Renal AT2 Receptors in Hypertension
Renal AT2 Receptors in Hypertension
批准号:
9460298
负责人:
ROBERT MUNSON CAREY
金额:
$56.66万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-04-01 至 2020-03-31
关键词:
5&apos-NucleotidaseAGTR2 geneAcuteAdultAffectAgonistAngiotensin IIAngiotensin IIIApicalBlood PressureBlood VesselsBradykininCell membraneCellsCessation of lifeChronicCyclic AMPCyclic GMPDefectDeltastabDependenceDiseaseDopamineEssential HypertensionExcretory functionFenoldopamFunctional disorderGoalsHeartHumanHypertensionImpairmentInbred SHR RatsInbred WKY RatsInfusion proceduresKidneyLaboratoriesLeadMeasurementMediatingMetabolismMicrotubulesMolecularNa(+)-K(+)-Exchanging ATPaseNatriuresisNitric OxidePathogenesisPeptidesPopulationProtein phosphataseProximal Kidney TubulesRattusReceptor ActivationReninRenin-Angiotensin SystemRisk FactorsRoleSignal PathwaySiteSodiumSodium ChlorideSprague-Dawley RatsSystemTechniquesTestingTransducersTransplantationWaterWestern Worldalanine aminopeptidasecGMP productiondisabilityhypertension preventionin vivomolecular targeted therapiesnew therapeutic targetnormotensiveprematurepreventpublic health relevancereceptorrecruitresponsesaluretic
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Angiotensin (Ang) II, the primary transducer peptide of the renin-Ang system (RAS), acts at two major receptors: type-1 (AT1R) and type-2 (AT2R). The majority of Ang II actions occur via AT1Rs, including antinatriuresis. Renal cross-transplantation studies have demonstrated that renal AT1Rs are both necessary and sufficient for the induction and sustainability of hypertension during Ang II infusion and that increased Na+ reabsorption in the renal proximal tubule (RPT) is the major determinant of this response. In contrast, the role of AT2Rs in the control of Na+ excretion and hypertension is less clearly defined. Recent studies from our laboratory have provided evidence for a major role of RPT AT2Rs in the inhibition of Na+ reabsorption. These studies have provided evidence that, instead of Ang II, des-aspartyl1-Ang II (Ang III) is the preferred AT2R agonist inducing natriuresis. Furthermore, we now have evidence for a defect in AT2R-mediated natriuresis in spontaneously hypertensive rats (SHR) that pre-dates the hypertension and is due, at least in part, to accelerated intrarenal Ang III metabolism. Overall, our results suggest that AT2R-induced natriruesis is defective and contributes to the pathogenesis of hypertension in SHR. The overall goal of this project is to elucidate the mechanisms of defective AT2R-mediated natriuresis in SHR. The project will focus on three specific aims: (1) To test the hypothesis that defective AT2R-mediated natriuresis is important in the pathogenesis of HT in SHR; (2) To test the hypothesis that impaired natriuresis in SHR is due to reduction of Ang III; and (3) To test the hypothesis that chronic AT2R activation can restore normal natriuresis and prevent HT in SHR. The project will apply a combination of state-of-the-art in vivo and cell and molecular techniques, including intrarenal Ang II and III measurements, to clarify the role of the AT2R in sodium excretion in hypertension. These studies will help define the pathophysiology of human primary hypertension, a disorder affecting one-quarter after adult population in the Western world.
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Renal AT2 Receptors in Hypertension
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批准号:10320944
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项目类别:
-
资助金额:$68.2万
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财政年份:2021
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负责人:ROBERT MUNSON CAREY
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依托单位:
Renal AT2 Receptors in Hypertension
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批准号:9249632
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项目类别:
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资助金额:$56.66万
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财政年份:2016
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负责人:ROBERT MUNSON CAREY
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依托单位:
D1, AT1 RECEPTORS IN HUMAN HYPERTENSION: SODIUM SENSITIVITY OF BLOOD PRESSURE
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批准号:8167153
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项目类别:
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资助金额:$1.6万
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财政年份:2010
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负责人:ROBERT MUNSON CAREY
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依托单位:
Renal AT2 Receptors in Hypertension
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批准号:7887245
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项目类别:
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资助金额:$44.88万
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财政年份:2010
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负责人:ROBERT MUNSON CAREY
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依托单位:
URINARY ANGIOTENSINOGEN EXCRETION IN NORMALS AND PATIENTS WITH TYPE II DM
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批准号:8167172
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项目类别:
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资助金额:$10.56万
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财政年份:2010
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负责人:ROBERT MUNSON CAREY
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依托单位:
Renal AT2 Receptors in Hypertension
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批准号:8242704
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项目类别:
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资助金额:$42.58万
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财政年份:2010
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负责人:ROBERT MUNSON CAREY
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依托单位:
Renal AT2 Receptors in Hypertension
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批准号:8441622
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项目类别:
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资助金额:$40.24万
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财政年份:2010
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负责人:ROBERT MUNSON CAREY
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依托单位:
Renal AT2 Receptors in Hypertension
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批准号:8058747
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项目类别:
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资助金额:$43.18万
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财政年份:2010
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负责人:ROBERT MUNSON CAREY
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依托单位:
Natriuretic mechanisms of AT2 receptors
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批准号:7894698
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项目类别:
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资助金额:$45.21万
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财政年份:2009
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负责人:ROBERT MUNSON CAREY
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依托单位:
CLINICAL TRIAL: EFFECT OF GENE VARIANTS ON DOPAMINE RECEPTOR NATRIURETIC RESPONS
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批准号:7951502
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项目类别:
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资助金额:$8.97万
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财政年份:2009
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负责人:ROBERT MUNSON CAREY
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依托单位:
D1, AT1 RECEPTORS IN HUMAN HYPERTENSION: SODIUM SENSITIVITY OF BLOOD PRESSURE
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批准号:7951466
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项目类别:
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资助金额:$25.64万
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财政年份:2009
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负责人:ROBERT MUNSON CAREY
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依托单位:
Natriuretic mechanisms of AT2 receptors
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批准号:7523729
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项目类别:
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资助金额:$44.48万
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财政年份:2009
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负责人:ROBERT MUNSON CAREY
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依托单位:
URINARY ANGIOTENSINOGEN EXCRETION IN NORMALS AND PATIENTS WITH TYPE II DM
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批准号:7951495
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项目类别:
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资助金额:$4.58万
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财政年份:2009
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负责人:ROBERT MUNSON CAREY
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依托单位:
CLINICAL TRIAL: EFFECT OF GENE VARIANTS ON DOPAMINE RECEPTOR NATRIURETIC RESPONS
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批准号:7718595
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项目类别:
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资助金额:$25.08万
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财政年份:2008
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负责人:ROBERT MUNSON CAREY
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依托单位:
D1, AT1 RECEPTORS IN HUMAN HYPERTENSION: SODIUM SENSITIVITY OF BLOOD PRESSURE
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批准号:7718548
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项目类别:
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资助金额:$48.78万
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财政年份:2008
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负责人:ROBERT MUNSON CAREY
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依托单位:
D1, AT1 RECEPTORS IN HUMAN HYPERTENSION: SODIUM SENSITIVITY OF BLOOD PRESSURE
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批准号:7606694
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项目类别:
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资助金额:$94.97万
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财政年份:2007
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负责人:ROBERT MUNSON CAREY
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依托单位:
PRESSURE NATRIURESIS MEDIATED BY EXTRACELLULAR cGMP
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批准号:7471463
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项目类别:
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资助金额:$42.52万
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财政年份:2005
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负责人:ROBERT MUNSON CAREY
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依托单位:
PRESSURE NATRIURESIS MEDIATED BY EXTRACELLULAR cGMP
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批准号:7103661
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项目类别:
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资助金额:$42.75万
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财政年份:2005
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负责人:ROBERT MUNSON CAREY
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依托单位:
D1, AT1 RECEPTORS IN HUMAN HYPERTENSION: SODIUM SENSITIVITY OF BLOOD PRESSURE
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批准号:7205516
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项目类别:
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资助金额:$4.81万
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财政年份:2005
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负责人:ROBERT MUNSON CAREY
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依托单位:
PRESSURE NATRIURESIS MEDIATED BY EXTRACELLULAR cGMP
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批准号:7261427
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项目类别:
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资助金额:$42.13万
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财政年份:2005
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负责人:ROBERT MUNSON CAREY
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依托单位:
国内基金
海外基金
鼠伤寒沙门菌5'-nucleotidase在致病过程中的作用机制研究
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批准号:--
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项目类别:--
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资助金额:50万元
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批准年份:2023
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负责人:廖成水
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依托单位: