Use of insulin sensitizers to offset skeletal muscle dysfunction during immobility
使用胰岛素增敏剂来抵消不动期间的骨骼肌功能障碍
基本信息
- 批准号:9805099
- 负责人:
- 金额:$ 22.88万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-08-01 至 2022-04-30
- 项目状态:已结题
- 来源:
- 关键词:AcuteAdultAgeAnabolismAttenuatedBed OccupancyBed restCeramidesCharacteristicsClinical ResearchDataDevelopmentDiseaseDistressDoseElderlyEnzymesEventFoundationsFunctional disorderGenetic TranscriptionGoalsGrantGrowthHealthHindlimb SuspensionHospitalizationImmobilizationImpairmentInflammationInflammatoryInjuryInsulinInterventionLegLinkLipidsMetforminMusMuscleMuscle CellsMuscle FibersMuscle WeaknessMuscle functionMuscular AtrophyNon-Insulin-Dependent Diabetes MellitusOperative Surgical ProceduresOralPathway interactionsPatientsPharmaceutical PreparationsPharmacologyPhysical FunctionPhysical activityPlacebosPopulationPrevention strategyPreventive therapyRandomizedRecoveryRiskRodentSignal TransductionSkeletal MuscleTestingThigh structureTimeTissuesUp-Regulationanti agingattenuationbasecell growthcost effectivecytokinegastrointestinalimprovedinsulin sensitivityinsulin sensitizing drugsmuscle formmuscle strengthnovelnovel therapeutic interventionphysical inactivityphysical modelpreservationpreventsarcopeniasedentary lifestyleside effectskeletal muscle wasting
项目摘要
Abstract
Hospitalizations for disease, injury, and/or surgery in older adults are likely to impair physical mobility and,
therefore, the older adults capacity to be physically active both during hospitalization and beyond. The resulting
sedentary lifestyle is likely to be accepted as the new normal, ultimately increasing the risk of skeletal muscle
dysfunction (e.g. sarcopenia).
Muscle atrophy and loss in strength is an unfortunate consequence with disuse in older adults. We have
observed with our bed rest studies in healthy older adults that in addition to muscle and strength changes,
there is a substantial increase in skeletal muscle inflammation and an upregulation of enzymes related to de
novo ceramide biosynthesis. The accumulation of local inflammation and ceramide, a toxic lipid intermediate,
can impair muscle growth. Metformin treatment may attenuate muscle loss by blunting inflammatory pathways
and ceramide accumulation. Though metformin has traditionally served as an insulin sensitizer, its use as a
preventive strategy to maintain muscle health during a period of physical inactivity in older adults has not been
investigated.
Therefore, we have proposed to conduct a clinical study in older adults to test whether metformin treatment
during bed rest will attenuate muscle atrophy, weakness and muscle inflammatory mechanisms. These
findings will be foundational in the development of novel treatments, such as metformin, to prevent muscle
dysfunction in older adults during disuse periods.!
摘要
老年人因疾病、受伤和/或手术而住院可能会损害身体活动能力,
因此,老年人在住院期间和住院后都有能力进行体育活动。由此产生的
久坐的生活方式可能会被接受为新的常态,最终增加骨骼肌的风险
功能障碍(如骨质疏松症)。
肌肉萎缩和力量丧失是老年人不使用运动的不幸后果。我们有
通过我们对健康老年人的卧床休息研究观察到,除了肌肉和力量的变化外,
骨骼肌炎症显著增加,与De相关的酶上调。
新神经酰胺生物合成。局部炎症和神经酰胺的积累,神经酰胺是一种有毒的脂质中间体,
会损害肌肉的生长。二甲双胍治疗可能通过钝化炎症途径来减轻肌肉损失
和神经酰胺的积累。虽然二甲双胍传统上是胰岛素增敏剂,但它的用途是
在老年人缺乏运动期间保持肌肉健康的预防性策略尚未得到
调查过了。
因此,我们建议在老年人中进行一项临床研究,以测试二甲双胍治疗
卧床休息会减轻肌肉萎缩、虚弱和肌肉发炎的机制。这些
这些发现将为开发新的治疗方法奠定基础,例如二甲双胍,以防止肌肉
老年人在停用期间的功能障碍。
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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Micah J Drummond其他文献
Micah J Drummond的其他文献
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{{ truncateString('Micah J Drummond', 18)}}的其他基金
MicroRNA regulation of chronic inflammation during aging
MicroRNA对衰老过程中慢性炎症的调节
- 批准号:
10817445 - 财政年份:2022
- 资助金额:
$ 22.88万 - 项目类别:
Regulation of macrophage metabolism in aged muscle during recovery
衰老肌肉恢复过程中巨噬细胞代谢的调节
- 批准号:
10622569 - 财政年份:2022
- 资助金额:
$ 22.88万 - 项目类别:
Regulation of macrophage metabolism in aged muscle during recovery
衰老肌肉恢复过程中巨噬细胞代谢的调节
- 批准号:
10460028 - 财政年份:2022
- 资助金额:
$ 22.88万 - 项目类别:
MicroRNA regulation of chronic inflammation during aging
MicroRNA对衰老过程中慢性炎症的调节
- 批准号:
10531053 - 财政年份:2022
- 资助金额:
$ 22.88万 - 项目类别:
Targeting macrophage polarization to optimize muscle regrowth from disuse atrophy
靶向巨噬细胞极化以优化废用性萎缩的肌肉再生
- 批准号:
10228828 - 财政年份:2020
- 资助金额:
$ 22.88万 - 项目类别:
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