The objective of this research proposal is to define the relationship between defects at the level of adipose tissue and regulation of hepatic glucose production (HGP) in the pathophysiology of NIDDM. In order to accomplish these goals, studies will be carried out in normal individuals and in patients with NIDDM of varying degrees of severity. These subjects will be matched in terms of age, gender, degree of general obesity, regional fat distribution, and level of habitual physical activity. Plasma free fatty acid (FFA) concentration will be either decreased (nicotinic acid infusion) or increased (intralipid plus heparin infusion) and the resultant changes in plasma glucose concentration, hepatic glucose production, and glucose disposal will be quantified. These experiments will be performed in the presence of somatostatin, both in the absence and the presence of basal concentrations of glucagon, growth hormone, and insulin. The results of these experiments should provide considerable new information as to the pathophysiology of NIDDM, a disease which is responsible for considerable morbidity and mortality not just in the United States, but in the remainder of the world as well.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK030732-10
Application #
3229623
Study Section
Metabolism Study Section (MET)
Project Start
1983-01-01
Project End
1995-03-31
Budget Start
1993-04-01
Budget End
1994-03-31
Support Year
10
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Abbasi, Fahim; Chu, James W; McLaughlin, Tracey et al. (2004) Effect of metformin treatment on multiple cardiovascular disease risk factors in patients with type 2 diabetes mellitus. Metabolism 53:159-64
Chu, James W; Abbasi, Fahim; Beatty, George W et al. (2003) Methods for quantifying insulin resistance in human immunodeficiency virus-positive patients. Metabolism 52:858-61
McLaughlin, T; Abbasi, F; Lamendola, C et al. (2001) Metabolic changes following sibutramine-assisted weight loss in obese individuals: role of plasma free fatty acids in the insulin resistance of obesity. Metabolism 50:819-24
Santos, R F; Nomizo, R; Oliveira, E et al. (2000) Erythrocyte insulin receptor tyrosine kinase activity is increased in glyburide-treated patients with type 2 diabetes in good glycaemic control. Diabetes Obes Metab 2:237-41
Abbasi, F; McLaughlin, T; Lamendola, C et al. (2000) The relationship between glucose disposal in response to physiological hyperinsulinemia and basal glucose and free fatty acid concentrations in healthy volunteers. J Clin Endocrinol Metab 85:1251-4
Rosolova, H; Mayer Jr, O; Reaven, G M (2000) Insulin-mediated glucose disposal is decreased in normal subjects with relatively low plasma magnesium concentrations. Metabolism 49:418-20
Abbasi, F; McLaughlin, T; Lamendola, C et al. (2000) Insulin regulation of plasma free fatty acid concentrations is abnormal in healthy subjects with muscle insulin resistance. Metabolism 49:151-4
Chen, N G; Reaven, G M (1999) Fatty acid inhibition of glucose-stimulated insulin secretion is enhanced in pancreatic islets from insulin-resistant rats. Metabolism 48:1314-7
Abbasi, F; Carantoni, M; Chen, Y D et al. (1998) Further evidence for a central role of adipose tissue in the antihyperglycemic effect of metformin. Diabetes Care 21:1301-5
Maheux, P; Chen, Y D; Polonsky, K S et al. (1997) Evidence that insulin can directly inhibit hepatic glucose production. Diabetologia 40:1300-6

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