β1-Blockade increases maximal apnea duration in elite breath-hold divers

被引:14
|
作者
Hoiland, Ryan L. [1 ]
Ainslie, Philip N. [1 ]
Bain, Anthony R. [1 ]
MacLeod, David B. [2 ]
Stembridge, Mike [3 ]
Drvis, Ivan [4 ]
Madden, Dennis [5 ]
Barak, Otto [6 ]
MacLeod, Douglas M. [7 ]
Dujic, Zeljko [5 ]
机构
[1] Univ British Columbia Okanagan, Sch Hlth & Exercise Sci, Ctr Heart Lung & Vasc Hlth, 3333 Univ Way, Kelowna, BC V1V 1V7, Canada
[2] Duke Univ, Med Ctr, Dept Anesthesiol, Durham, NC 27710 USA
[3] Cardiff Metropolitan Univ, Cardiff Sch Sport, Cardiff, S Glam, Wales
[4] Univ Zagreb, Sch Kinesiol, Zagreb, Croatia
[5] Univ Split, Sch Med, Dept Integrat Physiol, Split, Croatia
[6] Univ Novi Sad, Sch Med, Dept Physiol, Novi Sad, Serbia
[7] Emory Univ, Atlanta, GA 30322 USA
基金
加拿大自然科学与工程研究理事会;
关键词
esmolol; rate pressure product; breath-hold diving; cerebral blood flow; MYOCARDIAL OXYGEN-CONSUMPTION; CARDIAC-FUNCTION; ULTRASOUND; ESMOLOL; O-2; CO2;
D O I
10.1152/japplphysiol.00127.2016
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We hypothesized that the cardioselective beta(1)-adrenoreceptor antagonist esmolol would improve maximal apnea duration in elite breath-hold divers. In elite national-level divers (n = 9), maximal apneas were performed in a randomized and counterbalanced order while receiving either iv esmolol (150 mu g.kg(-1).min(-1)) or volume-matched saline (placebo). During apnea, heart rate (ECG), beat-by-beat blood pressure, stroke volume (SV), cardiac output (CO), and total peripheral resistance (TPR) were measured (finger photoplethysmography). Myocardial oxygen consumption (M(V)over dotO(2)) was estimated from rate pressure product. Cerebral blood flow through the internal carotid (ICA) and vertebral arteries (VA) was assessed using Duplex ultrasound. Apnea duration improved in the esmolol trial when compared with placebo (356 +/- 57 vs. 323 +/- 61 s, P < 0.01) despite similar end-apnea peripheral oxyhemoglobin saturation (71.8 +/- 10.3 vs. 74.9 +/- 9.5%, P = 0.10). The HR response to apnea was reduced by esmolol at 10-30% of apnea duration, whereas MAP was unaffected. Esmolol reduced SV (main effect, P < 0.05) and CO (main effect; P < 0.05) and increased TPR (main effect, P < 0.05) throughout apnea. Esmolol also reduced M(V)over dotO(2) throughout apnea (main effect, P < 0.05). Cerebral blood flow through the ICA and VA was unchanged by esmolol at baseline and the last 30 s of apnea; however, global cerebral blood flow was reduced in the esmolol trial at end-apnea (P < 0.05). Our findings demonstrate that, in elite breath-hold divers, apnea breakpoint is improved by beta(1)-blockade, likely owing to an improved total body oxygen sparring through increased centralization of blood volume (up arrow TPR) and reduced M(V)over dotO(2). NEW & NOTEWORTHY The governing bodies for international apnea competition, the Association Internationale pour le Developpment de l'Apnee and La Confederation Mondaile des Activites Subaquatiques, have banned the use of beta-blockers based on anecdotal reports that they improve apnea duration. Using a randomized placebo-controlled trial, we are the first to empirically confirm that beta-blockade improves apnea duration. This improvement in apnea duration coincided with a reduced myocardial oxygen consumption.
引用
收藏
页码:899 / 906
页数:8
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