Department of Internal Medicine

Endocrine-Metabolism Faculty


Robert Bar photo

Medical School:
Ohio State University

Residency:
Pennsylvania Hospital

Fellowship:
Ohio State University

Special Training:
Staff Fellow, Diabetes Branch,
National Institute of Arthritis
and Metabolic Diseases, NIH

Robert S. Bar, M.D.
Professor Emeritus
Director, Iowa Diabetes-Endocrinology Research Center
Director, VA/JDF Diabetes Research Center

Dr. Bar's research interests focus on the interactions of vascular endothelium with the insulin-like growth factors (IGFs) and their binding proteins (IGFBPs). Of the six IGFBPs, IGFBP-3 is of particular interest since IGFBP-3 is present in the highest concentration in the circulation, is synthesized and secreted by endothelial cells in vitro and in vivo, specifically adheres to endothelial cells and potentially can be degraded into bioactive fragments at the endothelial cell surface. It has recently been demonstrated that IGFBP-3 can be digested by plasmin thrombin and pregnancy serum into fragments with different properties than IGFBP-3, including potent intrinsic bioactivity. Studies are designed to determine the effects of specific IGFBP-3 fragments on IGF-I function and, in separate studies, assess the regulation of the IGFBP-3 gene in endothelial cells. Four model systems will be utilized, cultured endothelial cells, vascular rings, perfused organ preparations (rat heart and rat kidney) and the intact rat. Therapy with IGF-I and IGF-I/IGFBP complexes are presently being tested in clinical conditions ranging from diabetes mellitus to states of malnutrition. It is hoped that results of these studies will indicate methods to both selectively target and maximize specific IGF-I bioactivities.

Honors, Awards, and Organizations

Representative Publications

  1. Mazerbourg, S., Zapf, J., Bar, R.S., Brigstock, D.R., Lalou, C., Binoux, M., and Monget, P.: Insulin-like Growth Factor Binding Protein-4 Proteolytic Degradation in Ovine Preovulatory Follicles: Studies of Underlying Mechanisms. Endocrinology, 140:4175-4184, 1999.
  2. Oltman, C.L., Kane, N.L., Gutterman, D.D., Bar, R.S., and Dellsperger, K.C.: Mechanism of Coronary Vasodilation to Insulin and Insulin-like Growth Factor - 1 is Dependent on Vessel Size. American Journal of Physiology, 279:E176-E181, 2000.
  3. Booth, B.A., Boes, M., Dake, B.L., Caldwell, E.E.O., Weiler, J.M., and Bar, R.S.: Effect of IGFBP-derived Peptides on Incorporation of 35 SO 4 into Proteoglycans. Growth Hormone and IGF Research, 10:224-229, 2000.

PubMed publications list

Links of Interest

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