Influences of the prenatal environment on metabolic programming
Influences of the prenatal environment on metabolic programming
批准号:
7223832
负责人:
KELLIE L. K. TAMASHIRO
金额:
$6.71万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-12-01 至 2008-11-30
关键词:
AdolescenceAdultAffectAnimal ModelAppetitive BehaviorBehavioralBirthBody WeightCardiovascular DiseasesCharacteristicsClinicalConditionConsumptionDNA MethylationDataDevelopmentDietDiseaseEndocrineEnvironmentEpigenetic ProcessEtiologyExposure toFatty acid glycerol estersFeeding behaviorsFetusFoundationsGenesGoalsHealthHomeostasisHumanHypertensionInsulin ResistanceInterventionLactationLeadLife StyleLong-Term EffectsMentorsMetabolicMetabolic DiseasesMethylationModelingModificationMolecularMolecular GeneticsNeonatalNeurobiologyNeuroendocrinologyNeuropeptidesNon-Insulin-Dependent Diabetes MellitusObesityOrganismPhenotypePhysiologicalPotassium HydroxidePregnancyPublic HealthRattusRegulationResearchResearch PersonnelRiskRodent ModelRoleSolidStressStructureSystemTestingTimeTrainingWeaningWorkdayfeedinghypothalamic-pituitary-adrenal axisneuropsychiatrynutritionprenatalprenatal influenceprenatal stresspreventprogramsresearch studyresponse
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Obesity is a major public health problem worldwide and recent work has suggested that exposure to a suboptimal early environment may increase the risk of becoming obese. Epidemiological data show that an unfavorable intrauterine environment has long-term consequences in offspring including hypertension, cardiovascular disease, type 2 diabetes, obesity and neuropsychiatric disease. Specifically, prenatal stress and/or consumption of a high fat diet, characteristics of modern day human lifestyle, have been shown to lead to metabolic disorders such as obesity and insulin resistance in offspring. However, the mechanisms involved are not well understood. The overall goal of this proposal is to characterize the short- and long-term effects of changes in the prenatal environment - stress and nutrition - on the behavioral and physiological development of offspring and to explore the possible neuropeptide and epigenetic mechanisms involved using a rat animal model. Specific aims are: 1) To determine the developmental time course of behavioral and endocrine alterations resulting from prenatal stress. We will also test the hypothesis that prenatal stress will accentuate diet-induced obesity. Time points during lactation, adolescence, and adulthood will be examined to characterize the phenotype and to direct examination of possible mechanisms; 2) To test the hypothesis that prenatal stress, high fat diet, or both result in alterations in neuropeptide systems regulating energy homeostasis that are consistent with other rodent models of obesity; and 3) To test the hypothesis that prenatal stress and nutrition results in obesity in offspring through epigenetic modifications via differential DNA methylation of genes that are critical to energy homeostasis. These experiments will enhance our understanding of the etiology of obesity and metabolic disease ultimately allowing the development of rational clinical interventions for such conditions. This proposal has also been structured to provide a rich and diverse training opportunity. The trainee has assembled a mentoring committee that will provide expertise in the development and regulation of ingestive behavior (Dr. Timothy Moran), neurobiology of stress and the hypothalamic-pituitary-adrenal axis (Dr. James Koenig) and the role of epigenetics in the etiology of disease (Dr. Andrew Feinberg and Dr. James Potash). The guidance of this committee in conjunction with the trainee's previous work in behavioral and molecular neuroendocrinology, will provide a solid foundation for the trainee to develop a multi-disciplinary program of research including behavioral, physiological, cellular/molecular, and genetic/epigenetic studies that will facilitate her transition to an independent investigator.
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科研奖励(0)
会议论文
Maternal diet and programming of offspring gut-brain axis
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批准号:10438957
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项目类别:
-
资助金额:$57.26万
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财政年份:2022
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Maternal diet and programming of offspring gut-brain axis
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批准号:10656194
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项目类别:
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资助金额:$55.85万
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财政年份:2022
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Maternal diet and programming of offspring gut-brain axis
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批准号:10764183
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项目类别:
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资助金额:$9.64万
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财政年份:2022
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Epigenetic Mechanisms in the Perpetuation of Anorexia Nervosa-like Behavior
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批准号:8443813
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项目类别:
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资助金额:$19.44万
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财政年份:2012
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Epigenetic Mechanisms in the Perpetuation of Anorexia Nervosa-like Behavior
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批准号:8281794
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项目类别:
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资助金额:$24.3万
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财政年份:2012
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Influences of the prenatal environment on metabolic programming
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批准号:7938446
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项目类别:
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资助金额:$4.27万
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财政年份:2009
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Influences of the prenatal environment on metabolic programming
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批准号:8052835
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项目类别:
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资助金额:$24.4万
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财政年份:2007
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Influences of the prenatal environment on metabolic programming
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批准号:7744778
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项目类别:
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资助金额:$24.9万
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财政年份:2007
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Influences of the prenatal environment on metabolic programming
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批准号:7754852
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项目类别:
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资助金额:$24.65万
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财政年份:2007
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Influences of the prenatal environment on metabolic programming
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批准号:7324839
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项目类别:
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资助金额:$6.84万
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财政年份:2006
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Social stress-induced changes in energy homeostasis
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批准号:6737637
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项目类别:
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资助金额:$3.57万
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财政年份:2004
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
Social stress-induced changes in energy homeostasis
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批准号:6874364
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项目类别:
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资助金额:$2.29万
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财政年份:2004
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负责人:KELLIE L. K. TAMASHIRO
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依托单位:
海外基金