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Oksana Gavrilova, Ph.D.

Oksana Gavrilova.
Scientific Focus Areas: Genetics and Genomics, Health Disparities, Neuroscience, Social and Behavioral Sciences

Professional Experience

  • Staff Scientist and Core Director, Mouse Metabolism Core Laboratory, NIDDK, NIH, 2002-present
  • Staff Scientist, Diabetes, Endocrinology, and Obesity Branch, NIDDK, NIH, 2000-2002
  • Visiting Research Fellow, Diabetes, Endocrinology, and Obesity Branch, NIDDK, NIH, 1994-2000
  • Research Fellow, University of Texas Southwestern Medical Center, 1993-1994
  • Research Scientist, Institute of Genetics and Selection of Industrial Microorganisms, 1987-1993
  • Ph.D., Institute of Genetics and Selection of Industrial Microorganisms, 1989
  • M.S., Moscow State University, 1983

Research Goal

Our goal is to understand how environmental and genetic causes affect metabolism.

Current Research

The primary objective of the Mouse Metabolism Core is to support research in the area of obesity and diabetes by providing standardized, high-quality phenotyping services for mouse models of diabetes, obesity, and related disorders. Our services include analysis of body composition, food intake, energy expenditure, body temperature, as well as glucose and lipid metabolism. We also perform measurements of major metabolites and hormones in mouse serum and provide hands-on training in methods commonly used for analyses of energy and glucose metabolism in rodents.

Applying our Research

This research will help us understand the mechanisms underlying obesity and diabetes. It will also facilitate the development of treatments for these diseases.

Need for Further Study

In spite of the prevalence of obesity and diabetes in modern society, our understanding of their molecular basis is rudimentary. In particular, we need to learn more about the role of the central nervous system in the regulation of energy balance and glucose metabolism.

Select Publications

Intestinal peroxisome proliferator-activated receptor α-fatty acid-binding protein 1 axis modulates nonalcoholic steatohepatitis.
Yan T, Luo Y, Yan N, Hamada K, Zhao N, Xia Y, Wang P, Zhao C, Qi D, Yang S, Sun L, Cai J, Wang Q, Jiang C, Gavrilova O, Krausz KW, Patel DP, Yu X, Wu X, Hao H, Liu W, Qu A, Gonzalez FJ.
Hepatology (2023 Jan 1) 77:239-255. Abstract/Full Text
Adipocyte G(q) signaling is a regulator of glucose and lipid homeostasis in mice.
Kimura T, Pydi SP, Wang L, Haspula D, Cui Y, Lu H, König GM, Kostenis E, Steinberg GR, Gavrilova O, Wess J.
Nat Commun (2022 Mar 29) 13:1652. Abstract/Full Text
View More Publications

Research in Plain Language

We characterize various aspects of obesity and diabetes in mice. We use special instruments to measure body composition, body temperature, food intake, metabolic rates, and activity in mice. To study diabetes, we test how well mice respond to insulin, and whether they secrete enough insulin to control their glucose levels.

Last Reviewed August 2023