Search results for "Bromo"

showing 10 items of 936 documents

Chronic social stress inhibits cell proliferation in the adult medial prefrontal cortex: hemispheric asymmetry and reversal by fluoxetine treatment.

2006

Profound neuroplastic changes have been demonstrated in various limbic structures after chronic stress exposure and antidepressant treatment in animal models of mood disorders. Here, we examined in rats the effect of chronic social stress and concomitant antidepressant treatment on cell proliferation in the medial prefrontal cortex (mPFC). We also examined possible hemispheric differences. Animals were subjected to 5 weeks of daily social defeat by an aggressive conspecific and received concomitant, daily, oral fluoxetine (10 mg/kg) during the last 4 weeks. Bromodeoxyuridine (BrdU) labeling and quantitative stereological techniques were used to evaluate the treatment effects on proliferatio…

MaleCell SurvivalPrefrontal CortexCell CountFunctional Laterality03 medical and health sciences0302 clinical medicineHemispheric asymmetryFluoxetinemedicineAnimalsRats WistarPrefrontal cortexSocial Behavior030304 developmental biologyCell ProliferationPharmacologySocial stressNeurons0303 health sciencesFluoxetineDepressive DisorderCell growthStem CellsBody WeightCell DifferentiationOrgan SizeRatsPsychiatry and Mental healthBromodeoxyuridineChronic DiseaseDentate GyrusPsychologyNeuroscienceNeuroglia030217 neurology & neurosurgerySelective Serotonin Reuptake InhibitorsStress Psychologicalmedicine.drugNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology
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A population of prenatally generated cells in the rat paleocortex maintains an immature neuronal phenotype into adulthood.

2008

New neurons in the adult brain transiently express molecules related to neuronal development, such as the polysialylated form of neural cell adhesion molecule, or doublecortin (DCX). These molecules are also expressed by a cell population in the rat paleocortex layer II, whose origin, phenotype, and function are not clearly understood. We have classified most of these cells as a new cell type termed tangled cell. Some cells with the morphology of semilunar-pyramidal transitional neurons were also found among this population, as well as some scarce cells resembling semilunar, pyramidal. and fusiform neurons. We have found that none of these cells in layer II express markers of glial cells, m…

MaleCell typeDoublecortin ProteinAntimetabolitesCognitive NeuroscienceNeurogenesisPopulationMice Inbred StrainsNeural Cell Adhesion Molecule L1Receptors N-Methyl-D-AspartateImmunophenotypingRats Sprague-DawleyCellular and Molecular Neurosciencechemistry.chemical_compoundMiceReceptors GlucocorticoidPregnancyAnimalsEntorhinal CortexCyclic adenosine monophosphateeducationeducation.field_of_studyArc (protein)biologyPyramidal CellsStem CellsNeurogenesisAge FactorsPhenotypeDoublecortinCell biologyRatsMicroscopy ElectronchemistryBromodeoxyuridinebiology.proteinSialic AcidsNeural cell adhesion moleculeFemaleNeuroscienceNeurogliaBiomarkersCerebral cortex (New York, N.Y. : 1991)
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Lack of the Cell-Cycle Inhibitor p27Kip1 Results in Selective Increase of Transit-Amplifying Cells for Adult Neurogenesis

2002

The subventricular zone (SVZ) is the largest germinal layer in the adult mammalian brain and comprises stem cells, transit-amplifying progenitors, and committed neuroblasts. Although the SVZ contains the highest concentration of dividing cells in the adult brain, the intracellular mechanisms controlling their proliferation have not been elucidated. We show here that loss of the cyclin-dependent kinase inhibitor p27Kip1 has very specific effects on a population of CNS progenitors responsible for adult neurogenesis. Using bromodeoxyuridine and [3H]thymidine incorporation to label cells in S phase and cell-specific markers and electron microscopy to identify distinct cell types, we compared th…

MaleCell typePopulationSubventricular zoneApoptosisCell CountCell Cycle ProteinsMice TransgenicBiologyMicechemistry.chemical_compoundNeuroblastLateral VentriclesSpheroids CellularIn Situ Nick-End LabelingmedicineAnimalsARTICLEProgenitor celleducationCells CulturedNeuronseducation.field_of_studyStem CellsTumor Suppressor ProteinsGeneral NeuroscienceCell CycleNeurogenesisCell DifferentiationImmunohistochemistryCell biologyMice Inbred C57BLmedicine.anatomical_structureBromodeoxyuridinenervous systemchemistryStem cellCell DivisionCyclin-Dependent Kinase Inhibitor p27BromodeoxyuridineThymidineThe Journal of Neuroscience
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High-performance liquid chromatography with fluorimetric detection in biological tissues of the 4-bromomethyl-7-methoxycoumarin ester derivative of 5…

1985

MaleChemical PhenomenaMetaboliteCarboxylic acidPeptideKidneyHigh-performance liquid chromatographyMicechemistry.chemical_compoundDrug StabilityAnimalsUmbelliferonesChromatography High Pressure LiquidBrain Chemistrychemistry.chemical_classificationChromatographyGeneral ChemistryGlutamic acid4-bromomethyl-7-methoxycoumarinPyrrolidinonesPyrrolidonecarboxylic AcidChemistrySpectrometry FluorescenceLiverchemistryIndicators and ReagentsDerivative (chemistry)Journal of Chromatography B: Biomedical Sciences and Applications
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Mildronate enhances learning/memory and changes hippocampal protein expression in trained rats.

2013

Previously we demonstrated that mildronate [3-(2,2,2-trimethylhydrazinium) propionate dihydrate], a representative of the aza-butyrobetaine class of compounds, protects mitochondrial metabolism under conditions such as ischemia. Mildronate also acted as a neuroprotective agent in an azidothymidine-induced mouse model of neurotoxicity, as well as in a rat model of Parkinson's disease. These observations suggest that mildronate may stimulate processes involved in cell survival and change expression of proteins involved in neurogenic processes. The present study investigated the influence of mildronate on learning and memory in the passive avoidance response (PAR) test and the active condition…

MaleClinical BiochemistryGlutamate decarboxylaseBlotting WesternNerve Tissue ProteinsPharmacologyHippocampal formationToxicologyBiochemistryNeuroprotectionHippocampusBehavioral Neurosciencechemistry.chemical_compoundMemorymedicineAnimalsLearningRats WistarBiological PsychiatryPharmacologyChemistryGlutamate DecarboxylaseNeurotoxicitymedicine.diseaseAcetylcholinesteraseNeural stem cellRatsBromodeoxyuridineAcetylcholinesteraseCholinergicNeuroscienceBromodeoxyuridineMethylhydrazinesPharmacology, biochemistry, and behavior
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Properties of the microsomal and cytosolic glutathione transferases involved in hexachloro-1:3-butadiene conjugation

1989

Hexachloro-1,3-butadiene (HCBD) is a substrate for the hepatic microsomal glutathione transferases and is metabolised at higher rates by these enzymes than their cytosolic counterparts. Conjugation reactions catalysed by the microsomal and cytosolic transferases have been studied and characterized using this substrate and 1-chloro-2,4-dinitrobenzene (CDNB). In rat liver microsomes the Km values for HCBD and CDNB were 0.91 and 0.012 mM and in cytosol 0.51 and 0.10 mM respectively. Vmax values for HCBD were 1.39 and 0.35 nmol conjugate formed/min/mg protein for microsomes and cytosol respectively. In microsomal systems HCBD was a potent competitive inhibitor of the metabolism of CDNB with a K…

MaleDetergentsGuinea PigsCholic AcidBiochemistrySulfobromophthaleinchemistry.chemical_compoundCytochrome P-450 Enzyme SystemCricetinaeButadienesDinitrochlorobenzeneAnimalsHumansGlutathione transferase activityGlutathione TransferasePharmacologychemistry.chemical_classificationbiologyEndoplasmic reticulumBilirubinCholic AcidsGlutathioneMetabolismbiology.organism_classificationRatsKineticsCytosolEnzymeSolubilitychemistryBiochemistryMicrosomaMicrosomes LiverMicrosomeRabbitsBiochemical Pharmacology
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Alterations in striatal neuropeptide mRNA produced by repeated administration of L-DOPA, ropinirole or bromocriptine correlate with dyskinesia induct…

2002

Chronic administration of L-DOPA to MPTP-treated common marmosets induces marked dyskinesia while repeated administration of equivalent antiparkisonian doses of ropinirole and bromocriptine produces only mild involuntary movements. The occurrence of dyskinesia has been associated with an altered balance between the direct and indirect striatal output pathways. Using in situ hybridisation histochemistry, we now compare the effects of these drug treatments on striatal preproenkephalin-A (PPE-A) and adenosine A(2a) receptor mRNA expression as markers of the indirect pathway and striatal preprotachykinin (PPT) mRNA and preproenkephalin-B (PPE-B, prodynorphin) mRNA expression as markers of the d…

MaleDyskinesia Drug-Inducedmedicine.medical_specialtyIndolesCaudate nucleusStriatumIndirect pathway of movementAntiparkinson AgentsLevodopachemistry.chemical_compoundDopamine Uptake InhibitorsParkinsonian DisordersTachykininsInternal medicineNeural PathwaysmedicineAnimalsheterocyclic compoundsRNA MessengerProtein PrecursorsBromocriptineGeneral NeuroscienceMPTPPutamenNeuropeptidesReceptors Purinergic P1CallithrixEnkephalinsMazindoldopamine agonists peptide mRNAs L-DOPA 1-methyl-4-phenyl-1236-tetrahydropyridine primates dyskinesiaBromocriptinenervous system diseasesNeostriatumRopiniroleEndocrinologynervous systemchemistryDyskinesiaSettore BIO/14 - FarmacologiaFemalemedicine.symptommedicine.drugNeuroscience
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Drinking water disinfection by-products during pregnancy and child neuropsychological development in the INMA Spanish cohort study.

2017

Background: Disinfection by-products (DBPs) constitute a complex mixture of prevalent chemicals in drinking water and there is evidence of neurotoxicity for some of them. Objectives: We evaluated the association between estimates of DBP exposure during pregnancy and child neuropsychological outcomes at 1 and 4–5 years of age. Methods: We conducted a population-based mother-child cohort study in Spain with recruitment at first trimester of gestation (INMA Project, 2003–2008). Neuropsychological development was measured at 1 year of age using the Bayley Scales of Infant Development and at 4–5 years with the McCarthy Scales of Children's Abilities. Modeled tap water concentrations of trihalome…

MaleHaloacetic acidsBathingNeurodevelopmentPhysiology010501 environmental sciencesBromodichloromethane01 natural sciencesBayley Scales of Infant DevelopmentCohort Studieschemistry.chemical_compound0302 clinical medicineDisinfection by-productsChild DevelopmentPregnancyIngestionChildrenlcsh:Environmental sciencesGeneral Environmental Science2. Zero hungerlcsh:GE1-350education.field_of_study3. Good healthMaternal ExposureEnvironmental chemistryChild PreschoolFemalemedicine.drugTrihalomethanesAdultDibromochloromethanePopulation03 medical and health sciencesWater SupplymedicineHumanseducation0105 earth and related environmental sciencesPregnancyHaloacetic acidsDrinking WaterWaterInfantmedicine.diseasechemistrySpainNervous System Diseases030217 neurology & neurosurgeryWater Pollutants ChemicalDisinfectantsEnvironment international
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Sevoflurane affects neurogenesis after forebrain ischemia in rats.

2007

BACKGROUND: The effect of sevoflurane on the neuroregenerative potential after neuronal injury is unclear. We investigated the effect of low and high concentrations of sevoflurane on endogenous neurogenesis after cerebral ischemia. METHODS: Anesthetized and ventilated rats were randomized to four different treatment groups. Groups 1 and 2: 1.4% sevoflurane; Groups 3 and 4: 2.8% sevoflurane. In Groups 1 and 3, no cerebral ischemia was induced (sham-operated). In Groups 2 and 4, 10 min of forebrain ischemia was induced by bilateral carotid artery occlusion plus hemorrhagic hypotension. Physiological variables were maintained constant. Bromodeoxyuridine was given as a marker of neurogenesis. A…

MaleMethyl EthersIschemiaH&E stainHippocampusHippocampusSevofluraneBrain IschemiaRats Sprague-Dawleychemistry.chemical_compoundRandom AllocationSevofluraneProsencephalonmedicineAnimalsCell ProliferationNeuronsDose-Response Relationship Drugbusiness.industryDentate gyrusNeurogenesismedicine.diseaseNerve RegenerationRatsDose–response relationshipDisease Models AnimalAnesthesiology and Pain MedicinechemistryAnesthesiaAnesthetics InhalationDentate GyrusbusinessBromodeoxyuridinemedicine.drugAnesthesia and analgesia
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Effects of a single-dose hypertonic saline hydroxyethyl starch on cerebral blood flow, long-term outcome, neurogenesis, and neuronal survival after c…

2012

The beneficial effects of hypertonic saline on neuronal survival and on cerebral blood flow have been shown in several animal models of global and focal brain ischemia. Because of the potential benefits of hypertonic solutions, it is hypothesized that hydroxyethyl starch enhances cerebral blood flow and improves long-term outcome after cardiac arrest and cardiopulmonary resuscitation in an animal model.Laboratory animal study.University animal research laboratory.Fifty-nine male Sprague-Dawley rats.Rats were randomized to receive either 7.2% saline/6% hypertonic saline hydroxyethyl starch (4 mL/kg) or vehicle (NaCl 0.9 %) after 9 mins of asphyxic cardiac arrest and cardiopulmonary resuscita…

MaleNeurogenesismedicine.medical_treatmentPlasma Substitutesmacromolecular substancesHydroxyethyl starchCritical Care and Intensive Care MedicineHydroxyethyl Starch DerivativesRats Sprague-DawleyBrain ischemiaRandom AllocationAnimalsMedicineCardiopulmonary resuscitationBeneficial effectsNeuronsbusiness.industryNeurogenesisBrainmedicine.diseaseCardiopulmonary ResuscitationRatsHypertonic salineBromodeoxyuridineCerebral blood flowCerebrovascular CirculationAnesthesiaHeart Arrest InducedTonicitybusinessmedicine.drugCritical Care Medicine
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