Key result
Exogenous dopamine and D2-receptor blockade had no effect on pulmonary diffusing capacity, but dopamine blockade reduced time-to-exhaustion by 47% (P=0.04).
Why the study?
Recent studies suggest dopamine may regulate pulmonary capillary blood volume via vascular tone, but its contribution to pulmonary diffusing capacity, capillary blood volume responses, and exercise tolerance was unclear.
Does exogenous dopamine or dopamine blockade alter pulmonary diffusing capacity, capillary blood volume, or time-to-exhaustion during exercise in young healthy humans?
RCT (n=14)
Double-blind
Randomly assigned
Does exogenous dopamine or dopamine blockade alter pulmonary diffusing capacity, capillary blood volume, or time-to-exhaustion during exercise in young healthy humans?
Endogenous dopamine is important for maintaining exercise tolerance in healthy humans, though it does not appear to regulate pulmonary diffusing capacity or capillary blood volume during exercise.
Answers are grounded in this paper and cite their sources.
Dopamine D2 blockade may impair exercise tolerance independent of pulmonary diffusion; leaves open its clinical relevance.
New Findings What is the Central question? Does dopamine, a pulmonary vascular vasodilator, contribute to the regulation of pulmonary diffusing capacity and capillary blood volume responses to exercise and exercise tolerance? What are the main findings and their importance? Dopamine appears not to be important for regulating pulmonary diffusing capacity or pulmonary capillary blood volume during exercise in healthy participants. Dopamine blockade trials demonstrated that endogenous dopamine is important for maintaining exercise tolerance; however, exogenous dopamine does not improve exercise tolerance. Abstract Pulmonary capillary blood volume ( V c ) and diffusing membrane capacity ( D m ) expansion are important contributors to the increased pulmonary diffusing capacity (DL CO ) observed during upright exercise. Dopamine is a pulmonary vascular vasodilator, and recent studies suggest that it may play a role in V c regulation through changes in pulmonary vascular tone. The purpose of this study was to examine the effect of exogenous dopamine and dopamine receptor‐2 (D 2 ‐receptor) blockade on DL CO , V c and D m at baseline and during cycle exercise, as well as time‐to‐exhaustion at 85% of . We hypothesized that dopamine would increase DL CO , V c , D m and time‐to‐exhaustion, while D 2 ‐receptor blockade would have the opposite effect. We recruited 14 young, healthy, recreationally active subjects ( 45.8 ± 6.6 ml kg −1 min −1 ). DL CO , V c and D m were determined at baseline and during exercise at 60% and 85% of under the following randomly assigned and double blinded conditions: (1) intravenous saline and placebo pill, (2) intravenous dopamine (2 µg kg −1 min −1 ) and placebo pill, and (3) intravenous saline and D 2 ‐receptor antagonist (20 mg oral metoclopramide). Exogenous dopamine and dopamine blockade had no effect on DL CO , V c and D m responses at baseline or during exercise. Dopamine blockade reduced time‐to‐exhaustion by 47% ( P = 0.04), but intravenous dopamine did not improve time‐to‐exhaustion. While dopamine modulation did not affect DL CO , V c or D m , the reduction in time‐to‐exhaustion with D 2 ‐receptor blockade suggests that endogenous dopamine is important for exercise tolerance.
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Michaelchuk et al. (2019) conducted an RCT in Healthy (n=14). Dopamine and metoclopramide vs. Intravenous saline and placebo pill was evaluated on Pulmonary diffusing capacity (DLCO), capillary blood volume (Vc), diffusing membrane capacity (Dm), and time-to-exhaustion (p=0.04). Exogenous dopamine and D2-receptor blockade had no effect on pulmonary diffusing capacity, but dopamine blockade reduced time-to-exhaustion by 47% (P=0.04).
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