Search results for "developmental neuroscience"

showing 10 items of 360 documents

Episodic memories: how do the hippocampus and the entorhinal ring attractors cooperate to create them?

2020

AbstractThe brain is capable of registering a constellation of events, encountered only once, as an episodic memory that can last for a lifetime. As evidenced by the clinical case of the patient HM, memories preserving their episodic nature still depend on the hippocampal formation, several years after being created, while semantic memories are thought to reside in neocortical areas. The neurobiological substrate of one-time learning and life-long storing in the brain, that must exist at the cellular and circuit level, is still undiscovered. The breakthrough is delayed by the fact that studies jointly investigating the rodent hippocampus and entorhinal cortex are mostly targeted at understa…

Functional observationsComputer sciencehippocampusCognitive NeuroscienceNeuroscience (miscellaneous)Hippocampusgrid cellsHippocampal formationlcsh:RC321-57103 medical and health sciencesCellular and Molecular Neuroscience0302 clinical medicineDevelopmental NeuroscienceEncoding (memory)Semantic memoryEpisodic memorylcsh:Neurosciences. Biological psychiatry. Neuropsychiatry030304 developmental biology0303 health sciencesentorhinal cortexepisodic memoryphase precessionEntorhinal cortexplasticityClinical caseNeuroscience030217 neurology & neurosurgery
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Do we need algebraic-like computations? A reply to Bonatti, Pena, Nespor, and Mehler (2006).

2006

L. L. Bonatti, M. Pena, M. Nespor, and J. Mehler (2006) argued that P. Perruchet, M. D. Tyler, N. Galland, and R. Peereman (2004) confused the notions of segmentation and generalization by ignoring the evidence for generalization in M. Pena, L. L. Bonatti, M. Nespor, and J. Mehler (2002). In this reply, the authors reformulate and complement their initial arguments, showing that their way of dealing with segmentation and generalization is not due to confusion or ignorance but rather to the fact that the tests used in Pena et al. make it likely that neither segmentation nor generalization were captured in their experiments. Finally, the authors address the challenge posed by Pena et al. of a…

GeneralizationComputationmedia_common.quotation_subjectExperimental and Cognitive PsychologyIgnorance[ SCCO.PSYC ] Cognitive science/Psychology050105 experimental psychology03 medical and health sciences0302 clinical medicineDevelopmental Neurosciencemedicine0501 psychology and cognitive sciencesAlgebraic numberGeneral PsychologyComputingMilieux_MISCELLANEOUSConfusionmedia_commonComplement (set theory)Cognitive science05 social sciences[SCCO.PSYC]Cognitive science/Psychology[SCCO.PSYC] Cognitive science/Psychologymedicine.symptomPsychologyMathematical economics030217 neurology & neurosurgery
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P3‐039: Axonal neuritic pathology induces early presynaptic alterations in ps1/APP Alzheimer's mice hippocampus

2011

Loss of neurons in the hippocampus correlates with memory impairment in AD. Significant early reduction in the numerical density of hippocampal SOM interneurons was found in single (APPswe) and double (APPswe/ PS1dE9 and APPswe/TauP301S-G272V) transgenic models based on APP over expression and amyloid production. However, this inhibitory population was unaffected in age-matched single PS1 and tau transgenic mice as well as nontransgenic controls. Whereas SOM neuron loss in APPswe/PS1dE9 was associated to the onset of extracellular amyloid pathology in double APP/ tau mice this loss preceded plaque formation. Conclusions: As in human AD, somatostatin cell loss is a common early pathological …

Genetically modified mouseeducation.field_of_studyAmyloidEpidemiologyHealth PolicyTransgenePopulationHippocampusBiologyHippocampal formationInhibitory postsynaptic potentialPsychiatry and Mental healthCellular and Molecular NeuroscienceSomatostatinnervous systemDevelopmental Neurosciencemental disordersNeurology (clinical)Geriatrics and GerontologyeducationNeuroscienceAlzheimer's & Dementia
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P2‐077: Identification of potential modifiers of Alzheimer's disease pathology by quantitative mass spectrometry and drosophila genetics

2015

GeneticsPathologymedicine.medical_specialtybiologyEpidemiologyHealth PolicyDiseasebiology.organism_classificationMass spectrometryPsychiatry and Mental healthCellular and Molecular NeuroscienceDevelopmental NeurosciencemedicineIdentification (biology)Neurology (clinical)Geriatrics and GerontologyDrosophila (subgenus)Alzheimer's & Dementia
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Prevalence of cognitive frailty and associations with other frailty domains in a Spanish community‐dwelling sample

2020

GerontologyCognitive frailtyPsychiatry and Mental healthCellular and Molecular NeuroscienceDevelopmental NeuroscienceEpidemiologyHealth PolicySample (statistics)Neurology (clinical)Geriatrics and GerontologyPsychologyAlzheimer's & Dementia
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P2‐310: MIDLIFE SELF‐RATED HEALTH AND FITNESS IN RELATION TO WHITE MATTER LESIONS AND GREY MATTER VOLUME 20 YEARS LATER

2014

Midlife self-rated health and fitness in relation to white matter lesions and grey matter volume 20 years later

GerontologyEpidemiologybusiness.industryHealth PolicyGrey matterHyperintensityPsychiatry and Mental healthCellular and Molecular Neurosciencemedicine.anatomical_structureDevelopmental NeurosciencemedicineNeurology (clinical)Geriatrics and GerontologybusinessSelf-rated healthVolume (compression)Alzheimer's & Dementia
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P2-551: MIGRAINE, COGNITIVE DECLINE, AND DEMENTIA IN OLD AGE: A POPULATION-BASED STUDY

2019

GerontologyEpidemiologybusiness.industryHealth Policymedicine.diseasePopulation based studyPsychiatry and Mental healthCellular and Molecular NeuroscienceDevelopmental NeuroscienceMigrainemedicineDementiaNeurology (clinical)Geriatrics and GerontologyCognitive declinebusinessAlzheimer's & Dementia
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Leisure-time physical activity from mid- to late life, body mass index, and risk of dementia

2013

Abstract Background Physical activity may be beneficial for cognition, but the effect may vary depending on personal characteristics. Methods We investigated the associations between leisure-time physical activity (LTPA) from mid- to late life, the risk of dementia, and the role of body mass index, sex, and APOE in the CAIDE study during 28-year follow-up. Cognitive function of a random subsample was assessed at a mean age of 78.8 years (n = 1511), and dementia/Alzheimer's disease (AD) diagnoses were identified from national registers for the entire target population (n = 3559). Results Moderate (hazard ratio [HR], 1.46; 95% confidence interval [CI], 1.08–1.99) and low levels of midlife LTP…

GerontologyMaleEpidemiologyNeuroimagingOverweightMotor ActivityNeuropsychological TestsCommunity Health PlanningBody Mass IndexCellular and Molecular NeuroscienceLeisure ActivitiesDevelopmental NeuroscienceRisk FactorsmedicineDementiaHumansLongitudinal StudiesObesityExerciseFinlandAgedProportional Hazards Models2. Zero hungerAged 80 and overPsychiatric Status Rating ScalesPhysical activityHealth PolicyHazard ratioAge FactorsLife courseta3142Middle Agedmedicine.diseaseObesityConfidence interval3. Good healthPsychiatry and Mental healthDisease ProgressionLife course approachFemaleDementiaNeurology (clinical)Geriatrics and Gerontologymedicine.symptomPsychologyCohort studyBody mass indexCohort studyAlzheimers and Dementia
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Exposure to N-ethyl-N-nitrosourea in adult mice alters structural and functional integrity of neurogenic sites.

2011

BackgroundPrevious studies have shown that prenatal exposure to the mutagen N-ethyl-N-nitrosourea (ENU), a N-nitroso compound (NOC) found in the environment, disrupts developmental neurogenesis and alters memory formation. Previously, we showed that postnatal ENU treatment induced lasting deficits in proliferation of neural progenitors in the subventricular zone (SVZ), the main neurogenic region in the adult mouse brain. The present study is aimed to examine, in mice exposed to ENU, both the structural features of adult neurogenic sites, incorporating the dentate gyrus (DG), and the behavioral performance in tasks sensitive to manipulations of adult neurogenesis.Methodology/principal findin…

GerontologyMaleHippocampusHippocampuschemistry.chemical_compoundMiceMolecular Cell BiologyStem Cell NicheNeuronsMultidisciplinaryStem CellsNeurogenesisQAge FactorsRCell DifferentiationEnvironmental exposureAnimal ModelsAdult Stem Cellsmedicine.anatomical_structureMedicineCellular TypesBromodeoxyuridineAdult stem cellResearch Articlemedicine.medical_specialtyAlkylating AgentsNeurogenesisScienceImmunologySubventricular zoneBiologyModel OrganismsDevelopmental NeuroscienceInternal medicinemedicineotorhinolaryngologic diseasesAnimalsBiologyMemory DisordersDentate gyrusEnvironmental ExposureBarnes mazeEndocrinologychemistryEthylnitrosoureaDentate GyrusImmunologic TechniquesClinical ImmunologyDevelopmental BiologyNeurosciencePLoS ONE
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P3‐315: MID‐LIFE WORK‐RELATED STRESS INCREASES DEMENTIA RISK IN LATE‐LIFE: THE CAIDE 30‐YEAR STUDY

2014

Background: The associations between work-related stress and various health outcomes in mid-life are well documented, yet less is known about the effects on late-life cognitive process and dementia. The current study investigated the associations between work-related stress in mid-life and the development of cognitive impairment and Alzheimer’s disease in late-life. Methods: The data was derived from the Cardiovascular Risk Factors, Aging, and Incidence of Dementia (CAIDE) study; a prospective cohort study. Participants were randomly selected from four independent population-based samples that completed cardiovascular surveys. First baseline examinations occurred when participants were 50 y…

Gerontologyeducation.field_of_studyEpidemiologybusiness.industryHealth PolicyPopulationNeuropsychologyLonelinessCognitionOdds ratiomedicine.diseaseConfidence intervalPsychiatry and Mental healthCellular and Molecular NeuroscienceDevelopmental NeuroscienceMedicineDementiaNeurology (clinical)Geriatrics and Gerontologymedicine.symptomProspective cohort studyeducationbusinessAlzheimer's & Dementia
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