Adenosine receptor-dependent signaling is not obligatory for normobaric and hypobaric hypoxia-induced cerebral vasodilation in humans

J Appl Physiol (1985). 2017 Apr 1;122(4):795-808. doi: 10.1152/japplphysiol.00840.2016. Epub 2017 Jan 12.

Abstract

Hypoxia increases cerebral blood flow (CBF) with the underlying signaling processes potentially including adenosine. A randomized, double-blinded, and placebo-controlled design, was implemented to determine if adenosine receptor antagonism (theophylline, 3.75 mg/Kg) would reduce the CBF response to normobaric and hypobaric hypoxia. In 12 participants the partial pressures of end-tidal oxygen ([Formula: see text]) and carbon dioxide ([Formula: see text]), ventilation (pneumotachography), blood pressure (finger photoplethysmography), heart rate (electrocardiogram), CBF (duplex ultrasound), and intracranial blood velocities (transcranial Doppler ultrasound) were measured during 5-min stages of isocapnic hypoxia at sea level (98, 90, 80, and 70% [Formula: see text]). Ventilation, [Formula: see text] and [Formula: see text], blood pressure, heart rate, and CBF were also measured upon exposure (128 ± 31 min following arrival) to high altitude (3,800 m) and 6 h following theophylline administration. At sea level, although the CBF response to hypoxia was unaltered pre- and postplacebo, it was reduced following theophylline (P < 0.01), a finding explained by a lower [Formula: see text] (P < 0.01). Upon mathematical correction for [Formula: see text], the CBF response to hypoxia was unaltered following theophylline. Cerebrovascular reactivity to hypoxia (i.e., response slope) was not different between trials, irrespective of [Formula: see text] At high altitude, theophylline (n = 6) had no effect on CBF compared with placebo (n = 6) when end-tidal gases were comparable (P > 0.05). We conclude that adenosine receptor-dependent signaling is not obligatory for cerebral hypoxic vasodilation in humans.NEW & NOTEWORTHY The signaling pathways that regulate human cerebral blood flow in hypoxia remain poorly understood. Using a randomized, double-blinded, and placebo-controlled study design, we determined that adenosine receptor-dependent signaling is not obligatory for the regulation of human cerebral blood flow at sea level; these findings also extend to high altitude.

Keywords: adenosine; cerebral blood flow; high-altitude; transcranial Doppler; ultrasound.

MeSH terms

  • Acclimatization / drug effects
  • Acclimatization / physiology
  • Adult
  • Altitude
  • Blood Flow Velocity / drug effects
  • Blood Flow Velocity / physiology
  • Blood Pressure / drug effects
  • Blood Pressure / physiology
  • Brain / drug effects
  • Brain / metabolism*
  • Brain / physiopathology*
  • Carbon Dioxide / metabolism
  • Cerebrovascular Circulation / drug effects
  • Cerebrovascular Circulation / physiology
  • Female
  • Heart Rate / drug effects
  • Heart Rate / physiology
  • Humans
  • Hypoxia, Brain / drug therapy
  • Hypoxia, Brain / metabolism*
  • Hypoxia, Brain / physiopathology*
  • Male
  • Oxygen / metabolism
  • Purinergic P1 Receptor Antagonists / administration & dosage
  • Receptors, Purinergic P1 / metabolism*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • Theophylline / administration & dosage
  • Vasodilation / drug effects
  • Vasodilation / physiology*

Substances

  • Purinergic P1 Receptor Antagonists
  • Receptors, Purinergic P1
  • Carbon Dioxide
  • Theophylline
  • Oxygen