The role of NADPH oxidase in chronic intermittent hypoxia-induced respiratory plasticity in adult male mice

Respir Physiol Neurobiol. 2021 Oct:292:103713. doi: 10.1016/j.resp.2021.103713. Epub 2021 Jun 8.

Abstract

Reactive oxygen species (ROS) are proposed as mediators of chronic intermittent hypoxia (CIH)-induced respiratory plasticity. We sought to determine if NADPH oxidase 2 (NOX2)-derived ROS underpin CIH-induced maladaptive changes in respiratory control. Adult male mice (C57BL/6 J) were assigned to one of three groups: normoxic controls (sham); chronic intermittent hypoxia-exposed (CIH, 12 cycles/hour, 8 h/day for 14 days); and CIH + apocynin (NOX2 inhibitor, 2 mM) given in the drinking water throughout exposure to CIH. In addition, we studied sham and CIH-exposed NOX2-null mice (B6.129S-CybbTM1Din/J). Whole-body plethysmography was used to measure breathing and metabolic parameters. Ventilation (V̇I/V̇CO2) during normoxia was unaffected by CIH, but apnoea index was increased, which was prevented by apocynin, but not by NOX2 deletion. The ventilatory response to hypercapnia following exposure to CIH was potentiated in NOX2-null mice. Our results reveal ROS-dependent influences on the control of breathing and point to antioxidant intervention as a potential adjunctive therapeutic strategy in respiratory control disorders.

Keywords: Apnoea; Apocynin; Breathing; Chronic intermittent hypoxia; NADPH oxidase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetophenones / pharmacology*
  • Animals
  • Antioxidants / administration & dosage
  • Antioxidants / pharmacology*
  • Apnea / drug therapy
  • Apnea / metabolism*
  • Disease Models, Animal
  • Hypoxia / drug therapy
  • Hypoxia / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • NADPH Oxidases / drug effects
  • NADPH Oxidases / metabolism*
  • Respiration* / drug effects

Substances

  • Acetophenones
  • Antioxidants
  • acetovanillone
  • NADPH Oxidases