Heme oxygenase-1-dependent central cardiorespiratory adaptations to chronic intermittent hypoxia in mice

J Appl Physiol (1985). 2016 Oct 1;121(4):944-952. doi: 10.1152/japplphysiol.00036.2016. Epub 2016 Sep 8.

Abstract

Chronic intermittent hypoxia (CIH) increases sympathetic tone and respiratory instability. Our previous work showed that chronic hypoxia induces the oxygen-sensing enzyme heme oxygenase-1 (HO-1) within the C1 sympathoexcitatory region and the pre-Bötzinger complex (pre-BötC). We therefore examined the effect of CIH on time course of induced expression of HO-1 within these regions and determined whether the induction of HO-1 correlated with changes in respiratory, sigh frequency, and sympathetic responses (spectral analysis of heart rate) to acute hypoxia (10% O2) during 10 days of exposure to CIH in chronically instrumented awake wild-type (WT) and HO-1 null mice (HO-1-/-). HO-1 was induced within the C1 and pre-BötC regions after 1 day of CIH. There were no significant differences in the baseline respiratory parameters between WT and HO-1-/- Prior to CIH, acute hypoxia increased respiratory frequency in both WT and HO-1-/-; however, minute diaphragm electromyogram activity increased in WT but not HO-1-/- The hypoxic respiratory response after 1 and 10 days of CIH was restored in HO-1-/- CIH resulted in an initial significant decline in 1) the hypoxic sigh frequency response, which was restored in WT but not HO-1-/-, and 2) the baseline sympathetic activity in WT and HO-1-/-, which remained stable subsequently in WT but not in HO-1-/- We conclude that 1) CIH induces expression of HO-1 in the C1 and pre-BötC regions within 1 day and 2) HO-1 is necessary for hypoxia respiratory response and contributes to the maintenance of the hypoxic sigh responses and baseline sympathetic activity during CIH.

Keywords: C1 sympathoexcitatory region; chronic intermittent hypoxia; heme oxygenase; pre-Bötzinger complex; sighs; spectral analysis of heart rate variability.

MeSH terms

  • Adaptation, Physiological
  • Animals
  • Chronic Disease
  • Diaphragm / innervation
  • Diaphragm / physiopathology*
  • Heart Rate*
  • Heme Oxygenase-1 / metabolism*
  • Hypoxia / physiopathology*
  • Medulla Oblongata / metabolism*
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Oxygen / metabolism*
  • Respiratory Mechanics
  • Sympathetic Nervous System / physiopathology*

Substances

  • Membrane Proteins
  • Heme Oxygenase-1
  • Hmox1 protein, mouse
  • Oxygen