About Marius
Research Associate, Deborah Research Institute, 1995-96
NSERC Postdoctoral Fellow, Deborah Research Institute, Browns Mills, New Jersey 1993-95
Ph.D. University of Western Ontario, 1993
BSc. University of Western Ontario, 1987
BA. University of Western Ontario, 1984
Dr. Marius Locke's current research focuses on understanding how skeletal muscle adapts to stress, injury, exercise, and disease, with particular emphasis on the protective role of heat shock proteins (HSPs). His work explores the cellular mechanisms that help muscle tissue resist damage and recover from inflammation following strenuous activity, advancing knowledge with implications for health, aging, and physical performance. Using innovative experimental models, he investigates how stress responses are influenced by conditions such as exercise, diabetes, muscle hypertrophy, and environmental stressors.
An award-winning exercise physiologist, Dr. Locke received a Natural Sciences and Engineering Research Council of Canada (NSERC) Postdoctoral Fellowship and the American College of Sports Medicine’s New Investigator Award. Through his research, publications, and ongoing scientific collaborations, he continues to contribute to a deeper understanding of muscle protection, adaptation, and recovery. Full profile on DiscoverResearch.
The cellular response to muscle damage, including the regulation, expression and protection of stress/heat shock proteins/damage associated molecular patterns in striated muscle.
Cells respond to stressful conditions by rapidly synthesizing protective proteins known as Heat Shock Proteins (HSPs) or Stress Proteins (SPs). An elevated expression of HSPs has been shown to provide protection to cells and tissues during episodes of stress. HSPs are known to be involved in numerous processes and are likely to regulate important cell functions. I am currently examining the relationship between the content of HSPs and their ability to protect skeletal muscle from the damage associated with eccentric (lengthening) muscle contractions and the inflammatory response that follows. We use an ASI servo motor to induce skeletal muscle damage in the rat tibialis anterior muscle. We use this model in conjunction with other mammalian models (diabetes, hypertrophy, exercise, heat stress, cold stress, etc) to answer questions regarding the role that HSPs play in skeletal muscle protection.
Locke, M. & Salerno, S. (2020). Ovariectomy alters lengthening contraction induced heat shock protein expression. Applied Physiology, Nutrition, and Metabolism. 45. 1-9.
Waskiw-Ford, M., Hannaian, S., Kato, H., Abou Sawan, S., Locke, M., Kumbhare, D., & Moore, D. (2020). Leucine-Enriched Essential Amino Acids Improve Recovery from Post-Exercise Muscle Damage Independent of Increases in Integrated Myofibrillar Protein Synthesis in Young Men. Nutrients. 12.
Bonello, J. & Locke, M. (2019). HSP72 expression is specific to skeletal muscle contraction type. Cell Stress and Chaperones. 24
Locke, M. & Celotti, C. (2014). The effect of heat stress on skeletal muscle contractile proteins. Cell Stress and Chaperones 19:519-527.
Holwerda AM, Locke M. (2014). Hsp25 and Hsp72 content in rat skeletal muscle following controlled shortening and lengthening contractions. Applied Physiology, Nutrition and Metabolism 39(12):1380-7.
American College of Sports Medicine
Canadian Society for Exercise Physiology
International Cell Stress Society