Search results for "Motor activity"

showing 10 items of 486 documents

Dose-dependent impairing effects of morphine on avoidance acquisition and performance in male mice.

1998

The effects of morphine (6.3, 12.6, and 25.2 mg/kg) on active avoidance behavior of BALB/C mice are explored in three acquisition sessions and in two subsequent performance sessions. Morphine-treated animals showed an increase in avoidance acquisition with respect to control group without differences in performance. However, a dramatical, concomitant rise in the locomotor activity of the animals (increase in the number of crossings during the intertrial intervals) prompted us to transform the data employing a formula with which a measure of actual learning was obtained. Applying this formula, we have observed that morphine administration impairs, dose-dependently, acquisition and performanc…

MaleNarcoticsTime FactorsCognitive Neurosciencemedicine.medical_treatmentDose dependenceMale miceExperimental and Cognitive PsychologyPharmacologyLocomotor activityDevelopmental psychologyBehavioral NeuroscienceMicemedicineAnimal activityAvoidance LearningAnimalsMice Inbred BALB CBehavior AnimalDose-Response Relationship DrugMorphineStimulantDose–response relationshipMorphinePsychologyNeurosciencemedicine.drugNeurobiology of learning and memory
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Memantine presents different effects from MK-801 in motivational and physical signs of morphine withdrawal

2003

Adaptive changes in neural systems due to chronic opiate exposure are related to the neural plasticity phenomenon, NMDA receptors being implicated in these processes, e.g. tolerance, dependence or withdrawal. In this work, we investigated the effect of two non-competitive NMDA antagonists, memantine and MK-801, in motivational (Conditioned Place Aversion paradigm, CPA) and physical aspects of morphine withdrawal. After the induction of morphine dependence, animals in which the CPA was studied, received memantine (5 and 10 mg/kg) or MK-801 (0.3-0.006 mg/kg) either during the acquisition (conditioning) or expression (test) phase of this procedure. Both drugs were capable of inhibiting conditi…

MaleNarcoticsTime FactorsNarcotic AntagonistsMotor ActivityPharmacologyMiceBehavioral NeuroscienceMemantineConditioning PsychologicalNeuroplasticitymedicineAnimalsDrug InteractionsBehavior AnimalDose-Response Relationship DrugMorphineNaloxoneKindlingMemantineSubstance Withdrawal SyndromeBlockadeMorphineNMDA receptorConditioningDizocilpine MaleateOpiatePsychologyExcitatory Amino Acid AntagonistsMorphine Dependencemedicine.drugBehavioural Brain Research
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GHB differentially affects morphine actions on motor activity and social behaviours in male mice

2003

There are several reports suggesting that gamma-hydroxybutyric acid (GHB) influences the endogenous opioid system. The present study aimed to investigate the effects of GHB on motor and social activities and to examine its influence on morphine's actions on these behaviours. In a first experiment, several doses of GHB were studied but only the highest (200 and 400 mg/kg) produced a decrease in spontaneous motor activity measured in an actimeter cage. When hyperactivity induced by injecting 50 mg/kg of morphine was evaluated, all the GHB doses efficiently counteracted this morphine action. Using the paradigm of isolation-induced aggression, administration of 200 mg/kg of GHB significantly de…

MaleNarcoticsmedicine.drug_classClinical BiochemistryMale miceMotor ActivityPharmacologyToxicologyBiochemistryMiceBehavioral NeuroscienceOpioid receptormedicineAnimalsDrug InteractionsMotor activitySocial BehaviorBiological PsychiatryEndogenous opioidPharmacologyMorphineAggressionBiological activityAggressionOpioidExploratory BehaviorMorphinemedicine.symptomSodium OxybatePsychologyAnesthetics Intravenousmedicine.drugPharmacology Biochemistry and Behavior
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Lack of Specific Effects of Selective D1 and D2 Dopamine Antagonists vs. Risperidone on Morphine-Induced Hyperactivity

2000

Abstract RODRIGUEZ-ARIAS, M., I. BROSETA, M. A. AGUILAR AND J. MINARRO. Lack of specific effects of selective D 1 and D 2 dopamine antagonists on morphine-induced hyperactivity. PHARMACOL BIOCHEM BEHAV 66 (1) 189–197, 2000.—In the present study, three different dopamine antagonists were challenged in order to counteract hyperactivity induced by 50 mg/kg of morphine. A wide range of doses of morphine (50, 25, 12.5, 6.25, or 3.12 mg/kg) were evaluated on spontaneous locomotor activity. A significant increase was observed only with the two higher doses tested (25 and 50 mg/kg). No decrease was found with any of the doses used at any period of time. After analyzing doses of SCH 23390 (0.5, 0.1,…

MaleNarcoticsmedicine.medical_specialtyClinical BiochemistryMotor ActivityPharmacologyCatalepsyToxicologyBiochemistryMiceBehavioral Neurosciencechemistry.chemical_compoundDopamineInternal medicinemedicineAnimalsBiological PsychiatryPharmacologyRacloprideCatalepsySCH-23390RisperidoneMorphineChemistryReceptors Dopamine D1AntagonistDopamine antagonistBenzazepinesRisperidonemedicine.diseaseDopamine D2 Receptor AntagonistsEndocrinologyRacloprideMorphineDopamine Antagonistsmedicine.drugPharmacology Biochemistry and Behavior
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The effects of dopamine D 2 and D 3 antagonists on spontaneous motor activity and morphine-induced hyperactivity in male mice

1999

Rationale: Dopaminergic neurotransmission, in particular the mesolimbic pathway, is involved in spontaneous locomotor activity and in morphine-induced hyperactivity, since the drugs acting on DA receptors can modify the action of morphine and this effect could be dependent on the type of DA receptor affected. Objective: In this study, the action of U-99194A maleate, haloperidol, sulpiride and morphine (5, 10, 20, 40 mg/kg) on locomotor activity in male mice was evaluated. Likewise, the effects of these dopaminergic antagonists on morphine-induced hyperactivity were studied. Methods: Animals treated with U-99194A maleate (2.5, 5, 10, 20 mg/kg), haloperidol (0.075, 0.1 mg/kg), sulpiride (20, …

MaleNarcoticsmedicine.medical_specialtyMesolimbic pathwayMotor ActivityPharmacologyMiceDopamine receptor D2Internal medicineHaloperidolmedicineAnimalsPharmacologyMorphineChemistryDopaminergicReceptors Dopamine D3AntagonistDopamine D2 Receptor AntagonistsEndocrinologyMechanism of actionIndansMorphineDopamine AntagonistsHaloperidolSulpiridemedicine.symptomSulpiridemedicine.drugPsychopharmacology
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Effects of nicotinamide on central cholinergic transmission and on spatial learning in rats

1996

High-dose nicotinamide (1000 mg/kg) leads to a minor increase of plasma choline but to a major increase of the choline concentrations in the intra- and extracellular spaces of the brain. In the hippocampus, the nicotinamide-induced increase in choline was associated with an increase in the release of acetylcholine under stimulated conditions. In young rats, nicotinamide in doses between 10 and 1000 mg/kg did not influence spatial learning, as tested in the Morris water maze. In old rats, low doses of nicotinamide were ineffective whereas the high dose of 1000 mg/kg even impaired spatial learning. The combined administration of choline and nicotinamide had a synergistic effect on brain choli…

MaleNiacinamideAgingClinical BiochemistryHippocampusMorris water navigation taskMotor ActivityPharmacologyToxicologyHippocampusSynaptic TransmissionBiochemistryCholineBehavioral Neurosciencechemistry.chemical_compoundCognitionParasympathetic Nervous SystemmedicineExtracellularAnimalsCholineRats WistarMaze LearningBiological PsychiatryBrain ChemistryPharmacologyNicotinamideBiological activityAcetylcholineRatschemistryBiochemistryCholinergicExtracellular SpaceAcetylcholinemedicine.drugPharmacology Biochemistry and Behavior
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A specific anti-aggressive effect of repeatedly administered lobeline.

2002

The effects of chronic treatments with nicotinic agonists on agonistic encounters have received little attention. The effects of repeated (for 10 days) SC administration of (-)-lobeline (9.3, 18.6 and 37.2 micromol/kg) and (-)-nicotine (0.93, 1.86 and 3.72 micromol/kg) were evaluated using the mouse isolation-induced aggression model. Individually housed OF1 male mice served as experimental animals and were confronted by 'standard opponents'. Each mouse was tested only once on the last day of the repeated drug treatment. Videotaped agonistic encounters were analysed estimating the times allocated to 11 behavioural categories. Repeated treatment with the highest dose of lobeline diminished a…

MaleNicotineMedicine (miscellaneous)Male micePharmacologyMotor ActivityDrug Administration ScheduleNicotinechemistry.chemical_compoundMiceRepeated treatmentAgonistic behaviourmedicineAnimalsLobelineMotor activityNicotinic AgonistsPharmacologyDose-Response Relationship DrugAggressionAggressionPsychiatry and Mental healthNicotinic agonistchemistrySocial IsolationLobelinemedicine.symptomPsychologyAgonistic Behaviormedicine.drugAddiction biology
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Effects of housing and nicotine on shuttle-box avoidance in male NMRI mice

2005

The present study aimed to evaluate whether housing condition could interact with nicotine administration in influencing the acquisition of a two-way active avoidance task. Male NMRI mice were either group- or individually housed for 30 days and, after this period, evaluated both in the actimeter and, 24h later, in the elevated plus-maze. On the basis of the percentage of time spent in the open arms of the plus-maze, both group- and individually housed mice were sub-classified into three groups with high, moderate or low anxiety baseline levels. Effects of nicotine on the acquisition of the two-way active avoidance task was assessed in each of these groups of mice using an automated shuttle…

MaleNicotinePhysiologyAnxietyMotor ActivitySocial EnvironmentDevelopmental psychologyNicotineMiceBehavioral NeuroscienceStatistical significanceAvoidance LearningmedicineAnimal activityAnimalsNicotinic AgonistsMotor activityAnalysis of VarianceHousing AnimalSocial IsolationNmri miceShuttle boxAnxietyAnalysis of variancemedicine.symptomPsychologymedicine.drugBehavioural Brain Research
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Effects of chronic nicotine on the temporal structure of anxiety-related behavior in rats tested in hole-board.

2019

Abstract The present study aimed to assess the behavioral effects of chronic treatments of different doses of nicotine by using both quantitative and multivariate T-pattern analysis (TPA), which can reveal hidden behavioral structures, in Sprague-Dawley rats tested in the hole-board apparatus. To this purpose, nicotine ditartrate was administered at the doses of 0.1, 0.5 and 1 mg/kg i.p., three times per day, for 14 consecutive days. As to quantitative evaluations, we observed significant reductions in the mean durations and mean frequencies of walking, climbing, immobile-sniffing and rearing in comparison to control. A significant reduction of edge-sniff and head-dip mean frequencies was a…

MaleNicotineTime FactorsHole-boardmedicine.medical_treatmentQuantitative EvaluationsPhysiologyAnxietyMotor ActivityT-pattern analysisSettore BIO/09 - FisiologiaAnxiety; Chronic nicotine; Hole-board; Sprague-Dawley rats; T-pattern analysis; Animals; Anxiety; Dose-Response Relationship Drug; Drug Administration Schedule; Exploratory Behavior; Male; Motor Activity; Nicotine; Random Allocation; Rats; Rats Sprague-Dawley; Time FactorsDrug Administration ScheduleNicotineDose-Response RelationshipRats Sprague-Dawley03 medical and health sciencesSprague-Dawley ratRandom Allocation0302 clinical medicineSprague dawley ratsMedicineAnimalsBiological PsychiatryPharmacologyDose-Response Relationship Drugbusiness.industrySprague-Dawley rats030227 psychiatryRatsChronic nicotineChronic nicotineExploratory BehaviorSmoking cessationAnxietySprague-Dawleymedicine.symptomDrugbusinessmedicine.drugProgress in neuro-psychopharmacologybiological psychiatry
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Spatial learning in male mice with different levels of aggressiveness: effects of housing conditions and nicotine administration

2003

The main aim of the present investigation was to evaluate the possible modulation of spatial learning ability by housing conditions and level of aggressiveness in mice, also testing whether differences in locomotion and anxiety could influence this relationship. Additionally, we have examined effects of nicotine in the acquisition and retention of a spatial learning task in groups of mice differing in these variables. NMRI male mice were either group-housed or individually housed for 30 days and then classified into mice with short (SAL) and long (LAL) attack latency after a pre-screening agonistic encounter. Locomotor activity and baseline levels of anxiety of these groups were evaluated i…

MaleNicotinemedicine.medical_specialtyElevated plus mazeTime Factorsmedicine.drug_classSpatial BehaviorEscape responseWater mazeAnxietyMotor ActivitySocial EnvironmentAnxiolyticDevelopmental psychologyDiscrimination LearningNicotineMiceBehavioral NeuroscienceEscape ReactionInternal medicineReaction TimemedicineAnimalsNicotinic AgonistsMaze LearningAnalysis of VarianceBehavior AnimalDose-Response Relationship DrugHousing AnimalAggressionEndocrinologyNicotinic agonistSocial IsolationAnxiogenicAnalysis of variancePsychologymedicine.drugBehavioural Brain Research
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