Sex and stress: effects on the brain - gut axis
Sex and stress: effects on the brain - gut axis
批准号:
10455424
负责人:
Kirsteen Nairn Browning
金额:
$34.49万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-07-01 至 2024-04-30
关键词:
AddressAdultAnatomyBasal GangliaBehavioralBindingBrain StemCell NucleusCentral Nervous SystemChronicConsultationsCorticotropin-Releasing HormoneDataDiseaseDyspepsiaElectrophysiology (science)Estrogen ReceptorsEstrogensEtiologyFemaleFunctional Gastrointestinal DisordersFunctional disorderGABA ReceptorGastric EmptyingGastrointestinal DiseasesGastrointestinal MotilityGastrointestinal TransitGeneticHormonesHuman ResourcesHypothalamic structureImpairmentIn VitroIncidenceLaboratoriesMediatingMembraneMenstrual cycleModelingMorphologyMotorMotor NeuronsNeonatalNeural PathwaysNeuronal PlasticityNeuronsNorepinephrineNuclearOutputOxytocinPerimenopausePhysiciansPhysiologicalPlayPositioning AttributePredispositionPrimary CareRattusRegulationReportingRodent ModelRoleSensorySeveritiesSex DifferencesSliceSpecialistStomachStressSymptomsSynapsesTechniquesTestingTherapeutic InterventionThyrotropin-Releasing HormoneWomanWorkacute stresscell motilitydesigner receptors exclusively activated by designer drugsdorsal motor nucleusexperienceexperimental studygamma-Aminobutyric Acidgastrointestinalgastrointestinal functiongut-brain axisin vivoinsightirritationmalemenmotility disorderneural circuitneuromechanismneuronal excitabilitynovelpatch clampreceptor expressionresilienceresponsesensory inputsexsex disparitytherapeutically effectivetool
中文摘要
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英文摘要
PROJECT SUMMARY
Women display higher incidence of gastrointestinal disorders, including functional dyspepsia (FD), and
report a higher severity of dyspeptic symptoms compared to men. Although physiological mechanisms that
mediate this sex disparity in gastrointestinal (GI) disorders are not fully understood, it has been suggested that
they may be mediated by circulating estrogen.
Gastric motility is modulated by neurons of the dorsal motor nucleus of the vagus (DMV) and the activity of
these neurons is regulated by a robust tonic GABAergic input. Estrogen has been shown to increase GABA
expression and release in several regions of the central nervous system (CNS), as well as to modulate
neuronal morphology and synaptic activity.
Based on our preliminary studies that indicate an estrogen-dependent modulation of vagal output to the
stomach, we will test the following novel hypothesis: “Functional gastrointestinal disorders are increased in
severity and incidence in females due, in part, to an estrogen mediated decrease in vagal outflow to the
stomach”. To investigate this novel hypothesis, we will use a combination of in vitro and in vivo
electrophysiological, behavioral, chemogenetic, and anatomical approaches in a rodent model aimed at
interrogating the role of stress and estrogen on the brain-gut axis.
The results of the experiments outlined in this proposal will provide a deeper understanding of the cellular
and neural mechanisms by which estrogen influences the etiology of FD, help identify potential targets for
more effective therapeutic interventions directed specifically towards women, and provide novel insights into
changes in GI functions that occur in the perimenopausal period.
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