Calbet, J A L2; Boushel, Robert Christopher7; Robach, P4; Hellsten, Ylva8; Saltin, Bengt9; Lundby, Carsten6
1 Integrated Physiology, Department of Nutrition, Exercise and Sports, Faculty of Science, Københavns Universitet2 Copenhagen Muscle Research Center, Rigshospitalet, Copenhagen, Denmark; Department of Physical Education, University of Las Palmas de Gran Canaria, Canary Islands, Spain; Research Institute of Biomedical and Health Sciences (IUIBS), Las Palmas de Gran Canaria, Canary Islands, Spain.3 Section of Systems Biology Research, Department of Biomedical Sciences, Faculty of Health and Medical Sciences, Københavns Universitet4 Ecole Nationale de Ski et D’Alpinisme, Chamonix5 The Staff-Student Committee of the Bachelor/Master of Science in Public Health, Faculty of Health and Medical Sciences, Københavns Universitet6 Copenhagen Muscle Research Center, Rigshospitalet, Copenhagen7 Section of Systems Biology Research, Department of Biomedical Sciences, Faculty of Health and Medical Sciences, Københavns Universitet8 Integrated Physiology, Department of Nutrition, Exercise and Sports, Faculty of Science, Københavns Universitet9 The Staff-Student Committee of the Bachelor/Master of Science in Public Health, Faculty of Health and Medical Sciences, Københavns Universitet
AIMS: To determine the role played by adenosine, ATP and chemoreflex activation on the regulation of vascular conductance in chronic hypoxia. METHODS: The vascular conductance response to low and high doses of adenosine and ATP was assessed in ten healthy men. Vasodilators were infused into the femoral artery at sea level and then after 8-12 days of residence at 4559 m above sea level. At sea level, the infusions were carried out while the subjects breathed room air, acute hypoxia (FI O2 = 0.11) and hyperoxia (FI O2 = 1); and at altitude (FI O2 = 0.21 and 1). Skeletal muscle P2Y2 receptor protein expression was determined in muscle biopsies after 4 weeks at 3454 m by Western blot. RESULTS: At altitude, mean arterial blood pressure was 13% higher (91 ± 2 vs. 102 ± 3 mmHg, P < 0.05) than at sea level and was unaltered by hyperoxic breathing. Baseline leg vascular conductance was 25% lower at altitude than at sea level (P < 0.05). At altitude, the high doses of adenosine and ATP reduced mean arterial blood pressure by 9-12%, independently of FI O2 . The change in vascular conductance in response to ATP was lower at altitude than at sea level by 24 and 38%, during the low and high ATP doses respectively (P < 0.05), and by 22% during the infusion with high adenosine doses. Hyperoxic breathing did not modify the response to vasodilators at sea level or at altitude. P2Y2 receptor expression remained unchanged with altitude residence. CONCLUSIONS: Short-term residence at altitude increases arterial blood pressure and reduces the vasodilatory responses to adenosine and ATP.
Acta Physiologica (print), 2014, Vol 211, Issue 4, p. 574-584