Postnatal Actions of Maternal Obesity on Neonatal Metabolic Health
Postnatal Actions of Maternal Obesity on Neonatal Metabolic Health
批准号:
8841796
负责人:
Paul S. Maclean
金额:
$31.46万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-08-01 至 2016-05-31
关键词:
Acetyl-CoA CarboxylaseAdultAffectAnimalsBreast Epithelial CellsBreast FeedingCarbohydratesCellsChronicConsumptionDataDevelopmentDietDiscipline of NursingDiseaseEnergy IntakeEnergy MetabolismEnvironmentEpidemicExhibitsFatty acid glycerol estersFoodFosteringFoundationsFutureGoalsGoldGrowthHealthHealthcareHumanHuman MilkImageImpairmentIncidenceInsulin ResistanceInterventionInvestigationKnock-outLactationLeadLifeLinkLipidsMacronutrients NutritionMammary glandMetabolicMetabolic DiseasesMetabolic syndromeMetabolismMilkMolecularNeonatalNon-Insulin-Dependent Diabetes MellitusObese MiceObesityOutcomePhenotypePhysiologicalPredispositionProductionPropertyProteinsPublishingRiskRoleSolidSourceStagingTestingTimeTracerTransgenic MiceUnited StatesWeaningWorkcare burdenenergy balancefeedingfetalgenetic manipulationin uteroinnovationinsightlipid biosynthesismeetingsmortalitymouse modelneonatal humanneonatenutritionobesity in childrenobesity riskobesogenicoffspringpostnatalpreventprogramspupresearch study
中文摘要
描述(由申请人提供):母亲肥胖增加后代肥胖的风险,有大量证据表明胎儿和新生儿发育过程中的编程有助于这种易感。母乳喂养是公认的人类新生儿营养的“黄金标准”,与降低儿童肥胖风险有关。然而,来自人类和动物研究的新证据表明,母亲肥胖可能会超过母乳喂养对代谢健康和哺乳后代肥胖风险的益处。我们的研究旨在了解母亲肥胖影响其后代肥胖代谢倾向的机制。我们建立了一个小鼠模型,使我们能够确定母亲肥胖对新生儿代谢健康和肥胖易感性的产后贡献,区分母亲肥胖的特定影响与母亲食用高脂肪(HF)肥胖饮食所带来的影响。我们的数据证明,来自肥胖母鹿的乳汁选择性地改变了新生儿代谢中的肥胖变化。在最近的工作中,我们将这些变化与由于乙酰辅酶a羧化酶-1 (ACC1)的抑制而导致的新生牛奶脂合成受损以及肥胖母牛产生低脂牛奶联系起来。本提案的总体目标是利用肥胖小鼠模型结合创新的遗传操作和定量代谢和成像方法:(1)确定母亲肥胖对后代肥胖易感性的影响;(2)详细阐述了乳FRM肥胖坝对新生儿代谢的影响;(3)确定ACC1和新生脂肪生成在牛奶中促进新生儿肥胖的肥胖相关改变中的作用。本研究对产妇肥胖对新生儿代谢健康影响的生理和分子机制进行了详细系统的研究,为制定预防肥胖的新干预策略奠定了基础。
英文摘要
DESCRIPTION (provided by applicant): Maternal obesity increases the risk for offspring to become obese, and there is substantial evidence to suggest that programming during both fetal and neonatal development contributes to this predisposition. Breastfeeding, the recognized "gold standard" for human neonatal nutrition, is associated with reduced childhood obesity risk. However, emerging evidence from human and animal studies suggests that maternal obesity may override the benefits of breastfeeding on the metabolic health and obesity risk of nursing offspring. Our study is directed at understanding the mechanisms by which maternal obesity influences the metabolic predisposition of their off-spring to obesity. We established a mouse model that allows us to define postnatal contributions of maternal obesity to neonatal metabolic health and obesity predisposition, distinguishing the specific effects of maternal obesity from those imparted by maternal consumption of a high fat (HF) obesigenic diet. Our data document that milk from obese dams selectively programs obesigenic changes in neonatal metabolism. In recent work we linked these changes to impaired de novo milk lipid synthesis due to inhibition of acetyl- CoA carboxylase-1 (ACC1), and the production of lipid-poor milk by obese dams. The overall goals of this proposal are to use obese mouse models in conjunction with innovative genetic manipulation and quantitative metabolic and imaging approaches to: (1) define the effects of maternal obesity on off-spring obesity predisposition; (2) detail the effects of milk frm obese dams on neonatal metabolism; (3) define the roles ACC1 and de novo lipogenesis in the obesity-associated alterations in milk that promote neonatal obesity. The detailed systematic investigation of the physiological and molecular mechanisms underlying postnatal effects of maternal obesity on neonatal metabolic health, as outlined in this proposal, form the foundation for development of new intervention strategies to prevent obesity.
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会议论文
Postnatal Actions of Maternal Obesity on Neonatal Metabolic Health
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批准号:8584601
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负责人:Paul S. Maclean
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依托单位:
Functional aspects of SREBP1c in intact skeletal muscle
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批准号:7235738
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财政年份:2005
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依托单位:
Functional aspects of SREBP1c in intact skeletal muscle
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Functional aspects of SREBP1c in intact skeletal muscle
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Functional aspects of SREBP1c in intact skeletal muscle
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依托单位:
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依托单位:
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资助金额:$116.63万
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资助金额:$116.63万
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海外基金