Search results for "elevated plus maze"

showing 10 items of 53 documents

Effects of acute amitriptyline administration on memory, anxiety and activity in male and female mice

2002

The effects of acute administration of amitriptyline on memory consolidation in male and female CD1 mice were investigated. Three doses of this tricyclic antidepressant (7.5, 15 and 30 mg/kg) were administered immediately after inhibitory avoidance training. Forty-five minutes after injection, subjects explored the elevated plus-maze for five minutes. Subjects were tested for avoidance twenty-four hours later. Amitriptyline impaired inhibitory avoidance consolidation at doses 7.5, 15 and 30 mg/kg in males, and at doses 7.5 and 30 mg/kg in females. In the elevated plus-maze, amitriptyline had no effect on anxiety (percentage of open arm entries) and induced a dose-dependent impairment of act…

Elevated plus mazemedicine.medical_specialtymedicine.drug_classGeneral NeuroscienceTricyclic antidepressantRetrograde amnesiaInhibitory postsynaptic potentialmedicine.diseaseAnxiolyticEndocrinologyAnesthesiaInternal medicinemedicineAnxietyMemory consolidationAmitriptylinemedicine.symptomPsychologymedicine.drugNeuroscience Research Communications
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Behavioral effects of different enriched environments in mice treated with the cholinergic agonist PNU-282987.

2013

Abstract Environmental enrichment is an experimental model in which rodents are housed in complex environments that favor lower levels of anxiety-like behavior. PNU-282987 (PNU) is a α7 nicotinic acetylcholine receptor agonist with beneficial effects on learning though its effects on anxiety are unclear. Our main aim was to carry out a study of its effects in NMRI ( n  = 96) mice reared in different environments: environmental enrichment (EE), Marlau™ cages (MC) and standard environment (SE). After a 4-month period, mice received acute treatment of PNU (2.5, 5 and 10 mg/kg) and were evaluated in the elevated plus-maze (EPM) and hole-board (HB). In the EPM, both EE and MC reared mice showed …

AgonistMalemedicine.medical_specialtyElevated plus mazealpha7 Nicotinic Acetylcholine Receptormedicine.drug_classAnxietyEnvironmentMotor ActivityDevelopmental psychologyBehavioral NeuroscienceBridged Bicyclo CompoundsMiceα7 nicotinic acetylcholine receptorInternal medicinemedicineAnimalsNicotinic AgonistsBeneficial effectsEnvironmental enrichmentBehavior AnimalExperimental modelGeneral MedicineNicotinic agonistEndocrinologyBenzamidesExploratory BehaviorCholinergicAnimal Science and ZoologyPsychologyInjections IntraperitonealBehavioural processes
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Acute behavioural and neurotoxic effects of MDMA plus cocaine in adolescent mice.

2008

The poly-drug pattern is the most common among those observed in MDMA users, with cocaine being a frequently associated drug. This study evaluates the acute effects of MDMA (5, 10 and 20 mg/kg), alone or in combination with cocaine (25 mg/kg), on motor activity, anxiety (elevated plus maze and social interaction test), memory and brain monoamines in adolescent mice, Both drugs, administered alone or concurrently, produced hyperactivity and a decrease in social contacts. However, an anxiolytic effect, studied by means of the elevated plus maze and expressed as an increase in the time spent on the open arms, was observed only in those animals treated with cocaine and MDMA. The passive avoidan…

MaleSerotoninElevated plus mazeMDMAmedicine.drug_classDopamineN-Methyl-34-methylenedioxyamphetamineStriatumPharmacologyAnxietyMotor ActivityToxicologyAnxiolyticHippocampusCellular and Molecular NeuroscienceMiceSerotonin AgentsDevelopmental NeuroscienceCocaineDopaminemental disordersmedicineAvoidance LearningAnimalsBiogenic MonoaminesInterpersonal RelationsBrain ChemistryCerebral CortexBehavior AnimalMDMACortex (botany)NeostriatumSocial behaviourAnxietyNeurotoxicity SyndromesSerotoninmedicine.symptomElevated plus mazePsychologypsychological phenomena and processesmedicine.drugNeurotoxicology and teratology
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The effects of different basal levels of anxiety on the behavioral shift analyzed in the central platform of the elevated plus maze.

2015

The aim of the present research was to study the effects of different basal levels of anxiety on the behavioral shift studied in the central platform of the elevated plus maze. To this purpose, quantitative and multivariate analyses, the latter based on transition matrix elaboration, were carried out on Wistar and on DA/Han rats the latter belonging to a strain characterized by different reactivity to anxiogenic stimuli. Wistar rats spent 74.11 ± 5.11 s in the central platform, whereas DA/Han significantly more: 127.08 ± 9.87. Per cent distributions evidenced a clear-cut difference in walking activities (46.25% in Wistar, 28.4% in DA/Han rats) and in the sniffing activities (45.82% in Wista…

Malemedicine.medical_specialtyElevated plus mazeMaze learningWistar ratAnxietyMotor ActivitySettore BIO/09 - FisiologiaBehavioral NeuroscienceBasal (phylogenetics)SniffingInternal medicinemedicineAnimalsMotor activityRats WistarMaze LearningBehavioral shiftBehavior AnimalMultivariate analysiRats Inbred StrainsDA/Han ratRatsEndocrinologyAnxiogenicMultivariate AnalysisExploratory BehaviorAnxietyTransition matricesmedicine.symptomElevated plus mazePsychologyDecision makingNeuroscienceBehavioural brain research
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Anxiolytic-like effects of acute and chronic GABA transporter inhibition in rats.

2002

Acute GABA transporter inhibition can induce anxiolytic-like behaviors. The present analysis addressed whether chronic treatment (23 days via drinking water) with a GABA transporter inhibitor affects rat behavior similar to acute treatment and interferes with additional benzodiazepine-receptor agonistic treatment. Seventy-one rats divided into seven groups were acutely treated with either vehicle, diazepam (2 mg/kg), zolpidem (0.05 mg/kg), tiagabine (19 mg/kg) or chronically with tiagabine with or without acute diazepam or zolpidem. Animals were behaviorally characterized in an elevated plus-maze. None of the treatments induced changes in the activity of the animals. Acute and chronic treat…

AgonistMalemedicine.medical_specialtyElevated plus mazeZolpidemGABA Plasma Membrane Transport ProteinsTime FactorsTiagabinemedicine.drug_classPyridinesNipecotic AcidsOrganic Anion TransportersPharmacologyAnxiolyticDrug Administration Schedulechemistry.chemical_compoundInternal medicinemedicineGABA transporterAnimalsNeurotransmitterMaze LearningTiagabineBiological PsychiatryDiazepambiologyBehavior Animalbusiness.industryMembrane ProteinsMembrane Transport ProteinsDrug SynergismRats Inbred StrainsRatsZolpidemPsychiatry and Mental healthEndocrinologyNeurologychemistryAnti-Anxiety Agentsbiology.proteinNeurology (clinical)businessCarrier ProteinsDiazepammedicine.drugJournal of neural transmission (Vienna, Austria : 1996)
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Cocaine exposure during adolescence affects anxiety in adult mice.

2006

Psychostimulant drugs such as cocaine have profound and long-lasting neurobiological effects, which may affect anxiety or social behaviors. These actions could be greater when cocaine is administered during a developmental period such as adolescence. The present work attempts to further clarify the long-lasting effects of cocaine administration on mice, examining three major variables: age; pattern of drug administration; and housing conditions. Adolescent (postnatal day 26) or early adult mice (postnatal day 46) were exposed to a daily or binge cocaine administration and 15 days later their behavior was evaluated, the mice being housed either in isolation or in groups during this stage. Af…

MaleElevated plus mazemedicine.medical_specialtyAgingDose-Response Relationship DrugGeneral NeuroscienceDrug administrationPhysiologyAnxietyMotor ActivityAffect (psychology)Social relationCocaine-Related DisordersMiceCocainemedicineAnxietyAnimalsInterpersonal RelationsMotor activitymedicine.symptomPsychiatryPsychologyPostnatal daySocial behaviorBrain research bulletin
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The novelty-seeking phenotype modulates the long-lasting effects of intermittent ethanol administration during adolescence.

2013

The aim of the present study was to investigate if a novelty-seeking phenotype mediates the long-lasting consequences of intermittent EtOH intoxication during adolescence. The hole board test was employed to classify adolescent mice as High- or Low-Novelty Seekers. Subsequently, animals were administered ethanol (1.25 or 2.5 g/kg) on two consecutive days at 48-h intervals over a 14-day period. Anxiety levels - measured using the elevated plus maze- spontaneous motor activity and social interaction test were studied 3 weeks later. A different set of mice underwent the same procedure, but received only the 2.5 g/kg dose of ethanol. Three weeks later, in order to induce CPP, the same animals w…

MaleAginglcsh:MedicinePoison controlSocial SciencesAnxietyToxicologychemistry.chemical_compoundMiceBehavioral NeuroscienceCocaineMedicine and Health SciencesPsychologyPublic and Occupational Healthlcsh:ScienceHole-board testMultidisciplinaryAlcohol ConsumptionBehavior AnimalMDMAPhenotypeBehavioral PharmacologyAnxietymedicine.symptomBehavioral and Social Aspects of HealthReinforcement Psychologymedicine.drugResearch Articlemedicine.medical_specialtyElevated plus mazeAdolescentmedicine.drug_classN-Methyl-34-methylenedioxyamphetamineBiologyAnxiolyticInternal medicineMental Health and PsychiatrymedicineAnimalsHumansMaze LearningNutritionPharmacologyBehaviorEthanolEthanollcsh:RNovelty seekingBiology and Life SciencesDietEndocrinologychemistryExploratory Behaviorlcsh:QClinical MedicineNeurosciencePloS one
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Assessment of the abuse potential of MDMA in the conditioned place preference paradigm: Role of CB1 receptors

2013

Numerous reports have highlighted the role of the endocannabinoid system in the addictive potential of MDMA (3,4-methylenedioxy-methamphetamine). A previous report showed that CB1 knockout (KOCB1) mice do not acquire MDMA self-administration, despite developing conditioned place preference (CPP). This contradiction could be due to the particular procedure of place conditioning used. The present work compares MDMA-induced CPP in KOCB1 mice using unbiased and biased procedures of place conditioning. In the unbiased procedure, MDMA induced CPP and reinstatement of the extinguished preference in wild type (WT) mice, but not in KOCB1 mice. In contrast, in a biased protocol of CPP, MDMA produced …

MaleElevated plus mazeTime FactorsSubstance-Related Disordersmedicine.drug_classDopamineN-Methyl-34-methylenedioxyamphetamineNucleus accumbensPharmacologyAnxiolyticDevelopmental psychologyMiceNeurochemicalReceptor Cannabinoid CB1mental disordersmedicineAnimalsMaze LearningBiological PsychiatryMice KnockoutPharmacologyAnalysis of VarianceDose-Response Relationship DrugBrainHomovanillic AcidMDMAConditioned place preferenceDisease Models AnimalMonoamine neurotransmitternervous systemHallucinogens34-Dihydroxyphenylacetic AcidConditioning OperantSerotoninPsychologyReinforcement Psychologypsychological phenomena and processesmedicine.drugProgress in Neuro-Psychopharmacology and Biological 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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Adolescent but not adult ethanol binge drinking modulates cocaine withdrawal symptoms in mice.

2016

Background Ethanol (EtOH) binge drinking is an increasingly common behavior among teenagers that induces long-lasting neurobehavioral alterations in adulthood. An early history of EtOH abuse during adolescence is highly correlated with cocaine addiction in adulthood. Abstinence of cocaine abuse can cause psychiatric symptoms, such as anxiety, psychosis, depression, and cognitive impairments. This study assessed the consequences of adolescent exposure to EtOH on the behavioral alterations promoted by cocaine withdrawal in adulthood. Methods We pretreated juvenile (34-47 days old) or adult (68-81 days old) mice with EtOH (1.25 g/kg) following a binge-drinking pattern. Then, after a three-week…

MalePhysiologylcsh:MedicineAdolescentsOpen fieldMice0302 clinical medicineCocaineMedicine and Health Scienceslcsh:SciencePrepulse inhibitionmedia_commonMammalsMultidisciplinaryAlcohol ConsumptionAnimal BehaviorDepressionAge FactorsSubstance Withdrawal SyndromeChemistryBehavioral PharmacologyPhysical SciencesVertebratesResearch Articlemedicine.medical_specialtyElevated plus mazeAlcohol Drinkingmedia_common.quotation_subjectBinge drinkingRodents03 medical and health sciencesAlkaloidsInternal medicineRecreational Drug Usemental disordersMental Health and PsychiatrymedicineAnimalsAdultsNutritionPharmacologyBehaviorbusiness.industryMood DisordersBiological LocomotionAddictionlcsh:RChemical CompoundsOrganismsBiology and Life SciencesAbstinenceTail suspension test030227 psychiatryDietEndocrinologyAnxiogenicAge GroupsAmniotesPeople and Placeslcsh:QPopulation GroupingsbusinessZoology030217 neurology & neurosurgeryPloS one
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