A few minutes of high-intensity interval or sprinting exercise may be as effective as much longer exercise sessions in spurring beneficial improvements in mitochondrial function, according to new research. The small study is published ahead of print in the American Journal of Physiology—Regulatory, Integrative and Comparative Physiology.
Mitochondria, the energy centers of the cells, are essential for good health. Previous research has found that exercise creates new mitochondria and improves the function of existing mitochondria. Altered mitochondrial function in response to a single session of exercise generates signals that may lead to beneficial changes in the cells, lowering the risk for chronic disease. High-intensity interval exercise consists of short bursts of high-intensity aerobic exercise—physical activity that raises the heart rate—alternating with brief recovery periods. Whether the intensity of a workout affects mitochondrial response is unclear.
A team of researchers studied eight young adult volunteers as they participated in cycling workouts of varying intensity.
- Moderate intensity consisted of 30 minutes of continuous exercise at 50 percent peak effort.
- High-intensity interval exercise consisted of five four-minute cycling sessions at 75 percent peak effort, each separated by one minute of rest.
- Sprint cycling consisted of four 30-second sessions at maximum effort, each separated by 4.5 minutes of recovery time.
The research team measured the amount of energy the volunteers spent on each workout and compared mitochondrial changes in the participants’ thigh muscles before and after each exercise session. The researchers found that levels of hydrogen peroxide—a type of molecule involved in cell signaling called “reactive oxygen species” that contains oxygen and hydrogen—in different parts of the mitochondria change after exercise. While too much reactive oxygen species can be damaging to the cells, the researchers noted that the volunteers’ levels were an appropriate amount to potentially promote cell responses that benefit metabolic function rather than cause damage.
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