Elliot S. Vesell
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Academic title Evan Pugh Professor of Pharmacology, and Professor of Medicine
College College of Medicine
Campuses Penn State Milton S. Hershey Medical Center
Department Pharmacology
Joint departments Medicine
Graduate programs Genetics
Pharmacology
Email Phone
  esv1@psu.edu
  717 531 8285
 
Educational background
  M.D., Harvard Medical School, 1959
Sc.D., Philadelphia College of Pharmacy and Science, 1988 (honorary)
Research Associate and Assistant Physician, Rockefeller University, 1960-1962; National Institute of Arthritis and Metabolic Diseases, NIH 1963-1965
Research interests
 

Drug Metabolism; Drug Disposition; Development of New Drugs; Pharmacogenetics; Host Factors that Influence Drug Metabolism and Disposition

Dr. Vesell's research interests include fundamental aspects of drug action from the molecular to the clinical. He has identified specific host factors, both genetic and environmental, that cause large variations in drug response. He has developed new methodology to facilitate such investigations, including several model drugs now widely used for this purpose. In addition, he has worked to develop a new drug, pyrazinoylguanidine (PZG), for the treatment of hypertensive diabetic patients. This drug has remarkable properties. It corrects fundamental metabolic abnormalities of diabetes mellitus by decreasing blood concentrations of glucose, free fatty acids and cholesterol, thereby enhancing the insulin mediated passage of glucose across cell membranes.

Graphic
  Graphic
  A. Concentration-dependent reduction by PZG of isoproterenol-stimulated cyclic AMP concentrations in isolated rat adipocytes. Adipocyte suspensions were incubated for 5 min at 37�C with incremental concentrations of PG in the presence of 1mmol/l isoproterenol. The results are expressed as percentage of maximal response determined in the absence of PZG. B. Concentration-dependent reduction by PZG of forskolin-stimulated cyclic AMP concentrations in isolated rat adipocytes. Adipocyte suspensions were incubated for 5 min at 37�C with incremental concentrations of PZG in the presence of 1 mmol/l forskolin. The results are expressed as percentage of maximal response determined in the absence of PZG. (from Pharmacology 53:197-210, 1997)
Areas of expertise
 
PharmacogeneticsPharmacokinetics
PharmacologyGenetics
GenomicsPharmacology, Clinical
MetabolismBiotransformation
Aryl Hydrocarbon HydroxylasesOrgan Size
Ethylmorphine-N-DemethylaseMicrosomes, Liver
Aniline HydroxylaseOxidoreductases, N-Demethylating
Cytochrome P-450 Enzyme SystemLiver
Dietary CarbohydratesGlucose
Fructose
Publication author name
  Vesell ES
Select publications
  Vesell ES. Advances in pharmacogenetics and pharmacogenomics. 2000 Sep. J Clin Pharmacol. 40(9):930-8.
A-Rahim YI. Beyer KH. Vesell ES. Studies on pyrazinoylguanidine. 3. Downregulation of lipolysis in isolated adipocytes. 1996 Oct. Pharmacology. 53(4):197-210.
A-Rahim YI. Rannels SL. Kimball SR. Beyer KH. Vesell ES. Studies on pyrazinoylguanidine. 4. Upregulation of phosphodiesterase activity in rat adipose tissue and downregulation of gluconeogenesis and adenosine 3',5'-monophosphate concentrations in perfused rat liver. 1996 Oct. Pharmacology. 53(4):211-8.
Follansbee MH. Beyer KH. Griffith JW. Vesell ES. Studies on pyrazinoylguanidine. 5. Temporal effects over 24 weeks demonstrating attenuation of diabetic nephropathy in STZ-diabetic rats. 1997 May. Pharmacology. 54(5):241-55.
Follansbee MH. Beyer KH. Vesell ES. Studies on pyrazinoylguanidine. 6. Prevention of cataracts in STZ-diabetic rats. 1997 May. Pharmacology. 54(5):256-60.

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