2010
Post-weaning chronic social isolation produces profound behavioral dysregulation with decreases in prefrontal cortex synaptic-associated protein expression in female rats
Hermes G, Li N, Duman C, Duman R. Post-weaning chronic social isolation produces profound behavioral dysregulation with decreases in prefrontal cortex synaptic-associated protein expression in female rats. Physiology & Behavior 2010, 104: 354-359. PMID: 21185848, PMCID: PMC3387788, DOI: 10.1016/j.physbeh.2010.12.019.Peer-Reviewed Original ResearchMeSH KeywordsAge FactorsAnimalsAnimals, NewbornBehavioral SymptomsBody WeightDisks Large Homolog 4 ProteinEstriolEstrusExploratory BehaviorFemaleFood DeprivationGene Expression Regulation, DevelopmentalIntracellular Signaling Peptides and ProteinsMembrane ProteinsPrefrontal CortexPregnancyRatsRats, Sprague-DawleyReceptors, AMPAReceptors, N-Methyl-D-AspartateSocial IsolationSynapsinsConceptsFemale ratsNovelty-suppressed feeding testPrefrontal cortexSocial isolationPost-weaning social isolationSynapse-related proteinsChronic social isolationFemale Sprague-DawleyEarly life stressorsSerotonergic functionGlutamate receptorsSprague-DawleyMale rodentsMaternal separationProtein PSD95Profound dysregulationNeuropsychiatric disordersBrain developmentRatsAnxiety disordersMarked deficitDeprivation resultsProtein expressionAdult animalsBiochemical effects
2008
Neurological and behavioral abnormalities, ventricular dilatation, altered cellular functions, inflammation, and neuronal injury in brains of mice due to common, persistent, parasitic infection
Hermes G, Ajioka JW, Kelly KA, Mui E, Roberts F, Kasza K, Mayr T, Kirisits MJ, Wollmann R, Ferguson D, Roberts CW, Hwang JH, Trendler T, Kennan RP, Suzuki Y, Reardon C, Hickey WF, Chen L, McLeod R. Neurological and behavioral abnormalities, ventricular dilatation, altered cellular functions, inflammation, and neuronal injury in brains of mice due to common, persistent, parasitic infection. Journal Of Neuroinflammation 2008, 5: 48. PMID: 18947414, PMCID: PMC2588578, DOI: 10.1186/1742-2094-5-48.Peer-Reviewed Original ResearchMeSH KeywordsAge FactorsAnimalsAtrophyBehavior, AnimalBiomarkersBrainCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChronic DiseaseDisease Models, AnimalEncephalitisFemaleLateral VentriclesMagnetic Resonance ImagingMiceMicrogliaNerve DegenerationNerve Tissue ProteinsNeuronsToxoplasmaToxoplasmosis, CerebralConceptsT. gondii infectionAqueduct of SylviusPerivascular inflammationVentricular dilatationGondii infectionResistant miceInflammatory cellsBrain weightBrain parenchymaBrain MRIBehavioral abnormalitiesChronic T. gondii infectionLower brain weightPersistent brain infectionBrains of micePD-1LResultsTwelve monthsNeurologic findingsNeurological deficitsNeuronal injuryStudy of markersNeurologic functionNeuronal damageBrain infectionFree tachyzoitesIsolation and the timing of mammary gland development, gonadarche, and ovarian senescence: Implications for mammary tumor burden
Hermes GL, McClintock MK. Isolation and the timing of mammary gland development, gonadarche, and ovarian senescence: Implications for mammary tumor burden. Developmental Psychobiology 2008, 50: 353-360. PMID: 18393277, DOI: 10.1002/dev.20295.Peer-Reviewed Original ResearchConceptsMammary tumor burdenTumor burdenOvarian functionMammary gland developmentOvarian systemGreater tumor burdenGland developmentSpontaneous mammary tumorsSocial isolationMammary tissue developmentRisk factorsBreast cancerMammary tumorsOvarian senescenceEpidemiological studiesBreast parenchymaEarly pubertyRatsYoung adulthoodNorway ratsPubertyPsychosocial experiencesBurdenAgeEstropause