Resistance Training Modulation of Fat Metabolism in Obese Postmenopausal Women
抗阻训练对肥胖绝经后妇女脂肪代谢的调节
基本信息
- 批准号:10383752
- 负责人:
- 金额:$ 60.97万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-05-01 至 2026-04-30
- 项目状态:未结题
- 来源:
- 关键词:AbdomenAcuteAdipocytesAdipose tissueAdrenergic AgentsAffectAge-YearsAreaBody CompositionBody WeightBody fatCaloriesCardiometabolic DiseaseCatecholaminesChronicClosure by clampDataDiseaseEffectivenessEnergy MetabolismEnvironmental Risk FactorEquilibriumExerciseFatty acid glycerol estersFutureGlucoseGlucose ClampGlycerolGoalsHealthHeart AtriumHourImpairmentIndirect CalorimetryIndividualInsulinInsulin ResistanceInvestigationKnowledgeLaboratoriesLinkLipolysisMeasuresMediatingMenopauseMetabolic DiseasesMetabolic syndromeMetabolismMethodologyMicrodialysisMonitorMuscleNon obeseNon-Insulin-Dependent Diabetes MellitusObesityPalmitatesParticipantPathway interactionsPersonsPhentolaminePhysical activityPlayPostmenopausePrediabetes syndromePropranololProteinsPublishingRegulationReportingResistanceRestRiskRoleSkeletal MuscleSomatotropinStimulusSystemTestingThigh structureTrainingTraining ProgramsWalkingWaterWeightWeight GainWeight maintenance regimenWomanbehavior measurementbeta-adrenergic receptorblood glucose regulationcomorbiditydisorder riskendurance exerciseevidence baseexercise prescriptionexercise trainingexperimental studyflexibilityglycemic controlimprovedin vivolipid biosynthesislipid metabolismmalemenmode of exerciseobese personoxidationpreventresistance exerciseresponsesalureticstable isotopestrength trainingsubcutaneousweight maintenance
项目摘要
Project Summary
Prediabetes, a comorbidity of obesity and a precursor of type 2 diabetes, affects more than one-half of women over
60 years of age. Obesity has multiple causes; however, it is known that obese insulin resistant individuals have a
reduced ability to alter resting and stimulated lipolysis (fat breakdown). This lack of flexibility to respond to stimuli
that regulate lipolysis has been attributed, almost entirely through studies in males, to changes in the predominant
(catecholamine-mediated) lipolytic pathway. Our published preliminary data demonstrate that acute resistance
exercise increases lipolysis in non-obese women. Published data also indicate that resistance exercise, like
endurance exercise, increases lipolytic sensitivity in men. However, the alterations in lipolytic response due to
resistance, as compared to endurance, training matched for energy expenditure have not been investigated. It is
also unknown how training alters lipolysis during general physical activity (walking), which accounts for the majority
of activity people engage in during a typical day outside of planned exercise. Furthermore, the lack of prior
investigations in this area in women points to the need for resistance training studies of fat metabolism in women
to determine if resistance training is as effective as endurance training. Therefore, the overall objective of this
study is to compare the effects of 12 weeks of resistance training to endurance training with respect to fat
metabolism, with a focus on lipolysis in postmenopausal women with obesity and prediabetes. Our central
hypothesis is that both 12 weeks of resistance training and 12 weeks of endurance training will increase lipolytic
flexibility. We will compare the effects of endurance training to the effects imparted by calorie-matched endurance
exercise training. We will determine with powerful in-vivo microdialysis and stable isotope methodologies the extent
to which 12 weeks of resistance training, as compared to calorie-matched endurance training: a) increases physical
activity (walking)-stimulated whole-body and regional lipolysis (Aim 1); b) increases local adrenergic regulation of
lipolysis in subcutaneous abdominal and gluteal adipose tissue (Aim 2); and c) increases insulin-mediated
suppression of whole-body and regional lipolysis (Aim 3) in postmenopausal women with obesity and prediabetes.
Secondarily, fat oxidation, lipogenesis and adipogenesis in adipose tissue, as well as lipolytic activity in skeletal
muscle, will also be studied to develop a global understanding of fat metabolism response to resistance exercise
training. In addition, we will investigate the influence of resistance and endurance training on glucose profile under
laboratory as well as free-living conditions, as poor glucose control is linked to the aberrant lipid metabolism
commonly associated with obesity. These studies will provide a greater understanding of how these exercise
modalities affect metabolism in women with obesity and prediabetes, allowing practitioners to make more evidence-
based exercise prescriptions intended to improve body composition, glycemic control, and weight management.
项目摘要
糖尿病前期是肥胖的一种共病,也是2型糖尿病的先兆,超过一半的女性会受到影响。
60岁。肥胖有多种原因;然而,众所周知,肥胖的胰岛素抵抗者有一个
改变休息和刺激脂肪分解的能力降低(脂肪分解)。这种对刺激缺乏反应的灵活性
几乎完全通过对男性的研究,这种调节脂肪分解的作用被归因于主要的
(儿茶酚胺介导的)脂解途径。我们公布的初步数据表明,急性耐药
运动会增加非肥胖女性的脂肪分解。公布的数据还表明,抵抗力练习,如
耐力运动,增加男性对脂类的敏感性。然而,脂解反应的改变是由于
与耐力相比,耐力与能量消耗相匹配的训练尚未得到调查。它是
也不知道训练如何改变一般体力活动(步行)中的脂肪分解,这是主要的
人们在计划的锻炼之外的典型一天中进行的活动。此外,缺乏事前
在妇女这一领域的调查表明,有必要对妇女的脂肪代谢进行抵抗训练研究。
以确定阻力训练是否与耐力训练一样有效。因此,这一总体目标是
研究是比较12周抗阻训练和耐力训练对脂肪的影响
代谢,重点是肥胖症和糖尿病前期绝经后妇女的脂肪分解。我们的中央
假设是12周的抗阻训练和12周的耐力训练都会增加脂解作用
灵活性。我们将比较耐力训练的效果和卡路里匹配耐力所带来的效果
运动训练。我们将用强大的体内微透析和稳定同位素方法来确定
与卡路里匹配的耐力训练相比,12周的耐力训练:a)增加了体能
活动(步行)刺激的全身和局部脂肪分解(目标1);b)增加局部肾上腺素能调节
腹部和臀部皮下脂肪组织的脂肪分解(目标2);以及c)增加胰岛素介导的
肥胖和糖尿病前期绝经后妇女的全身和局部脂肪分解抑制(目标3)。
其次,脂肪组织中的脂肪氧化、脂肪生成和脂肪生成以及骨骼中的脂解活性
肌肉,也将进行研究,以发展对抵抗运动的脂肪代谢反应的全球理解
训练。此外,我们还将研究耐力和耐力训练对血糖的影响。
实验室和自由生活条件,因为血糖控制不佳与脂肪代谢异常有关
通常与肥胖有关。这些研究将提供对这些练习如何进行更好的理解
治疗方式会影响患有肥胖症和糖尿病前期的女性的新陈代谢,从而使医生能够提出更多证据--
基于运动处方,旨在改善身体成分、血糖控制和体重管理。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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ROBERT C HICKNER其他文献
ROBERT C HICKNER的其他文献
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{{ truncateString('ROBERT C HICKNER', 18)}}的其他基金
Resistance Training Modulation of Fat Metabolism in Obese Postmenopausal Women
抗阻训练对肥胖绝经后妇女脂肪代谢的调节
- 批准号:
10211863 - 财政年份:2021
- 资助金额:
$ 60.97万 - 项目类别:
Resistance Training Modulation of Fat Metabolism in Obese Postmenopausal Women
抗阻训练对肥胖绝经后妇女脂肪代谢的调节
- 批准号:
10617221 - 财政年份:2021
- 资助金额:
$ 60.97万 - 项目类别:
NADPH Oxidase and Microvascular Dysfunction in Obesity
肥胖中的 NADPH 氧化酶和微血管功能障碍
- 批准号:
8434433 - 财政年份:2013
- 资助金额:
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Reduction in CVD risk in children by physical activity
通过体力活动降低儿童心血管疾病风险
- 批准号:
7626363 - 财政年份:2006
- 资助金额:
$ 60.97万 - 项目类别:
Reduction in CVD risk in children by physical activity
通过体力活动降低儿童心血管疾病风险
- 批准号:
7214827 - 财政年份:2006
- 资助金额:
$ 60.97万 - 项目类别:
Regulation of lipolysis by nitric oxide and adenosine
一氧化氮和腺苷调节脂肪分解
- 批准号:
7072473 - 财政年份:2006
- 资助金额:
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Reduction in CVD risk in children by physical activity
通过体力活动降低儿童心血管疾病风险
- 批准号:
7026895 - 财政年份:2006
- 资助金额:
$ 60.97万 - 项目类别:
Reduction in CVD risk in children by physical activity
通过体力活动降低儿童心血管疾病风险
- 批准号:
7425088 - 财政年份:2006
- 资助金额:
$ 60.97万 - 项目类别:
Exercise, muscle nutritive blood flow and eNOS in aging
衰老过程中的运动、肌肉营养性血流和 eNOS
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6544416 - 财政年份:2002
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Exercise, muscle nutritive blood flow and eNOS in aging
衰老过程中的运动、肌肉营养性血流和 eNOS
- 批准号:
6649673 - 财政年份:2002
- 资助金额:
$ 60.97万 - 项目类别:
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