Therapeutically Modified Gut Bacteria for Treatment of Obesity
Therapeutically Modified Gut Bacteria for Treatment of Obesity
批准号:
8656665
负责人:
SEAN Stephen DAVIES
金额:
$35.94万
依托单位:
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:
2013-05-01 至 2018-04-30
关键词:
AcyltransferaseAdherenceAdverse effectsAmericanAnimalsArabidopsisAwardBacteriaBehaviorBiochemicalBody CompositionBody Weight decreasedBody fatCaloriesCalorimetryCardiovascular DiseasesCellsCholecystokininConsumptionDataDiabetes MellitusDietDietary InterventionDiseaseEatingEffectivenessEnergy MetabolismEngineeringEnteroendocrine CellEscherichia coliExposure toFamilyFatty acid glycerol estersFeedbackFeeding behaviorsFoodFood EnergyGeneticHealthHormonesHumanHungerIndividualInflammationIntakeIntestinesLife StyleLipidsMeasuresMediatingMedicalMetabolic DiseasesMetabolismMethodsModelingMolecularMolecular Mechanisms of ActionMonitorMusMyocardial InfarctionNeuronsNeurosecretory SystemsObesityPPAR alphaPharmaceutical PreparationsPhosphatidylethanolaminePredispositionProbioticsProcessRegimenRewardsSatiationSignal TransductionSignaling MoleculeTestingTherapeuticTreatment ProtocolsUnited StatesUnited States National Institutes of HealthWeightWithholding Treatmentdrinking waterenergy balancefeedingfollow-upfood surveillanceglucagon-like peptide 1glucose monitorglucose tolerancegut microbiotaimprovednovel strategiesobesity treatmentpreventpublic health relevancereceptorresponsesuccesstreatment strategy
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Metabolic disorders including obesity, diabetes, and cardiovascular disease have become widespread in the United States. Unfortunately, adherence to effective medical and lifestyle treatment regimens for metabolic disorders is often poor as the result of poorly satisfying the hunger drive when limiting food calories and the labor intensiveness of food and glucose monitoring. Therefore, simple treatments strategies that do not require ignoring hunger drive or performing labor intensive monitoring and medication are vitally needed. Because gut microbiota composition has recently been shown to impact susceptibility to metabolic disease, we have pursued a novel strategy of genetically modifying the gut microbiota to secrete satiety factors. Because of the stability of gut bacteria, this stratgy may provide highly sustainable reductions in food intake without requiring treated individuals to ignore hunger drive or to perform labor intensive medication regimens. Our preliminary data demonstrate that when mice fed a high fat diet were administered E. coli Nissle 1917 modified to secrete N-acylphosphatidylethanolamine (NAPE), these mice were protected against obesity. Importantly, this protection against obesity was sustained for the 4 week follow-up period after stopping administration of the modified bacteria demonstrating that at least some level of stable colonization was achieved. These exciting results demonstrate the feasibility of this approach, but also raise important questions, the answers to which will help us understand whether this strategy could be used to treat human obesity. The aims of this proposal are: To determine the duration of protection afforded by treatment with NAPE secreting bacteria and if this will reverse already established obesity that arises both as the result of highly palatable diets or genetics. To determine the effect of the NAPE secreting bacteria on both short and long term neuronal processes regulating feeding behavior. To determine the molecular mechanism of action in the intestine of these NAPE secreting bacteria. If we successfully complete these studies, we will know if this strategy to remodel the gut microbiota is likely to \be successful i obese humans and we will have a better understanding of how gut microbiota interact with their host to regulate host metabolic processes.
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Lipid Peroxidation Analytical Core
-
批准号:10327713
-
项目类别:
-
资助金额:$24.65万
-
财政年份:2014
-
负责人:SEAN Stephen DAVIES
-
依托单位:
Modification of HDL and Macrophage Function in Atherosclerosis
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批准号:10544067
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项目类别:
-
资助金额:$36.48万
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财政年份:2014
-
负责人:SEAN Stephen DAVIES
-
依托单位:
Lipid Peroxidation Analytical Core
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批准号:10544053
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项目类别:
-
资助金额:$24.65万
-
财政年份:2014
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负责人:SEAN Stephen DAVIES
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依托单位:
Lipid Peroxidation Analytical Core
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批准号:10089338
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项目类别:
-
资助金额:$26.44万
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财政年份:2014
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负责人:SEAN Stephen DAVIES
-
依托单位:
Modification of HDL and Macrophage Function in Atherosclerosis
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批准号:10089343
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项目类别:
-
资助金额:$38.21万
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财政年份:2014
-
负责人:SEAN Stephen DAVIES
-
依托单位:
Modification of HDL and Macrophage Function in Atherosclerosis
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批准号:10327718
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项目类别:
-
资助金额:$36.48万
-
财政年份:2014
-
负责人:SEAN Stephen DAVIES
-
依托单位:
Therapeutically Modified Gut Bacteria for Treatment of Obesity
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批准号:8843716
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项目类别:
-
资助金额:$35.94万
-
财政年份:2013
-
负责人:SEAN Stephen DAVIES
-
依托单位:
Therapeutically Modified Gut Bacteria for Treatment of Obesity
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批准号:9042948
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项目类别:
-
资助金额:$37.05万
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财政年份:2013
-
负责人:SEAN Stephen DAVIES
-
依托单位:
Therapeutically Modified Gut Bacteria for Treatment of Obesity
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批准号:8481874
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项目类别:
-
资助金额:$37.05万
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财政年份:2013
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负责人:SEAN Stephen DAVIES
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依托单位:
Transformed Probiotic Bacteria for Treatment of Chronic Diseases
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批准号:7431222
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项目类别:
-
资助金额:$230.25万
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财政年份:2007
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负责人:SEAN Stephen DAVIES
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依托单位:
EFFECTS OF AGE ON THE RESPONSE TO OXIDATIVE STRESS
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批准号:7605577
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项目类别:
-
资助金额:$0.05万
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财政年份:2006
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负责人:SEAN Stephen DAVIES
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依托单位:
EFFECTS OF AGE ON THE RESPONSE TO OXIDATIVE STRESS
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批准号:7731402
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项目类别:
-
资助金额:$0.0万
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财政年份:2006
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负责人:SEAN Stephen DAVIES
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依托单位:
EFFECTS OF AGE ON THE RESPONSE TO OXIDATIVE STRESS
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批准号:7375655
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项目类别:
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资助金额:$0.84万
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财政年份:2005
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负责人:SEAN Stephen DAVIES
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依托单位:
EFFECTS OF AGE ON THE RESPONSE TO OXIDATIVE STRESS
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批准号:7207312
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项目类别:
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资助金额:$0.41万
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财政年份:2004
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负责人:SEAN Stephen DAVIES
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依托单位:
Chemical Synthesis and Lipid Peroxidation Analytical Core
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批准号:8852698
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项目类别:
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资助金额:$23.7万
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财政年份:--
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负责人:SEAN Stephen DAVIES
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依托单位:
Chemical Synthesis and Lipid Peroxidation Analytical Core
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批准号:8693117
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项目类别:
-
资助金额:$24.03万
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财政年份:--
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负责人:SEAN Stephen DAVIES
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依托单位:
Chemical Synthesis and Lipid Peroxidation Analytical Core
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批准号:9276739
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项目类别:
-
资助金额:$24.21万
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财政年份:--
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负责人:SEAN Stephen DAVIES
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依托单位:
海外基金