Effect of Ischemic Preconditioning on the Recovery of Cardiac Autonomic Control From Repeated Sprint Exercise

Autor(es)

Lopes, Thiago R. ^{[1, 2, 3, 4]} ; Sabino-Carvalho, Jeann L. ^{[1, 3]} ; Ferreira, Thiago H. N. ^{[1, 3]} ; Succi, Jose E. ^[5] ; Silva, Antonio C. ^{[1, 2]} ; Silva, Bruno M. ^{[1, 2, 3]}

Afiliação do(s) autor(es)

^[1] Univ Fed Sao Paulo, Dept Physiol, Sao Paulo - Brazil

^[2] Olymp Ctr Training & Res, Lab Exercise Physiol, Sao Paulo - Brazil

^[3] Univ Fed Sao Paulo, Postgrad Program Translat Med, Sao Paulo - Brazil

^[4] Sao Paulo Assoc Med Dev, Sao Paulo - Brazil

^[5] Univ Fed Sao Paulo, Dept Surg, Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: FRONTIERS IN PHYSIOLOGY; v. 9, OCT 26 2018.
• Citações Web of Science: 1

Resumo

Repeated sprint exercise (RSE) acutely impairs post-exercise heart rate (HR) recovery (HRR) and time-domain heart rate variability (i. e., RMSSD), likely in part, due to lactic acidosis-induced reduction of cardiac vagal reactivation. In contrast, ischemic preconditioning (IPC) mediates cardiac vagal activation and augments energy metabolism efficiency during prolonged ischemia followed by reperfusion. Therefore, we investigated whether IPC could improve recovery of cardiac autonomic control from RSE partially via improved energy metabolism responses to RSE. Fifteen men team-sport practitioners (mean +/- SD: 25 +/- 5 years) were randomly exposed to IPC in the legs (3 x 5 min at 220 mmHg) or control (CT; 3 x 5 min at 20 mmHg) 48 h, 24 h, and 35 min before performing 3 sets of 6 shuttle running sprints (15 + 15 m with 180 degrees change of direction and 20 s of active recovery). Sets 1 and 2 were followed by 180 s and set 3 by 3608 of inactive recovery. Short-term HRR was analyzed after all sets via linear regression of HR decay within the first 30 s of recovery (130) and delta from peak HR to 60 s of recovery (HRR60s). Long-term HRR was analyzed throughout recovery from set 3 via first-order exponential regression of HR decay. Moreover, RMSSD was calculated using 30-s data segments throughout recovery from set 3. Energy metabolism responses were inferred via peak pulmonary oxygen uptake ((V) over dotO(2)peak), peak carbon dioxide output ((V) over dotCO(2)peak), peak respiratory exchange ratio (RERpeak), first-order exponential regression of (V) over dotO(2) decay within 360 s of recovery and blood lactate concentration ({[}Lac-]). IPC did not change 130, but increased HRR6Os after all sets (condition main effect: P = 0.03; partial eta square (eta(2)p) = 0.27, i.e., large effect size). IPC did not change long-term HRR and RMSSD throughout recovery, nor did IPC change any energy metabolism parameter. In conclusion, IPC accelerated to some extent the short-term recovery, but did not change the long-term recovery of cardiac autonomic control from RSE, and such accelerator effect was not accompanied by any IPC effect on surrogates of energy metabolism responses to RSE. (AU)

• Processo FAPESP: 14/15877-8 - Efeito de pré-condicionamento isquêmico sobre mecanismos determinantes do desempenho aeróbio em corredores de alto nível
• Beneficiário: Jeann Luccas de Castro Sabino de Carvalho
• Modalidade de apoio: Bolsas no Brasil - Mestrado