Skip to main navigation Skip to search Skip to main content

Characterisation of the ventilatory response to hypoxia in a model of transgenic anemic mice

  • J. L. Macarlupú
  • , A. Buvry
  • , O. E. Morel
  • , F. León-Velarde
  • , J. P. Richalet
  • , F. Favret
  • Sorbonne Paris Nord University

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Both polycythemia and the increase in hypoxic ventilatory response (HVR) are considered as important factors of acclimatization to hypoxia. The objective of this study was to characterise the ventilation pattern at different inspired oxygen fraction in a model of chronic anemic mice. These mice have a targeted disruption in the 5′ untranslated region of the Epo gene that reduces Epo expression such that the homozygous animal is severely anemic. Ventilation in normoxia in Epo-TAgh mice was significantly greater than in wild type, and the difference was mainly due to a higher tidal volume. HVR was higher in Epo-TAgh mice at every FIO2 suggesting a higher chemosensitivity. Resting oxygen consumption was maintained in anemic mice. Maximal oxygen consumption was 30% lower while hemoglobin was 60% lower in anemic mice compared to wild type. This small decrease in maximal oxygen consumption is probably due a greater cardiac output and/or a better tissue oxygen extraction and would allow these anemic mice to acclimatize to hypoxia in spite of low oxygen carrying capacity. In conclusion, Epo-TAgh anemic mice showed increased ventilation and hypoxic ventilatory response. However, whether these adaptations will contribute to acclimatization in chronic hypoxia remains to be determined.

Original languageEnglish
Pages (from-to)19-26
Number of pages8
JournalRespiratory Physiology and Neurobiology
Volume150
Issue number1
DOIs
StatePublished - 25 Jan 2006

Keywords

  • Anemia
  • Hypoxic ventilatory response
  • Oxygen consumption
  • Transgenic mice

Fingerprint

Dive into the research topics of 'Characterisation of the ventilatory response to hypoxia in a model of transgenic anemic mice'. Together they form a unique fingerprint.

Cite this