Search results for "conditioning"

showing 10 items of 632 documents

Induction of conditioned place preference and dopamine release by salsolinol in posterior VTA of rats: involvement of μ-opioid receptors.

2011

Salsolinol (Sal), locally administered into the posterior VTA (pVTA) of rats, produces psychomotor responses and reinforcing effects, probably, through the activation of μ-opioid receptors (MORs). The neurochemical correlates of these phenomena are, however, practically unknown. In this paper, we explore the neurochemical events and the mechanisms involved in these behaviors. To do that, we test the ability of Sal, directly microinjected into the pVTA, to induce conditioned place preference (CPP) and to increase dopamine levels in the nucleus accumbens shell. Bilateral injections of 30 pmol of Sal induced a strong CPP (rats spent around 70% of the total test time), a result that could be ex…

MaleMicrodialysismedicine.medical_specialtyMicroinjectionsDopamineMicrodialysisNarcotic AntagonistsReceptors Opioid muNucleus accumbensNucleus AccumbensCellular and Molecular NeuroscienceNeurochemicalDopamineInternal medicineparasitic diseasesmedicineLimbic SystemAnimalsRats WistarChemistryVentral Tegmental AreaAntagonistCell BiologyIsoquinolinesConditioned place preferenceNaltrexoneRatsVentral tegmental areamedicine.anatomical_structureEndocrinologynervous systemOpioidConditioning OperantNeurosciencemedicine.drugNeurochemistry international
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Dose-dependent induction of CPP or CPA by intra-pVTA ethanol: Role of mu opioid receptors and effects on NMDA receptors.

2020

AbstractThe neurobiological mechanisms underlying alcohol motivational properties are still not fully understood, however, the mu-opioid receptors (MORs) have been evidenced as central elements in the manifestation of the alcohol reinforcing properties. Drug-associated environmental stimuli can trigger alcohol relapse and promote alcohol consumption whereby N-methyl-D-aspartate (NMDA) receptors play a pivotal role. Here we sought to demonstrate, for the first time, that ethanol induces conditioned place preference or aversion (CPP or CPA) when administered locally into the ventral tegmental area (VTA) and the associated role of MORs. We further analyzed the changes in the expression and mRN…

MaleMicroinjectionsReceptors Opioid muHippocampusNucleus accumbensPharmacologyReceptors N-Methyl-D-AspartateArticle03 medical and health scienceschemistry.chemical_compound0302 clinical medicineConditioning PsychologicalmedicineAvoidance LearningAnimalsRats WistarReceptorBiological Psychiatry030304 developmental biologyPharmacology0303 health sciencesEthanolDose-Response Relationship DrugEthanolChemistryVentral Tegmental AreaConditioned place preference030227 psychiatryRatsVentral tegmental areamedicine.anatomical_structureInfusions Intraventricularnervous systemNMDA receptorμ-opioid receptor030217 neurology & neurosurgeryProgress in neuro-psychopharmacologybiological psychiatry
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Role of the dopaminergic system in the acquisition, expression and reinstatement of MDMA-induced conditioned place preference in adolescent mice.

2012

Background The rewarding effects of 3,4-methylenedioxy-metamphetamine (MDMA) have been demonstrated in conditioned place preference (CPP) procedures, but the involvement of the dopaminergic system in MDMA-induced CPP and reinstatement is poorly understood. Methodology/Principal Findings In this study, the effects of the DA D1 antagonist SCH 23390 (0.125 and 0.250 mg/kg), the DA D2 antagonist Haloperidol (0.1 and 0.2 mg/kg), the D2 antagonist Raclopride (0.3 and 0.6 mg/kg) and the dopamine release inhibitor CGS 10746B (3 and 10 mg/kg) on the acquisition, expression and reinstatement of a CPP induced by 10 mg/kg of MDMA were evaluated in adolescent mice. As expected, MDMA significantly increa…

MaleMouseThiazepinesDopaminelcsh:MedicineStriatumPharmacologychemistry.chemical_compoundBehavioral NeuroscienceHabitsMiceHaloperidolMedicinePsychologylcsh:ScienceRacloprideSCH-23390MultidisciplinaryAnimal BehaviorDopaminergicMDMAAnimal ModelsNeurotransmittersMental HealthMedicinepsychological phenomena and processesmedicine.drugResearch ArticleSerotoninN-Methyl-34-methylenedioxyamphetamineBlotting WesternModel OrganismsAnimalsBiologyBehaviorbusiness.industrylcsh:RAntagonistBenzazepinesAdjustment (Psychology)Conditioned place preferencechemistrynervous systemRacloprideDevelopmental PsychologyConditioning OperantDopamine AntagonistsHaloperidollcsh:QbusinessZoologyNeurosciencePLoS ONE
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Results of a HOVON/SAKK donor versus no-donor analysis of myeloablative HLA-identical sibling stem cell transplantation in first remission acute myel…

2007

Abstract The Dutch-Belgian Hemato-Oncology Cooperative Group and the Swiss Group for Clinical Cancer Research (HOVON-SAKK) collaborative study group evaluated outcome of patients (pts) with acute myeloid leukemia (AML) in first remission (CR1) entered in 3 consecutive studies according to a donor versus no-donor comparison. Between 1987 and 2004, 2287 pts were entered in these studies of whom 1032 pts (45%) without FAB M3 or t(15;17) were in CR1 after 2 cycles of chemotherapy, received consolidation treatment, and were younger than 55 years of age and therefore eligible for allogeneic hematopoietic stem cell transplantation (allo-SCT). An HLA-identical sibling donor was available for 326 pt…

MaleMyeloidTransplantation Conditioningmedicine.medical_treatmentHematopoietic stem cell transplantationBiochemistryGastroenterologyRecurrenceRisk FactorsUNRELATED DONORSLiving DonorsMedicineTOTAL-BODYACUTE MYELOGENOUS LEUKEMIAHistocompatibility TestingAge FactorsHematopoietic Stem Cell TransplantationMyeloid leukemiaHematologyCOLONY-STIMULATING FACTORMiddle AgedChemotherapy regimenSurvival RateLeukemiaLeukemia Myeloid Acutemedicine.anatomical_structureFemalePOSTREMISSION THERAPYAdultmedicine.medical_specialtyAcute myeloblastic leukemiaAdolescentImmunologymacromolecular substancesDisease-Free SurvivalMeta-Analysis as TopicInternal medicineotorhinolaryngologic diseasesHumansTransplantation HomologousSurvival rateRetrospective StudiesEUROPEAN GROUPbusiness.industryACUTE MYELOBLASTIC-LEUKEMIACell Biologymedicine.diseaseBONE-MARROW-TRANSPLANTATIONINTENSIVE CHEMOTHERAPYSurgeryTransplantationAML-10 TRIALbusinessFollow-Up StudiesBlood
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Effects of risperidone on the acquisition and reinstatement of the conditioned place preference induced by MDMA

2013

Some users of 3,4-methylenedioxymethylamphetamine (MDMA or ecstasy) abuse this drug and/or become concerned about their use. These individuals would benefit greatly from the development of pharmacological strategies to reduce MDMA consumption. We have previously observed that antipsychotics block acquisition and expression of the conditioned place preference (CPP) induced by MDMA, though they do not modify priming-induced reinstatement of MDMA-induced CPP after extinction. In the present study we have evaluated the capacity of the mixed serotonin (5-HT2A)/dopamine (DA D2) antagonist risperidone to block acquisition and reinstatement of MDMA induced-CPP. Adolescent male mice conditioned with…

MaleN-Methyl-34-methylenedioxyamphetamineEcstasyPharmacologyMiceRewardDopamineConditioning Psychologicalmental disordersmedicineAnimalsDrug InteractionsSerotonin Plasma Membrane Transport ProteinsDopamine Plasma Membrane Transport ProteinsRisperidoneDose-Response Relationship DrugGeneral NeuroscienceAge FactorsAntagonistMDMAExtinction (psychology)RisperidoneCorpus StriatumConditioned place preferenceAnimals NewbornHallucinogensSerotoninPsychologypsychological phenomena and processesAntipsychotic Agentsmedicine.drugBrain Research Bulletin
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Involvement of NMDA glutamate receptors in the acquisition and reinstatement of the conditioned place preference induced by MDMA.

2015

Some 3,4-methylenedioxymethamphetamine (MDMA) users become dependent as a result of chronic consumption. A greater understanding of the neurobiological basis of the rewarding effects of MDMA could contribute to developing effective pharmacotherapies for MDMA-related problems. The present study evaluated the role of N-methyl-D-aspartate (NMDA) glutamate receptors (NMDARs) in the acquisition and reinstatement of conditioned place preference (CPP) induced by MDMA. Adolescent male mice were conditioned with 1 or 10 mg/kg MDMA and pretreated with 5 or 10 mg/kg of the NMDAR antagonist memantine during acquisition of conditioning (experiment 1), or before a reinstatement test (experiment 2). In ad…

MaleN-Methyl-34-methylenedioxyamphetamineMale miceSpatial BehaviorPharmacologyReceptors N-Methyl-D-AspartateMiceSerotonin AgentsMemantineMemorymental disordersConditioning PsychologicalAvoidance LearningMedicineAnimalsPharmacologyCacaoMotivationDose-Response Relationship Drugbusiness.industrymusculoskeletal neural and ocular physiologyGlutamate receptorMemantineAntagonistMDMAExtinction (psychology)Conditioned place preferencePsychiatry and Mental healthnervous systemNMDA receptorbusinessExcitatory Amino Acid Antagonistspsychological phenomena and processesmedicine.drugBehavioural pharmacology
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Role of acute social stress in the rewarding effects of MDMA in adolescent mice

2021

Drug use among adolescents is a serious problem in our society, as some individuals develop dependence and addiction. MDMA/Esctasy is one of the most typically used substances by this age group. It is well known that environmental factors can alter the rewarding properties of drugs and the propensity to drug-related disorders. In this sense, exposure to social stress induces long-term effects in mice, enhancing the rewarding effects of MDMA in the conditioned place preference (CPP) paradigm. On the other hand, previous research has not provided conclusive results regarding the short-term effects of social defeat on MDMA reward in adolescent animals, probably due to the use of very low or ve…

MaleN-Methyl-34-methylenedioxyamphetaminemedia_common.quotation_subjectConditioning ClassicalSocial DefeatSocial defeatMice03 medical and health sciencesBehavioral Neuroscience0302 clinical medicineRewardmental disordersHigh dosesAnimalsMedicine030304 developmental biologymedia_commonSocial stress0303 health sciencesBehavior Animalbusiness.industryAddictionAge FactorsMDMAConditioned place preferenceDisease Models AnimalCentral Nervous System StimulantsbusinessStress Psychologicalpsychological phenomena and processes030217 neurology & neurosurgerymedicine.drugClinical psychologyBehavioural Brain Research
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Pattern analyses reveal separate experience-based fear memories in the human right Amygdala

2017

Learning fear via the experience of contingencies between a conditioned stimulus (CS) and an aversive unconditioned stimulus (US) is often assumed to be fundamentally different from learning fear via instructions. An open question is whether fear-related brain areas respond differently to experienced CS–US contingencies than to merely instructed CS–US contingencies. Here, we contrasted two experimental conditions where subjects were instructed to expect the same CS–US contingencies while only one condition was characterized by prior experience with the CS–US contingency. Using multivoxel pattern analysis of fMRI data, we found CS-related neural activation patterns in the right amygdala (but…

MaleNEUROBIOLOGYFACESFunctional LateralityPREPAREDNESSNeural Pathway0302 clinical medicineConditioning PsychologicalinstructionsFear conditioningResearch Articlesinstructions ; amygdala ; fear ; learningGeneral Neuroscience05 social sciencesamygdalaFUNCTIONAL CONNECTIVITYMagnetic Resonance Imagingmedicine.anatomical_structurePattern Recognition VisualSIMILARITYfearFemalePsychologyPHOBIASCognitive psychologyAdultAWARENESSAdolescentNeuroscience(all)Amygdala050105 experimental psychologyYoung Adult03 medical and health sciencesNeuroimagingMemorymedicineEMOTIONHumansLearning0501 psychology and cognitive sciencesAnterior cingulate cortexFear processing in the brainPhobiasClassical conditioningAnticipation Psychologicalmedicine.diseaseElectric StimulationANTERIOR CINGULATE CORTEXPhotic Stimulation030217 neurology & neurosurgery
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Morphine potentiates the impairing effects of neuroleptics on two-way active conditioned avoidance response in male mice

2004

The dopaminergic and opioid systems have effects on the conditioned avoidance response (CAR), although the possible interaction between these systems on this behaviour has not been studied. The effects of morphine (12.6 mg/kg), haloperidol (0.075 mg/kg), sulpiride (20 mg/kg) and risperidone (0.1 mg/kg) alone as well as morphine combined with these dopamine (DA) antagonists on the acquisition and performance of the CAR were explored in mice. Morphine increased avoidances but this seemed secondary to a rise in activity levels. All DA antagonists impaired CAR in the acquisition phase but only haloperidol disrupted performance. The combination of morphine plus neuroleptics impaired acquisition …

MaleNarcoticsConditioning ClassicalPharmacologyAvoidance responseMiceEscape ReactionDopamineAvoidance LearningmedicineHaloperidolAnimalsBiological PsychiatryPharmacologyAnalysis of VarianceMice Inbred BALB CRisperidoneBehavior AnimalMorphinebusiness.industryDopaminergicDrug SynergismOpioidMorphineDopamine AntagonistsSulpiridebusinesshuman activitiesAntipsychotic Agentsmedicine.drugProgress in Neuro-Psychopharmacology and Biological Psychiatry
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Involvement of nitric oxide synthesis in sensitization to the rewarding effects of morphine

2009

Abstract Knowledge about the specific brain changes and neural plasticity processes produced by repeated exposure to a drug is essential to progress in the field of neurobiology of addiction and the development of effective medication. In the present study, the influence of nitric oxide synthesis on sensitization to the rewarding effects of morphine has been evaluated. The effects of pre-treatment of mice with saline or 20 mg/kg of morphine plus the nitric oxide synthase inhibitor 7-nitroindazole (7NI) (12.5 or 25 mg/kg) on the place conditioning induced by a low dose of morphine (2 mg/kg) were assessed. The dose of 2 mg/kg of morphine was ineffective in animals pre-treated with saline but …

MaleNarcoticsIndazoles7-Nitroindazolemedia_common.quotation_subjectConditioning ClassicalPharmacologyNitric OxideNitric oxideMicechemistry.chemical_compoundRewardmedicineAnimalsSensitizationmedia_commonMorphinebiologybusiness.industryGeneral NeuroscienceAddictionConditioned place preferenceNitric oxide synthasemedicine.anatomical_structurechemistryNitric Oxide PathwayMorphinebiology.proteinNitric Oxide Synthasebusinessmedicine.drugNeuroscience Letters
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