ROLE OF ENPP1 IN INSULIN RESISTANCE WITHOUT OBESITY

ENPP1 在无肥胖的胰岛素抵抗中的作用

• 批准号: 7606349
• 负责人: Nicola Abate
• 金额: $ 0.85万
• 依托单位: UT SOUTHWESTERN MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-04-01 至 2007-09-16
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7606349
• 关键词: Adipose tissue; Cardiovascular Diseases; Cell membrane; Computer Retrieval of Information on Scientific Projects Database; Data; Diabetes Mellitus; Disease; Epidemic; Funding; Gene Proteins; Genetic Polymorphism; Glucose; Glycoproteins; Grant; Individual; Institution; Insulin; Insulin Receptor; Insulin Resistance; Literature; Mediating; Metabolic; Metabolic syndrome; Muscle; Non obese; Non-Insulin-Dependent Diabetes Mellitus; Obesity; Pathogenesis; Peripheral; Persons; Population; Predisposition; Principal Investigator; Research; Research Personnel; Resources; Risk; Role; Skeletal system; Source; Testing; United States National Institutes of Health; cell type; ethnic minority population; gain of function; glucose disposal; insulin sensitivity; insulin signaling; intervention program; non-diabetic; prevent; protein expression

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The objective of this study is to evaluate the role of ENPP1 (also known as PC-1) in the pathogenesis of insulin resistance in non-obese persons. The effects of obesity on insulin resistance are of importance in the growing epidemic of the metabolic syndrome, type 2 diabetes and cardiovascular disease in the US population. However, it is recognized that groups of persons, often part of ethnic minorities of the US population, have excessive insulin resistance and risk for its associated metabolic complications, even without significant obesity. These individuals are more likely not to be captured in intervention programs to prevent diabetes and cardiobasculat disease. Although the role of ENPP1 in the pathogenesis of insulin resistance and prediction of type 2 diabetes is still controversial, both data available from the literature and preliminary data by the principal investigator support the possibility that it could be a determinant of insulin resistance even in absence of obesity. ENPP1 is a glycoprotein that is located in the plasma membrane of most cell types and interacts with the insulin receptor so to determine a reduction in insulin signaling when it is over-expressed. A common polymorphism, the K121Q, associates with a "gain of function" so that higher susceptibility to insulin resistance appears to be present in the 121Q carriers. The overall hypothesis of this study is that ENPP1 over-expression and K121Q polymorphism act synergistically in determining adipose tissue insulin resistance and defective systemic insulin-mediated glucose utilization, even in absence of obesity. To test this hypothesis we propose to take the approach of evaluating ENPP1 K121Q polymorphism and gene/protein expression in adipose tissue and skeletal muscle of non-diabetic and non-obese persons who will be carefully studied for adipose tissue insulin resistance and insulin sensitivity to peripheral glucose disposal.

该副本是利用众多研究子项目之一 由NIH/NCRR资助的中心赠款提供的资源。子弹和 调查员（PI）可能已经从其他NIH来源获得了主要资金， 因此可以在其他清晰的条目中代表。列出的机构是 对于中心，这不一定是调查员的机构。 这项研究的目的是评估ENPP1（也称为PC-1）在非肥胖者胰岛素抵抗发病机理中的作用。 肥胖对胰岛素抵抗的影响在美国人群中代谢综合征，2型糖尿病和心血管疾病的流行病中至关重要。 但是，人们认识到，即使没有明显的肥胖症，也经常是美国人口中少数族裔的一群人，对其相关代谢并发症具有过多的胰岛素抵抗和风险。 这些人更有可能在预防糖尿病和心脏疾病的干预计划中被捕获。 尽管ENPP1在胰岛素抵抗的发病机理中的作用和2型糖尿病的预测仍然是有争议的，但主要研究者的文献和初步数据可获得的数据，即使在肥胖症的情况下，也可能是胰岛素抵抗的可能性。 ENPP1是一种位于大多数细胞类型的质膜中的糖蛋白，并与胰岛素受体相互作用，因此确定胰岛素信号过表达时的降低。 K121Q是一种常见的多态性，它与“功能的增益”相关，因此在121Q载体中似乎存在更高的胰岛素抵抗易感性。 这项研究的总体假设是，即使在没有肥胖症的情况下，ENPP1过表达和K121Q多态性在确定脂肪组织胰岛素抵抗和有缺陷的全身性胰岛素介导的葡萄糖利用方面具有协同作用。 为了检验这一假设，我们建议采取评估脂肪组织中的ENPP1 K121Q多态性和基因/蛋白质表达的方法，这些方法将仔细研究非糖尿病和非肥胖者的非糖尿病和非肥胖者的骨骼肌肉，以确保脂肪组织的抗胰岛素耐药性和胰岛素抗胰岛素敏感性对外周的葡萄糖粘液糖性敏感性。