Search results for "ACL"

showing 10 items of 906 documents

Construct validity and reliability of the Finnish version of the Knee Injury and Osteoarthritis Outcome Score

2018

Background The Knee Injury and Osteoarthritis Outcome Score (KOOS) is a commonly used knee assessment and outcome tool in both clinical work and research. However, it has not been formally translated and validated in Finnish. The purpose of this study was to translate and culturally adapt the KOOS questionnaire into Finnish and to determine its validity and reliability among Finnish middle-aged patients with knee injuries. Methods KOOS was translated and culturally adapted from English into Finnish. Subsequently, 59 patients with knee injuries completed the Finnish version of KOOS, Western Ontario and McMaster Osteoarthritis Index (WOMAC), Short-Form 36 Health Survey (SF-36) and Numeric Pai…

Malelcsh:Diseases of the musculoskeletal systemSports medicineIntraclass correlationpolvetmedicine.medical_treatmentValiditySeverity of Illness Index0302 clinical medicineOrthopedics and Sports Medicine030212 general & internal medicineReliability (statistics)FinlandPain MeasurementHEALTH-STATUSRELEVANTRehabilitationKOOSPAINMiddle AgedOsteoarthritis KneeReliabilityCOMMUNITYTreatment OutcomevalidointiFemaleKnee osteoarthritisKnee injuryResearch ArticleAdultCross-Cultural Comparisonmedicine.medical_specialtynivelrikkoWOMACarviointimenetelmätKnee InjuriesVALIDATIONknee osteoarthritisValidity03 medical and health sciencesRheumatologyCronbach's alphamedicineQUALITYCOSMINHumans030203 arthritis & rheumatologyreliabilitybusiness.industryFinnishConstruct validityReproducibility of Results3126 Surgery anesthesiology intensive care radiologyHealth Surveysknee injuryvaliditeettiCROSS-CULTURAL ADAPTATIONPhysical therapyvammatlcsh:RC925-935business
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Benzodiazepine receptor binding: the interactions of some non-benzodiazepine drugs with specific [3H] diazepam binding to rat brain synaptosomal memb…

1978

The interaction of several non-benzodiazepine drugs with [3H] diazepam binding to benzodiazepine receptors in rat brain synaptosomal membranes was investigated. Baclofen, benzoctamine, hydroxyzine, chlorpromazine, haloperidol, imipramine, and amitriptyline displace specific [3H] diazepam binding, but the concentrations needed are too high to explain pharmacological effects of these drugs by an interaction with benzodiazepine receptors. The most potent non-benzodiazepine drug for inhibiting specific [3H] diazepam binding was methaqualone (IC50 value of 150 micrometer). It is suggested that interactions with benzodiazepine receptors may account for the anxiolytic and anticonvulsive side effec…

Malemedicine.drug_classReceptors DrugPharmacologyIn Vitro TechniquesAnxiolyticBinding Competitivechemistry.chemical_compoundmedicineAnimalsDrug InteractionsBenzodiazepine receptor bindingPharmacologyBenzodiazepineDiazepam bindingDiazepamMembranesGABAA receptorBrainGeneral MedicineRatsBaclofenAnalepticchemistryBenzoctaminemedicine.drugSynaptosomesNaunyn-Schmiedeberg's archives of pharmacology
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Measuring patient experiences in Fabry disease: validation of the Fabry-specific Pediatric Health and Pain Questionnaire (FPHPQ)

2012

Abstract Introduction Common symptoms for children with Anderson-Fabry Disease (FD) such as acroparaesthesia and gastrointestinal manifestations can only be objectively assessed in patients using a valid instrument. To date, no such instrument exists. Methods A preliminary 40-item measure of symptoms and experience with FD, the Fabry-specific Paediatric Health and Pain Questionnaire (FPHPQ) was developed, but lacked a formal assessment of its measurement properties. The FPHPQ was used in the Fabry Outcome Survey (FOS), a registry for all patients with a confirmed diagnosis of FD who are receiving agalsidase alfa, or are treatment naïve and who are managed by physicians participating in FOS.…

Malemedicine.medical_specialtyAdolescentIntraclass correlation610 Medicine & healthlcsh:Computer applications to medicine. Medical informaticsSeverity of Illness IndexPsychometrics validationCronbach's alphaQuality of lifeSurveys and QuestionnairesSeverity of illnessmedicineHumansBrief Pain InventoryChildChildrenPain MeasurementFabry diseaseItem analysisbusiness.industryResearchPublic Health Environmental and Occupational HealthReproducibility of ResultsConstruct validity2739 Public Health Environmental and Occupational HealthGeneral MedicinePaediatric Health and Pain Questionnairemedicine.diseaseFabry disease10036 Medical ClinicChild PreschoolEnzyme replacement therapyQuality of LifePhysical therapylcsh:R858-859.7FemalebusinessHealth and Quality of Life Outcomes
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Concurrent validation of the OMNI-Resistance Exercise Scale of perceived exertion with elastic bands in the elderly.

2018

Purpose:\ud To examine the concurrent validity of the OMNI-Resistance Exercise Scale of perceived exertion using elastic bands in elder population.\ud \ud Methods:\ud Twenty-six participants performed three separate sets of 15 repetitions (low- medium- and high-intensity) for 4 different exercises (2 for the upper-limb and 2 for the lower limb), over two different testing sessions. The criterion variables were heart rate and applied force (average and maximum). In addition to these dependent variables, the active muscle and overall body OMNI-RES for elastic bands scores were collected at the end of each repetition.\ud \ud Results:\ud Significant differences in heart rate, applied force and …

Malemedicine.medical_specialtyAgingScale (ratio)Intraclass correlationConcurrent validityPopulationPhysical ExertionPerceived exertion030204 cardiovascular system & hematologyBiochemistry03 medical and health sciences0302 clinical medicineEndocrinologyPhysical medicine and rehabilitationHeart RateHeart rateTask Performance and AnalysisGeneticsmedicineHumanseducationMuscle SkeletalMolecular BiologyMathematicsAgedRating of perceived exertioneducation.field_of_study030229 sport sciencesCell BiologyMiddle AgedQPCross-Sectional StudiesExercise intensityExercise TestFemalePerceptionPsychomotor PerformanceExperimental gerontology
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Cholinergic and GABAergic regulation of nitric oxide synthesis in the guinea pig ileum.

1999

Nitric oxide (NO) synthesis was examined in intact longitudinal muscle-myenteric plexus preparations of the guinea pig ileum by determining the formation of [3H]citrulline during incubation with [3H]arginine. Spontaneous [3H]citrulline production after 30 min was 80–90 dpm/mg, which constituted ∼1% of the tissue radioactivity. Electrical stimulation (10 Hz) led to a threefold increase in [3H]citrulline formation. Removal of calcium from the medium or addition of N G-nitro-l-arginine strongly inhibited both spontaneous and electrically induced production of [3H]citrulline. TTX reduced the electrically induced but not spontaneous [3H]citrulline formation. The electrically induced formation o…

Malemedicine.medical_specialtyBaclofenArgininePhysiologyGuinea PigsScopolamineMyenteric PlexusTubocurarineTetrodotoxinBiologyCholinergic AgonistsIn Vitro TechniquesMecamylamineBicucullineNitric OxideNitroarginineCholinergic Antagonistschemistry.chemical_compoundIleumPhysiology (medical)Internal medicineIsometric ContractionMuscarinic acetylcholine receptorMecamylaminemedicineCitrullineAnimalsEgtazic AcidGABA AgonistsMyenteric plexusgamma-Aminobutyric AcidHepatologyGABAA receptorMuscimolOxotremorineGastroenterologyMuscle SmoothBicucullineElectric StimulationEndocrinologychemistryMuscimolCitrullineFemalemedicine.drugThe American journal of physiology
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Sex differences in escape-avoidance response in mice after acute administration of raclopride, clozapine, and SCH 23390.

1998

Sex differences in the effects of haloperidol in the escape-avoidance response in mice have previously been found in various studies carried out in our laboratory. Males were more affected than females by the disruptive effects of this neuroleptic. The work described herein extended the study of these sex differences to raclopride, clozapine, and SCH 23390, using several doses of each drug in acute administration. The results showed dose-dependent sex differences in the deteriorating effects of these dopamine antagonists in the escape-avoidance response. Male mice were more affected by the inhibitory effects of these drugs, showing fewer escape responses and more nonresponses than females. …

Malemedicine.medical_specialtyClinical BiochemistryEscape responsePharmacologyToxicologyBiochemistryBehavioral NeuroscienceMiceDopamineEscape ReactionInternal medicineSalicylamidesmedicineHaloperidolAvoidance LearningAnimalsClozapineBiological PsychiatryPharmacologyRacloprideSex CharacteristicsDose-Response Relationship DrugReceptors Dopamine D1DopaminergicDopamine antagonistBenzazepinesDopamine D2 Receptor AntagonistsEndocrinologyDopamine receptorRacloprideDopamine AntagonistsFemalePsychologymedicine.drugSex characteristicsPharmacology, biochemistry, and behavior
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Sex differences in the effects of neuroleptics on escape-avoidance behavior in mice: a review.

1999

Abstract The literature of the effects of dopamine antagonists on escape-avoidance, focusing on data obtained in our laboratory with male and female mice, is reviewed. The acute administration of haloperidol, raclopride, clozapine, and SCH 23390 impaired escape-avoidance behavior more in males than in females, and the subchronic administration of haloperidol had a similar effect. This appeared to be a reliable phenomenon, because it was observed in both kinds of administration, in two mouse strains, and with several drugs and doses. The observed results were dose dependent, although the dose–effect relationship was not the same in all drugs. The sex differences in escape avoidance did not s…

Malemedicine.medical_specialtyClinical BiochemistryToxicologyBiochemistryBehavioral Neurosciencechemistry.chemical_compoundMiceDopamineEscape ReactionInternal medicinemedicineHaloperidolAvoidance LearningAnimalsBiological PsychiatryClozapinePharmacologyRacloprideSCH-23390Sex CharacteristicsDopamine antagonistAntagonistEndocrinologychemistryDopamine receptorRacloprideHaloperidolFemalePsychologymedicine.drugAntipsychotic AgentsPharmacology, biochemistry, and behavior
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Effects of dopamine antagonists with different receptor blockade profiles on morphine-induced place preference in male mice.

2001

The effects of dopamine (DA) antagonists with different selectivity for the DA receptors (SCH 23390, 0.5, 0.25, 0.125 mg/kg; haloperidol, 0.2, 0.1 mg/kg; raclopride, 1.2, 0.6, 0.3 mg/kg; risperidone, 0.4, 0.2, 0.1 mg/kg; U-99194A maleate, 40, 20 mg/kg; clozapine, 2.5, 1.25, 0.625 mg/kg) on the acquisition of place conditioning and morphine-induced conditioned place preference (CPP) were explored in male mice. Morphine (40 mg/kg) produced CPP while SCH 23390, haloperidol and clozapine (highest dose) and risperidone (lowest dose) produced conditioned place aversion (CPA). Raclopride and U-99194A maleate did not produce CPP or CPA. Morphine-induced CPP was reversed by the administration of SCH…

Malemedicine.medical_specialtyConditioning ClassicalPharmacologyChoice BehaviorReceptors DopamineBehavioral Neurosciencechemistry.chemical_compoundMiceDopamineInternal medicineOrientationpolycyclic compoundsmedicineHaloperidolAvoidance LearningAnimalsRacloprideSCH-23390MotivationDose-Response Relationship DrugMorphineChemistryAntagonistBrainConditioned place preferenceEndocrinologyDopamine receptorMorphineDopamine Antagonistsmedicine.drugBehavioural brain research
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Sensitization to the rewarding effects of morphine depends on dopamine

2005

The influence of dopamine (DA) on sensitization to the rewarding effects of morphine was evaluated. The effects of pre-treatment with saline or morphine plus naloxone, CGS 10746B, haloperidol, SCH 23390 and raclopride, on the place conditioning induced by 2 mg/kg morphine were evaluated. This dose was ineffective in saline pre-treated animals but induced a clear conditioned place preference in mice pre-treated with morphine, CGS 10746B or haloperidol. Conversely, animals pre-treated with morphine plus naloxone, CGS 10746B, SCH 23390, raclopride and the high dose of haloperidol did not acquire place preference. Our results demonstrated that DA release and subsequent DA D1 and D2 receptor act…

Malemedicine.medical_specialtyDopamine(+)-NaloxonePharmacologyReceptors DopamineMicechemistry.chemical_compoundRewardInternal medicineDopamine receptor D2Conditioning PsychologicalHaloperidolmedicineAnimalsSensitizationRacloprideSCH-23390MorphineNaloxoneGeneral NeuroscienceBenzazepinesConditioned place preferenceEndocrinologymedicine.anatomical_structurechemistryMorphinemedicine.drugNeuroReport
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Role of dopamine neurotransmission in the long-term effects of repeated social defeat on the conditioned rewarding effects of cocaine

2016

Numerous studies report that social defeat stress alters dopamine (DA) neurotransmission in several areas of the brain. Alterations of the mesolimbic dopaminergic pathway are believed to be responsible for the increased vulnerability to drug use observed as a result of social stress. In the present study, we evaluated the influence of DA receptors on the long-term effect of repeated social defeat (RSD) on the conditioned rewarding and reinstating effects of cocaine. For this purpose, the D1R antagonist SCH 23390 and the D1R antagonist raclopride were administered 30 min before each social defeat and a cocaine-induced CPP procedure was initiated three weeks later. The expression of the D1R a…

Malemedicine.medical_specialtyHippocampusStatistics NonparametricReceptors DopamineSocial defeatMice03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDopamine Uptake InhibitorsRewardCocaineInternal medicineDopamine receptor D2medicineAnimalsDopamine receptorsBiological PsychiatryCerebral CortexPharmacologyRacloprideSocial stressSCH-23390Dose-Response Relationship DrugDopaminergicAge FactorsBenzazepinesConditioned place preferenceConditioned place preference030227 psychiatryDisease Models AnimalEndocrinologychemistryRacloprideDopamine receptorAnesthesiaConditioning OperantDopamine AntagonistsPsychologySocial defeat stressStress Psychological030217 neurology & neurosurgerymedicine.drug
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