Chronic hypoxia increases blood pressure and noradrenaline spillover in healthy humans

Chronic hypoxia is associated with elevated sympathetic activity and hypertension in patients with chronic pulmonary obstructive disease. However, the effect of chronic hypoxia on systemic and regional sympathetic activity in healthy humans remains unknown. To determine if chronic hypoxia in healthy humans is associated with hyperactivity of the sympathetic system, we measured intra-arterial blood pressure, arterial blood gases, systemic and skeletal muscle noradrenaline (norepinephrine) spillover and vascular conductances in nine Danish lowlanders at sea level and after 9 weeks of exposure at 5260 m. Mean blood pressure was 28% higher at altitude (P < 0.01) due to increases in both systolic (18% higher, P < 0.05) and diastolic (41% higher, P < 0.001) blood pressures. Cardiac output and leg blood flow were not altered by chronic hypoxia, but systemic vascular conductance was reduced by 30 % (P < 0.05). Plasma arterial noradrenaline (NA) and adrenaline concentrations were 3.7- and 2.4-fold higher at altitude, respectively (P < 0.05). The elevation of plasma arterial NA concentration was caused by a 3.8-fold higher whole-body NA release (P < 0.001) since whole-body noradrenaline clearance was similar in both conditions. Leg NA spillover was increased similarly (× 3.2, P < 0.05). These changes occurred despite the fact that systemic O2 delivery was greater after altitude acclimatisation than at sea level, due to 37 % higher blood haemoglobin concentration. In summary, this study shows that chronic hypoxia causes marked activation of the sympathetic nervous system in healthy humans and increased systemic arterial pressure, despite normalisation of the arterial O2 content with acclimatisation.

[1]  S. Lahiri Role of arterial O2 flow in peripheral chemoreceptor excitation. , 1980, Federation proceedings.

[2]  G. Jennings,et al.  Adverse consequences of high sympathetic nervous activity in the failing human heart. , 1995, Journal of the American College of Cardiology.

[3]  B. Saltin,et al.  Pulmonary gas exchange and acid-base state at 5,260 m in high-altitude Bolivians and acclimatized lowlanders. , 2002, Journal of applied physiology.

[4]  Y Cinar,et al.  Effect of hematocrit on blood pressure via hyperviscosity. , 1999, American journal of hypertension.

[5]  A. Quyyumi,et al.  Cardiac sympathetic nerve function in congestive heart failure. , 1996, Circulation.

[6]  J. Floras,et al.  Reducing cardiac filling pressure lowers norepinephrine spillover in patients with chronic heart failure. , 2000, Circulation.

[7]  A. Cymerman,et al.  Operation Everest II: metabolic and hormonal responses to incremental exercise to exhaustion. , 1992, Journal of applied physiology.

[8]  M. Fatemian,et al.  Selected contribution: chemoreflex responses to CO2 before and after an 8-h exposure to hypoxia in humans. , 2001, Journal of applied physiology.

[9]  F. Abboud,et al.  Interaction of baroreceptor and chemoreceptor reflex control of sympathetic nerve activity in normal humans. , 1991, The Journal of clinical investigation.

[10]  E. Golanov,et al.  Sympatho-excitatory neurons of the rostral ventrolateral medulla are oxygen sensors and essential elements in the tonic and reflex control of the systemic and cerebral circulations. , 1994, Journal of hypertension. Supplement : official journal of the International Society of Hypertension.

[11]  J. Skatrud,et al.  Exposure to hypoxia produces long-lasting sympathetic activation in humans. , 2001, Journal of applied physiology.

[12]  A. Trzebski,et al.  Increased sensitivity of the arterial chemoreceptor drive in young men with mild hypertension. , 1982, Cardiovascular research.

[13]  B. Saltin,et al.  The re‐establishment of the normal blood lactate response to exercise in humans after prolonged acclimatization to altitude , 2001, The Journal of physiology.

[14]  M. Sander,et al.  Sympathetic neural overactivity in healthy humans after prolonged exposure to hypobaric hypoxia , 2003, The Journal of physiology.

[15]  J. Dempsey,et al.  Influence of lung volume on sympathetic nerve discharge in normal humans. , 1990, Circulation research.

[16]  A Boczek-Funcke,et al.  Respiratory modulation of the activity in sympathetic neurones supplying muscle, skin and pelvic organs in the cat. , 1992, The Journal of physiology.

[17]  P. Dow Estimations of cardiac output and central blood volume by dye dilution. , 1956, Physiological reviews.

[18]  C. Zwillich,et al.  Norepinephrine clearance is increased during acute hypoxemia in humans. , 1991, The American journal of physiology.

[19]  B. Saltin,et al.  Maximal perfusion of skeletal muscle in man. , 1985, The Journal of physiology.

[20]  J. Calbet,et al.  Oxygen tension and content in the regulation of limb blood flow. , 2000, Acta physiologica Scandinavica.

[21]  M. Rostrup Catecholamines, hypoxia and high altitude. , 1998, Acta physiologica Scandinavica.

[22]  C. Zoccali,et al.  Plasma Norepinephrine Predicts Survival and Incident Cardiovascular Events in Patients With End-Stage Renal Disease , 2002, Circulation.

[23]  J. Richalet,et al.  Adrenergic status of humans during prolonged exposure to the altitude of 6,542 m. , 1994, Journal of applied physiology.

[24]  J. Alexander,et al.  Mechanism of reduced cardiac stroke volume at high altitude , 1983, Clinical cardiology.

[25]  S. Takagi,et al.  Effects of incomplete ionization of impurities in poly-Si gate and band gap narrowing on direct tunneling gate leakage current , 2001 .

[26]  B. Groves,et al.  Arterial catecholamine responses during exercise with acute and chronic high-altitude exposure. , 1991, The American journal of physiology.

[27]  S. Gangopadhyay,et al.  Characterization of fluorinated hydrogenated amorphous silicon nitride (a‐SiNx:H) alloys , 1994 .

[28]  C. G. Blomqvist,et al.  Regulation of muscle sympathetic nerve activity after bed rest deconditioning. , 2001, American journal of physiology. Heart and circulatory physiology.

[29]  J. Marshall,et al.  Peripheral chemoreceptors and cardiovascular regulation. , 1994, Physiological reviews.

[30]  P. Korner,et al.  Determination of norepinephrine apparent release rate and clearance in humans. , 1979, Life sciences.

[31]  J. Stamler,et al.  Export by red blood cells of nitric oxide bioactivity , 2001, Nature.

[32]  M. Esler,et al.  The sympathetic system and hypertension. , 2000, American journal of hypertension.

[33]  N. Christensen,et al.  Blood pressure and plasma catecholamines in acute and prolonged hypoxia: effects of local hypothermia. , 1999, Journal of applied physiology.

[34]  J. Dempsey,et al.  Respiratory influences on sympathetic vasomotor outflow in humans , 2002, Respiratory Physiology & Neurobiology.

[35]  G. Brooks,et al.  Acclimatization to high altitude increase muscle sympathetic activity both at rest and during exercise. , 1995, The American journal of physiology.

[36]  F. Abboud,et al.  Impaired reflex vasoconstriction in chronically hypoxemic patients. , 1972, The Journal of clinical investigation.

[37]  G. Jennings,et al.  Contribution of individual organs to total noradrenaline release in humans. , 1984, Acta physiologica Scandinavica. Supplementum.

[38]  L. Rowell,et al.  Hypoxemia raises muscle sympathetic activity but not norepinephrine in resting humans. , 1989, Journal of applied physiology.

[39]  G. Hasenfuss,et al.  Marked sympathetic activation in patients with chronic respiratory failure. , 2001, American journal of respiratory and critical care medicine.

[40]  M. Dwinell,et al.  Effects of carotid body hypocapnia during ventilatory acclimatization to hypoxia. , 1997, Journal of applied physiology.

[41]  C. Clar,et al.  Ventilatory effects of 8 h of isocapnic hypoxia with and without beta-blockade in humans. , 1999, Journal of applied physiology.

[42]  A. Delabays,et al.  Augmented sympathetic activation during short-term hypoxia and high-altitude exposure in subjects susceptible to high-altitude pulmonary edema. , 1999, Circulation.

[43]  M. Joyner,et al.  Effects of regional phentolamine on hypoxic vasodilatation in healthy humans , 2001, The Journal of physiology.

[44]  N. Montano,et al.  Selective potentiation of peripheral chemoreflex sensitivity in obstructive sleep apnea. , 1999, Circulation.

[45]  E. Fletcher,et al.  highlighted topics Physiological and Genomic Consequences of Intermittent Hypoxia Invited Review: Physiological consequences of intermittent hypoxia: systemic blood pressure , 2001 .

[46]  Kevin Gleeson,et al.  Obstructive apnea during sleep is associated with peripheral vasoconstriction. , 2002, American journal of respiratory and critical care medicine.

[47]  Constancio González,et al.  Carotid body chemoreceptors: from natural stimuli to sensory discharges. , 1994, Physiological reviews.

[48]  B. Hamberger,et al.  A sensitive method for the determination of plasma catecholamines using liquid chromatography with electrochemical detection. , 1978, Life sciences.

[49]  B. Saltin,et al.  Why is VO2 max after altitude acclimatization still reduced despite normalization of arterial O2 content? , 2003, American journal of physiology. Regulatory, integrative and comparative physiology.

[50]  P. Baud,et al.  Decreased cardiac response to isoproterenol infusion in acute and chronic hypoxia , 1988 .

[51]  B. Walker,et al.  Attentuation of systemic vasoreactivity in chronically hypoxic rats. , 1991, The American journal of physiology.

[52]  P. Timmermans,et al.  Modulation of Noradrenaline Release by Peripheral Presynaptic α2‐Adrenoceptors in Humans , 1987 .

[53]  D. Reis,et al.  Decerebration does not alter hypoxic sympathoexcitatory responses in rats. , 1995, Journal of the autonomic nervous system.

[54]  R Hilton,et al.  The influence of chemical factors on the coronary circulation , 1925, The Journal of physiology.