Search results for "Place preference"

showing 10 items of 104 documents

Adolescent pre-exposure to ethanol and 3,4-methylenedioxymethylamphetamine (MDMA) increases conditioned rewarding effects of MDMA and drug-induced re…

2011

Many adolescents often take ethanol (EtOH) in combination with 3,4-methylenedioxymethylamphetamine (MDMA). In the present work, we used a mouse model to study the effect of repeated pre-exposure during adolescence to EtOH (2 g/kg), MDMA (10 or 20 mg/kg) or EtOH + MDMA on the rewarding and reinstating effects of MDMA in the conditioned place preference (CPP) paradigm. Pre-exposure to EtOH, MDMA or both increased the rewarding effects of a low dose of MDMA (1.25 mg/kg). These pre-treatments did not affect the acquisition of the CPP induced by 5 mg/kg of MDMA. However, the CPP was more persistent in mice pre-exposed to both doses of MDMA or to EtOH + MDMA20. After extinction of the CPP induced…

PharmacologyEthanolHomovanillic acidMedicine (miscellaneous)MDMAExtinction (psychology)StriatumPharmacologyConditioned place preferencePsychiatry and Mental healthchemistry.chemical_compoundchemistryDopaminemental disordersmedicineSerotoninpsychological phenomena and processesmedicine.drugAddiction Biology
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Dopamine D2 receptors mediate the increase in reinstatement of the conditioned rewarding effects of cocaine induced by acute social defeat

2017

Social stress modifies the activity of brain areas involved in the rewarding effects of psychostimulants, inducing neuroadaptations in the dopaminergic mesolimbic system and modifying the sensitivity of dopamine receptors. In the present study we evaluated the effect of the dopamine D1- and D2-like receptor antagonists (SCH23390 and raclopride, respectively) on the short-time effects of acute social defeat (ASD). Male OF1 mice were socially defeated before each conditioning session of the conditioned place preference (CPP) induced by 1mg/kg or 25mg/kg of cocaine plus the corresponding dopamine antagonist. A final experiment was designed to evaluate the effect of the dopamine antagonists on …

PharmacologyRaclopridebusiness.industryDopaminergicDopamine antagonistPharmacologyConditioned place preference030227 psychiatry03 medical and health sciences0302 clinical medicineDopamine receptor D1Dopamine receptorDopamineDopamine receptor D2AnesthesiaMedicinebusiness030217 neurology & neurosurgerymedicine.drugEuropean Journal of Pharmacology
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Antagonism of corticotropin-releasing factor CRF 1 receptors blocks the enhanced response to cocaine after social stress

2018

Numerous studies have shown that social defeat stress induces an increase in the rewarding effects of cocaine. In this study we have investigated the role played by the main hypothalamic stress hormone, corticotropin-releasing factor (CRF), in the effects that repeated social defeat (RSD) induces in the conditioned rewarding effects and locomotor sensitization induced by cocaine. A total of 220 OF1 mice were divided into experimental groups according to the treatment received before each social defeat: saline, 5 or 10 mg/kg of the nonpeptidic corticotropin-releasing factor CRF1 receptor antagonist CP-154,526, or 15 or 30 µg/kg of the peptidic corticotropin-releasing factor CRF2 receptor ant…

PharmacologySocial stressbusiness.industrymedicine.drug_classAntagonistPharmacologyReceptor antagonistConditioned place preference030227 psychiatryCorticotropin-releasing hormone receptor 1Social defeat03 medical and health sciences0302 clinical medicinemedicine.anatomical_structureAnxiogenicmedicinebusiness030217 neurology & neurosurgerySensitizationEuropean Journal of Pharmacology
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Effects of repeated social defeat on adolescent mice on cocaine-induced CPP and self-administration in adulthood: integrity of the blood-brain barrier

2015

Social stress in adulthood enhances cocaine self-administration, an effect that has been related with an increase in extracellular signal-regulated kinase and p38α mitogen-activated protein kinase phosphorylation. A detrimental effect of cocaine on blood-brain barrier (BBB) integrity has also been reported. This study evaluates the effects of repeated social defeat (RSD) during adolescence on the reinforcing and motivational effects of cocaine in adult mice and the changes induced by RSD on BBB permeability. Cocaine self-administration, conditioned place preference and quantitative analysis of claudin-5, laminin, collagen-IV and IgG immunoreactivity took place 3 weeks after RSD. Mice social…

PharmacologySocial stressmedicine.medical_specialtyMedicine (miscellaneous)HippocampusNucleus accumbensBlood–brain barrierConditioned place preference030227 psychiatrySocial defeat03 medical and health sciencesPsychiatry and Mental health0302 clinical medicinemedicine.anatomical_structureEndocrinologyInternal medicinemedicineSelf-administrationProtein kinase APsychologyNeuroscience030217 neurology & neurosurgeryAddiction Biology
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Rewarding Properties of Testosterone in Intact Male Mice

2000

The present study examined the rewarding properties of 4-androsten-17β-ol-3-one testosterone in intact male mice using the conditioned place preference (CPP) technique. In Experiment 1, the pharmacokinetics of 0.8 and 1.2 mg/kg of testosterone were studied to determine the most appropriate temporal interval to test behavior. Additionally, the locomotor activity was recorded to control a possible interfering effect on CPP. The maximum testosterone concentration was registered at 45 min of administration, and no effects on activity were found. In Experiment 2, three groups of male OF-1 mice received four pairings of the least-preferred compartment with testosterone (0.8, 1, or 1.2 mg/kg, SC) …

Pharmacologymedicine.medical_specialtyChemistrymedicine.drug_classRatónClinical BiochemistryTestosterone (patch)ToxicologyAndrogenBiochemistryConditioned place preferenceBehavioral NeuroscienceEndocrinologyPharmacokineticsInternal medicineBlood plasmamedicineCompartment (pharmacokinetics)Intact maleBiological PsychiatryPharmacology Biochemistry and Behavior
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Pre-treatment with high doses of cocaine decreases the reinforcing effects of cocaine in the conditioned place preference paradigm.

2012

The aim of the present study was to determine if pre-exposure to high doses of cocaine can subsequently alter the rewarding effects of this drug. Adult male mice received a pretreatment of physiological saline, or 12.5 or 25 mg/kg of cocaine (one injection a day for five days). After an interval of six days without injections, the rewarding effects of low doses of cocaine (0.5, 1 or 1.5 mg/kg) were evaluated in the conditioned place preference (CPP) paradigm. Doses of 1 and 1.5 mg/kg induced a clear CPP in animals pre-treated with saline but were ineffective in those pre-treated with 25 mg/kg of cocaine. Only the dose of 1.5 mg/kg induced CPP in mice pre-treated with 12.5 mg/kg of cocaine. …

Pre treatmentMaleAdult maleDose-Response Relationship Drugbusiness.industryGeneral Neurosciencemedicine.medical_treatmentLow doseConditioning ClassicalDrug SynergismDrug TolerancePharmacologyConditioned place preferenceMiceCocaineDrug toleranceHigh dosesMedicineAnimalsbusinessSalinePhysiological salineNeuroscience letters
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Prepulse inhibition can predict the motivational effects of cocaine in female mice exposed to maternal separation

2020

The prepulse inhibition (PPI) of the startle response can identify the rodents that are more sensitive to the effects of cocaine. Mice with a lower PPI presented a higher vulnerability to the effects of cocaine and a higher susceptibility to developing a substance use disorder (SUD). Maternal separation with early weaning (MSEW) is a relevant animal model to induce motivational alterations throughout life. Nevertheless, only a few studies on females exist, even though they are more vulnerable to stress- and cocaine-related problems. Hence, the aim of the present study was to evaluate the ability of PPI to identify females with a greater vulnerability to the long-term consequences of early s…

Reflex StartleStartle responseAnhedoniaPhysiologySelf AdministrationWeaningReinforcing effectsMiceBehavioral NeuroscienceAnimal modelCocaineDopamine Uptake InhibitorsMaternal separation with early weaningFemale micemedicineAnimalsPrepulse inhibitionMotivationmedicine.diagnostic_testPrepulse Inhibitionbusiness.industryMaternal Deprivationmedicine.diseaseAnhedonia-like behavioursConditioned place preferenceSubstance abuseDisease Models AnimalLocomotor sensitizationConditioning OperantBiomarker (medicine)FemalePassive avoidancebusinessBehavioural Brain Research
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Caracterización conductual y neuroinmune de la resiliencia al estrés social: Efectos reforzantes de la cocaína

2020

Numerosos estudios preclínicos han demostrado que el estrés social incrementa la vulnerabilidad a los efectos reforzantes de la cocaína. Sin embargo, los resultados obtenidos no son homogéneos, observándose siempre una subpoblación que no muestra dicho incremento. Utilizando el modelo de derrota social (DS) repetida en ratones, en este trabajo hemos querido caracterizar conductualmente a los ratones resilientes al incremento de los efectos reforzantes de la cocaína inducido por el estrés social. Utilizamos ratones adultos macho de la cepa C57/BL6 a los que sometimos al protocolo de DS repetida y tres semanas más tarde, realizamos el Condicionamiento de Preferencia de Lugar (CPL) inducido po…

Social stressCoping (psychology)business.industryAddictionmedia_common.quotation_subjectMedicine (miscellaneous)PhysiologyConditioned place preferenceSocial defeatPsychiatry and Mental healthAnimal modelHomogeneousMedicineConditioningbusinessmedia_common
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Correction: Indomethacin blocks the increased conditioned rewarding effects of cocaine induced by repeated social defeat

2019

It is well established that repeated social defeat stress can induce negative long-term consequences such as increased anxiety-like behavior and enhances the reinforcing effect of psychostimulants in rodents. In the current study, we evaluated how the immune system may play a role in these long-term effects of stress. A total of 148 OF1 mice were divided into different experimental groups according to stress condition (exploration or social defeat) and pre-treatment (saline, 5 or 10 mg/kg of the anti-inflammatory indomethacin) before each social defeat or exploration episode. Three weeks after the last social defeat, anxiety was evaluated using an elevated plus maze paradigm. After this tes…

Social stressmedicine.medical_specialtyElevated plus mazeMultidisciplinarybusiness.industryAddictionmedia_common.quotation_subjectlcsh:Rlcsh:MedicineHippocampusConditioned place preference030227 psychiatrySocial defeat03 medical and health sciences0302 clinical medicineEndocrinologyAnxiogenicInternal medicinemedicinelcsh:Qlcsh:SciencePrefrontal cortexbusiness030217 neurology & neurosurgerymedia_commonPLOS ONE
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Lesions of the dopaminergic innervation of the nucleus accumbens medial shell delay the generation of preference for sucrose, but not of sexual phero…

2011

Male sexual pheromones are rewarding stimuli for female mice, able to induce conditioned place preference. To test whether processing these natural reinforcing stimuli depends on the dopaminergic innervation of the nucleus accumbens, as for other natural rewards, we compare the effects of specific lesions of the dopaminergic innervation of the medial shell of the nucleus accumbens on two different appetitive behaviours, ‘pheromone seeking’ and sucrose preferential intake. Female mice, with no previous experience with either adult male chemical stimuli or with sucrose, received injections of 6-hydroxydopamine (or vehicle) in the medial shell of the accumbens. Then, we analyzed their preferen…

Sucrosemedicine.medical_specialtyTime FactorsVomeronasal organMotor ActivityNucleus accumbensNucleus Accumbensnatural rewardvomeronasal systemFood PreferencesMiceBehavioral Neurosciencechemistry.chemical_compoundRewardmotivationDopamineInternal medicinemedicineAnimalsSex AttractantsOxidopamineAccumbensSucrose preferenceNeophobiaDopaminergicmedicine.diseaseConditioned place preferenceEndocrinologychemistryNerve DegenerationPheromoneFemaledopaminePsychologyNeuroscienceOxidopaminemedicine.drug
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