Search results for "Muscle relaxant"

showing 10 items of 13 documents

Evidence of competitive inhibition for the intestinal absorption of baclofen by phenylalanine

1996

Abstract Previous studies showed that the absorption of the antispastic drug baclofen, in the rat middle intestine, is inhibited by β-alanine, γ-aminobutyric acid (GABA) and leucine. It was concluded that baclofen intestinal transport was mediated, at least in part, by the β-, γ- and α-amino acid carriers. We therefore focused our next studies on the analysis of the possible inhibition of drug absorption by an aromatic α-amino acid model compound, phenylalanine. An in situ study in the rat small intestine was undertaken in order to evaluate the effect of phenylalanine on baclofen absorption and to establish the inhibition model. Assays using isotonic perfusion solutions of 0.5 mM baclofen w…

Absorption (pharmacology)medicine.drug_classChemistryPharmaceutical SciencePhenylalanineMuscle relaxantPharmacologyIntestinal absorptionchemistry.chemical_compoundBaclofenNon-competitive inhibitionnervous systemPharmacokineticsmedicineLeucineInternational Journal of Pharmaceutics
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Economic aspects of different muscle relaxant regimens.

2000

Objective At a time of cost reduction in medical care efforts to manage the ever-increasing costs of new pharmaceutical drugs become increasingly important. Costs of four different muscle relaxant regimens including the new intermediate-acting neuromuscular blocking drugs (NMBD) cisatracurium and rocuronium will be analyzed. Methods Eighty patients undergoing laparoscopic cholecystectomy were prospectively studied. All patients received standardized general anaesthesia with desflurane/fentanyl. Muscle relaxation was achieved with atracurium, cisatracurium, vecuronium, or rocuronium with 20 patients in each group. Intraoperatively muscle relaxants were added to maintain two twitches of the t…

AdultMaleTime Factorsmedicine.drug_classCritical Care and Intensive Care MedicineDrug CostsPacuFentanylDesfluraneIntraoperative PeriodMedicineHumansGeneral anaesthesiaAnesthesiaAndrostanolsProspective StudiesRocuroniumAgedAged 80 and overPostoperative CareNeuromuscular BlockadeVecuronium Bromidebiologybusiness.industryMuscle Relaxants CentralMuscle relaxantGeneral MedicineMiddle Agedbiology.organism_classificationAnesthesiology and Pain MedicineMuscle relaxationTreatment OutcomeCholecystectomy LaparoscopicAnesthesiaEmergency MedicineAtracuriumFemaleRocuroniumbusinessmedicine.drugNeuromuscular Nondepolarizing AgentsAnasthesiologie, Intensivmedizin, Notfallmedizin, Schmerztherapie : AINS
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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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Effects of dantrolene on the responses to methylxanthines in the isolated guinea-pig trachea.

1991

The effect of dantrolene on the responses to methylxanthines (caffeine and theophylline) and a beta-adrenoceptor agonist (salbutamol) was studied in isolated guinea-pig trachea. Caffeine and theophylline (1 microM-10 mM) and salbutamol (1 nM-10 microM) produced concentration-dependent relaxation of spontaneous and stimulated (acetylcholine 1 mM) tone. Responses to high concentrations (10 mM) of caffeine and theophylline added to tracheal strips either unstimulated (spontaneous tone) or indomethacin (2.8 microM)-treated were reversed to contractions in the presence of dantrolene (3 microM-0.3 mM). This effect was not observed for salbutamol or when relaxant responses to the agonists were gen…

AgonistMalemedicine.drug_classGuinea PigsIndomethacinPharmacologyDantrolene SodiumDantroleneDantrolenechemistry.chemical_compoundTheophyllineCaffeinemedicineAnimalsTheophyllineAlbuterolPharmacologyMuscle relaxantMuscle SmoothAcetylcholineTracheachemistryAnesthesiaCalciumFemalemedicine.symptomCaffeineAcetylcholinemedicine.drugMuscle contractionMuscle ContractionEuropean journal of pharmacology
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Mechanical and electrophysiological effects of cromakalim on the human urinary bladder.

1994

The effects of cromakalim on spontaneous and induced mechanical activity of human detrusor muscle were investigated in vitro. Cromakalim produces a concentration-related decrease of spontaneous as well as carbachol- and K(+)-evoked contractions. This is the first study to utilize the patch clamp technique to elucidate the mechanism of action of cromakalim on human detrusor cells. Cromakalim hyperpolarizes the detrusor cells by increasing the net outward current which is most likely carried by potassium ions. In the human urinary bladder, this effect is mediated by a glibenclamide-sensitive potassium channel, as glibenclamide is able to diminish the relaxant effect of cromakalim and to preve…

Detrusor muscleAdultMalemedicine.medical_specialtyCromakalimCarbacholPatch-Clamp TechniquesPotassium Channelsmedicine.drug_classUrologyGuinea PigsUrinary BladderIn Vitro Techniquesurologic and male genital diseasesMembrane Potentialschemistry.chemical_compoundInternal medicineMedicineAnimalsHumansBenzopyransPyrrolesPatch clampUrinary bladderbusiness.industryParasympatholyticsMuscle relaxantMuscle SmoothHyperpolarization (biology)Middle Agedmusculoskeletal systemfemale genital diseases and pregnancy complicationsPotassium channelRatsElectrophysiologyEndocrinologymedicine.anatomical_structurechemistrycardiovascular systemFemaleStress MechanicalbusinessCromakalimmedicine.drugMuscle ContractionInvestigative urology (Berlin, Germany)
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Zur Wirkung von Muskelrelaxantien auf den intraokularen Druck

1988

Since general anesthesia is being used increasingly in ophthalmic surgery, the effects of anesthetic drugs on intraocular pressure (IOP) have to be considered. Competitive neuromuscular blocking drugs either do not affect IOP or produce a slight decrease. Depolarizing muscle relaxants increase IOP. This effect, which is pronounced with succinylcholine, cannot be reliably prevented by any concomitant medication. The new competitive relaxants atracurium and vecuronium provide stable conditions with respect to IOP and systemic circulation, combined with fast onset and intermediate duration of action.

Intraocular pressuregenetic structuresbusiness.industryDepolarizing muscle relaxantsFast onsetSystemic circulationeye diseasesOphthalmologyAnesthesiaAnestheticMedicinesense organsbusinessOphthalmic surgerymedicine.drugKlinische Monatsblätter für Augenheilkunde
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Interaction of Taurine on Baclofen Intestinal Absorption: A Nonlinear Mathematical Treatment using Differential Equations to Describe Kinetic Inhibit…

1996

Previous studies showed that the in situ absorption of baclofen in rat jejunum was inhibited by beta-alanine, a nonessential amino acid, and therefore mediated, at least in part, by some beta-amino acid carrier. In this paper a similar study was undertaken using taurine, a sulfonic beta-amino acid, in order to evaluate its effect and to establish a general inhibition model. To achieve this goal, remaining concentrations of inhibitor were also measured and incorporated into the model. Previously, kinetic absorption in situ parameters for taurine in free solution were obtained: Vm = 27.73 +/- 9.99 mM h-1, K(m) = 8.06 +/- 2.82 mM, Ka (passive difussion component) = 0.40 +/- 0.28 h-1. Isotonic …

MaleAbsorption (pharmacology)BaclofenTaurineTaurinePharmaceutical ScienceIntestinal absorptionchemistry.chemical_compoundNon-competitive inhibitionLeucineAnimalsRats Wistargamma-Aminobutyric Acidchemistry.chemical_classificationChromatographyMuscle Relaxants CentralRatsAmino acidKineticsBaclofenIntestinal AbsorptionModels ChemicalchemistryBiochemistrybeta-AlanineLeucinePerfusionJournal of Pharmaceutical Sciences
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Deep dry needling of trigger points located in the lateral pterygoid muscle: efficacy and safety of treatment for management of myofascial pain and t…

2014

Background To determine whether deep dry needling (DDN) of trigger points (TPs) in the lateral pterygoid muscle (LPM) would significantly reduce pain and improve function, compared with methocarbamol/paracetamol medication. Material and Methods Forty-eight patients with chronic myofascial pain located in the LPM were selected and randomly assigned to one of two groups (DDN test group, n=24; drug-treated control group, n=24). The test group received three applications of needling of the LPM once per week for three weeks, while control group patients were given two tablets of a methocarbamol/paracetamol combination every six hours for three weeks. Assessments were carried out pretreatment, 2 …

MaleAcupuncture TherapyLateral pterygoid musclelaw.inventionRandomized controlled triallawMyofascial Pain SyndromesDry needlingMethocarbamolMuscle Relaxants CentralEquipment DesignAnalgesics Non-NarcoticMiddle AgedTemporomandibular Joint Disorders:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludTreatment OutcomeNeedlesAnesthesiaUNESCO::CIENCIAS MÉDICASFemalePterygoid Musclesmedicine.drugAdultmedicine.medical_specialtyAdolescentOdontologíaMyofascial pain syndromeYoung AdultmedicineHumansPain ManagementGeneral DentistryMasticationAcetaminophenAgedOral Medicine and Pathologybusiness.industryResearchTrigger PointsPterygoid Musclesmedicine.diseaseSurgeryAcetaminophenOtorhinolaryngologySurgerybusinessAcupuncture PointsMethocarbamol
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Synergistic Effect of Physical Therapy Plus Pharmacological Therapy with Eperisone in Tension-Type Cervicalgia

2019

Background. This study assessed the effect of eperisone + physical therapy compared with physical therapy alone on the alleviation of pain and disability experienced by patients with tension-type cervicalgia. Methods. Patients with tension-type cervicalgia were randomized to eperisone + physical therapy (Group A) or physical therapy alone (Group B). Patients were assessed at baseline (T0), after 4-weeks’ treatment (T1), and at 2 months’ follow-up (T2). Outcome measures included the Numerical Rating Scale, the Italian version of the Neck Pain and Disability Scale, the Short Form-McGill Pain Questionnaire, and the Italian version of the Neck Disability Index. Results. Ninety-eight patients (5…

Pharmacological therapyTension (physics)business.industrySettore MED/34 - Medicina Fisica E RiabilitativaMedicinemultimodal treatment approachOrthopedics and Sports MedicinePharmacologymuscle relaxantneck pain.businessEperisonemedicine.drugMuscle Ligaments and Tendons Journal
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The triaminopyridine flupirtine prevents cell death in rat cortical cells induced by N-methyl-D-aspartate and gp120 of HIV-1.

1994

Abstract Flupirtine, a triaminopyridine derivative, is a non-opiate centrally acting analgesic agent with muscle relaxant properties. Now we show that this drug displays a potent cytoprotective effect on neurons (rat cortical cells) treated with (i) the excitatory amino acid N-methyl- d -aspartate (NMDA) or (ii) with the human immunodeficiency virus type 1 (HIV-1) coat protein gp120. In the absence of the drug the two agents cause a >90% reduction of cell viability after a 18 h incubation. During this period the DNA in the cells undergoes fragmentation and shows a pattern which is typical for cell death. If the neurons were preincubated with flupirtine for 2 h and subsequently exposed to th…

Programmed cell deathAIDS Dementia ComplexN-Methylaspartatemedicine.drug_classCell SurvivalAnalgesicAminopyridinesBiologyPharmacologyHIV Envelope Protein gp120medicineAnimalsViability assayFragmentation (cell biology)Rats WistarCells CulturedPharmacologyCerebral CortexNeuronsAnalgesicsCell DeathMuscle relaxantRatsMolecular Weightmedicine.anatomical_structureImmunologyHIV-1NMDA receptorNeuronFlupirtinemedicine.drugEuropean journal of pharmacology
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