In this study in normal subjects (n=20), we will examinethe dynamic relationship between the fatty acid acylated insulin, [LysB29-tetradecanoyl, des-(B30) human insulin], or NN304, and the rate of heptic gluclose production, measured directly with the artiovenous difference technique via heptatic vein catherization. We will also examine the potency (steady state action based upon gluclose turnover and suppression of non-esterified fatty acids) of NN304 in comparison to an equimolar intravenous continous infusion of native insulin (Novolin-R). We will directly determine the splanchic (hepatic) extraction of NN304, native insulin, and C-peptide by the liver via heptic vein catherization. Finally, we will determine to what extent any difference in potency between NN304 and human insulin can be explained by the hepatic extraction of NN304.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000043-40
Application #
6408235
Study Section
Special Emphasis Panel (ZRR1)
Project Start
1974-10-01
Project End
2002-11-30
Budget Start
Budget End
Support Year
40
Fiscal Year
2000
Total Cost
Indirect Cost
Name
University of Southern California
Department
Type
DUNS #
041544081
City
Los Angeles
State
CA
Country
United States
Zip Code
90033
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