1 of 2

*

  • Background: The autonomic nervous system regulates involuntary functions through two divisions: the sympathetic division raises heart rate, contractility, and blood pressure, and the parasympathetic division lowers them. During exercise, sympathetic activation redistributes blood flow to working muscles; during recovery, parasympathetic reactivation restores cardiovascular balance. Heart rate variability (HRV), the variation in time between heartbeats, is a non-invasive marker of cardiac autonomic modulation. High HRV reflects ANS adaptability and health; low HRV is linked to cardiac disease, aging, poor inflammatory regulation, and mental health disorders
  • Sex Differences: Evidence is mixed on whether HRV differs by sex at rest or after exercise. Other postexercise responses do differ: postexercise hypotension occurs through vasodilation in females but through reduced cardiac output in males
  • Knowledge Gap: Sex-specific postexercise autonomic responses to HIIE vs. CE are not well understood
  • Purpose: Compare the acute effects of HIIE and CE on postexercise cardiovascular and autonomic nervous system dynamics between sexes
  • Hypotheses: HIIE will elicit greater sympathetic dominance and slower parasympathetic reactivation than CE. The HIIE vs. CE difference will vary between males and females

Study Design

3 visits to the Exercise Physiology Laboratory, Dept. of Kinesiology

Visit 1: maximal exercise test to determine aerobic capacity (VO₂ max)

Visits 2 & 3: HIIE or CE, in randomized order

Exercise Protocols

  • HIIE (28 min total):
    • Four 4-min high-intensity bouts (85-95% VO₂ reserve)
    • Four 3-min moderate-intensity recovery phases (40-50% VO₂ reserve)
  • CE (25 min total):
    • Steady-state exercise at 65% VO₂ reserve

Postexercise Measurements

Participants seated for 30 min after each exercise bout

VO₂ and ECG recorded continuously, BP, VO₂ analyzed in 5 min windows

HIIE was followed by lower vagal-related HRV (ln RMSSD, ln HF) than CE throughout 30 min of recovery, with no difference at baseline, suggesting greater and more sustained parasympathetic withdrawal. Slower reactivation after HIIE was supported only as a trend (condition × time, p = 0.028-0.064). HRV recovery was similar in males and females, apart from a trend toward lower ln LF in males. Males had higher diastolic BP after CE only. Larger studies of sex-specific ANS recovery are needed.

  • After both workouts, the heart beat faster and the time between beats was shorter, as expected.
  • Heart rate variability (HRV), a sign of how well the body’s calming system is working, dropped after exercise. It tended to drop more after interval exercise, but that difference was only a trend, not a firm result.
  • A measure of the body’s calming (“rest and digest”) system was lower after the interval workout than after the steady workout.
  • Another HRV measure (low-frequency power) was also lower after the interval workout.
  • The balance between the body’s “stress” and “calm” systems tipped toward stress after both workouts.
  • Men and women responded similarly overall. One measure (low-frequency power) tended to be lower in men after exercise.

Influence Of High-Intensity Interval Exercise On Postexercise Autonomic Nervous System Dynamics Between Sexes

CESAR A. CARRERA JR., B.S., ACSM-EP, MATT LEE, PH.D, FACSM, KENT A. LORENZ, PH.D, JAMES R. BAGLEY, PH.D

Exercise & Muscle Physiology Laboratory; Department of Kinesiology; San Francisco State University; San Francisco, CA 

EXERCISE

PHYSIOLOGY LAB

Figure 1. Experimental protocol. After a 5-min seated baseline, participants completed either high-intensity interval exercise (HIIE; 28 min) or continuous exercise (CE; 25 min) on separate visits, followed by 30 min of postexercise recovery. ECG and VO₂ were recorded continuously. Heart rate variability (HRV), blood pressure (BP), and VO₂ were analyzed during the baseline and the 5-10, 15-20, and 25-30 min postexercise windows (blue). The intervention block is not drawn to scale.

  • Main effect of time on RR interval, which decreased postexercise (p<0.001)
  • Main effect of time on ln LF/ln HF showed it was higher postexercise (p<0.001)

ln HF was lower after HIIE (condition effect, p < 0.001); condition × time trend (p = 0.047)

ln RMSSD was lower after HIIE (condition effect, p < 0.001); �condition × time trend (p = 0.064)

ln LF tended to be lower in males postexercise�(sex × time trend, p = 0.043)

ln LF was lower after HIIE (condition effect, p < 0.001); condition × time trend (p = 0.028)

ln RMSSD was lower in males overall (sex effect, p < 0.001); sex × time, p = 0.517

LFnu was higher in males overall (sex effect, p = 0.003); sex × time, p = 0.628.

Panel 1. Postexercise (A) ln RMSSD and (B) ln HF following HIIE and CE. Values are estimated marginal means from the linear mixed model (sex × condition × time; diagonal covariance; VO₂ max covariate for ln RMSSD and ln HF). Effects were evaluated at a Bonferroni-adjusted α = 0.025. (n = 23; 22 per condition, 21 at the 15–20 min window). Error bars represent the 95% confidence interval. * CE significantly different from HIIE (p < 0.05, pairwise).

​

Panel 2. Postexercise (C) ln LF power following HIIE and CE. Values are estimated marginal means; error bars represent the 95% CI. * CE significantly different from HIIE (p < 0.05, pairwise). Postexercise (D) ln LF power in males and females, collapsed across conditions. Values are estimated marginal means; error bars represent the 95% CI. † Females significantly different from males at 5-10 min (p < 0.05, pairwise).

​

Panel 3. Postexercise (E) ln RMSSD and (F) LFnu in males and females, collapsed across conditions. Values are estimated marginal means; error bars represent the 95% CI. † Females significantly different from males (p < 0.05, pairwise).

A

B

Effect sizes: Partial η² for the CE vs HIIE comparison in ln RMSSD, ln HF, and ln LF at each time point. Dashed lines mark conventional thresholds for medium (.06) and large (.14) effects.

Diastolic blood pressure: DBP mean values following HIIE and CE in males and females. Values are estimated marginal means; error bars represent the 95% CI. † Males had higher diastolic BP than females after CE (p < 0.001), but not after HIIE (sex × condition, p = 0.021).

Table 1. Values are mean ± SD; VO₂ max range in parentheses. BMI = body mass index. Hedges’ g = standardized effect size (male vs female). P values from independent-samples t-tests.

​

C

D

E

F

INTRO/BACKGROUND

METHODS

RESULTS

BOTTOM LINE

Variable

Male�(n=12)

Female�(n=11)

Hedges’ g�(Male − Female)

P value

Age�(year)

23.0 ± 2.4

23.1 ± 2.3

−.037

.927

BMI�(kg·m−2)

26.6 ± 3.8

24.5 ± 4.9

.464

.262

VO2 max�(mL·kg−1·min−1)

42.1 ± 6.7

(32.6–55.1)

37.4 ± 7.4

(27.1–51.3)

.632

.131

Bottom line: The interval workout turned the body’s calming system down more, and it stayed lower through the 30-minute recovery. Whether it switched back on more slowly was only a trend, not a firm result. Men and women recovered mostly the same.

CONCLUSION

2 of 2

References

​

  1. Aeschbacher, S., Schoen, T., Dörig, L., Kreuzmann, R., Neuhauser, C., Schmidt-Trucksäss, A., Probst-Hensch, N. M., Risch, M., Risch, L., & Conen, D. (2017). Heart rate, heart rate variability and inflammatory biomarkers among young and healthy adults. Annals of Medicine, 49(1), 32–41. https://doi.org/10.1080/07853890.2016.1226512
  2. Alansare, A., Alford, K., Lee, S., Church, T., & Jung, H. C. (2018). The Effects of High-Intensity Interval Training vs. Moderate-Intensity Continuous Training on Heart Rate Variability in Physically Inactive Adults. International Journal of Environmental Research and Public Health, 15(7), 1508. https://doi.org/10.3390/ijerph15071508
  3. Bassareo, P. P., & Crisafulli, A. (2020). Gender Differences in Hemodynamic Regulation and Cardiovascular Adaptations to Dynamic Exercise. Current Cardiology Reviews, 16(1), 65–72. https://doi.org/10.2174/1573403X15666190321141856
  4. Bellocchi, C., Carandina, A., Montinaro, B., Targetti, E., Furlan, L., Rodrigues, G. D., Tobaldini, E., & Montano, N. (2022). The Interplay between Autonomic Nervous System and Inflammation across Systemic Autoimmune Diseases. International Journal of Molecular Sciences, 23(5), 2449. https://doi.org/10.3390/ijms23052449
  5. Borresen, J., & Lambert, M. I. (2008). Autonomic Control of Heart Rate during and after Exercise: Measurements and Implications for Monitoring Training Status. Sports Medicine, 38(8), 633–646. https://doi.org/10.2165/00007256-200838080-00002
  6. Buchheit, M., Laursen, P. B., & Ahmaidi, S. (2007). Parasympathetic reactivation after repeated sprint exercise. American Journal of Physiology-Heart and Circulatory Physiology, 293(1), H133–H141. https://doi.org/10.1152/ajpheart.00062.2007
  7. Carter, R., Watenpaugh, D. E., & Smith, M. L. (2001). Selected Contribution: Gender differences in cardiovascular regulation during recovery from exercise. Journal of Applied Physiology, 91(4), 1902–1907. https://doi.org/10.1152/jappl.2001.91.4.1902
  8. Coates, A. M., Millar, P. J., & Burr, J. F. (2023). Investigating the roles of exercise intensity and biological sex on postexercise alterations in cardiac function. Journal of Applied Physiology, 134(2), 455–466. https://doi.org/10.1152/japplphysiol.00570.2022
  9. Cooper, T. M., McKinley, P. S., Seeman, T. E., Choo, T.-H., Lee, S., & Sloan, R. P. (2015). Heart rate variability predicts levels of inflammatory markers: Evidence for the vagal anti-inflammatory pathway. Brain, Behavior, and Immunity, 49, 94–100. https://doi.org/10.1016/j.bbi.2014.12.017
  10. Daniela, M., Catalina, L., Ilie, O., Paula, M., Daniel-Andrei, I., & Ioana, B. (2022). Effects of Exercise Training on the Autonomic Nervous System with a Focus on Anti-Inflammatory and Antioxidants Effects. Antioxidants, 11(2), 350. https://doi.org/10.3390/antiox11020350
  11. Dart, A. (2002). Gender, sex hormones and autonomic nervous control of the cardiovascular system. Cardiovascular Research, 53(3), 678–687. https://doi.org/10.1016/S0008-6363(01)00508-9
  12. De Oliveira Carpes, L., Domingues, L. B., Schimitt, R., Fuchs, S. C., Alhalimi, T., Tanaka, H., & Ferrari, R. (2021). Sex Differences in Post-exercise Hypotension, Ambulatory Blood Pressure Variability, and Endothelial Function After a Power Training Session in Older Adults. Frontiers in Physiology, 12, 657373. https://doi.org/10.3389/fphys.2021.657373
  13. Dutra, S. G. V., Pereira, A. P. M., Tezini, G. C. S. V., Mazon, J. H., Martins-Pinge, M. C., & Souza, H. C. D. (2013). Cardiac Autonomic Modulation Is Determined by Gender and Is Independent of Aerobic Physical Capacity in Healthy Subjects. PLoS ONE, 8(10), e77092. https://doi.org/10.1371/journal.pone.0077092
  14. Edwards, J. J., Wiles, J. D., Vadaszy, N., Taylor, K. A., & O’Driscoll, J. M. (2022). Left ventricular mechanical, cardiac autonomic and metabolic responses to a single session of high intensity interval training. European Journal of Applied Physiology, 122(2), 383–394. https://doi.org/10.1007/s00421-021-04840-z
  15. Gorostiaga, E. M., Walter, C. B., Foster, C., & Hickson, R. C. (1991). Uniqueness of interval and continuous training at the same maintained exercise intensity. European Journal of Applied Physiology and Occupational Physiology, 63(2), 101–107. https://doi.org/10.1007/BF00235177
  16. Hottenrott, L., Möhle, M., Ide, A., Ketelhut, S., Stoll, O., & Hottenrott, K. (2021). Recovery from Different High-Intensity Interval Training Protocols: Comparing Well-Trained Women and Men. Sports, 9(3), 34. https://doi.org/10.3390/sports9030034
  17. Jandackova, V. K., Scholes, S., Britton, A., & Steptoe, A. (2019). Healthy Lifestyle and Cardiac Vagal Modulation Over 10 Years: Whitehall II Cohort Study. Journal of the American Heart Association, 8(19), e012420. https://doi.org/10.1161/JAHA.119.012420
  18. Kamath, M. V., Fallen, E. L., & McKelvie, R. (1991b). Effects of steady state exercise on the power spectrum of heart rate variability. Medicine &amp; Science in Sports &amp; Exercise, 23(4). https://doi.org/10.1249/00005768-199104000-00007
  19. Lynn, B. M., McCord, J. L., & Halliwill, J. R. (2007). Effects of the menstrual cycle and sex on postexercise hemodynamics. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, 292(3), R1260–R1270. https://doi.org/10.1152/ajpregu.00589.2006
  20. Marçal, I. R., Goessler, K. F., Buys, R., Casonatto, J., Ciolac, E. G., & Cornelissen, V. A. (2021). Post-exercise Hypotension Following a Single Bout of High Intensity Interval Exercise vs. a Single Bout of Moderate Intensity Continuous Exercise in Adults With or Without Hypertension: A Systematic Review and Meta-Analysis of Randomized Clinical Trials. Frontiers in Physiology, 12, 675289. https://doi.org/10.3389/fphys.2021.675289
  21. Mariano, I. M., Domingos, D. C., Ribeiro, A. L. A., Peçanha, T., Simões, H. G., & Puga, G. M. (2019). Sex and exercise-mode differences in post-exercise blood pressure and heart rate variability responses during a workday. Motriz: Revista de Educação Física, 25(1), e101930. https://doi.org/10.1590/s1980-6574201900010030
  22. Michael, S., Graham, K. S., & Davis, G. M. (2017). Cardiac Autonomic Responses during Exercise and Post-exercise Recovery Using Heart Rate Variability and Systolic Time Intervals—A Review. Frontiers in Physiology, 8, 301. https://doi.org/10.3389/fphys.2017.00301
  23. Professional, C. C. medical. (2026, September 16). What is heart rate variability?. Cleveland Clinic. https://my.clevelandclinic.org/health/symptoms/21773-heart-rate-variability-hrv
  24. Olivieri, F., Biscetti, L., Pimpini, L., Pelliccioni, G., Sabbatinelli, J., & Giunta, S. (2024). Heart rate variability and autonomic nervous system imbalance: Potential biomarkers and detectable hallmarks of aging and inflammaging. Ageing Research Reviews, 101, 102521. https://doi.org/10.1016/j.arr.2024.102521
  25. Pierpont, G. L., Adabag, S., & Yannopoulos, D. (2013). Pathophysiology of Exercise Heart Rate Recovery: A Comprehensive Analysis. Annals of Noninvasive Electrocardiology, 18(2), 107–117. https://doi.org/10.1111/anec.12061
  26. Salih, T. R., & Abdulateef, D. S. (2026). Correlation between heart rate variability and estradiol, progesterone, and the estradiol/progesterone ratio across menstrual phases in healthy women. Physiological Reports, 14(8), e70887. https://doi.org/10.14814/phy2.70887
  27. Senitko, A. N., Charkoudian, N., & Halliwill, J. R. (2002). Influence of endurance exercise training status and gender on postexercise hypotension. Journal of Applied Physiology, 92(6), 2368–2374. https://doi.org/10.1152/japplphysiol.00020.2002
  28. Seo, M.-W., Park, T.-Y., & Jung, H. (2023). Sex Differences in Heart Rate Variability and Vascular Function Following High-Intensity Interval Training in Young Adults. Journal of Human Kinetics, 90, 89–100. https://doi.org/10.5114/jhk/170964
  29. Serrano, H. M., Gueugneau, N., & Ravier, G. (2026). Influence of menstrual cycle on autonomic nervous system, muscular strength and mood states. Scientific Reports, 16(1), 28294. https://doi.org/10.1038/s41598-026-56802-0
  30. Varzideh, F., Jankauskas, S. S., Mone, P., Kansakar, U., & Santulli, G. (2026). Autonomic neurotransmission in cardiovascular regulation and pathophysiology. Frontiers in Neuroscience, 19, 1739330. https://doi.org/10.3389/fnins.2025.1739330
  31. Waghmare, S., Whitaker‐Hilbig, A. A., Chertoff, M., & Billinger, S. A. (2024). Blood pressure and heart rate variability to assess autonomic response to an acute bout of high intensity interval exercise in healthy young adults. Physiological Reports, 12(14), e16142. https://doi.org/10.14814/phy2.16142
  32. Wichi, R. B., De Angelis, K., Jones, L., & Irigoyen, M. C. (2009). A Brief Review of Chronic Exercise Intervention to Prevent Autonomic Nervous System Changes During the Aging Process. Clinics, 64(3), 253–258. https://doi.org/10.1590/S1807-59322009000300017
  33. Williams, D. P., Koenig, J., Carnevali, L., Sgoifo, A., Jarczok, M. N., Sternberg, E. M., & Thayer, J. F. (2019). Heart rate variability and inflammation: A meta-analysis of human studies. Brain, Behavior, and Immunity, 80, 219–226. https://doi.org/10.1016/j.bbi.2019.03.009