Skip Navigation LinksHome > July 2002 - Volume 34 - Issue 7 > Cerebral hemodynamics and resistance exercise
Medicine & Science in Sports & Exercise:
APPLIED SCIENCES: Physical Fitness and Performance

Cerebral hemodynamics and resistance exercise

EDWARDS, MICHAEL R.; MARTIN, DONNY H.; HUGHSON, RICHARD L.

Free Access
Article Outline
Collapse Box

Author Information

Cardiorespiratory and Vascular Dynamics Laboratory, Faculty of Applied Health Sciences, University of Waterloo, Ontario, CANADA

Submitted for publication July 2001.

Accepted for publication February 2002.

Collapse Box

Abstract

EDWARDS, M. R., D. H. MARTIN, and R. L. HUGHSON. Cerebral hemodynamics and resistance exercise. Med. Sci. Sports Exerc., Vol. 34, No. 7, pp. 1207–1211, 2002.

Purpose: Repetitive resistance exercise with large muscle mass causes rapid fluctuations in mean arterial blood pressure (MAP). We sought to determine the effect of these fluctuations on the cerebrovasculature response determined by mean flow velocity (Vmean) of the middle cerebral artery.

Methods: Nine subjects performed 10-repetition maximum leg press exercise. MAP was estimated by finger photoplethysmography, Vmean by Doppler ultrasound, and end-tidal CO2 (PETCO2) by mass spectrometry.

Results: Vmean fluctuated with MAP with each repetition however averaged over the 10 repetitions, Vmean was unchanged from resting baseline values (66.9 ± 10.8 vs 67.7 ± 12.3 cm·s−1, baseline vs exercise, P > 0.05) despite an increased MAP (89.5 ± 8.4 vs 105.0 ± 4.9 Torr, P < 0.05). PETCO2 also remained unchanged from rest to exercise (37.7 ± 2.8 vs 36.6 ± 2.7 Torr, P > 0.05). Vmean decreased below resting levels for the first 5 s of recovery (59.8 ± 9.1 cm·s−1, P < 0.05) as MAP returned rapidly to slightly below baseline (83.3 ± 6.1, P > 0.05). MAP/Vmean, an index of cerebrovascular resistance, was elevated during exercise and returned to baseline after exercise. An increase in Vmean at 30 s post exercise (78.4 ± 10.6 cm·s−1, P < 0.05) corresponded with elevated PETCO2 (43.0 ± 4.8 Torr, P > 0.05).

Conclusion: The results suggest that fluctuations in MAP with individual muscle contractions during resistance exercise appear to be too rapid to be countered by cerebrovascular autoregulation. However, the progressive increase in MAP over a number of contractions was effectively countered to maintain Vmean near baseline values before a decrease in Vmean immediately after exercise.

Cerebral blood flow remains relatively constant across a range of mean arterial pressure (MAP) from 50 to 140 mm Hg by the process called autoregulation (14,18). In healthy individuals, the autoregulatory response to step changes in MAP returns cerebral blood flow within 3 to 5 s (28). Heavy resistance exercise might challenge the ability of the autoregulatory system due to both the rapid changes in MAP and the fact that MAP might exceed the autoregulatory zone (15). Injuries such as stroke, subarachnoid hemorrhage, and retinal hemorrhage may be associated with resistance exercise.

Recent measurements of mean flow velocity (Vmean) of the middle cerebral artery (MCA) with Doppler ultrasound in a group of elite power athletes revealed a significant reduction in Vmean from the resting levels during a single maximal lift (7). Loss of consciousness, commonly referred to by weight lifters as “blackouts,” has been reported during heavy resistance exercise (6), suggesting that cerebral blood flow and autoregulation may be critically impaired under these circumstances. Anecdotally, some recreational athletes complain of presyncopal symptoms when performing resistance exercise. The mechanism for the decreased Vmean or insufficient autoregulation, which may lead to syncope, remains elusive; however, it is likely due to an interaction among MAP, intracranial pressure, and cerebrovascular resistance. To date, there is no information on cerebral blood flow during repetitive resistance exercise that might be performed by recreational athletes.

The objective of the present study was to characterize the Vmean response to the double leg press, a common resistance exercise, in a group of recreationally active subjects. Double leg press was selected as it involves a large muscle mass and generates high physiological changes in MAP (15,16). We hypothesized that the rapid fluctuations in MAP with each leg press would be transmitted into oscillations in Vmean, while any systematic increase in MAP would be met by an increase in cerebrovascular resistance to keep Vmean close to baseline. To obtain an indicator of cerebrovascular resistance, we determined MAP/Vmean at rest and during resistance exercise to explore autoregulation and factors including arterial CO2 that influence the control of cerebral circulation.

Back to Top | Article Outline

METHODS

Subjects

Nine healthy subjects (six females) were tested after being fully informed of the experimental details. Their mean age was 21.0 ± 3.6 yr (mean ± standard deviation), height 167.5 ± 8.0 cm and weight 67.3 ± 11.0 kg. All subjects had at least 3 months of resistance exercise experience and were presently involved in regular training at least 3 times/wk. The Office of Research Ethics at the University of Waterloo approved all procedures, and written consent was obtained.

Back to Top | Article Outline
Procedure

Subjects were instrumented and seated in a 45° inclined bilateral leg press apparatus with the back supported and the feet resting on foot plates. The load selected for testing was designed to allow the subjects to complete 10 and only 10 repetitions of the leg press exercise. This load is equivalent to ∼75% of each subject’s theoretical maximum voluntary contraction (MVC) (23). To determine the test load, subjects self-selected a weight based on their own experience. Weights were added or removed so that the 10-repetition criterion was achieved within 2 to 3 trials. After a 5-min rest period, 5 min of continuous baseline data were collected, followed by the 10-repetition leg press exercise. All subjects were instructed to breathe normally and avoid holding their breath. Vmean, MAP, end-tidal CO2 (PETCO2) and heart rate (HR), were continuously recorded for resting baseline collection, exercise, and recovery.

Back to Top | Article Outline
Experimental measures

MAP was determined from the finger placed at the level of the heart using noninvasive arterial photoplethysmography (Finapres Ohmeda, Englewood, CO) and corrected using standard cuff measurements. Vmean of the middle cerebral artery was estimated from transcranial Doppler ultrasonsography (Transpect TCD MedaSonics, Freemont, CA) as previously described (2). Briefly, a 2 MHz probe was used to isolate the right middle cerebral artery through the temporal bone window and held in place with the use of a headband. Breath-by-breath PETCO2 was collected continuously using an ultrasonic flow meter (Kou Consulting Inc., Redmond, WA) and mass spectrometry (MGA-1100, Perkin-Elmer Medical Gas Analyzer, Pomona, CA). HR was determined by a 3-lead electrocardiograph.

Back to Top | Article Outline
Data Analysis

Data were recorded on digital format tape (TEAC Instruments, Montebello, CA), then transferred for analysis by a computer based system to yield a data set sampled at 100 Hz. Vmean was determined from the outer envelope of the fast Fourier transformed Doppler signal. The ratio, MAP/Vmean, was calculated as an index of averaged cerebrovascular resistance.

Back to Top | Article Outline
Statistics

Differences among mean values during rest, exercise, and three recovery periods (first 5 s, 5 to15 s, and 15 to 30 s of recovery) were assessed with a one-way repeated measures ANOVA for the dependent variables Vmean, MAP, MAP/Vmean, HR, and PETCO2. If significance was obtained (P < 0.05), a Bonferoni post hoc was used to assess the differences from baseline.

Back to Top | Article Outline

RESULTS

A representative data set from one subject is illustrated in Figure 1. The MAP response to resistance exercise followed a distinct sinusoidal oscillatory pattern with each repetition that increased with successive repetitions. Vmean followed a similar sinusoidal oscillatory pattern to MAP with each repetition, but unlike MAP it did not increase with successive repetitions. The first solid, vertical line in Figure 1 shows the correspondence between MAP and Vmean. MAP/Vmean progressively increased with successive repetitions. PETCO2 remained near baseline levels throughout the exercise. Following a brief reduction, Vmean increased in recovery and appeared to correspond to the increased PETCO2.

Figure 1
Figure 1
Image Tools

Averaged data are shown in Table 1. Compared to resting values, averaged Vmean was unchanged during exercise (P > 0.05), depressed during the first 5 s of recovery (P < 0.05), and increased within 15 to 30 s of recovery (P < 0.05). The MAP increased from resting levels during exercise (P < 0.05) but returned to baseline values during recovery (P > 0.05), although there was a trend for MAP to be decreased at the first 5 s of recovery. The data for a single subject (Fig. 1) shows with the second solid vertical line that the decrease in Vmean corresponded to the rapid drop in MAP. MAP/Vmean was elevated during exercise (P < 0.05) and declined toward baseline within the first 5 s of recovery. PETCO2 was increased at 5 to 15 s, and 15 to 30 s of recovery (P < 0.05). HR was increased above baseline during exercise as well as in the first 5 s, 5 to 15 s, and 15 to 30 s of recovery (P < 0.05).

Table 1
Table 1
Image Tools
Back to Top | Article Outline

DISCUSSION

The major new observations from this study were that the average value of Vmean remained constant during leg press exercise, yet Vmean oscillated directly with the changes in MAP during the exercise. Further, we observed that Vmean decreased significantly below baseline in the first 5 s after exercise. These observations during and immediately after exercise were consistent with our hypotheses that rapid oscillations in MAP transmit directly to Vmean but that systematic increases in MAP are countered by an efficient autoregulatory response to maintain Vmean. The reason that Vmean declined significantly after exercise appeared to be that MAP decreased more rapidly than the change in cerebrovascular resistance could counter. The oscillations and progressive rise in MAP during leg press exercise are consistent with previous observations (15,24). The increase in MAP at the onset of resistance exercise has been ascribed to a number of factors including the overcoming of inertia, a body position with a biomechanical disadvantage, and contribution from the Valsalva maneuver, if allowed. The progressive rise in MAP with successive contractions is thought to reflect an increase in motor unit recruitment or chemoreflex activation (15,24).

The observation that Vmean appeared to be dependent on and in phase with the sinusoidal oscillations in MAP during the resistance exercise (Fig. 1) was consistent with Pott et al. (19) who found that Vmean fluctuated in phase with MAP during a rowing cycle. The cerebrovascular system operates as a high pass filter allowing rapid changes in MAP to cause changes in Vmean (8,29). Cerebrovascular autoregulation is initiated almost immediately with a change in MAP, but the full response requires 3 to 5 s in healthy individuals and up to 10 to 15 s with impaired autoregulation (28). Thus, the cerebral circulation can effectively minimize changes in Vmean in response to slowly developing changes in MAP.

Interpretation of the cerebrovascular resistance response has to be made with caution because resistance is calculated from perfusion pressure gradient divided by blood flow. Consistent with all other studies of cerebrovascular control in humans, we were unable to measure either of these variables directly. At least for the baseline period and the recovery period it would be anticipated that venous or intracranial pressure would be relatively constant so that changes in MAP would reliably reflect changes in perfusion pressure gradient, and MAP/Vmean would provide an index of cerebrovascular resistance. Thus, our observation of somewhat elevated MAP/Vmean immediately after exercise suggests that cerebrovascular resistance probably increased during the exercise to counter the progressive rise in MAP. On the other hand, it is not appropriate to interpret MAP/Vmean directly as an index of cerebrovascular resistance during the leg press exercise, as the venous and intracranial pressures were almost certainly increased at some phase of the activity. Although our subjects did not perform a Valsalva maneuver against a closed glottis, as evidenced by the expired air profile, they probably had some increase in intrathoracic pressure that could alter central venous pressure (19,20) and thus affect the pressure gradient across the cerebrovascular system (4,22).

During the 10-repetion leg press exercise there was no change in average Vmean compared with baseline. This differed from an observation of reduced Vmean in elite power athletes during a single maximal lift (7). There are several differences between experiments that might account for this. A simple explanation might be the timing of measurements. While average Vmean was not affected (Fig. 1, Tab. 1), there were large fluctuations about the mean value during the leg press exercise of the current study as well as during a rowing cycle (19). An apparent under perfusion is immediately followed by an over perfusion: the physiological significance of this finding to cerebral function/metabolism is unknown. During a single maximal lift MAP is markedly elevated, probably in part from the contribution of a Valsalva maneuver. When performed in the absence of weight lifting exercise the Valsalva causes a reduction in Vmean (20).

The arterial partial pressure of CO2 has an important role in the regulation of cerebrovascular resistance (13,26,27). It has been suggested that the increase in Vmean during dynamic exercise might (10) or might not (12) be related to arterial PCO2. We observed that PETCO2 was constant during resistance exercise but that it increased to its highest point at 30 s into recovery. This was followed after a short delay by the peak response of Vmean during the recovery period. It seems reasonable to suggest that the observed amplitude and time delay between PETCO2 and Vmean indicated that during recovery, PETCO2 resulted in cerebral vasodilation. The cerebrovascular response to PETCO2 from baseline to 30 s recovery (% change Vmean/change in PETCO2) was 3.2% per Torr PETCO2, similar to other Doppler studies reported in the literature under resting conditions (5,17). In addition, Poulin et al. (21) recently found the vascular response of Vmean to step changes in PETCO2 was initiated after a 6-s delay, much more rapid that previously thought.

None of our subjects experienced dizziness or syncope during the testing protocol. Syncopal symptoms are probably related to a reduction in cerebral blood flow that could be due to some combination of increased cerebrovascular resistance or decreased MAP. It has been suggested that hyperventilation before or during heavy resistance exercise might be linked to the syncope experienced by some athletes (6). Based on PETCO2 values, none of our subjects hyperventilated before exercise. Given the decline in Vmean immediately after exercise in individuals with normal PETCO2, it would seem prudent to recommend that individuals taking part in resistance exercise avoid voluntary hyperventilation before or during exercise as this would further elevate cerebrovascular resistance, potentially causing a more marked decline in Vmean.

Back to Top | Article Outline
Limitations

Doppler ultrasound of the middle cerebral artery measures velocity and not flow, and therefore relies on the assumption that the diameter of the artery does not change. This assumption has been considered extensively (1,3,29), including in studies with magnetic resonance imaging (MRI) of the cerebral artery during lower body negative pressure and modest changes in PETCO2 (25), and comparisons with 133Xe clearance during dynamic cycle exercise (12). However, flow indices calculated by spectral weighed sums of the transcranial Doppler signal have questioned this assumption. Giller et al. (9) evaluated the cerebral blood flow response to rhythmic handgrip exercise and found that their calculated cerebral blood flow index was heterogeneous between subjects and concluded that ordinary cerebral Doppler velocities obtained during exercise may be invalid. To date this issue has not been resolved. In the study of Giller, it appeared from the typical subject presented that during the first 100 s of exercise, as MAP increased Vmean and their indicator of MCA diameter remained constant. It was only in the final 200 s of exercise that the indicator of diameter changed. Thus, it is not apparent how their data might affect our interpretation as the current exercise lasted approximately 40 s (Fig. 1). If there were any reduction in MCA diameter at the end of exercise, then our observed decrease in Vmean would underestimate the decline in cerebral blood flow.

As considered above, calculation of MAP/Vmean to provide an index of cerebrovascular resistance to study autoregulation is appropriate during steady state conditions, but should be viewed with caution during exercise or Valsalva maneuver. With repetitive resistance exercise or dynamic exercise, MAP, cerebrovascular resistance, intracranial pressure, and cerebral venous outflow might be expected to change. Pott et al. (19) found that Vmean increased by 10 cm·s−1, MAP increased by 11 Torr, and central venous pressure by 8 Torr during rowing exercise. Similar to the present study, intracranial pressure could not be assessed, yet the authors concluded that Vmean was dominated by MAP. Furthermore, under a resistance exercise protocol such as ours, numerous other factors such as brain metabolism, blood volume, and thermoregulation may have also influenced cerebral blood flow (11). In spite of these limitations, the main measured variable, Vmean, did fluctuate markedly during exercise and showed a postexercise pattern that was consistent with an elevated cerebrovascular resistance within the first 5 s after exercise, and a reduced MAP/Vmean subsequently as PETCO2 increased.

Back to Top | Article Outline

CONCLUSION

The results of the present study indicate that Vmean was dependent on the fluctuations in MAP that occur during individual repetitions of resistance exercise but independent of the progressive rise in MAP with successive repetitions. These findings suggest that each muscle contraction during resistance exercise may be too fast to engage an effective autoregulatory response, but that systematic changes in MAP are countered to maintain mean cerebral blood flow close to the baseline value.

M. R. Edwards was supported by the Natural Sciences and Engineering Council of Canada postgraduate scholarship and by a Canadian Space Agency graduate supplement. This research was supported by the Heart and Stroke Foundation of Ontario NA-4387.

Address for correspondence: Professor Richard L. Hughson, Cardiorespiratory and Vascular Dynamics Laboratory, Faculty of Applied Health Sciences, University of Waterloo, Waterloo, ON N2 L 3G1, Canada; E-mail: hughson@uwaterloo.ca

Back to Top | Article Outline

REFERENCES

1. Aaslid, R., K. F. Lindegaard, W. Sorteberg, and H. Nornes. Cerebral autoregulation dynamics in humans. Stroke 20: 45–52, 1989.

2. Aaslid, R., T. Markwalder, and H. Nornes. Noninvasive transcranial Doppler ultrasound recording of flow velocity in basal cerebral arteries. J. Neurosurg. 57: 769–774, 1982.

3. Birch, A. A., M. J. Dirnhuber, R. Hartley-Davies, F. Iannotti, and G. Neil-Dwyer. Assessment of autoregulation by means of periodic changes in blood pressure. Stroke 26: 834–837, 1995.

4. Bloomfield, G. L., P. C. Ridings, C. R. Blocher, A. Marmarou, and H. J. Sugerman. A proposed relationship between increased intra-abdominal, intrathoracic, and intracranial pressure. Crit. Care Med. 25: 496–503, 1997.

5. Cencetti, S., G. Bandinelli, and A. Lagi. Effect of PCO2 changes induced by head-upright tilt on transcranial Doppler recordings. Stroke. 28: 1195–1197, 1997.

6. Compton, D, P. M. Hill, and J. D. Sinclair. Weight-lifters’ blackout. Lancet 12: 1234–1237, 1973.

7. Dickerman, R. D., W. J. McConathy, G. H. Smith, J. W. East, and L. Rudder. Middle cerebral artery blood flow velocity in elite power athletes during maximal weight-lifting. Neurol. Res. 22: 337–340, 2000.

8. Diehl, R. R., D. Linden, D. Lücke, and P. Berlit. Phase relationship between cerebral blood flow velocity and blood pressure. Stroke 26: 1801–1804, 1995.

9. Giller, C. A., A. M. Giller, C. R. Cooper, and M. R. Hatab. Evaluation of the cerebral hemodynamic response to rhythmic handgrip. J. Appl. Physiol. 88: 2205–2213, 2000.

10. Hellström, G., W. Fischer-Colbrie, N. G. Wahlgren, and T. Jogestrand. Carotid artery blood flow and middle cerebral artery blood flow velocity during physical exercise. J. Appl. Physiol. 81: 413–418, 1996.

11. Ide, K., and N. H. Secher. Cerebral blood flow and metabolism during exercise. Prog. Neurobiol. 61: 397–414, 2000.

12. Jørgensen, L. G., M. Perko, B. Hanel, T. V. Schroeder, and N. H. Secher. Middle cerebral artery flow velocity and blood flow during exercise and muscle ischemia in humans. J. Appl. Physiol. 72: 1123–1132, 1992.

13. Lambertsen, C. J., S. J. G. Semple, M. G. Smyth, and R. Gelfand. H+ and pCO2 as chemical factors in respiratory and cerebral circulatory control. J. Appl. Physiol. 16: 473–484, 1961.

14. Lassen, N. A. Cerebral blood flow and oxygen consumption in man. Physiol. Rev. 39: 183–233, 1959.

15. MacDougall, J. D., R. S. McKelvie, D. E. Moroz, D. G. Sale, N. McCartney, and F. Buick. Factors affecting blood pressure during heavy weight lifting and static contractions. J. Appl. Physiol. 73: 1590–1597, 1992.

16. Narloch, J. A., and M. E. Brandstater. Influence of breathing technique on arterial blood pressure during heavy weight lifting. Arch. Phys. Med. Rehabil. 76: 457–462, 1995.

17. Panerai, R. B., S. T. Deverson, P. Mahony, P. Hayes, and D. H. Evans. Effect of CO2 on dynamic cerebral autoregulation measurement. Physiol. Meas. 20: 265–275, 1999.

18. Paulson, O. B., S. Strandgaard, and L. Edvinsson. Cerebral autoregulation. Cerebrovasc. Brain Metab. Rev. 2: 161–192, 1990.

19. Pott, F, L. Knudsen, M. Nowak, H. B. Nielsen, B. Hanel, and N. H. Secher. Middle cerebral artery blood velocity during rowing. Acta Physiol. Scand. 160: 251–255, 1997.

20. Pott, F., J. J. Van Lieshout, K. Ide, P. Madsen, and N. H. Secher. Middle cerebral artery blood velocity during a Valsalva maneuver in the standing position. J. Appl. Physiol. 88: 1545–1550, 2000.

21. Poulin, M. J., P. J. Liang, and P. A. Robbins. Dynamics of the cerebral blood flow response to step changes in end-tidal PCO2 and PO2 in humans. J. Appl. Physiol. 81: 1084–1095, 1996.

22. Rosenthal, R. J., R. L. Friedman, A. Chidambaram, A. M. Khan, J. Martz, Q. Shi, and M. Nussbaum. Effects of hyperventilation and hypoventilation on PaCO2 and intracranial pressure during acute elevations of intraabdominal pressure with CO2 pneumoperitoneum: large animal observations. J. Am. Coll. Surg. 187: 32–38, 1998.

23. Sale, D. G., and J. D. MacDougall. Specificity in strength training: a review for the coach and athlete. Can. J. Sport Sci. 6: 87–92, 1981.

24. Sale, D. G., D. E. Moroz, R. S. McKelvie, J. D. MacDougall, and N. McCartney. Comparison of blood pressure response to isokinetic and weight-lifting exercise. Eur. J. Appl. Physiol. Occup. Physiol. 67: 115–120, 1993.

25. Serrador, J. M., P. A. Picot, B. K. Rutt, J. K. Shoemaker, and R. L. Bondar. MRI measures of middle cerebral artery diameter in conscious humans during simulated orthostasis. Stroke 31: 1672–1678, 2000.

26. Severinghaus, J. W., and N. Lassen. Step hypocapnia to separate arterial from tissue Pco2 in the regulation of cerebral blood flow. Circ Res. 20: 272–278, 1967.

27. Shapiro, W., A. J. Wasserman, and J. L. Patterson, Jr. Human cerebrovascular response time to elevation of arterial carbon dioxide tension. Arch. Neurol. 13: 130–138, 1965.

28. Tiecks, F. P., A. M. Lam, R. Aaslid, D. W. Newell. Comparison of static and dynamic cerebral autoregulation measurements. Stroke 26: 1014–1019, 1995.

29. Zhang, R., J. H. Zuckerman, C. A. Giller, and B. D. Levine. Transfer function analysis of dynamic cerebral autoregulation in humans. Am. J. Physiol. 274: H233–H241, 1998.

Cited By:

This article has been cited 13 time(s).

Acta Physiologica
Dynamic blood pressure control and middle cerebral artery mean blood velocity variability at rest and during exercise in humans
Ogoh, S; Dalsgaard, MK; Secher, NH; Raven, PB
Acta Physiologica, 191(1): 3-14.
10.1111/j.1748-1716.2007.01708.x
CrossRef
Sports Medicine
Regulation of cerebral blood flow during exercise
Querido, JS; Sheel, AW
Sports Medicine, 37(9): 765-782.

Chest
Mechanisms of periodic breathing during exercise in patients with chronic heart failure
Agostoni, P; Apostolo, A; Albert, RK
Chest, 133(1): 197-203.
10.1378/chest.07-1439
CrossRef
American Journal of Physiology-Heart and Circulatory Physiology
Middle cerebral artery flow velocity and pulse pressure during dynamic exercise in humans
Ogoh, S; Fadel, PJ; Zhang, R; Selmer, C; Jans, O; Secher, NH; Raven, PB
American Journal of Physiology-Heart and Circulatory Physiology, 288(4): H1526-H1531.
10.1152/ajpheart.00979.2004
CrossRef
Clinical Autonomic Research
Cerebral autoregulation is temporarily disturbed in the early recovery phase after dynamic resistance exercise
Koch, A; Ivers, M; Gehrt, A; Schnoor, P; Rump, A; Rieckert, H
Clinical Autonomic Research, 15(2): 83-91.
10.1007/s10286-005-0249-8
CrossRef
Oxygen Transport to Tissue Xxxi
Cerebrovascular Response During Heavy Upper Body Exercise: Effect of Mode of Ventilation on Blood Flow Velocity in the Middle Cerebral Artery
Sato, K; Hirasawa, A; Tsunoda, N; Taniguchi, Y; Sadamoto, T
Oxygen Transport to Tissue Xxxi, 662(): 347-352.
10.1007/978-1-4419-1241-1_50
CrossRef
Journal of Applied Physiology
Regulation of middle cerebral artery blood velocity during recovery from dynamic exercise in humans
Ogoh, S; Fisher, JP; Purkayastha, S; Dawson, EA; Fadel, PJ; White, MJ; Zhang, R; Secher, NH; Raven, PB
Journal of Applied Physiology, 102(2): 713-721.
10.1152/japplphysiol.00801.2006
CrossRef
Journal of Applied Physiology
Cerebral blood flow during exercise: mechanisms of regulation
Ogoh, S; Ainslie, PN
Journal of Applied Physiology, 107(5): 1370-1380.
10.1152/japplphysiol.00573.2009
CrossRef
Scandinavian Journal of Medicine & Science in Sports
Middle cerebral artery blood velocity during running
Lyngeraa, TS; Pedersen, LM; Mantoni, T; Belhage, B; Rasmussen, LS; van Lieshout, JJ; Pott, FC
Scandinavian Journal of Medicine & Science in Sports, 23(1): e32-e37.
10.1111/sms.12009
CrossRef
Medicine & Science in Sports & Exercise
Resistance Exercise, the Valsalva Maneuver, and Cerebrovascular Transmural Pressure
HAYKOWSKY, MJ; EVES, ND; R. WARBURTON, DE; FINDLAY, MJ
Medicine & Science in Sports & Exercise, 35(1): 65-68.

PDF (131)
Journal of Hypertension
Resistance training and arterial compliance: keeping the benefits while minimizing the stiffening
Kawano, H; Tanaka, H; Miyachi, M
Journal of Hypertension, 24(9): 1753-1759.
10.1097/01.hjh.0000242399.60838.14
PDF (125) | CrossRef
Medicine & Science in Sports & Exercise
Hyperventilation before Resistance Exercise: Cerebral Hemodynamics and Orthostasis
ROMERO, SA; COOKE, WH
Medicine & Science in Sports & Exercise, 39(8): 1302-1307.
10.1249/mss.0b013e3180653636
PDF (260) | CrossRef
Medicine & Science in Sports & Exercise
Autonomic Control of Cerebral Circulation: Exercise
OGOH, S
Medicine & Science in Sports & Exercise, 40(12): 2046-2054.
10.1249/MSS.0b013e318180bc6f
PDF (609) | CrossRef
Back to Top | Article Outline
Keywords:

DOPPLER ULTRASOUND; ARTERIAL BLOOD PRESSURE; LEG PRESS

©2002The American College of Sports Medicine

Login

Article Tools

Images

Share

Search for Similar Articles
You may search for similar articles that contain these same keywords or you may modify the keyword list to augment your search.

Connect With Us