4310 Institute For Human Performance
505 Irving Ave.
Syracuse, NY 13210

315 464-9841

Current Appointments

• Professor of Medicine
• Professor of Pharmacology

Hospital Campus

• Downtown

Web Resources

• Linked In

Education & Fellowships

• PhD: University of Illinois College of Medicine at Chicago, 1984, Pharmacology
• BS: Cornell University, 1975, Physiology

Previous Appointments

• Harvard Medical School, 1990–1998
• New York University School of Medicine, 1998–2007
• Tufts University School of Medicine, 1984–1990

Web Resources

• Linked In

Publications

Link to PubMed (Opens new window. Close the PubMed window to return to this page.)

Research Abstract

Our laboratory is performing studies of the "Incretin Mimetics", a newly recognized class of blood glucose-lowering agents that stimulate pancreatic insulin secretion, and which are likely to be the next line of defense for the treatment of type 2 diabetes mellitus. Incretin mimetics mimic the action of GLP-1 (glucagon-like peptide-1), a naturally-occurring incretin hormone secreted by L-cells of the intestine, and which when administered to type 2 diabetic subjects, lowers concentrations of blood glucose.

Why are GLP-1 and the incretin mimetics of special interest? Perhaps most remarkable is the finding that the immediate blood glucose-lowering action of these compounds in type 2 diabetic subjects is self-terminating once normoglycemia is achieved. Thus, unlike administered insulin, there exists a natural safeguard such that these agents are less likely to produce hypoglycemia when they are adminstered for therapeutic purposes. One such incretin mimetic is Amylin Pharmaceutical's Byetta. It is an insulin secretagogue that is structurally-related to GLP-1, but unlike GLP-1 it exhibits an extended duration of action. Understanding how the beneficial "antidiabetogenic" actions of GLP-1 and Byetta are achieved is a primary focus of my research.