Biological differences between sexes—particularly due to fluctuating levels of 17β-estradiol and menstrual cycle dynamics—may influence exercise-induced reactive oxygen species (ROS) formation, inflammation and exercise performance. Despite these considerations, there is a lack of research exploring how estradiol and menstrual cycle phases may impact exercise performance, exercise-induced ROS formation and inflammation. This study aimed to examine whether estradiol concentration or menstrual cycle phase may be significantly associated with resistance circuit high-intensity interval training (HIIT) performance, as well as exercise-induced formation of ROS and Interleukin-6 (IL-6). A total of 30 young healthy female participants completed a single bout of resistance-based HIIT in a fasted state. Blood samples were collected at four time points: at baseline after overnight fasting, two hours after consumption of 0.5 L of water (pre-HIIT), immediately post exercise (post-HIIT) and after 15 min of recovery (15-post-HIIT). Additionally, participants attended six fasting baseline assessments scheduled across various menstrual cycle days. These sessions enabled the assessment of estradiol, ROS and IL-6 concentrations throughout the menstrual cycle without being confounded by nutritional factors. Neither baseline levels of ROS nor IL-6 differed significantly between menstrual cycle phases (luteal vs. follicular ROS: 0.013 µmol/min, p = 0.716; IL-6: 0.052, p = 0.679) menstruation status (yes vs. no ROS: −0.056 µmol/min, p = 0.259; IL-6: −0.302 pg/mL, p = 0.088) or 17β-estradiol concentrations (low (11–≤72.5 pg/mL) vs. high (>72.5–394 pg/mL) ROS: −0.038 µmol/min, p = 0.266; IL-6: +0.015 pg/mL, p = 0.906). On the resistance-circuit-HIIT intervention day, no significant differences in ROS or IL-6 were observed between estradiol concentrations (ROS: p = 0.477; IL-6: p = 0.249), menstrual cycle phase (ROS; p = 0.752; IL-6: p = 0.557) or menstruation status (ROS: p = 0.383; IL-6: p = 0.808) from baseline to pre-HIIT, post-HIIT or 15-post-HIIT. These findings should be interpreted with caution, as the menstrual cycle phases were assigned using a calendar-based approach without biochemical ovulation confirmation and the subgroup sizes were relatively small. These findings suggest that natural 17-beta-Estradiol fluctuations within the menstrual cycle, as well as differences in the menstrual cycle itself, may not substantially modulate ROS or IL-6 responses to acute resistance-based HIIT in young healthy female adults.
Gassner et al. (Wed,) studied this question.
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