Search results for "muscle relaxation"

showing 10 items of 94 documents

Modulatory role of magnesium on the contractile response of rat aorta to several agonists in normal and calcium-free medium.

1993

Abstract Acute withdrawal of external Mg2+ increased basal tone of rat isolated aorta incubated in the presence of Ca2+. Above normal levels of Mg2+ (1–4 Mm) inhibited basal tone while much higher levels of the divalent cation (64–256 Mm) evoked contractile responses regardless of the presence of Ca2+. Contractile responses to noradrenaline (1μm) and KCl (80 Mm) were inhibited by addition of cumulative concentrations of Mg2+. Acetylcholine-induced contractions in the presence of physiological concentrations of Mg2+ (1 Mm) decreased gradually to the basal tone, but a sustained contraction was observed in the absence of this ion. In Ca2+-free medium, acetylcholine-induced phasic responses ind…

Malemedicine.medical_specialtyContraction (grammar)Muscle RelaxationPharmaceutical Sciencechemistry.chemical_elementAorta ThoracicCalciumIn Vitro TechniquesMuscle Smooth VascularDivalentPotassium ChlorideNorepinephrineInternal medicinemedicineExtracellularAnimalsMagnesiumRats WistarPharmacologychemistry.chemical_classificationAcetylcholineCulture MediaRatsKineticsMuscle relaxationEndocrinologychemistryCalciummedicine.symptomIsotonic SolutionsExtracellular SpaceMagnesium DeficiencyVasoconstrictionAcetylcholinemedicine.drugMuscle contractionMuscle ContractionThe Journal of pharmacy and pharmacology
researchProduct

Neurotensin: dual effect on the motor activity of rat duodenum

1992

The effects of neurotensin on mechanical activity of rat duodenum were investigated using an isometric-isovolumic preparation. Neurotensin (1 pM to 10 nM) induced a concentration-dependent, tetrodotoxin (TTX)-insensitive fall in both endoluminal pressure and isometric tension. At higher concentrations of neurotensin (1 nM to 1 microM) the relaxation was followed by a concentration-dependent TTX-insensitive contraction, detected only by an increase in endoluminal pressure. Different concentrations of neurotensin were required to desensitize the relaxant and the contractile actions of the neuropeptide. The relaxation was antagonized by apamin, while the contractile response was blocked by nif…

Malemedicine.medical_specialtyContraction (grammar)NifedipineDuodenumMuscle RelaxationNeuropeptideIn Vitro TechniquesBiologyApamincomplex mixturesdigestive systemchemistry.chemical_compoundNifedipineInternal medicinemedicineAnimalsReceptors NeurotensinNeurotensinPharmacologymusculoskeletal neural and ocular physiologydigestive oral and skin physiologyRats Inbred StrainsElectric StimulationRatsReceptors NeurotransmitterMuscle relaxationEndocrinologyApaminnervous systemchemistryTetrodotoxinCalciummedicine.symptomGastrointestinal MotilityMuscle ContractionNeurotensinmedicine.drugMuscle contractionEuropean Journal of Pharmacology
researchProduct

On the peptidergic hypothesis for non-adrenergic non-cholinergic innervation in the rat duodenum

1992

1. The nature of the non-adrenergic, non-cholinergic (NANC) transmitter was studied in vitro in the rat duodenum, by use of an isometric-isovolumic preparation. 2. Electrical field stimulation (EFS) induced a tetrodotoxin (TTX)-sensitive fall both in luminal pressure and in isometric tension. 3. Neurotensin (NT) induced TTX-insensitive inhibitory responses similar to those induced by EFS. Vasoactive intestinal peptide (VIP) caused a delayed, slow, concentration-dependent, TTX-insensitive inhibitory effect, detected only by a change in luminal pressure. 4. alpha-chymotrypsin prevented the NT- and VIP-induced inhibitory effects and antagonized the response to EFS. 5. Apamin antagonized the EF…

Malemedicine.medical_specialtyDuodenumMuscle RelaxationVasoactive intestinal peptideIn Vitro TechniquesBiologyAutonomic Nervous SystemApaminInhibitory postsynaptic potentialchemistry.chemical_compoundDesensitization (telecommunications)Isometric ContractionInternal medicinemedicineAnimalsChymotrypsinReceptorNeurotensinPharmacologymusculoskeletal neural and ocular physiologyGeneral NeuroscienceNeuropeptidesMuscle SmoothRats Inbred StrainsElectric StimulationRatsmedicine.anatomical_structureEndocrinologyApaminchemistryTetrodotoxinDuodenumhormones hormone substitutes and hormone antagonistsVasoactive Intestinal PeptideNeurotensinJournal of Autonomic Pharmacology
researchProduct

Differential effects of isoliquiritigenin and YC-1 in rat aortic smooth muscle.

1997

We investigated the effects of isoliquiritigenin and YC-1 (3-(5'-hydroxymethyl-2'-furyl)-1-benzyl indazole) on tension in endothelial-free rat aortic rings precontracted with phenylephrine (3 microM). Both compounds induced a concentration-dependent relaxation (EC50 of YC-1 1.9 microM and of isoliquiritigenin 9.4 microM). The effects developed faster with YC-1 than with isoliquiritigenin, and the effects of YC-1 were potentiated by isoliquiritigenin (10 microM). 1H-[1,2,4]Oxadiazolo[4,3-a]quinoxalin-1-one (30 microM) inhibited the effect of YC-1, but not of isoliquiritigenin. These results suggest that the effects of YC-1 are due to stimulation of soluble guanylyl cyclase activity, whereas …

Malemedicine.medical_specialtyIndazolesPhosphodiesterase InhibitorsMuscle RelaxationStimulationMuscle Smooth VascularRats Sprague-Dawleychemistry.chemical_compoundChalconeChalconesAldehyde ReductaseInternal medicinemedicineAnimalsEnzyme InhibitorsPhenylephrinePharmacologybiologyDose-Response Relationship DrugChemistryBiological activityRatsDose–response relationshipEndocrinologyCarotid ArteriesMechanism of actionEnzyme inhibitorGuanylate Cyclasebiology.proteinFemalemedicine.symptomSoluble guanylyl cyclaseIsoliquiritigeninPlatelet Aggregation Inhibitorsmedicine.drugMuscle ContractionEuropean journal of pharmacology
researchProduct

The effects of phorbol 12,13-diacetate on responses of guinea-pig isolated trachea to methylxanthines, isoprenaline and ryanodine

1994

1. Using guinea-pig isolated trachea, we have studied how phorbol 12,13-diacetate (PDA) modulates mechanical responses of the tissue to methylxanthines, isoprenaline and ryanodine. 2. Caffeine (10 microM-5 mM), theophylline (10 microM-5 mM) and isoprenaline (1 nM-1 microM), each inhibited the spontaneous tone of the trachea. Pretreatment with PDA (0.1-10 microM) converted relaxant responses to high concentrations of the methylxanthines into contractions. PDA produced no equivalent effect against isoprenaline. Pretreatment with verapamil (1 or 10 microM), nifedipine (0.1 microM) or incubation with Ca(2+)-free, EGTA (0.1 mM)-containing physiological salt solution (PSS) suppressed the contract…

Malemedicine.medical_specialtyMuscle RelaxationGuinea PigsMepyramineIn Vitro TechniquesCalcium Chloridechemistry.chemical_compoundTheophyllineCaffeineIsoprenalineInternal medicinePhorbol EstersmedicineAnimalsDrug InteractionsTheophyllinePharmacologyRyanodineRyanodine receptorIsoproterenolMuscle SmoothCold TemperatureTracheaEndocrinologyMuscle relaxationVerapamilchemistryMuscle SpasticityXanthinesPotassiumTrachealis muscleVerapamilFemaleCaffeineResearch ArticleHistamineMuscle Contractionmedicine.drugBritish Journal of Pharmacology
researchProduct

Effects of sensitization on vasoactive intestinal polypeptide-induced relaxation and its concentration and binding in guinea-pig airways.

1993

We investigated the relaxant effect of vasoactive intestinal polypeptide (VIP) in trachea and lung parenchyma from normal and sensitized guinea-pigs. A technique by which drug access was restricted to either the mucosal or the adventitial surface of tracheal rings was used. In intact trachea, concentration-response curves for VIP entering from the mucosal surface (pD2 = 6.61 +/- 0.06) were displaced to the right compared with those for adventitial entry (pD2 = 6.78 +/- 0.04). Epithelium removal produced a leftward shift (approximately 2.8-fold) in the mucosal VIP concentration-response curve. Sensitization did not alter the responsiveness (maximal effect) or sensitivity (pD2 values) of trac…

Malemedicine.medical_specialtyMuscle RelaxationVasoactive intestinal peptideGuinea PigsRespiratory SystemBiologyIn Vitro TechniquesEpitheliumGuinea pigIodine RadioisotopesInternal medicineParenchymamedicineAnimalsRespiratory systemSensitizationPharmacologyMuscle Smoothrespiratory systemEpitheliumTracheaBronchodilatationmedicine.anatomical_structureEndocrinologyFemalehormones hormone substitutes and hormone antagonistsRespiratory tractMuscle ContractionVasoactive Intestinal PeptideEuropean journal of pharmacology
researchProduct

GABAergic inhibition of nitric oxide-mediated relaxation of guinea-pig ileum

1999

The effects of GABA receptor agonists were investigated on guinea-pig isolated ileum longitudinal muscle with intact myenteric plexus. Electrical field stimulation (1 Hz, 10 s) of the histamine (1 microM)-precontracted preparation caused a contraction followed by a relaxation. Relaxations were inhibited by L-N(G)-nitroarginine (L-NA; EC50 3 microM) in a concentration-dependent manner. The inhibitory action of 10 microM L-NA was blocked by 10 microM L-arginine but not by D-arginine, which indicates that the relaxation was largely mediated by endogenous nitric oxide (NO). Tetrodotoxin (1 microM) reduced the relaxation only by about 50%. GABA and the GABA(B) agonist, baclofen, inhibited the fi…

Malemedicine.medical_specialtyNitric Oxide Synthase Type IIIMuscle RelaxationGuinea PigsTetrodotoxinIn Vitro TechniquesGABAB receptorBicucullineNitric OxideNitroargininechemistry.chemical_compoundGABA receptorIleumInternal medicinemedicineAnimalsGABA-A Receptor AgonistsEnzyme InhibitorsGABA Agonistsgamma-Aminobutyric AcidMyenteric plexusPharmacologyMuscimolGABAA receptorMuscle SmoothGeneral MedicineBicucullineElectric StimulationBaclofenEndocrinologynervous systemchemistryMuscimolGABA-B Receptor AgonistsSaclofenBiophysicsFemaleNitric Oxide SynthaseHistaminemedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
researchProduct

Acute relaxant effects of 17-beta-estradiol through non-genomic mechanisms in rabbit carotid artery.

2002

Estrogens could play a cardiovascular protective role not only by means of systemic effects but also by means of direct effects on vascular structure and function. We have studied the acute effects and mechanisms of action of 17-beta-estradiol on vascular tone of rabbit isolated carotid artery. 17-Beta-estradiol (10, 30, and 100 microM) elicited concentration-dependent relaxation of 50 mM KCl-induced active tone in male and female rabbit carotid artery. The stereoisomer 17-alpha-estradiol showed lesser relaxant effects in male rabbits. Endothelium removal did not modify relaxation induced by 17-beta-estradiol. The NO synthase inhibitor L-NAME (100 microM) only reduced significantly relaxati…

Malemedicine.medical_specialtyVascular smooth muscleContraction (grammar)Potassium ChannelsCharybdotoxinEndotheliumMuscle RelaxationClinical BiochemistryNicardipineEstrogen receptorCycloheximideBiochemistrychemistry.chemical_compoundCalcium ChlorideNicardipineEndocrinologyInternal medicinemedicineAnimalsChannel blockerEnzyme InhibitorsMolecular BiologyPharmacologyEstradiolOrganic ChemistryCalcium Channel BlockersEndocrinologymedicine.anatomical_structureCarotid ArteriesNG-Nitroarginine Methyl EsterchemistryPotassiumCalciumFemaleCalcium ChannelsEndothelium VascularRabbitsNitric Oxide Synthasemedicine.drugSteroids
researchProduct

Evidence for a role of inducible nitric oxide synthase in gastric relaxation of mdx mice

2006

Alterations of gastric mechanical activity have been reported in mdx mouse, animal model for Duchenne muscular dystrophy. This study examined if alterations in the vasoactive intestinal polypeptide (VIP) system are present in mdx stomach. Gastric mechanical activity was recorded in vitro as changes of endoluminal pressure and neurally or pharmacologically evoked relaxations were analysed in mdxvs normal stomach. Reverse-transcription polymerase chain reaction was used to detect inducible nitric oxide synthase (iNOS) expression. Relaxations to sodium nitroprusside in mdx stomach showed no difference in comparison with normal preparations. In normal stomach, VIP produced relaxation, which was…

Malemedicine.medical_specialtymdx mousePhysiologyMuscle RelaxationVasoactive intestinal peptideNitric Oxide Synthase Type IIStimulationDUCHENNES MUSCULAR-DYSTROPHYSettore BIO/09 - FisiologiaNitric oxidechemistry.chemical_compoundMiceOrgan Culture TechniquesInternal medicineQuinoxalinesmedicineAnimalsRNA MessengerEnzyme InhibitorsReceptorOxadiazolesbiologyEndocrine and Autonomic SystemsReverse Transcriptase Polymerase Chain ReactionStomachStomachGastroenterologySMOOTH-MUSCLE CELLSMuscle SmoothPEPTIDE RELEASENitric oxide synthaseMuscular Dystrophy DuchenneDisease Models AnimalEndocrinologymedicine.anatomical_structureNG-Nitroarginine Methyl Esterchemistrybiology.proteinMice Inbred mdxReceptors Vasoactive Intestinal PeptideSodium nitroprussideIminesmedicine.drugVasoactive Intestinal Peptide
researchProduct

Functional evidence for different roles of GABAA and GABAB receptors in modulating mouse gastric tone

2010

Abstract The aims of the present study were to investigate, using mouse whole stomach in vitro , the effects of γ-aminobutyric acid (GABA) and GABA receptor agonists on the spontaneous gastric tone, to examine the subtypes of GABA receptors involved in the responses and to determine the possible site(s) of action. GABA induced gastric relaxation, which was antagonized by the GABA A -receptor antagonist, bicuculline, potentiated by phaclofen, GABA B -receptor antagonist, but not affected by 1,2,5,6-Tetrahydropyridin-4-yl methylphosphinic acid hydrate (TPMPA), GABA C -receptor antagonist. Muscimol, GABA A -receptor agonist, mimicked GABA effects inducing relaxation, which was significantly re…

Malemedicine.medical_specialtymedicine.drug_classMuscle RelaxationIn Vitro TechniquesGABAB receptorApaminSettore BIO/09 - FisiologiaMicePotassium Channels Calcium-ActivatedGABACellular and Molecular Neurosciencechemistry.chemical_compoundPhaclofenReceptors GABAGABA receptorNANC inhibitory nerves.GABA receptorInternal medicinemedicineAnimalsGABA-A Receptor AgonistsGABA-A Receptor Antagonistsgamma-Aminobutyric AcidPharmacologyGABAA receptorMuscle SmoothBicucullineReceptors GABA-AReceptor antagonistMice Inbred C57BLEndocrinologyReceptors GABA-Bnervous systemMuscimolchemistryGABA-B Receptor AgonistsMuscle Tonuscholinergic excitatory nerveNitric Oxide SynthaseGABA-B Receptor Antagonistsstomachmedicine.drugNeuropharmacology
researchProduct