Dr. Spriet's basic research examines how skeletal muscle generates the large amounts of energy needed to exercise and compete in work and sport situations. The pathways that metabolize carbohydrate and lipid as fuel to produce energy are studied in human skeletal muscle. His practical research examines whether compounds that are purported to be "ergogenic" or work enhancing agents actually augment muscle metabolism and/or improve human performance (e.g. blood doping, creatine, carnitine, pyruvate, taurine, caffeine and omega-3 fatty acids). He also conducts hydration/sweat testing and research aimed at counteracting the effects of dehydration in athletes engaging in stop-and-go sports like ice hockey, basketball, and soccer.Learn More
My current research blends my research backgrounds in biomechanics and visuomotor control to examine how postural control is integrated and coordinated with voluntary movement (e.g. reaching, stepping, whole-body reaching). I am interested in developing an understanding of balance and movement both from a fundamental level, and in application to the immense problem of impaired mobility and falls in older adults and other clinical populations (e.g. stroke).Learn More
My main research focus centres around the issue of how contracting skeletal muscle can communicate with blood vessels in order to ensure adequate blood flow to the working skeletal muscle cells. There is a direct relationship between skeletal muscle metabolic rate and blood flow. This type of relationship requires that active skeletal muscle cells communicate their need for blood flow to the cells of the vasculature, endothelial cells and vascular smooth muscle cells, and that these cells alter their function in order to ensure the proper blood flow delivery. I am interested in this intercellular communication.Learn More
My lab conducts research on several areas related to cardio-respiratory physiology and pathophysiology. For example, we are studying: 1) how the heart initially adapts to hypertension before the development of contractile dysfunction and heart failure; 2) skeletal and cardiomyocyte cell signalling during normal and hypoxic conditions; 3) proteomic alterations that occur in limb muscles during exercise; 4) key post-translational modifications of myofilament proteins that arise during the development of whole muscle dysfunction as a result of fatigue or ischemia; and, 5) dyastolic dysfunction in various physiological and pathological states, such as aging, sex differences, and models of heart failure.Learn More
To date, my research program has focused on strategies used to execute safe movement during adapted locomotor tasks (steering, obstacle circumvention, obstacle stepping) and the role of vision in these tasks. I am also interested in exploring the impact of cognitive or brain function on locomotor control. Given the commonness of dual tasking in our daily living, I hope to map patterns of cognitive-locomotor interference for multiple adapted locomotor (e.g. obstacle circumvention) and cognitive activities (e.g. visuo-spatial cognitive tasks) and ascertain optimal training strategies for dual-task performance.Learn More
The primary goals of my research program are 1) to understand where posture is controlled 2) to understand what sensory information contributes to successful movement and equilibrium.
By investigating these two key questions I believe we will have a better understanding of how sensory decline contributes to a loss of mobility as we age. My research program involves two key areas of study:
1) To perform direct recordings from sensory afferents and motor efferents in awake human subjects to investigate sensory contributions to movement, balance control, and reflex responses.
2) To elicit balance perturbations to test the function of these reflex loops, and sensory contributions to the maintenance of equilibrium and postural control.
More than 4 million Canadians have arthritis and the number of people living with arthritis continues to increase year after year. Osteoarthritis involves multiple tissues and often includes cartilage damage, bone sclerosis and synovial inflammation. A pressing need remains for joint localized therapies and interventions that could slow or ideally stop this debilitating disease.
In our research, we use genetic and surgical models of spontaneous osteoarthritis (with old age) and post-traumatic osteoarthritis (following injury). We follow the progression of disease in a joint in order to better understand how proteins such as TRPV4, integrin alpha1beta1 and cilia influence chondrocyte signal transduction and thus the development of osteoarthritis.
My research program adopts a broad and integrative approach to the study of chronic musculoskeletal pain, incorporating both basic and clinical sciences. A major arm to my research program is investigating the underlying pathophysiologic mechanisms using both animal and human models. My research also aims to advance reliable diagnostic criteria (imaging, biomarkers) and physical assessment techniques (quantitative sensory testing, electromyography) that enable effective and reliable treatment and management strategies. By emphasizing transdisciplinary and multi-institutional collaborations, my research program will continue to inform future clinical and experimental initiatives in the field of chronic musculoskeletal pain.Learn More
Skeletal muscle is a remarkable tissue which regulates many metabolic processes, generates heat and is the basic motor of locomotion allowing us to meaningfully interact with our environment. When a muscle is activated at various lengths it produces a given predictable amount of force. However, when that muscle is actively lengthened or shortened those predictions go out the window. We actually know very little regarding dynamic muscle contraction. My research program focuses on muscle contractile properties and gaining a deeper understanding of how muscle works. I use altered states to tease out some of these fine muscle details such as muscle fatigue, aging, and training.Learn More
Ongoing projects include:
1) Examining cardiac remodeling in zebrafish and trout in response to thermal acclimation.
2) Characterizing the role of the troponin complex in regulating the function of striated muscle.
3) Examining the function of the hagfish heart during prolonged anoxia exposure.
4) Examining the change in diaphragm function during the onset of heart failure.
5) Characterizing how bitumen exposure of sockeye salmon early life stages influences cardiac development and aerobic fitness.
Our research is dedicated to understanding mechanisms that dictate healthy function of the human spine, and ultimately the causes and consequences of low back injury and pain. To do this we study the mechanics and physiology of the lumbar spine and its musculature. We use both human and animal models to understand different aspects of how spine movement is achieved and what "normal" movement looks like, the role of muscle in producing this movement and stabilizing the spine, and how the spine and muscle both adapt to injury and how they can be rehabilitated from injury.Learn More