Increased ventilation in female erythropoietin-deficient mouse line is not progesterone and estrous stage-dependent

Respir Physiol Neurobiol. 2017 Nov:245:98-104. doi: 10.1016/j.resp.2017.07.002. Epub 2017 Jul 19.

Abstract

Previous studies suggest that chronic erythropoietin (Epo) deficiency in male mice does not alter normoxic/hypoxic ventilation. As effects of Epo are sex specific and as progesterone could be a respiratory stimulant, we evaluated the impact of Epo deficiency and its possible interaction with progesterone in ventilatory control in female mice during estrous cycle phases. Compared to wild type (WT) animals, Epo-TAgh female mice exhibited higher ventilation in hypoxia. However, when data were separated into luteal and follicular phases of the estrous cycle, basal ventilation and hypoxic ventilation were not different in both mice strains. As progesterone is known to be a potent respiratory stimulant, additional experiments were performed to elucidate its role. Interestingly, after mifepristone treatment, HVR was not modified in WT and Epo-TAgh mice, showing that the ventilatory stimulation observed in females was not directly mediated by progesterone. We conclude that Epo-TAgh female mice show no estrous stage-dependent increase of ventilatory control and progesterone independent response to hypoxia.

Keywords: Anemia; Erythropoietin; Estrus cycle; Hypoxia; Mifepristone; Progesterone.

MeSH terms

  • Animals
  • Erythropoietin / deficiency*
  • Erythropoietin / genetics
  • Estrous Cycle / drug effects
  • Estrous Cycle / physiology*
  • Female
  • Hormone Antagonists / pharmacology
  • Hyperventilation / metabolism*
  • Hypoxia / metabolism
  • Mice, Inbred CBA
  • Mice, Transgenic
  • Mifepristone / pharmacology
  • Plethysmography, Whole Body
  • Progesterone / metabolism*
  • Receptors, Progesterone / antagonists & inhibitors
  • Receptors, Progesterone / metabolism
  • Respiration* / drug effects

Substances

  • Epo protein, mouse
  • Hormone Antagonists
  • Receptors, Progesterone
  • Erythropoietin
  • Mifepristone
  • Progesterone