Search results for "4-Methylenedioxyamphetamine"

showing 10 items of 39 documents

Role of nitric oxide pathway in the conditioned rewarding effects of MDMA in mice.

2017

It is estimated that 2.1 million young adults used MDMA/Ecstasy in the last year in Europe. Vulnerable subjects can develop dependence after MDMA abuse but currently there does not exist an effective treatment for this disorder. The nitric oxide (NO) pathway seems to have an important role on the rewarding effects of different drugs and has been proposed as a new pharmacological treatment for psychostimulant addiction. In the present study, we intend to evaluate whether the blockade of the NO synthesis (NOS) interferes with the rewarding effects of MDMA in the conditioned preference place (CPP) paradigm in young adult male mice. Our results indicated that mice treated with 7-nitroindazole (…

0301 basic medicineHallucinogenMaleMDMA7-NitroindazoleIndazolesmedia_common.quotation_subjectN-Methyl-34-methylenedioxyamphetamineEcstasyConditioning ClassicalEnsayos clínicosPharmacologyNitric OxideNitric oxide03 medical and health sciencesBehavioral Neurosciencechemistry.chemical_compoundMice0302 clinical medicineRewardmental disordersConditioning PsychologicalmedicineAnimalsDrogasmedia_commonbiologyAddictionMDMABlockadeNitric oxide synthaseEfectos fisiológicos030104 developmental biologychemistrybiology.proteinHallucinogensConditioning OperantCentral Nervous System StimulantsNitric Oxide SynthasePsychologyEstupefacientepsychological phenomena and processes030217 neurology & neurosurgerymedicine.drugBehavioural brain research
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Blockade of nitric oxide signalling promotes resilience to the effects of social defeat stress on the conditioned rewarding properties of MDMA in mice

2020

Abstract MDMA abuse continues being a serious problem in our society. Environmental factors, such as stress, increase the vulnerability of individuals to develop drug abuse and we have observed that exposure to social defeat (SD) stress alters the sensitivity of mice to the rewarding effects of MDMA in the conditioned place preference (CPP) paradigm. In the present study, we evaluated the role of the nitric oxide (NO) pathway in the effects of SD on the rewarding properties of MDMA. Three groups of mice were treated with an inhibitor of NO synthesis, 7-nitroindazole (0, 7.25 and 12.5 mg/kg), before each exposure to SD and place conditioning with MDMA (1.25 mg/kg) on PND 54, 56, 58, and 60. …

0301 basic medicineMaleCancer Researchmedicine.medical_specialty7-NitroindazoleIndazolesMDMAPhysiologyN-Methyl-34-methylenedioxyamphetamineClinical BiochemistryHippocampusMice Inbred StrainsStriatum030204 cardiovascular system & hematologyNitric OxideBiochemistrySocial defeat03 medical and health scienceschemistry.chemical_compoundMice0302 clinical medicineSocial defeatInternal medicineConditioning Psychologicalmental disordersmedicineAnimalsPrefrontal cortex7-NitroindazoleSocial stressDose-Response Relationship Drugbusiness.industryMDMANitric oxideConditioned place preferenceConditioned place preference030104 developmental biologyEndocrinologychemistrybusinessStress Psychologicalpsychological phenomena and processesmedicine.drugSignal Transduction
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Increased visual cortical excitability in ecstasy users: a transcranial magnetic stimulation study

2003

To test the presence of abnormalities of visual cortical excitability in people using ecstasy as a recreational drug.Ecstasy users and control subjects underwent single pulse transcranial magnetic stimulation (TMS) of the occipital cortex. The phosphene threshold was analysed and compared in the two groups.Phosphene thresholds were significantly lower in ecstasy users compared with control subjects, and were correlated negatively with frequency of ecstasy use. Frequency of use was positively correlated with the presence of visual hallucinations. The phosphene threshold of subjects with hallucinations was significantly lower than that of subjects without hallucinations.The use of ecstasy as …

AdultMaleSerotoninmedicine.medical_specialtyHallucinationsSubstance-Related DisordersN-Methyl-34-methylenedioxyamphetaminemedicine.medical_treatmentPhosphenesEcstasyShort ReportStimulationAudiologyReference ValuesCortex (anatomy)Sensory thresholdmedicineHumansVisual CortexTranscranial Magnetic StimulationTranscranial magnetic stimulationPsychiatry and Mental healthVisual cortexmedicine.anatomical_structurePhospheneSensory ThresholdsFemaleSurgeryOccipital LobeNeurology (clinical)Occipital lobePsychologyNeuroscienceJournal of Neurology, Neurosurgery & Psychiatry
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Analysis of ecstasy in oral fluid by ion mobility spectrometry and infrared spectroscopy after liquid-liquid extraction.

2014

We developed and evaluated two different strategies for determining abuse drugs based on (i) the analysis of saliva by ion mobility spectrometry (IMS) after thermal desorption and (ii) the joint use of IMS and infrared (IR) spectroscopy after liquid-liquid microextraction (LLME) to enable the sensitivity-enhanced detection and double confirmation of ecstasy (MDMA) abuse. Both strategies proved effective for the intended purpose. Analysing saliva by IMS after thermal desorption, which provides a limit of detection (LOD) of 160μgL(-1), requires adding 0.2M acetic acid to the sample and using the truncated negative second derivative of the ion mobility spectrum. The joint use of IMS and IR spe…

AdultMaleSpectrophotometry InfraredIon-mobility spectrometryInfraredN-Methyl-34-methylenedioxyamphetamineLiquid-Liquid ExtractionThermal desorptionAnalytical chemistryInfrared spectroscopyBiochemistryAnalytical ChemistryIonLiquid–liquid extractionLimit of DetectionHumansSpectroscopySalivaDetection limitChromatographyChemistryIllicit DrugsOrganic ChemistryGeneral MedicineSubstance Abuse DetectionFemaleJournal of chromatography. A
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Effect of adolescent exposure to WIN 55212-2 on the acquisition and reinstatement of MDMA-induced conditioned place preference.

2009

The present study employs a conditioned place preference procedure (CPP) to examine the effects of exposure to the cannabinoid agonist WIN 55212-2 (WIN) (0.1 and 0.5mg/kg) during adolescence on the reinforcing properties of +/-3,4-methylenedioxymetamphetamine hydrochloride (MDMA) (1.25 and 2.5mg/kg) in mice. On postnatal day (PD) 27, animals received a daily injection of the assigned treatment on 5 consecutive days, and three days later the place conditioning procedure was initiated (PD 35). The results suggest that pre-exposure to cannabinoids strengthens the properties of MDMA and favors reinstatement of the craving for the drug, which endorses the gateway hypothesis.

AgonistMaleReinforcement ScheduleTime Factorsmedicine.drug_classmedicine.medical_treatmentMorpholinesN-Methyl-34-methylenedioxyamphetamineSpatial BehaviorCravingPharmacologyNaphthalenesDevelopmental psychologyExtinction PsychologicalMiceRimonabantPiperidinesmedicineAnimalsDrug InteractionsCannabinoid Receptor AntagonistsBiological PsychiatryPharmacologyAnalysis of VarianceDose-Response Relationship DrugMDMAExtinction (psychology)Calcium Channel BlockersConditioned place preferenceBenzoxazinesAnimals NewbornHallucinogensCannabinoid receptor antagonistConditioning OperantPyrazolesCannabinoidmedicine.symptomRimonabantPsychologypsychological phenomena and processesmedicine.drugProgress in neuro-psychopharmacologybiological psychiatry
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Determination of amphetamines in hair by integrating sample disruption, clean-up and solid phase derivatization

2016

The utility of matrix solid phase dispersion (MSPD) for the direct analysis of amphetamines in hair samples has been evaluated, using liquid chromatography (LC) with fluorescence detection and precolumn derivatization. The proposed approach is based on the employment of MSPD for matrix disruption and clean-up, followed by the derivatization of the analytes onto the dispersant-sample blend. The fluorogenic reagent 9-fluorenylmethyl chloroformate (FMOC) has been used for derivatization. Different conditions for MSPD, analyte purification and solid phase derivatization have been tested, using amphetamine (AMP), methamphetamine (MET), ephedrine (EPE) and 3,4-methylenedioxymethamphetamine (MDMA)…

AnalyteN-Methyl-34-methylenedioxyamphetamine02 engineering and technologyChloroformate01 natural sciencesBiochemistryMethamphetamineAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundmedicineHumansEphedrineDerivatizationFluorescent DyesEphedrineDetection limitFluorenesChromatographyAmphetamines010401 analytical chemistryOrganic ChemistryGeneral Medicine021001 nanoscience & nanotechnology0104 chemical sciencesClean-upAmphetaminechemistryReagent0210 nano-technologyChromatography LiquidHairmedicine.drugJournal of Chromatography A
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Sensitive determination of methylenedioxylated amphetamines by liquid chromatography.

2001

Different strategies for the liquid chromatographic determination of methylenedioxylated amphetamines were evaluated: separation and detection of underivatized analytes by (i) UV or (ii) fluorescence, (iii) derivatization with 3,5-dinitrobenzoyl chloride followed by separation and UV detection of the derivatives formed and (iv) derivatization with 9-fluorenylmethyl chloroformate (FMOC) and subsequent separation and fluorimetric detection of the derivatives. The compounds tested were 3,4-methylenedioxyamphetamine (MDA), 3,4-methylenedioxymethamphetamine (MDMA) and 3,4-methylenedioxyethylamphetamine (MDE). On the basis of these studies, a new procedure for the chromatographic determination of…

Detection limitReproducibilityAnalyteChromatographyChemistryN-Methyl-34-methylenedioxyamphetamineAmphetaminesChloroformateBiochemistryFluorescence spectroscopyAnalytical Chemistrychemistry.chemical_compoundElectrochemistryHallucinogensEnvironmental ChemistryHumansUv detectionDerivatizationQuantitative analysis (chemistry)Spectroscopy34-MethylenedioxyamphetamineChromatography LiquidThe Analyst
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Effects of acute social stress on the conditioned place preference induced by MDMA in adolescent and adult mice

2014

Exposure to social defeat stress increases the rewarding effects of psychostimulants in animal models, but its effect on 3,4-methylenedioxymethylamphetamine (MDMA) reward has received little attention. In the present study, we evaluated the influence of social defeat on the rewarding effects of MDMA in adolescent [postnatal day (PND) 29-40] and adult (PND 50-61) male mice using the conditioned place preference paradigm. Experimental mice were exposed to social defeat in an agonistic encounter before each session of conditioning with 1.25 or 10 mg/kg of MDMA. The effects of social defeat on corticosterone levels and the motor or the anxiogenic effects of MDMA were also evaluated. Mice expose…

Dominance-SubordinationMaleAgingmedicine.medical_specialtyN-Methyl-34-methylenedioxyamphetamineAnxietyMotor ActivityAffect (psychology)Social defeatMicechemistry.chemical_compoundRewardCorticosteroneInternal medicineConditioning Psychologicalmental disordersmedicineAgonistic behaviourAnimalsSocial BehaviorPharmacologySocial stressDose-Response Relationship Drugbusiness.industryMDMAConditioned place preferencePsychiatry and Mental healthEndocrinologychemistryAnxiogenicSpace PerceptionHallucinogensCorticosteronebusinessStress Psychologicalpsychological phenomena and processesmedicine.drugBehavioural Pharmacology
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Rewarding effects of 3,4-methylenedioxymethamphetamine (“Ecstasy”) in dominant and subordinate OF-1 mice in the place preference conditioning paradigm

2006

We tested the ability of 3,4-methylenedioxymethamphetamine (MDMA) to induce conditioned place preference (CPP) in dominant and subordinate OF-1 mice subjected to cohabitation and repeated sessions of agonistic confrontation, as well as in non-confronted mice. We selected doses of MDMA (2, 6, 10 mg/kg) previously reported to induce CPP in mice and we measured expression of c-Fos evoked by the treatments in non-confronted mice. MDMA induced c-Fos protein in several corticolimbic regions involved in drug-induced reward. Mice were exposed to brief sessions of agonistic confrontation on 5 consecutive days. Determinations of circulating hormones and drug conditioning tests were carried out on com…

Dominance-SubordinationMalemedicine.medical_specialtyN-Methyl-34-methylenedioxyamphetamineEcstasyGene ExpressionSocial EnvironmentMicechemistry.chemical_compoundSerotonin AgentsRewardCorticosteroneInternal medicinemedicineAnimalsTestosteroneBiological PsychiatryTestosteronePharmacologySocial stressGenes fosMDMAImmunohistochemistryConditioned place preferenceEndocrinologychemistryConditioning OperantCorticosteronePsychologyAgonistic BehaviorStress Psychologicalpsychological phenomena and processesGlucocorticoidmedicine.drugHormoneProgress in Neuro-Psychopharmacology and Biological Psychiatry
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Cognitive and behavioural effects induced by social stress plus MDMA administration in mice

2017

Adverse life experiences such as social stress may make an individual more vulnerable to drug addiction and mental disorders associated with drug consumption. The present work aimed to evaluate the effects of stress induced by acute social defeat combined with the administration of 3,4-methylenedioxymethamphetamine (MDMA) on depression-like behaviour, memory function and motor response to drug in late adolescent male mice. Two groups of mice were exposed to social defeat (SD) during four encounters with an aggressive co-specific, which took place on alternate days. Immediately after defeat, animals were treated with saline or MDMA 10mg/kg (SD+SAL and SD+MDMA). In control groups, mice were p…

Dominance-SubordinationMalemedicine.medical_specialtyN-Methyl-34-methylenedioxyamphetaminemedia_common.quotation_subjectPoison controlBehavioral SymptomsMotor ActivityBody TemperatureSocial defeatMice03 medical and health sciencesBehavioral Neurosciencechemistry.chemical_compound0302 clinical medicineCorticosteroneInternal medicinemental disordersAvoidance LearningmedicineAnimalsPsychiatrymedia_commonSocial stressAnalysis of VarianceAddictionRecognition PsychologyMDMAmedicine.diseaseTail suspension test030227 psychiatrySubstance abuseDisease Models AnimalEndocrinologyHindlimb SuspensionchemistryHallucinogensCognition DisordersCorticosteronePsychologyStress Psychologicalpsychological phenomena and processes030217 neurology & neurosurgerymedicine.drugBehavioural Brain Research
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