Purinergic P2Mouse stomachStomachAntagonistP2Y receptorThionucleotidesATPAdenosine DiphosphateMice Inbred C57BLEndocrinologychemistryP2X receptorReceptors Purinergic P2XTetrodotoxinmedicine.drugMuscle ContractionEuropean journal of pharmacology
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Involvement of purinergic nerves in the NANC inhibitory junction potentials in pigeon oesophageal smooth muscle.

2004

1. Electrical field stimulation (EFS) (0.5 ms in train of 2-32 Hz for 300 ms) in smooth muscle of pigeon oesophagus, in the presence of atropine (1 microm) and guanethidine (1 microm), elicited an inhibitory response consisting of a transient hyperpolarization (inhibitory junction potential, IJP) associated with muscle relaxation. 2. Sodium nitroprusside (SNP, 100 microm) induced hyperpolarization correlated to mechanical relaxation. 3. The nitric oxide (NO) synthase inhibitor N(omega)-nitro-l-arginine (from 0.1 to 100 microm) caused a concentration-dependent reduction of electromechanical response to EFS indicating a role for NO in this response. 4. Apamin (1 microm) reduced both IJP and r…

AtropineGuanethidineAdenosinePatch-Clamp TechniquesNeuromuscular JunctionMuscarinic AntagonistsPharmacologyIn Vitro TechniquesInhibitory postsynaptic potentialApaminAutonomic Nervous Systemchemistry.chemical_compoundAdrenergic AgentsEsophaguspigeon oesophageal smooth muscle NANC pathways electrical field stimulation IJPAdenine nucleotidemedicineAnimalsColumbidaePharmacologyAdenine NucleotidesPurinergic receptorMuscle SmoothHyperpolarization (biology)AdenosineElectric StimulationElectrophysiologyMuscle relaxationchemistryBiochemistryApaminPurinesmedicine.symptommedicine.drugMuscle contractionMuscle ContractionAutonomicautacoid pharmacology
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Evidence that adenosine is not involved in the non-adrenergic non-cholinergic relaxation in the rat duodenum.

1990

In rat isolated duodenal segments, adenosine induced, in the presence of atropine and guanethidine, a dose-dependent, long-lasting (about 20 s), tetrodotoxin (TTX)-resistant relaxation both in endoluminal pressure and in isometric tension. Electrical field stimulation (EFS) induced, in the presence of atropine and guanethidine, a TTX-sensitive short-lasting (about 6 s) relaxation followed by a sustained rebound contraction. Theophylline, a P1 receptor antagonist, at the concentration of 100 microM caused a marked inhibition of the adenosine-induced relaxation, while the EFS-induced relaxation was not modified. Our results suggest that adenosine induces relaxation of the rat duodenal smooth …

AtropineGuanethidinemedicine.medical_specialtyAdenosinePhysiologyDuodenumMuscle RelaxationTetrodotoxinIn Vitro TechniquesBiochemistrychemistry.chemical_compoundTheophyllineInternal medicineIsometric ContractionmedicinePressureAnimalsTheophyllineNeurotransmitterReceptorGuanethidineReceptors PurinergicMuscle SmoothAdenosineAdenosine receptorElectric StimulationRatsAtropineEndocrinologychemistryTetrodotoxinmedicine.drugArchives internationales de physiologie et de biochimie
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Comparative Analysis of the Vascular Actions of Diterpenes Isolated from Euphorbia canariensis

1998

Abstract We have analysed the effects of 2,3-diepiingol 7,12-diacetate-8-isobutyrate (compound 1), ingenol-3-angelate-17-benzoate (compound 2), ingenol-3-angelate-17-benzoate-20-acetate (compound 3) and 3,5,7,8,9,15-hexahydroxyjatropha-6(17),11-dien-14-one-5,8-bis(2-methylbutyrate)-7-(2-methylpropionate) (compound 4), four diterpenes isolated from E. canariensis, on the isometric tension developed by isolated rabbit basilar and carotid arteries. Concentration-response curves to these compounds were obtained cumulatively in both arteries at resting tension and active tone (KCl, 50 mM). At resting tension a concentration-dependent contraction was induced by the four compounds. In the basilar …

Contraction (grammar)Muscle RelaxationPharmaceutical ScienceVasodilationIn Vitro TechniquesPharmacologyMuscle Smooth VascularEuphorbia canariensismedicine.arteryBasilar arterymedicineAnimalsPotencyPharmacologyLagomorphabiologyPlant Extractsbusiness.industryEuphorbiaceaeAnatomybiology.organism_classificationKineticsCarotid ArteriesBasilar ArteryCirculatory systemRabbitsDiterpenesmedicine.symptombusinessVasoconstrictionMuscle ContractionJournal of Pharmacy and Pharmacology
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