TY - JOUR
T1 - Muscle Fatigue Is Attenuated When Applying Intermittent Compared With Continuous Blood Flow Restriction During Endurance Cycling
AU - Corvino, Rogério B.
AU - Scheffer, Débora L.
AU - Santos, Rafael P.
AU - Latini, Alexandra
AU - Oliveira, Anderson S.
AU - Caputo, Fabrizio
PY - 2022/7
Y1 - 2022/7
N2 - Purpose: The aim of this study was to identify a blood-flow-restriction (BFR) endurance exercise protocol that maximizes metabolic strain and minimizes muscle fatigue. Methods: Twelve healthy participants accomplished 5 different interval cycling endurance exercises (2-min work, 1-min rest) in a randomized order: (1) control, low intensity with unrestricted blood flow (CON30); (2) low intensity with intermittent BFR (i-BFR30, ∼150mmHg); (3) low intensity with continuous BFR (c-BFR, ∼100mmHg); (4) unloaded cycling with i-BFR0 (∼150mm Hg); and (5) high intensity (HI) with unrestricted blood flow. Force production, creatine kinase activity, antioxidant markers, blood pH, and potassium (K+) were measured in a range of 5 minutes before and after each cycling exercise protocol. Results: HI showed the highest reduction (Δ = -0.26 [0.05], d = 5.6) on blood pH. Delta pH for c-BRF30 (Δ = -0.02 [0.03], d = 0.8) and Δ pH for i-BRF30 (Δ = -0.04 [0.03], d = 1.6) were different fromeach other, and both were higher compared with CON30 (Δ = 0.03 [0.03]). There was significant before-to-after force loss following HI (Δ = 55 [40] N m-1, d = 1.5) and c-BFR30 (Δ = 27 [21] N m-1, d = 0.7) protocols only, which were accompanied by significant increases in K+ (HI: Δ = 0.94 [0.65] mmol L-1, d = 1.8; c-BFR30: Δ = 0.72 [0.85] mmol L-1, d = 1.2). Moreover, all BFR conditions elicited slight increases in plasma creatine kinase, but not for HI and CON30. Glutathione changes frombefore to after were significant for all BFR conditions andHI, but not for CON30. Conclusions: The attenuation in fatigue-induced reductions in maximal force suggests that i-BFR exercise could be preferable to c-BFR in improving exercise capacity, with considerably less biologic stress elicited from HI exercises.
AB - Purpose: The aim of this study was to identify a blood-flow-restriction (BFR) endurance exercise protocol that maximizes metabolic strain and minimizes muscle fatigue. Methods: Twelve healthy participants accomplished 5 different interval cycling endurance exercises (2-min work, 1-min rest) in a randomized order: (1) control, low intensity with unrestricted blood flow (CON30); (2) low intensity with intermittent BFR (i-BFR30, ∼150mmHg); (3) low intensity with continuous BFR (c-BFR, ∼100mmHg); (4) unloaded cycling with i-BFR0 (∼150mm Hg); and (5) high intensity (HI) with unrestricted blood flow. Force production, creatine kinase activity, antioxidant markers, blood pH, and potassium (K+) were measured in a range of 5 minutes before and after each cycling exercise protocol. Results: HI showed the highest reduction (Δ = -0.26 [0.05], d = 5.6) on blood pH. Delta pH for c-BRF30 (Δ = -0.02 [0.03], d = 0.8) and Δ pH for i-BRF30 (Δ = -0.04 [0.03], d = 1.6) were different fromeach other, and both were higher compared with CON30 (Δ = 0.03 [0.03]). There was significant before-to-after force loss following HI (Δ = 55 [40] N m-1, d = 1.5) and c-BFR30 (Δ = 27 [21] N m-1, d = 0.7) protocols only, which were accompanied by significant increases in K+ (HI: Δ = 0.94 [0.65] mmol L-1, d = 1.8; c-BFR30: Δ = 0.72 [0.85] mmol L-1, d = 1.2). Moreover, all BFR conditions elicited slight increases in plasma creatine kinase, but not for HI and CON30. Glutathione changes frombefore to after were significant for all BFR conditions andHI, but not for CON30. Conclusions: The attenuation in fatigue-induced reductions in maximal force suggests that i-BFR exercise could be preferable to c-BFR in improving exercise capacity, with considerably less biologic stress elicited from HI exercises.
KW - aerobic exercise
KW - biomarkers
KW - exercise training
KW - muscle damage
KW - muscle strength
KW - oxidative stress
UR - http://www.scopus.com/inward/record.url?scp=85134531766&partnerID=8YFLogxK
U2 - 10.1123/ijspp.2021-0523
DO - 10.1123/ijspp.2021-0523
M3 - Journal article
SN - 1555-0265
VL - 17
SP - 1126
EP - 1131
JO - International Journal of Sports Physiology and Performance
JF - International Journal of Sports Physiology and Performance
IS - 7
ER -