The proposed research is a continuation of studies completed and in progress which are designed to evaluate insulin action in the liver in normal and altered metabolic states.
The specific aims are to further characterize insulin action in the liver with regard to the acute and chronic effects of insulin on lipoprotein synthesis and secretion and the role of insulin resistance in altering insulin action on these parameters. We will further explore the role of glucocorticoids in modulating insulin action in regard to glycogen synthesis and lipid and apo B synthesis and secretion. Additional studies will include and evaluation of phosphorylation events in insulin action with regard to the phosphorylation of apo B by acute and chronic changes in insulin levels in vitro and in vivo. The role of the insulin receptor in phosphorylation of apo B will also be evaluated. Finally, we will pursue ongoing studies to evaluate the mechanisms of insulin resistance in nonketotic streptozotocin-induced diabetes mellitus by testing the hypothesis that the insulin receptor kinase is under intracellular regulation and is not identical in all subcellular fractions. Methodologies to be employed included primary cultures of rat hepatocytes, subcellular fractionation of rat liver, affinity chromatography of the insulin receptor, insulin receptor autophosphorylation and tyrosine kinase activity, synthesis of lipid using 3H20 and 14C- acetate, net glycogen production, 35S-methionine incorporation into apo B, apo B mass measurements by radioimmunoassay, SDS PAGE, 32P incorporation into apo B using immunoprecipitation and SDS PAGE, phosphoamino acid analysis, HPLC, and lipid mass measurements by TLC. The proposed studies will improve our understanding of insulin mediated hepatic metabolism and the interrelationships between insulin and glucocorticoids with regard to lipid, glycogen, and apo B metabolism. In addition, the proposed studies of insulin action in normal and altered metabolic states will allow us to better define mechanisms of insulin action and the pathophysiology of a group of disorders characterized by insulin """"""""resistance"""""""". Because of the central role of the liver in lipoprotein production and metabolism and the importance of lipoproteins in the development of atherosclerosis in Type II diabetes, an improved understanding of insulin effects on lipoprotein synthesis and secretion will enable us to mechanistically approach the relationships between diabetes and atherosclerosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK020948-13
Application #
3226851
Study Section
Metabolism Study Section (MET)
Project Start
1978-09-15
Project End
1993-03-31
Budget Start
1991-04-01
Budget End
1992-03-31
Support Year
13
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Rochester
Department
Type
Schools of Dentistry
DUNS #
208469486
City
Rochester
State
NY
Country
United States
Zip Code
14627
Salhanick, A I; Schwartz, S I; Amatruda, J M (1991) Insulin inhibits apolipoprotein B secretion in isolated human hepatocytes. Metabolism 40:275-9
Jackson, T K; Salhanick, A I; Elovson, J et al. (1990) Insulin regulates apolipoprotein B turnover and phosphorylation in rat hepatocytes. J Clin Invest 86:1746-51
Salhanick, A I; Leighty, S J; Amatruda, J M (1989) Postreceptor regulation of insulin action in primary cultures of rat hepatocytes by oral hypoglycemic agents: effects of linogliride and chlorpropamide. Horm Metab Res 21:596-601
Salhanick, A I; Chang, C L; Amatruda, J M (1989) Hormone and substrate regulation of glycogen accumulation in primary cultures of rat hepatocytes. Biochem J 261:985-92
Salhanick, A I; Amatruda, J M (1988) Role of sialic acid in insulin action and the insulin resistance of diabetes mellitus. Am J Physiol 255:E173-9