Mechanisms for Altered Glucose Homeostasis During HAART

HAART 期间改变血糖稳态的机制

• 批准号: 7840812
• 负责人: PAUL W HRUZ
• 金额: $ 3.82万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-06-10 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7840812
• 关键词: Acute; Adipocytes; Adipose tissue; Animals; Antibodies; Antibody Affinity; Atazanavir; Binding; Binding Proteins; Binding Sites; Cardiac; Chronic; Co-Immunoprecipitations; Continuous Intravenous Infusion; Control Animal; Coupled; Deoxyglucose; Development; Diabetes Mellitus; Epitopes; Euglycemic Clamping; Fatty acid glycerol esters; Funding; GLUT 4 protein; GLUT4 gene; Glucose Clamp; Glucose Transporter; Goals; HIV Protease Inhibitors; Heart; Hepatic; Highly Active Antiretroviral Therapy; Indinavir; Individual; Insulin; Insulin Resistance; Knockout Mice; Label; Leptin; Mass Spectrum Analysis; Measures; Mediating; Metabolic; Metabolic syndrome; Mitochondria; Molecular; Molecular Target; Morbidity - disease rate; Muscle; Mutation; Nonesterified Fatty Acids; Nucleosides; Patients; Peptides; Peripheral; Pharmaceutical Preparations; Post-Translational Protein Processing; Production; Proteins; RNA; Radiolabeled; Rattus; Retinol Binding Proteins; Reverse Transcriptase Inhibitors; Ritonavir; Role; SLC2A1 gene; Serum; Skeletal Muscle; Stavudine; System; Time; Tissues; Toxic effect; Transgenic Mice; Transgenic Organisms; Western Blotting; Work; Xenopus oocyte; Zidovudine; abacavir; adiponectin; basal insulin; blood glucose regulation; functional loss; glucose disposal; glucose production; glucose transport; glucose uptake; intraperitoneal; mortality; prevent; radiotracer; research study; resistin; uptake

DESCRIPTION (provided by applicant): The long term goal of this project is to understand the molecular mechanisms responsible for altered glucose homeostasis during highly active antiretroviral therapy (HAART). The metabolic changes that occur in association with the use of HIV protease inhibitors (Pis) have significant potential for increasing cardiac- associated morbidity and mortality. The immediate objectives of this proposal are to determine the specific contribution of GLUT4 inhibition to altered glucose uptake into insulin responsive tissues, to elucidate the role of altered glucose transport in the development of changes in adiocytokine production, and to identify the precise molecular interactions that mediate PI binding to GLUT4. The role of GLUT4 in Pi-induced effects on peripheral glucose disposal will be studied by measuring radiolabeled 2-deoxyglucose uptake into cardiac, skeletal muscle and adipose tissue under basal and hyperinsulinemic euglycemic clamp conditions in wild-type and transgenic mice with specific deletion of GLUT4 from muscle or fat. Changes in leptin, adiponectin and resistin RNA and protein levels, peripheral glucose disposal, and hepatic glucose production will be determined following semi-acute exposure of control and GLUT4 null mice to Pis in the presence and absence of semi-chronic treatment with NRTIs. The structural features in GLUT4 that mediate HIV protease inhibitor binding and inactivation will be determined in primary and/or cultured rat adipocytes labeled with a photoactivatable peptide containing the GLUT4 inhibiting epitope zHFF coupled to the FLAG epitope. Modified proteins will be isolated using a FLAG antibody affinity column and identified by mass spectrometry. The ability of Pis to influence the binding of proteins known to interact with the GLUT4 carboxy terminus will also be investigated by Western blot analysis and co-immunoprecipitation experiments using factor specific antibodies. Mutations will be introduced into the identified GLUT4 PI binding site and the resulting functional effects on transport activity and PI sensitivity will be determined. Taken together, these studies will provide crucial information about the mechanism(s) by which Pis contribute to the development of insulin resistance and diabetes mellitus. This will greatly assist efforts to develop effective strategies for preventing and/or treating the metabolic changes that occur both in patients on HAART and in the wider context of HIV-negative individuals with features of the metabolic syndrome.

描述(由申请人提供)：该项目的长期目标是了解在高效抗逆转录病毒治疗(HAART)过程中导致葡萄糖稳态改变的分子机制。与使用HIV蛋白酶抑制剂(PI)相关的代谢变化具有显著增加心脏相关发病率和死亡率的潜力。这一建议的直接目的是确定GLUT4抑制对胰岛素反应组织葡萄糖摄取改变的具体贡献，阐明葡萄糖运输改变在脂肪细胞因子产生变化中的作用，并确定介导PI与GLUT4结合的确切分子相互作用。GLUT4在肌肉或脂肪中特异性缺失的野生型和转基因小鼠的基础和高胰岛素正常血糖钳夹条件下，将通过测量放射性标记的2-脱氧葡萄糖在心肌、骨骼肌和脂肪组织中的摄取量来研究GLUT4在PI诱导的外周葡萄糖处置中的作用。瘦素、脂联素和抵抗素RNA和蛋白质水平、外周葡萄糖处置和肝脏葡萄糖产生的变化将在对照组和GLUT4基因缺失的小鼠半急性暴露于Pis后确定，其中存在和不存在NRTIs的半慢性治疗。在原代和/或培养的大鼠脂肪细胞中，将确定介导HIV蛋白酶抑制剂结合和失活的GLUT4的结构特征，该细胞标记的光激活肽包含与FLAG表位偶联的GLUT4抑制表位zHFF。修饰后的蛋白质将使用FLAG抗体亲和柱进行分离，并通过质谱仪进行鉴定。Pis影响已知与GLUT4羧基末端相互作用的蛋白质的结合的能力也将通过蛋白质印迹分析和使用因子特异性抗体的免疫共沉淀实验来研究。突变将被引入到已鉴定的GLUT4PI结合位点，并将确定由此产生的对转运活性和PI敏感性的功能影响。综上所述，这些研究将提供有关Pis促进胰岛素抵抗和糖尿病发展的关键信息(S)。这将极大地有助于制定有效的战略，预防和/或治疗在接受HAART治疗的患者和具有代谢综合征特征的艾滋病毒阴性个人中发生的代谢变化。