Search results for "PAM"

showing 10 items of 1768 documents

Long-lasting handling affects behavioural reactivity in adult rats of both sexes prenatally exposed to diazepam

2001

Environmental stressors can substantially affect the adaptive response of rats to novelty in a sexually dimorphic manner. Gender-related differences are also observed in neurochemical and behavioural patterns of adult rats following prenatal exposure to diazepam (DZ). In the present study the behavioural reactivity to novelty is investigated in open field (OF) and in acoustic startle reflex (ASR) tests, in non handled (NH), short-lasting handled (SLH) and long-lasting handled (LLH) adult male and female rats prenatally exposed to DZ. A single daily s.c. injection of DZ (1.5 mg/kg) over gestation days 14-20 decreases GABA/BDZ receptor function in both sexes, as shown by the decreased electro…

MaleReflex Startlemedicine.medical_specialtySettore BIO/14 - FARMACOLOGIAHippocampal formationHandling PsychologicalOpen fieldchemistry.chemical_compoundNeurochemicalPregnancyInternal medicinegendermedicineAnimalsprenatal diazepamRats Wistarprenatal diazepam; handling; gender; behavioral reactivitybehavioral reactivityMolecular BiologySex CharacteristicsDiazepamHandlingGeneral NeuroscienceRatsSexual dimorphismEndocrinologyAnti-Anxiety AgentschemistryPrenatal Exposure Delayed EffectsAcoustic Startle ReflexExploratory BehaviorRatGestationFemaleNeurology (clinical)PsychologyDiazepamDevelopmental Biologymedicine.drugPicrotoxinBrain Research
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Lateral differences in the GABAergic system of the rat striatum.

1985

Asymmetric differences have been found in the pre- and postsynaptic activity of the GABAergic system of the left and right striata of the rat. 3H-GABA binding shows a higher dissociation constant (KD) and a higher number of sites (Bmax) in the left striatum than in the right. Moreover, 3H-diazepam binding seems to be more extensively activated by GABA in the right striatum suggesting a more sensitive postsynaptic GABAergic activity than on the left side. However, when the presynaptic marker (GAD activity) was measured, the asymmetry was in the opposite direction. The results provide further neurochemical evidence of the functional asymmetry of the rat brain.

MaleRight striatumDermatologyStriatumSynaptic TransmissionRat striatumNeurochemicalPostsynaptic potentialBrain asymmetryAnimalsgamma-Aminobutyric AcidBinding SitesDiazepamChemistryGlutamate DecarboxylaseGeneral NeuroscienceRats Inbred StrainsGeneral MedicineCorpus StriatumRatsDissociation constantPsychiatry and Mental healthnervous system4-Aminobutyrate TransaminaseGABAergicNeurology (clinical)NeuroscienceItalian journal of neurological sciences
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The cost of a school based mass treatment of schistosomiasis in Ugu District, KwaZulu Natal, South Africa in 2012.

2020

Introduction The Neglected Tropical Diseases Roadmap of the WHO set targets for potential elimination as a "public health problem" for the period 2012-2020 in multiple countries in Africa, with the aim of global elimination of schistosomiasis as a "public health problem" by 2025. Aim The purpose of the study was to estimate the cost from a provider's perspective of the Department of Health's Schistosomiasis Mass Drug Administration (MDA) in Ugu District, KwaZulu-Natal in 2012, with a view to project the costs for the entire KwaZulu Natal Province. Methods A total of 491 public schools and 16 independent schools in Ugu District, a predominantly rural district in KwaZulu-Natal with a total of…

MaleRural PopulationBudgetsEndemic DiseasesFinancial ManagementTotal costEconomicsSocial SciencesPraziquantelGeographical locationsSouth AfricaFamilies0302 clinical medicineLearning and MemorySociologyMedicine and Health SciencesSchistosomiasisPsychology030212 general & internal medicineSocioeconomicsActivity-based costingChildChildrenAnthelminticsMultidisciplinarySchoolsPharmaceuticsQRHelminth InfectionsNeglected tropical diseasesMedicineMass Drug AdministrationFemaleResearch ArticleNeglected Tropical Diseasesmedicine.medical_specialtyDrug AdministrationAdolescentScience030231 tropical medicineDrug CostsSampling StudiesDirect Service CostsEducation03 medical and health sciencesHuman LearningDrug TherapymedicineParasitic DiseasesCapital costHumansLearningHuman resourcesUnit costCost databaseRetrospective StudiesSchool Health Servicesbusiness.industryPublic healthCognitive PsychologyBiology and Life SciencesTropical DiseasesAge GroupsCapital ExpendituresPeople and PlacesAfricaCognitive SciencePamphletsPopulation GroupingsbusinessVDP::Samfunnsvitenskap: 200::Urbanisme og fysisk planlegging: 230FinanceNeurosciencePloS one
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Transgenic expression and activation of PGC-1α protect dopaminergic neurons in the MPTP mouse model of Parkinson’s disease

2011

Mitochondrial dysfunction and oxidative stress occur in Parkinson’s disease (PD), but little is known about the molecular mechanisms controlling these events. Peroxisome proliferator-activated receptor-gamma coactivator-1α (PGC-1α) is a transcriptional coactivator that is a master regulator of oxidative stress and mitochondrial metabolism. We show here that transgenic mice overexpressing PGC-1α in dopaminergic neurons are resistant against cell degeneration induced by the neurotoxin MPTP. The increase in neuronal viability was accompanied by elevated levels of mitochondrial antioxidants SOD2 and Trx2 in the substantia nigra of transgenic mice. PGC-1α overexpression also protected against MP…

MaleSOD2Mice TransgenicSubstantia nigraMitochondrionBiologyNeuroprotectionCell LineMiceCellular and Molecular Neurosciencechemistry.chemical_compoundDopaminemedicineAnimalsNeurotoxinParkinson Disease SecondaryMolecular BiologyPGC-1α RSV SIRT1 MPTP Dopaminergic neurons Parkinson’s diseasePharmacologyMPTPDopaminergicBrainParkinson DiseaseCell BiologyPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaMitochondriaCell biologyDisease Models AnimalOxidative Stressnervous systemBiochemistrychemistry1-Methyl-4-phenyl-1236-tetrahydropyridineTrans-ActivatorsMolecular MedicineFemaleTranscription Factorsmedicine.drugCellular and Molecular Life Sciences
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THE EFFECTS OF AGING ON DOPAMINERGIC NEUROTRANSMISSION A microPET STUDY OF [11C]-raclopride BINDING IN THE AGED RODENT BRAIN

2010

Rodent models are frequently used in aging re search to investigate biochemical age effects and aid in the development of therapies for pathological and non pathological age related degenerative processes In order to validate the use of animal models in aging research and pave the way for longitudinal intervention based animal studies, the consistency of cerebral aging processes across species needs to be evaluated The dopaminergic system seems particularly susceptible to the aging process, and one of the most consistent findings in human brain aging research is a decline in striatal D2-like receptor (D2R) availability, quantifiable by positron emission tomography (PET) imaging In this stud…

MaleSenescenceAgingmedicine.medical_specialtyraclopride animal modelspositron emission tomographyDopamineDopamineDopamine receptor D2Internal medicinemedicineAnimalsRacloprideBrain MappingCarbon IsotopesGeneral NeuroscienceDopaminergicagingBrainHuman braindopamine D2 like receptorRatsEndocrinologymedicine.anatomical_structureRacloprideD2-like receptorPositron-Emission TomographyDopamine AntagonistsAnimal studiesPsychologyNeuroscienceProtein Bindingmedicine.drug
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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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Behavioural and neurotoxic long-lasting effects of MDMA plus cocaine in adolescent mice

2008

The poly-drug pattern is the most common among MDMA users, with cocaine being a frequently associated drug. The aim of the present work was to evaluate the behavioural and neurotoxic long-term effects of exposure during adolescence to MDMA alone or plus cocaine. Mice of 28 to 30 days of age received a treatment of two daily injections of an identical dose of MDMA (5, 10 or 20 mg/kg), alone or plus cocaine (25 mg/kg), for 3 days (6 administrations). Three weeks after receiving MDMA, an increase in the time dedicated by the animals to social contacts with their conspecifics was observed, whilst their behaviour in the elevated plus maze showed no differences from that of non-treated mice. Afte…

MaleSerotoninElevated plus mazemedicine.drug_classDopamineN-Methyl-34-methylenedioxyamphetamineMotor ActivityPharmacologyAnxiolyticBody TemperatureMicechemistry.chemical_compoundCocaineDopaminemental disordersmedicineAnimalsMaze LearningSocial BehaviorNeurotransmitterPharmacologyBehavior AnimalLocal anestheticDopaminergicBrainMDMACorpus StriatumchemistrySerotoninPsychologypsychological phenomena and processesmedicine.drugEuropean Journal of Pharmacology
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Neurochemical Substrates of MDMA Reward: Effects of the Inhibition of Serotonin Reuptake on the Acquisition and Reinstatement of MDMA-induced CPP

2013

Different neurotransmitter brain systems have been implicated in the rewarding effects of 3,4-methylenedioxymetamphetamine (MDMA), including dopamine or serotonin. Serotonin selective reuptake inhibitors (SSRI) are a commonly prescribed therapy for psychiatric disorders, and the SSRI fluoxetine is recommended for MDMA users due to its neuroprotective effect against MDMAinduced neurotoxicity. In the present work, we employed the conditioned place preference (CPP) paradigm to study how the inhibition of serotonin reuptake with fluoxetine affected the rewarding and reinstating effects of MDMA in adolescent male mice. Firstly, we evaluated the motivational effects of fluoxetine (1 and 10 mg/kg)…

MaleSerotoninN-Methyl-34-methylenedioxyamphetaminePharmacologyMicechemistry.chemical_compoundNeurochemicalRewardDopamineFluoxetineConditioning Psychologicalmental disordersDrug DiscoveryAnimalsMedicineNeurotransmitterPharmacologyFluoxetineDose-Response Relationship Drugbusiness.industryMDMAConditioned place preferencechemistryHallucinogensSerotoninbusinessReuptake inhibitorSelective Serotonin Reuptake Inhibitorspsychological phenomena and processesmedicine.drugCurrent Pharmaceutical Design
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Central serotonin depletion modulates the behavioural, endocrine and physiological responses to repeated social stress and subsequent c-fos expressio…

1999

Abstract Intraspecific confrontation has been used to study effect of depleting central serotonin on the adaptation of male rats to repeated social stress (social defeat). Four groups of adult male rats were used (serotonin depletion/sham: stressed; serotonin depletion/sham: non-stressed). Central serotonin was reduced (by 59–97%) by a single infusion of the neurotoxin 5,7-dihydroxtryptamine (150 μg) into the cerebral ventricles; levels of dopamine and noradrenaline were unaltered (rats received appropriate uptake blockers prior to neurotoxic infusions). Sham-operated animals received solute only. Rats were then either exposed daily for 10 days to a second larger aggressive male in the latt…

MaleSerotoninmedicine.medical_specialty57-DihydroxytryptamineHypothalamusMotor ActivityAmygdalac-FosRats Sprague-DawleySocial defeatchemistry.chemical_compoundSerotonin AgentsHeart RateStress PhysiologicalCorticosteroneDopamineInternal medicineAdaptation PsychologicalmedicineAnimalsNeurotransmitterSocial stressbiologyGeneral NeuroscienceHydroxyindoleacetic AcidAmygdalaRatsAggressionEndocrinologymedicine.anatomical_structureSocial Dominancechemistrybiology.proteinFemaleSerotoninCorticosteronePsychologyProto-Oncogene Proteins c-fosBody Temperature RegulationBrain Stemmedicine.drugNeuroscience
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Neurotransmitter receptor density changes in Pitx3ak mice – A model relevant to Parkinson’s disease

2014

Abstract Parkinson’s disease (PD) is the second most common neurodegenerative disorder, characterized by alterations of nigrostriatal dopaminergic neurotransmission. Compared to the wealth of data on the impairment of the dopamine system, relatively limited evidence is available concerning the role of major non-dopaminergic neurotransmitter systems in PD. Therefore, we comprehensively investigated the density and distribution of neurotransmitter receptors for glutamate, GABA, acetylcholine, adrenaline, serotonin, dopamine and adenosine in brains of homozygous aphakia mice being characterized by mutations affecting the Pitx3 gene. This genetic model exhibits crucial hallmarks of PD on the ne…

MaleSerotoninmedicine.medical_specialtyAdenosineEpinephrineDopamineMice TransgenicD1-like receptorKainate receptorBiologySerotonergicParkinsonian DisordersNeurotransmitter receptorInternal medicinemedicineAnimalsReceptorgamma-Aminobutyric Acid5-HT receptorHomeodomain ProteinsGeneral NeuroscienceHomozygoteGlutamate receptorBrainAcetylcholineReceptors NeurotransmitterMice Inbred C57BLEndocrinology5-HT6 receptorNeuroscienceTranscription FactorsNeuroscience
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