4.6 Article

On the contribution of group III and IV muscle afferents to the circulatory response to rhythmic exercise in humans

Journal

JOURNAL OF PHYSIOLOGY-LONDON
Volume 589, Issue 15, Pages 3855-3866

Publisher

WILEY
DOI: 10.1113/jphysiol.2011.209353

Keywords

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Funding

  1. US National Heart, Lung, and Blood Institute [HL-103786-02, HL-09183]

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We investigated the role of skeletal muscle afferent feedback in circulatory control during rhythmic exercise in humans. Nine healthy males performed single leg knee-extensor exercise (15/30/45 watts, 3 min each) under both control conditions (Ctrl) and with lumbar intrathecal fentanyl impairing mu-opioid receptor-sensitive muscle afferents. Cardiac output and femoral blood flow were determined, and femoral arterial/venous blood samples were collected during the final minute of each workload. To rule out cephalad migration of fentanyl to the brain-stem, we documented unchanged resting ventilatory responses to different levels of hypercapnia. There were no haemodynamic differences between conditions at rest. However, during exercise cardiac output was similar to 20% lower with fentanyl blockade compared to control (P < 0.05), secondary to a 6% and 13% reduction in heart rate and stroke volume, respectively. Throughout exercise mean arterial pressure (MAP) was reduced by 7% (P < 0.01) which is likely to have contributed to the 15% fall in femoral blood flow. However, MAP was not completely responsible for this peripheral haemodynamic change as vascular conductance was also attenuated (similar to 9%). Evidence of increasing noradrenaline spillover (P = 0.09) implicated an elevation in sympathetic outflow in this response. The attenuated femoral blood flow during exercise with fentanyl was associated witha 17% reduction in leg O-2 delivery (P < 0.01) and a concomitant rise in the arteriovenous O-2 difference (4-9%), but leg O-2 consumption remained 7-13% lower than control (P < 0.05). Our findings reveal an essential contribution of continuous muscle afferent feedback to ensure the appropriate haemodynamic and ultimately metabolic response to rhythmic exercise in humans.

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