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Hemodynamic Responses
and Perceived Exertion
During Continuous and
Discontinuous Resistance
Exercise
DOI 10.1055/s-0035-1549957
Int J Sports Med
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IJSM/4616/16.5.2015/MPS
Authors
Affiliations
Key words
muscle strength
strength training
photoplethysmography
blood pressure
borg scale
Abstract
Introduction
vessels and favoring the removal of local metabolites. Consequently, there would be a reduction of
vascular resistance and afferent stimulus from
the exercise pressor reflex, producing lower values of BP at the end of a given set of repetitions
vs. continuous sets.
Based on this premise, different strategies to
apply discontinuous sets have been investigated,
such as splitting sets in 2 halves using pauses of
215s [4,5,15], or interspersing pauses after
each repetition [1]. While some studies have
shown that cardiovascular responses might
decrease at the end of discontinuous sets in comparison to continuous sets [1,4,5], at least one
study revealed that BP after multiple discontinuous sets could be even higher than continuous
sets, therefore suggesting that the BP response to
discontinuous or continuous sets might rely on
the type of exercise [15]. Other issues that are
still unclear and warrant additional research
include the optimal pause to induce an attenuation of hemodynamic stress in different resistance exercises and the possible mechanisms
underlying the hemodynamic responses in discontinuous vs. continuous sets.
Methods
Participants
Study design
IJSM/4616/16.5.2015/MPS
The BP at rest was measured by an automatic sphygmomanometer (OnromTM, Matsusaka, Japan). Upon arrival at the laboratory, the subjects remained seated in a quiet environment for
10min. After this, 3 sequential measurements of BP were
obtained with 2min intervals and the average value was
recorded as BP at rest. Before each exercise session the BP at rest
was checked using the same device, to assure that pre-exercise
values were similar across conditions and consistent with the BP
at rest previously determined.
Beat-to-beat blood pressure during exercise was measured using
finger photoplethysmography (FinometerTM, Finapres Medical
Systems BV, Arnhem, the Netherlands) obtained from the middle finger of the left hand. The finger was supported at the level
of the right atrium by a sling, and the hip was stabilized through
a belt to prevent any unwanted movement that could jeopardize
the physiological sign. Subjects were instructed not to perform
any muscle contraction with the left lower limb and to avoid the
Valsalva maneuver, exhaling during the concentric phase and
inhaling in the eccentric phase of the movement. The stroke volume (SV) was calculated offline using a Modelflow offered by the
BeatScope software, version 1.0 (TNO Biomedical InstrumentationTM, Amsterdam, The Netherlands), which computed aortic
blood flow from arterial pressure wave by simulating a nonlinear, time-varying, 3-element model of aortic input impedance
[25]. This methodology has been shown to reliably estimate
rapid changes in CO during a variety of experimental protocols
[14,23], including both dynamic [23] and resistance exercise
[24]. In our lab, the operator reliability has been calculated and
was considered satisfactory (ICC=0.84). The Q was estimated by
the product between SV and HR, while the TPR was calculated as
the ratio between the mean arterial pressure (MAP) and Q.
Changes in mean arterial pressure measured by photoplethysmography are not different from direct arterial blood pressure
measurements both at rest and during exercise [10,22]. However, finger photoplethysmography may slightly overestimate
SBP and underestimate DBP vs. intrabrachial [9] and auscultation [16] methods. Therefore prior to data assessment the BP
values at rest provided by the Finometer were checked against
automatic sphygmomanometer (OnromTM, Matsusaka, Japan).
The tests were initiated only when the difference between BP
assessed by both methods was lower than 5%. Data assessed by
IJSM/4616/16.5.2015/MPS
1st moment
2nd moment
(pause)
40
3rd moment
SBP (%)
30
20
C
D5
D10
10
0
10
6
7
Repetitions
10
11
12
Fig. 1 Variation (%) of systolic blood pressure (SBP) during the repetitions in the continuous (C) and discontinuous protocols performed with
pauses of 5s (D5) and 10s (D10).
Statistical analysis
The normality of data was confirmed by the KolmogorovSmirnov test, and therefore results are expressed as meanstandard deviation. Possible BP differences at rest across the visits
were tested by ANOVA for repeated measurements. Differences
with regard to the percentage of variation (%) between the
resistance exercise protocols (C, D5 and D10) along the fourth
set (1st to 6th repetitions vs. pause vs. 8th to 12th repetitions)
were tested by 2-way ANOVA for repeated measurements. To
compare the Borg score at the end of the fourth set of each protocol, an ANOVA for repeated measurements was applied. Fisher
post hoc verifications were used in the event of significant F
ratios. For all treatments, the significance level was set at P0.05
and calculations were made using the software Statistica 7.0
(StatsoftTM, Tulsa, OK, USA).
Results
pressure (SBP) during the repetitions in the protocols and demonstrates every moment that was used for data analysis.
Fig. 2 illustrates data for the comparison of SBP and DBP per
centage of variation in the different protocols and moments.
Both SBP and DBP have shown similar response pattern across
Table 1 Absolute values of SBD (systolic blood pressure), DPB (diastolic blood pressure), Q (cardiac output), HR (heart rate), SV (systolic volume) and TPR
(total peripheral resistance) during each moment of exercise.
Variables
SBP (mmHg)
DBP (mmHg)
Q (l.min1)
HR (bpm)
SV (ml)
TPR (mmHg.
(l.min)1)
Protocol
Pre-exercise (10s)
C
D5
D10
C
D5
D10
C
D5
D10
C
D5
D10
C
D5
D10
C
D5
D10
143.9215.94
138.6310.98
137.4015.08
80.797.19
76.336.34
78.815.62
10.442.05
10.011.47
9.632.11
91.3813.38
88.0212.17
88.0813.95
114.8015.70
113.8814.72
110.5523.18
10.062.11
9.851.80
10.582.15
165.8616.73
158.0215.64
153.6715.64
100.6410.05
92.8110.27
93.058.7
10.042.08
10.311.65
10.381.79
95.2514.87
96.6514.79
98.0715.05
105.2611.15
107.7613.18
107.1916.89
12.762.33
11.451.88
11.221.88
163.9218.06*
134.5015.54
133.9918.01
101.4213.14*
69.668.78
72.668.58
10.812.35#
12.252.17
12.252.30
107.7018.59
107.0416.78
109.2815.77
101.2118.32#
115.5719.29
113.5221.44
11.962.52*
7.431.34
7.611.24
172.0619.98*
185.5418.48
183.5717.33
105.5213.20
107.5510.86
107.2511.17
11.352.26
10.932.08
10.421.99
115.9719.25#
105.6221.11
99.2718.21
98.7517.77
105.0014.86
106.2818.72
11.812.27
12.732.66
13.382.57
**Pause in discontinuous protocols and 7th repetition in the continuous protocol. Symbols indicate significant percentage differences between protocols at the same moments:*=P<0.001 (C vs. D5 and D10); #=P<0.05 (C vs. D10)
IJSM/4616/16.5.2015/MPS
40
30
SBP (%)
C
D5
D10
50
40
10
0
C
D5
D10
30
20
10
0
10
20
60
50
20
DBP (%)
10
1 to 6
pause
Repetitions
8 to 12
20
1 to 6
pause
Repetitions
and TPR in the different protocols. The Q was higher in discontinuous (during interspersed pauses) vs. continuous conditions
(P<0.05), which was probably due to a higher SV observed at the
same time (P<0.05). On the other hand, the HR tended to be
higher in continuous vs. discontinuous protocols (P<0.05) The
TPR remained stable during the continuous exercise, but varied
significantly along the discontinuous protocols, being lower during the pauses in comparison with values obtained during the
sets (P<0.05).
Table 1 contains the absolute values of SBD, DPB, Q, HR, SV, and
Discussion
8 to 12
cols [1,5], but at least one previous study concurred with our
results [15]. Baum et al. [1] analyzed the BP and rate product
pressure during the leg press performed intermittently and continuously (1.5s for concentric and eccentric phases, with 3s
pauses between each repetition) in protocols including 3 sets of
12, 10 and 8 repetitions with 50, 70 and 80% of 1RM loads,
respectively. At all intensities, the hemodynamic responses were
higher when exercise was performed continuously. Silva et al.
[5] assessed the effects of discontinuous and continuous protocols during the leg press and bench press performed with 3 sets
of 10 repetitions with load corresponding to 10RM. Although
the pauses between sets in the discontinuous protocol (5 and
15s) have been quite similar to those adopted in the present
study, in contrast to their results our data suggested that discontinuous exercise would be related to lower hemodynamic
responses.
A previous study by our group [15] could not confirm these findings. Similar to the present data, it has been shown that both SBP
and DBP were higher at the end of discontinuous over continuous sets performed with 8RM load (4 sets of 8 repetitions and 2s
pauses between the fourth and fifth repetitions). The exercise
protocols applied by Polito et al. [15] were quite similar to the
protocols used in this study the hemodynamic responses were
assessed during the knee extension performed continuously and
with pauses applied at the middle of each set. However, the
pauses presently applied were longer (5 and 10s) than in the
study by Polito et al. [15] (only 2s). It can be therefore claimed
that, at least for the knee extension exercise, pauses from 2 to
10s do not minimize the hemodynamic responses in comparison with continuous protocols.
Considering the type of exercises investigated by the studies
reporting lower hemodynamic responses in discontinuous vs.
continuous protocols, and those that did not concur with those
findings, it can be speculated that the type of muscle contraction
applied at the beginning of the exercises might have a determinant role. For instance, Silva et al. (2010) and Baum et al. (2003)
[5] used exercises which started with eccentric muscle contraction, while in the present and in Politos [15] studies, the exercise began with the concentric phase. The rationale for such a
hypothesis relies on the fact that, at the beginning of exercises
performed with concentric contraction, it is necessary to move
the load against gravity to overcome inertia with additional
recruitment of motor units [11,13,17], which could probably
lead to an up-regulated and centrally mediated increase in BP
[26,27]. On the other hand, when beginning the exercise with
eccentric contraction, the movement is not performed against
gravity and the number of recruited motor units would not be
influenced by inertia [11,13,17]. This may help to explain why
the increased hemodynamic responses, particularly BP, would
be greater after the pauses in the middle of each set in exercises
IJSM/4616/16.5.2015/MPS
40
30
HR (%)
Q (%)
30
10
0
10
0
20
10
1a6
pausa
Repetitions
C
D5
8 a 12
1a 6
D10
20
pausa
Repetitions
C
D5
60
8 a12
D10
40
10
0
TPR (%)
SV (%)
20
10
10
20
30
40
20
50
pausa
Repetitions
C
D5
0
20
40
*
1a6
20
8 a 12
D10
60
1a6
pausa
Repetitions
C
D5
8 a12
D10
cols confirm this premise [4], since higher RPE scores in continuous vs. discontinuous protocols were associated with greater
lactate concentration. An additional speculation from the present
findings, which dissociated the hemodynamic responses and
RPE, is that BP might be influenced rather by feed-forward reflex
mechanisms from neural regulation than by peripheral stimulation mediated by metaboreceptors. These mechanisms should
be better elucidated by future research.
The present study has limitations. First, SV and TPR were estimated and not directly measured. Second, EMG activity during
exercise was not quantified, and therefore it was not possible to
confirm whether a greater number of motor units have indeed
been recruited when resuming the exercise after interruption in
the discontinuous protocols. This would be an important strategy to be considered in future studies for a better understanding
of potential mechanisms underlying the hemodynamic
responses to continuous and discontinuous resistance exercise
protocols.
Conclusion
Acknowledgements
IJSM/4616/16.5.2015/MPS