Cardiovascular and autonomic responses after exercise sessions with different intensities and durations

Juliano Casonatto, Taís Tinucci, Antônio Carlos Dourado, Marcos Polito, Juliano Casonatto, Taís Tinucci, Antônio Carlos Dourado, Marcos Polito

Abstract

Background: Several studies have reported the phenomenon of post-exercise hypotension. However, the factors that cause this drop in blood pressure after a single exercise session are still unknown.

Objective: To investigate the effects of aerobic exercise on the acute blood pressure response and to investigate the indicators of autonomic activity after exercise.

Methods: Ten male subjects (aged 25 ± 1 years) underwent four experimental exercise sessions and a control session on a cycle ergometer. The blood pressure and heart rate variability of each subject were measured at rest and at 60 min after the end of the sessions.

Results: Post-exercise hypotension was not observed in any experimental sessions (P > 0.05). The index of parasympathetic neural activity, the RMSSD, only remained lower than that during the pre-exercise session after the high-intensity session (Δ = -19 ± 3.7 for 15-20 min post-exercise). In addition, this value varied significantly (P < 0.05) between the high- and low-intensity sessions (Δ = -30.7 ± 4.0 for the high intensity session, and Δ = -9.9 ± 2.5 for the low intensity session).

Conclusion: The present study did not find a reduction in blood pressure after exercise in normotensive, physically active young adults. However, the measurements of the indicators of autonomic neural activity revealed that in exercise of greater intensity the parasympathetic recovery tends to be slower and that sympathetic withdrawal can apparently compensate for this delay in recovery.

Figures

Figure 1
Figure 1
Post-exercise changes in the systolic and diastolic blood pressures. ISS  =  intense short session, MLS  =  moderate long session, MSS  =  moderate short session, LLS  =  light long session and CS  =  control session. * =  significantly different from the pre-exercise value.

References

    1. Kenney MJ, Seals DR. Postexercise hypotension. Key features, mechanisms, and clinical significance. Hypertension. 1993;22:653–64.
    1. Hill L. Arterial pressure in man while sleeping, resting, working and bathing. J Physiol Lond. 1897;22:xxvi–xxix.
    1. Halliwill JR. Mechanisms and clinical implications of post-exercise hypotension in humans. Exerc Sport Sci Rev. 2001;29:65–70.
    1. Ciolac EG, Guimaraes GV, D'Avila VM, Bortolotto LA, Doria EL, Bocchi EA. Acute aerobic exercise reduces 24-h ambulatory blood pressure levels in long-term-treated hypertensive patients. Clinics. 2008;63:753–8.
    1. Halliwill JR, Taylor JA, Eckberg DL. Impaired sympathetic vascular regulation in humans after acute dynamic exercise. J Physiol. 1996;495:279–88.
    1. Vanderlei LC, Pastre CM, Hoshi RA, Carvalho TD, Godoy MF. Basic notions of heart rate variability and its clinical applicability. Rev Bras Cir Cardiovasc. 2009;24:205–17.
    1. Jones H, George K, Edwards B, Atkinson G. Is the magnitude of acute post-exercise hypotension mediated by exercise intensity or total work done. Eur J Appl Physiol. 2007;102:33–40.
    1. Forjaz CL, Cardoso CG, Jr, Rezk CC, Santaella DF, Tinucci T. Postexercise hypotension and hemodynamics: the role of exercise intensity. J Sports Med Phys Fitness. 2004;44:54–62.
    1. Alderman BL, Arent SM, Landers DM, Rogers TJ. Aerobic exercise intensity and time of stressor administration influence cardiovascular responses to psychological stress. Psychophysiology. 2007;44:759–66.
    1. Forjaz CL, Santaella DF, Rezende LO, Barretto AC, Negrao CE. [Effect of exercise duration on the magnitude and duration of post-exercise hypotension] Arq Bras Cardiol. 1998;70:99–104.
    1. Mach C, Foster C, Brice G, Mikat RP, Porcari JP. Effect of exercise duration on postexercise hypotension. J Cardiopulm Rehabil. 2005;25:366–9.
    1. Forjaz CL, Matsudaira Y, Rodrigues FB, Nunes N, Negrao CE. Post-exercise changes in blood pressure, heart rate and rate pressure product at different exercise intensities in normotensive humans. Braz J Med Biol Res. 1998;31:1247–55.
    1. MacDonald J, MacDougall J, Hogben C. The effects of exercise intensity on post exercise hypotension. J Hum Hypertens. 1999;13(8):527–31.
    1. MacDonald JR, MacDougall JD, Hogben CD. The effects of exercise duration on post-exercise hypotension. J Hum Hypertens. 2000;14:125–9.
    1. V Brazilian Guidelines in Arterial Hypertension. Arq Bras Cardiol. 2007;89:e24–79.
    1. Heart rate variability: standards of measurement, physiological interpretation and clinical use. Task Force of the European Society of Cardiology and the North American Society of Pacing and Electrophysiology. Circulation. 1996;93:1043–65.
    1. Bird S, Davison R. Physiological testing guidelines. B.A.S.E.S, Leeds. 1997
    1. Pescatello LS, Miller B, Danias PG, Werner M, Hess M, Baker C, et al. Dynamic exercise normalizes resting blood pressure in mildly hypertensive premenopausal women. Am Heart J. 1999;138:916–21.
    1. Brownley KA, West SG, Hinderliter AL, Light KC. Acute aerobic exercise reduces ambulatory blood pressure in borderline hypertensive men and women. Am J Hypertens. 1996;9:200–6.
    1. Cleroux J, Kouame N, Nadeau A, Coulombe D, Lacourciere Y. Aftereffects of exercise on regional and systemic hemodynamics in hypertension. Hypertension. 1992;19:183–91.
    1. Brandao Rondon MU, Alves MJ, Braga AM, Teixeira OT, Barretto AC, Krieger EM, et al. Postexercise blood pressure reduction in elderly hypertensive patients. J Am Coll Cardiol. 2002;39:676–82.
    1. Moraes MR, Bacurau RF, Ramalho JD, Reis FC, Casarini DE, Chagas JR, et al. Increase in kinins on post-exercise hypotension in normotensive and hypertensive volunteers. Biol Chem. 2007;388:533–40.
    1. Harvey PJ, Morris BL, Kubo T, Picton PE, Su WS, Notarius CF, et al. Hemodynamic after-effects of acute dynamic exercise in sedentary normotensive postmenopausal women. J Hypertens. 2005;23:285–92.
    1. Wilder J. The law of initial value in neurology and psychiatry; facts and problems. J Nerv Ment Dis. 1957;125:73–86.
    1. Fagard RH. Physical fitness and blood pressure. J Hypertens Suppl. 1993;11:S47–52.
    1. Hagberg JM, Park JJ, Brown MD. The role of exercise training in the treatment of hypertension: an update. Sports Med. 2000;30:193–206.
    1. Pescatello LS, Kulikowich JM. The aftereffects of dynamic exercise on ambulatory blood pressure. Med Sci Sports Exerc. 2001;33:1855–61.
    1. Pescatello LS, Franklin BA, Fagard R, Farquhar WB, Kelley GA, Ray CA. American College of Sports Medicine position stand. Exercise and hypertension. Med Sci Sports Exerc. 2004;36:533–53.
    1. Pollock ML, Gaesser GA, Butchner JD, Despres JP, Dishman RK, Franklin BA, et al. American College of Sports Medicine Position Stand. The recommended quantity and quality of exercise for developing and maintaining cardiorespiratory and muscular fitness, and flexibility in healthy adults. Med Sci Sports Exerc. 1998;30:975–91.
    1. Pescatello LS, Bairos L, Vanheest JL, Maresh CM, Rodriguez NR, Moyna NM, et al. Postexercise hypotension differs between white and black women. Am Heart J. 2003;145:364–70.
    1. Senitko AN, Charkoudian N, Halliwill JR. Influence of endurance exercise training status and gender on postexercise hypotension. J Appl Physiol. 2002;92:2368–74.
    1. Birch K, Cable N, George K. Combined oral contraceptives do not influence post-exercise hypotension in women. Exp Physiol. 2002;87:623–32.
    1. Jones H, Pritchard C, George K, Edwards B, Atkinson G. The acute post-exercise response of blood pressure varies with time of day. Eur J Appl Physiol. 2008;104:481–9.
    1. Kaplan NM. Morning surge in blood pressure. Circulation. 2003;107:1347.
    1. Khoury AF, Sunderajan P, Kaplan NM. The early morning rise in blood pressure is related mainly to ambulation. Am J Hypertens. 1992;5:339–44.

Source: PubMed

Подписаться