Integrated Regulation of Bile Acids and Diabetes

胆汁酸与糖尿病的综合调节

• 批准号: 7393086
• 负责人: Timothy F Osborne
• 金额: $ 27.86万
• 依托单位: UNIVERSITY OF CALIFORNIA-IRVINE
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-04-01 至 2010-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7393086
• 关键词: Accounting; Affect; Animal Model; Atherosclerosis; Bile Acid Biosynthesis Pathway; Bile Acids; Biliary calculi; Binding; Biological Assay; CYP7A1 gene; Cell membrane; Cholelithiasis; Cholesterol; Cholesterol 7-alpha-Monooxygenase; Cholesterol Homeostasis; Complications of Diabetes Mellitus; Cultured Cells; DNA; DNA Binding; DNA-Binding Proteins; Defect; Development; Diabetes Mellitus; Diabetic mouse; Disease; Disease susceptibility; Energy Metabolism; Enzymes; Fasting; Fatty acid glycerol esters; Feedback; Gene Expression; Gene Expression Regulation; Genes; Genetic; Glucose; Hepatic; Human; In Vitro; Insulin; Insulin-Dependent Diabetes Mellitus; Link; Liver; Malignant Neoplasms; Mediating; Metabolism; Modeling; Molecular; Monitor; Mus; Muscle; Nervous System Physiology; Non-Insulin-Dependent Diabetes Mellitus; Nutrient; Obesity; Orphan; Pathway interactions; Phenotype; Physiological; Population; Predisposition; Process; Proteins; Publications; Rate; Regulation; Research; Role; Route; Serum; Signal Transduction; Societies; Solutions; Staging; Streptozocin; System; Techniques; Testing; Tetanus Helper Peptide; Tetracycline; Tetracyclines; Transfection; Work; base; cell growth; chromatin immunoprecipitation; genetic manipulation; glucose metabolism; glucose production; insight; lipid metabolism; mouse model; novel; prevent; programs; promoter; protein protein interaction; receptor; response; size; small heterodimer partner protein; steroid hormone biosynthesis

DESCRIPTION (provided by applicant): Cholesterol is a critical nutrient that is required as a structural component of cell membranes and is a precursor in the biosynthesis of steroid hormones and bile acids. It is important that cholesterol levels are properly regulated because aberrant metabolism causes molecular defects in development and neurological function, and contributes to obesity, diabetes, atherosclerosis, and cancer. Thus, a fundamental understanding of cholesterol metabolism is key to mechanisms that underlie many of the major diseases of modern society. This proposal is focused on one aspect of the regulation of cholesterol, its conversion into bile acids. In preliminary studies, partly included in a recent publication, we have uncovered a novel role for the transcriptional co-activator PGC-1alpha in converting bile acids. PGC-1a is up-regulated during diabetes and fasting. A key role for PGC-1alpha in both diabetes and bile acid metabolism would provide a new link between cholesterol metabolism and diabetes. Our studies have shown that the gene for the rate controlling enzyme of the classic bile acid pathway, CYP7A1, is also up-regulated along with PGC-1alpha during fasting and in an animal model of type I diabetes. Our central hypothesis is that PGC-1alpha links bile acid metabolism with diabetes and we are evaluating the molecular mechanism for this association. Here, we plan to use both pharmacological and genetic manipulation to evaluate PGC-1alpha in regulation of CYP7A1 expression, bile acid metabolism, and hepatic glucose metabolism.

描述（由申请人提供）：胆固醇是细胞膜结构成分所必需的关键营养素，是类固醇激素和胆汁酸生物合成的前体。适当调节胆固醇水平很重要，因为异常代谢会导致发育和神经功能中的分子缺陷，并导致肥胖、糖尿病、动脉粥样硬化和癌症。因此，对胆固醇代谢的基本理解是现代社会许多主要疾病背后机制的关键。