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Stephen J. Gardell, PhD

Stephen J. Gardell , PhD

Senior Investigator

Translational Research

Stephen Gardell

Overview

Dr. Gardell received his Ph.D. in Biochemistry from Cornell University Graduate School of Medical Sciences (NY, NY). His post-doctoral training in Molecule Biology was done at the University of California, San Francisco (UCSF), where he helped pioneer the use of site-directed mutagenesis to probe enzyme catalytic mechanisms. Dr. Gardell next spent 22 years in the drug discovery divisions of several major pharmaceutical companies (Merck, Bayer, Wyeth). The disease areas that were the target of his research pursuits included thrombosis, congestive heart failure, atherosclerosis, obesity, diabetes and Alzheimer’s disease. In 2009, Dr. Gardell joined the Sanford Burnham Prebys Medical Research Institute (SBP) in Orlando, Florida where he investigated an enzyme, nicotinamide phosphoribosyltransferase (NAMPT), which is the rate-determining step in NAD+ biosynthesis. He and his colleagues discovered small molecule activators of NAMPT that raise intracellular NAD+ levels, an effect with potential utility for a wide variety of diseases and healthy aging. While at SBP, Dr. Gardell also established a network of diverse technology cores and helped to direct the research operation. In May 2018, Dr. Gardell joined the Translational Research Institute in Orlando, Florida as a Senior Investigator where he continues his drug discovery research on NAMPT. In addition, Dr. Gardell established a Metabolomics Core at the TRI-MD which is a powerful technology platform to measure metabolites which serve to elucidate disease pathophysiology and unveil promising disease biomarkers..

Articles

Genetic drivers of human plasma metabolites that determine mortality in heart failure patients with reduced ejection fraction

FRONTIERS IN CARDIOVASCULAR MEDICINE

2024

The TAS1R2 G-protein-coupled receptor is an ambient glucose sensor in skeletal muscle that regulates NAD homeostasis and mitochondrial capacity

NATURE COMMUNICATIONS

2024

Source of nicotinamide governs its metabolic fate in cultured cells, mice, and humans

CELL REPORTS

2023

Exercise and ageing impact the kynurenine/tryptophan pathway and acylcarnitine metabolite pools in skeletal muscle of older adults

JOURNAL OF PHYSIOLOGY-LONDON

2023

Comprehensive interrogation of human skeletal muscle reveals a dissociation between insulin resistance and mitochondrial capacity

AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM

2023

NAD(+) and human muscle health

NATURE AGING

2022

A Metabolomic Signature of Glucagon Action in Healthy Individuals With Overweight/Obesity

JOURNAL OF THE ENDOCRINE SOCIETY

2021

Discovery of 1-[2-(1-methyl-1H-pyrazol-5-yl)-[1,2,4]triazolo[1,5-a] pyridin-6-yl]-3-(pyridin-4-ylmethyl)urea as a potent NAMPT (nicotinamide phosphoribosyltransferase) activator with attenuated CYP inhibition

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

2021

Optimization of a urea-containing series of nicotinamide phosphoribosyltransferase (NAMPT) activators

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

2021

Metabolic adaptation characterizes short-term resistance to weight loss induced by a low-calorie diet in overweight/obese individuals.

The American journal of clinical nutrition

2021

Education & Training

Education

Cornell University, Graduate School of Medical Sciences, NY, NY

Associated Clinical Trials