Circadian Clock Dysregulation in a Model of Obstructive Sleep Apnea
Circadian Clock Dysregulation in a Model of Obstructive Sleep Apnea
批准号:
10642895
负责人:
David F Smith
金额:
$16.35万
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:
2019-09-01 至 2024-06-30
关键词:
ATAC-seqAffectBiologyBlood PressureCardiopulmonaryCardiovascular systemCellsChIP-seqChildChromatinCircadian DysregulationCircadian gene expressionClock proteinCommunicationDNADataDependenceDevelopmentDiseaseDyslipidemiasEarly InterventionEventExposure toFive-Year PlansFunctional disorderGenomeHeartHeart DiseasesHypoxiaHypoxia Inducible FactorIndividualInflammatoryInjuryKnowledgeLinkLungLung diseasesMeasuresMedicineMetabolic dysfunctionModalityModelingMolecularMorbidity - disease rateMusNeurocognitiveObstructive Sleep ApneaOrganOutcomeOxidative StressOxygenPatientsPhasePhysiologicalPhysiological ProcessesPreventionProblem behaviorProcessPublishingRecoveryResearchRoleScientistSignal PathwaySleepSleep ArchitectureSortingStructure of parenchyma of lungSurgeonTestingTimeUp-RegulationWorkairway obstructionburden of illnesscandidate identificationcardiopulmonary systemcareer developmentcell typecircadiancircadian pacemakerendothelial dysfunctiongenome-wideinflammatory markerinnovationlaboratory experiencemalemolecular clockmouse modelnovel therapeuticsresponsesexsingle-cell RNA sequencingtargeted treatmenttranscription factortranscriptome sequencing
中文摘要
点击翻译按钮获取中文摘要
英文摘要
ABSTRACT
Obstructive sleep apnea (OSA) occurs in 4% of children in the US. OSA is characterized by
upper airway obstruction and intermittent hypoxia during sleep. Even in young children,
untreated OSA can lead to heart and lung conditions, metabolic dysfunction, and neurocognitive
problems. Without early intervention, these pathophysiologic changes may lead to a lifetime
burden of disease.
The disease processes associated with OSA are driven by upregulation of inflammatory
mechanisms, heightened oxidative stress, and endothelial dysfunction. Despite our
understanding of OSA and intermittent hypoxia, the upstream causal events remain poorly
characterized. An emerging hypothesis to explain other hypoxic-driven diseases is that low
oxygen levels reset the circadian clock. Hypoxia inducible factors (HIFs) are transcription factors
that are stabilized under low oxygen conditions to activate an array of physiologic processes.
These factors also communicate with the molecular clock at the genome level.
The link between hypoxia and the circadian clock may be an important, though
unexplored mechanism by which OSA leads to associated disease processes in the
cardiopulmonary system. I hypothesize that intermittent hypoxia results in circadian clock
dysregulation, resulting in molecular mechanisms that contribute to end-organ damage. I
will pursue this hypothesis by (1) determining the impact of circadian phase on physiologic
responses to intermittent hypoxia and recovery (IHR) as a model for OSA, (2) characterizing the
sex-dependency of IHR on mechanisms of end-organ damage, and (3) identifying specific
cardiopulmonary cell types that respond to IHR. Collectively, this work may enable new
management strategies and targeted therapies for OSA based on realignment of the circadian
clock.
In this proposal, I present a five-year plan for career development focused on didactic
coursework and hands-on laboratory experience. The research strategy and didactic work will
help me to become an independent surgeon-scientist, pursuing innovative discoveries in the
field of sleep medicine.
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DOI:
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发表时间:
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期刊:
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine
影响因子:
--
作者:
[Suurna,MariaV, Jacobowitz,Ofer, Chang,Jolie, Koutsourelakis,Ioannis, Smith,David, Alkan,Uri, D'Agostino,Mark, Boon,Maurits, Heiser,Clemens, Hoff,Paul, Huntley,Colin, Kent,David, Kominsky,Alan, Lewis,Richard, Maurer,JoachimT, Ravesloot,Ma]
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DOI:
10.1126/science.aax7621
发表时间:
2019-08-09
期刊:
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影响因子:
--
作者:
[Ruben MD, Smith DF, FitzGerald GA, Hogenesch JB]
通讯作者:
Hogenesch JB
DOI:
10.3390/genes12101627
发表时间:
2021-10-16
期刊:
Genes
影响因子:
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作者:
[Koritala BSC, Lee YY, Bhadri SS, Gaspar LS, Stanforth C, Wu G, Ruben MD, Francey LJ, Smith DF]
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Smith DF
Diurnal regulation of metabolism by Gs-alpha in hypothalamic QPLOT neurons.
下丘脑QPLOT神经元中GS-Alpha代谢的昼夜调节。
DOI:
10.1371/journal.pone.0284824
发表时间:
2023
期刊:
PLOS ONE
影响因子:
3.7
作者:
[Gaitonde, Kevin P., Andrabi, Mutahar, Burger, Courtney, D'Souza, Shane F., Vemaraju, Shruti A., Koritala, Bala S. C., Smith, David, Lang, Richard]
通讯作者:
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DOI:
10.1177/0194599820954383
发表时间:
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期刊:
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
影响因子:
--
作者:
[Sarber KM, von Allmen DC, Tikhtman R, Howard J, Simakajornboon N, Yu W, Smith DF, Ishman SL]
通讯作者:
Ishman SL
共 17 条
Circadian Clock Dysregulation in a Model of Obstructive Sleep Apnea
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批准号:10218268
-
项目类别:
-
资助金额:$16.36万
-
财政年份:2019
-
负责人:David F Smith
-
依托单位:
Circadian Clock Dysregulation in a Model of Obstructive Sleep Apnea
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批准号:10461776
-
项目类别:
-
资助金额:$16.35万
-
财政年份:2019
-
负责人:David F Smith
-
依托单位:
Circadian Clock Dysregulation in a Model of Obstructive Sleep Apnea
-
批准号:9805874
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项目类别:
-
资助金额:$16.36万
-
财政年份:2019
-
负责人:David F Smith
-
依托单位:
海外基金