Mechanisms linking the adipogenic phenotype of aging muscle to insulin resistance

衰老肌肉的脂肪形成表型与胰岛素抵抗之间的联系机制

• 批准号: 7907198
• 负责人: DEBORAH M MUOIO
• 金额: $ 15.21万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-09-15 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7907198
• 关键词: Adenoviruses; Adipocytes; Adipose tissue; Adverse effects; Aerobic; Aerobic Exercise; Age; Aging; Biochemical; Biological Assay; Cardiology; Carnitine; Ceramides; Chronic; Citric Acid Cycle; Clinical; Coculture Techniques; Data; Data Set; Deposition; Development; Diabetes Mellitus; Diet; Dimensions; Dyslipidemias; Educational Intervention; Esters; Event; Exercise; Fasting; Fatty Acids; Fatty acid glycerol esters; Functional disorder; Gender; Gene Expression; Genetic Engineering; Glucose Intolerance; Glycogen; Goals; Health; Homeostasis; Human; Hyperglycemia; Hyperinsulinism; Impairment; In Vitro; Infiltration; Insulin; Insulin Resistance; Interdisciplinary Study; Intramuscular; Investigation; Link; Lipids; Lower Extremity; Mass Spectrum Analysis; Metabolic; Metabolic syndrome; Metabolism; Mitochondria; Modality; Modeling; Molecular; Morbidity - disease rate; Muscle; Muscle Cells; Muscle Mitochondria; Musculoskeletal System; Obesity; Organelles; Outcome; Overnutrition; Oxidative Stress; Oxygen saturation measurement; Pathology; Performance; Phenotype; Physical activity; Physiological; Physiology; Principal Investigator; Recombinants; Regulation; Research; Respiration; Rodent; Sampling; Scanning; Series; Signal Transduction; Skeletal Muscle; Specimen; Staining method; Stains; Stress; Symptoms; System; Testing; Thigh structure; Time; Tissues; Training; Translating; Universities; Visceral; X-Ray Computed Tomography; acylcarnitine; age related; aged; base; blood glucose regulation; body system; combat; coping; fatty acid oxidation; feeding; functional outcomes; glucose metabolism; in vitro Model; in vivo; insight; insulin sensitivity; intravenous glucose tolerance test; lipid biosynthesis; lipid mediator; mimetics; muscle aging; muscle metabolism; novel; nutrition; oil red O; organic acid; oxidation; prevent; programs; research study; respiratory; response; skeletal; strength training; subcutaneous

DESCRIPTION (provided by applicant): In response to RFA-AG-06-003, this application proposes to investigate mechanisms that link the adipogenic phenotype of aging muscle to the development of insulin resistance. Based on our preliminary data, we hypothesize that increased perimuscular adipogenesis contributes to insulin resistance via mechanisms that link directly to fatty acid-induced mitochondrial stress. We have therefore proposed studies to determine how lipid deposits within and between skeletal myofibers impact mitochondrial performance, insulin sensitivity and the interplay between these two functional endpoints. We further hypothesize that habitual exercise combats the adverse effects of lipid infiltration by remodeling muscle mitochondria in manner that enables these organelles to better cope with a high lipid load. These hypotheses will be tested using a two-pronged approach that applies comprehensive mass-spectrometry (MS) based metabolic profiling strategies to both in vitro and in vivo studies of human muscle. First, our plan will employ a newly developed human adipocyte-myocyte co-culture system to investigate i) the impact of adipocytes on the metabolic function of neighboring myocytes; and ii) the underlying mechanisms that link increasing adipogenesis to impaired insulin action. We predict that lipid-induced mitochondrial stress will emerge as a primary event that connects adipogenic burden to impaired glucose homeostasis, and moreover, that this event might be exacerbated in myocytes from aged compared to young donors. Second, using existing data/specimens from the STRRIDE study we will translate findings from our in vitro model to human physiology. To this end, we will examine how lipid infiltration of muscle (both intramuscular and perimuscular) relates to both insulin sensitivity and metabolic/transcriptional markers of mitochondrial performance, in the context of an exercise training intervention. These goals will be accomplished by a multidisciplinary research team from the Duke University Stedman Nutrition and Metabolism Center. Completion of the aims of this study will not only provide mechanistic information about the relationship between lipid stores in and around skeletal muscle and whole body insulin action - a major determinant of morbidity related to obesity, diabetes and aging - but will also provide insight into the most efficacious exercise prescription for preventing and correcting deficient skeletal muscle insulin action in these conditions.

描述(由申请人提供)：作为对RFA-AG-06-003的响应，本申请建议研究衰老肌肉的成脂表型与胰岛素抵抗发展之间的联系。根据我们的初步数据，我们假设肌肉周围脂肪生成增加通过与脂肪酸诱导的线粒体应激直接相关的机制来促进胰岛素抵抗。因此，我们建议进行研究，以确定骨骼肌纤维内部和之间的脂肪沉积如何影响线粒体性能、胰岛素敏感性以及这两个功能终点之间的相互作用。我们进一步假设，习惯性运动通过重塑肌肉线粒体的方式对抗脂质渗透的不利影响，使这些细胞器能够更好地应对高脂负荷。这些假设将通过双管齐下的方法进行验证，该方法将基于全面的质谱学(MS)的代谢谱策略应用于人体肌肉的体外和体内研究。首先，我们的计划将使用一种新开发的人类脂肪细胞-心肌细胞共培养系统来研究i)脂肪细胞对邻近心肌细胞代谢功能的影响；ii)将增加脂肪生成与胰岛素作用受损联系起来的潜在机制。我们预测，脂质诱导的线粒体应激将成为将成脂负担与受损的葡萄糖稳态联系起来的主要事件，而且，与年轻捐赠者相比，这一事件在老年心肌细胞中可能会加剧。其次，利用STRRIDE研究的现有数据/样本，我们将把我们体外模型的发现转化为人类生理学。为此，我们将在运动训练干预的背景下，研究肌肉(肌肉内和肌周)的脂质渗透与胰岛素敏感性和线粒体性能的代谢/转录标记物之间的关系。这些目标将由杜克大学斯特德曼营养和新陈代谢中心的多学科研究团队来实现。完成这项研究的目的不仅将提供有关骨骼肌内和周围的脂肪储存与全身胰岛素作用之间的关系的机械信息--与肥胖、糖尿病和衰老相关的发病率的主要决定因素--而且还将为预防和纠正这些情况下骨骼肌胰岛素作用不足的最有效的运动处方提供洞察。