Search results for "Maze"

showing 10 items of 199 documents

Liver failure under valproic acid

2011

Valproic acid (VPA, 2-propylvaleric acid) is originally an antiepileptic drug, which has been in use for more than 30 years in over 100 countries. The clinical application of VPA has expanded in the last years. Approval has been granted by the FDA for treatment of migraine and cluster headache in 1996, and for treatment of mania and long-term prophylaxis of bipolar affective disorder in 1995. In ongoing studies, VPA has been reported to inhibit growth of several types of cancer cells; in addition, effects on neurodegeneration, and on virus replication in HIV infection have been demonstrated potentially expanding the application of VPA in the future. Despite a good tolerability of the drug, …

DrugTopiramateValproic Acidbusiness.industrymedia_common.quotation_subjectCarbamazepinePharmacologyLamotriginemedicine.diseasePsychiatry and Mental healthTolerabilityMigrainemedicinelipids (amino acids peptides and proteins)medicine.symptombusinessManiamedicine.drugmedia_commonEuropean Psychiatry
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Biowaiver Monograph for Immediate-Release Solid Oral Dosage Forms: Carbamazepine.

2020

Abstract Literature relevant to assessing whether BCS-based biowaivers can be applied to immediate release (IR) solid oral dosage forms containing carbamazepine as the single active pharmaceutical ingredient are reviewed. Carbamazepine, which is used for the prophylactic therapy of epilepsy, is a non-ionizable drug that cannot be considered “highly soluble” across the range of pH values usually encountered in the upper gastrointestinal tract. Furthermore, evidence in the open literature suggests that carbamazepine is a BCS Class 2 drug. Nevertheless, the oral absolute bioavailability of carbamazepine lies between 70 and 78% and both in vivo and in vitro data support the classification of ca…

Drugmedia_common.quotation_subjectPharmaceutical ScienceAdministration OralBiological Availability02 engineering and technologyBioequivalencePharmacology030226 pharmacology & pharmacyDosage formBiopharmaceuticsExcipients03 medical and health sciences0302 clinical medicineIVIVCTherapeutic indexmedicineImmediate releasemedia_commonActive ingredientDosage Formsbusiness.industryCarbamazepine021001 nanoscience & nanotechnologyCarbamazepineSolubilityTherapeutic Equivalency0210 nano-technologybusinessmedicine.drugJournal of pharmaceutical sciences
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Early handling effect on female rat spatial and non-spatial learning and memory

2014

This study aims at providing an insight into early handling procedures on learning and memory performance in adult female rats. Early handling procedures were started on post-natal day 2 until 21, and consisted in 15 min, daily separations of the dams from their litters. Assessment of declarative memory was carried out in the novel-object recognition task; spatial learning, reference- and working memory were evaluated in the Morris water maze (MWM). Our results indicate that early handling induced an enhancement in: (1) declarative memory, in the object recognition task, both at 1h and 24h intervals; (2) reference memory in the probe test and working memory and behavioral flexibility in the…

Early handling; maternal separationMorris water navigation taskHandling PsychologicalDevelopmental psychologyTask (project management)Behavioral NeuroscienceEarly handlingCognitionMemoryNon spatialDeclarative memoryAnimalsLearningFemale ratsRats WistarMaternal BehaviorMaze LearningDeclarative memoryWorking memoryMaternal DeprivationWorking memoryCognitive neuroscience of visual object recognitionFlexibility (personality)Recognition PsychologyCognitionGeneral MedicineRatsMemory Short-TermMaternal careFemaleAnimal Science and ZoologyBehavioral flexibilityPsychologyCognitive psychologyBehavioural Processes
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Social Housing Conditions Modulate the Long-Lasting Increase in Cocaine Reward Induced by Intermittent Social Defeat

2019

Social defeat is considered the most representative animal model for studying the consequences of social stress. Intermittent social defeat (ISD) has proved to enhance the response to cocaine hedonic properties. In the present research, we evaluated if different social housing conditions, as housing with a familiar conspecific or with a female, exert a protective effect modulating the negative consequences of ISD as the increased sensitivity to cocaine and the induction of anxiety-like behavior. To achieve this objective, non-stressed or ISD OF1 male mice were divided into five different experimental groups according to their social environment: standard housing (four adult males per cage);…

Elevated plus mazeCognitive Neurosciencemedia_common.quotation_subjectcocainePhysiologylcsh:RC321-571Social defeatsocial environment03 medical and health sciencesBehavioral NeuroscienceSocial support0302 clinical medicinesocial defeatoxytocinMedicinelcsh:Neurosciences. Biological psychiatry. NeuropsychiatryOriginal Research030304 developmental biologymedia_commonSocial stressIL-60303 health sciencesbusiness.industryAddictionSocial environmentconditioned place preferenceConditioned place preferenceNeuropsychology and Physiological PsychologyAnxiogenicbusiness030217 neurology & neurosurgeryNeuroscienceFrontiers in Behavioral Neuroscience
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Behavioural Consequences of P-Glycoprotein Deficiency in Mice, with Special Focus on Stress-Related Mechanisms

2012

P-glycoprotein (P-gp), an efflux transporter localised in the blood-brain barrier, limits the access of multiple xenobiotics to the central nervous system. Whether it is also implemented in the transport of the endogenous glucocorticoid corticosterone is a matter of debate. The P-gp knockout mouse model [abcb1a/b (-/-)] has been shown to differ in the functioning of the hypothalamic-pituitary adrenal (HPA) axis. In the present study, we investigated the behaviour of abcb1a/b (-/-) and wild-type mice with respect to stress-related tests and the effects of corticosterone. Behavioural activities were assessed in the open field (OF) test for 4 days, and in the forced swimming test (FST) and tai…

Elevated plus mazemedicine.medical_specialtyEndocrine and Autonomic SystemsEndocrinology Diabetes and MetabolismBiologyTail suspension testOpen fieldCellular and Molecular Neurosciencechemistry.chemical_compoundEndocrinologyGlucocorticoid receptorEndocrinologychemistryCorticosteroneInternal medicinemedicineHabituationGlucocorticoidBehavioural despair testmedicine.drugJournal of Neuroendocrinology
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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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Carbamazepine exposure in the sea anemones Anemonia sulcata and Actinia equina: Metabolite identification and physiological responses

2020

Trabajo presentado en el 11º Congreso Ibérico, 8º Iberoamericano de Contaminación y Toxicología (CICTA 2018) celebrado en la Escuela Técnica Superior de Ingeniería de Montes, Forestal y del Medio Natural, Madrid del 11 al 13 de julio de 2018

Environmental Engineering010504 meteorology & atmospheric sciencesMetaboliteZoologyCarbohydrate metabolism010501 environmental sciences01 natural scienceschemistry.chemical_compoundMediterranean seaBiotransformationBiotransformationsAnthozoaMediterranean SeaAnimalsEnvironmental ChemistryEcotoxicologyWaste Management and DisposalEcosystem0105 earth and related environmental sciencesMass spectrometrybiologyChemistryMetabolismAnthozoabiology.organism_classificationBioaccumulationPollutionCarbamazepineSea AnemonesBioaccumulationPharmaceuticalsWater Pollutants ChemicalActiniaScience of The Total Environment
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Effects of the benzodiazepine receptor agonist midazolam and antagonist flumazenil on 5-hydroxytryptamine release from guinea-pig intestine in vitro

1990

Isolated segments of the guinea-pig small intestine and the guinea-pig stomach were vascularly perfused and the release of 5-hydroxytryptamine (5-HT) and 5-hydroxyindoleacetic acid into the portal venous effluent determined by high pressure liquid chromatography with electrochemical detection. Test substances were applied intraarterially. The benzodiazepine receptor agonist, midazolam, concentration-dependently increased (by 58%, at 1 nmol/l) and decreased (by 32%, at 100 nmol/l) the release of 5-HT from small intestine preparations. Both effects were blocked by the benzodiazepine receptor antagonist flumazenil (10 nmol/l) The stimulatory effect of midazolam was also abolished in the presen…

FlumazenilMaleAgonistSerotoninmedicine.medical_specialtymedicine.drug_classMidazolamGuinea PigsTetrodotoxinIn Vitro TechniquesBiologychemistry.chemical_compoundInternal medicineIntestine SmallElectrochemistrymedicineAnimalsChromatography High Pressure LiquidPharmacologyBenzodiazepineGABAA receptorStomachAntagonistGeneral MedicineHydroxyindoleacetic AcidBicucullineReceptors GABA-ASmall intestinePerfusionEndocrinologymedicine.anatomical_structurechemistryGastric MucosaFlumazenilChromaffin SystemTetrodotoxinFemalemedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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[ 18 F]Fluoroethylflumazenil: a novel tracer for PET imaging of human benzodiazepine receptors

2001

5-(2'-[18F]Fluoroethyl)flumazenil ([18F]FEF) is a fluorine-18 labelled positron emission tomography (PET) tracer for central benzodiazepine receptors. Compared with the established [11C]flumazenil, it has the advantage of the longer half-life of the fluorine-18 label. After optimisation of its synthesis and determination of its in vitro receptor affinities, we performed first PET studies in humans. PET studies in seven healthy human volunteers were performed on a Siemens ECAT EXACT whole-body scanner after injection of 100-280 MBq [L8F]FEF. In two subjects, a second PET scan was conducted after pretreatment with unlabelled flumazenil (1 mg or 2.5 mg i.v., 3 min before tracer injection). A t…

FlumazenilMalemedicine.drug_classNuclear magnetic resonancemedicineHumansRadiology Nuclear Medicine and imagingReceptorTemporal cortexBenzodiazepineChemistrybusiness.industryGABAA receptorBrainHalf-lifeBinding potentialGeneral MedicineHuman brainReceptors GABA-Amedicine.anatomical_structureFlumazenilRadiopharmaceuticalsNuclear medicinebusinessTomography Emission-Computedmedicine.drugEuropean Journal of Nuclear Medicine and Molecular Imaging
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Benzodiazepines for catatonic symptoms, stupor, and mutism.

1988

FlumazenilPediatricsmedicine.medical_specialtyDepressive DisorderDiazepamMutismbusiness.industryStuporCatatoniaGeneral MedicineLorazepamPsychiatry and Mental healthBenzodiazepinesAnti-Anxiety AgentsmedicineHumansPharmacology (medical)Femalemedicine.symptombusinessPharmacopsychiatry
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